Yoshiki Sekijima, M.D., Ph.D. - Publications

Affiliations: 
Neurology and Rheumatology Shinshu University School of Medicine 
Area:
degenerative disease etiology
Website:
http://www.labome.org/expert/japan/shinshu/sekijima/yoshiki-sekijima-1375380.html

115 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Kinoshita M, Oyanagi K, Kondo Y, Ishizawa K, Ishihara K, Yoshida M, Inoue T, Mitsuyama Y, Yoshida K, Yamada M, Sekijima Y, Ikeda SI. Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP). Eneurologicalsci. 22: 100310. PMID 33553700 DOI: 10.1016/j.ensci.2021.100310  0.6
2017 Schonhoft JD, Monteiro C, Plate L, Eisele YS, Kelly JM, Boland D, Parker CG, Cravatt BF, Teruya S, Helmke S, Maurer M, Berk J, Sekijima Y, Novais M, Coelho T, et al. Peptide probes detect misfolded transthyretin oligomers in plasma of hereditary amyloidosis patients. Science Translational Medicine. 9. PMID 28904227 DOI: 10.1126/scitranslmed.aam7621  1
2017 Kobayashi Y, Shimojima Y, Kondo Y, Takamatsu R, Miyazaki D, Kishida D, Sekijima Y, Ikeda SI. Protein-losing Gastroenteropathy Related to Mixed Connective Tissue Disease: A Case Report of a Successful Outcome and Literature Review. Internal Medicine (Tokyo, Japan). 56: 2057-2062. PMID 28768981 DOI: 10.2169/internalmedicine.56.8391  0.6
2017 Ikeda J, Matsushima A, Ishii W, Goto T, Takahashi K, Nakamichi K, Saijo M, Sekijima Y, Ikeda SI. Brain Biopsy Is More Reliable than the DNA test for JC Virus in Cerebrospinal Fluid for the Diagnosis of Progressive Multifocal Leukoencephalopathy. Internal Medicine (Tokyo, Japan). 56: 1231-1234. PMID 28502942 DOI: 10.2169/internalmedicine.56.7689  0.6
2017 Nagamatsu K, Sekijima Y, Nakamura K, Nakamura K, Hattori K, Ota M, Shimizu Y, Endo F, Ikeda SI. Prevalence of Fabry disease and GLA c.196G>C variant in Japanese stroke patients. Journal of Human Genetics. PMID 28275245 DOI: 10.1038/jhg.2017.31  0.6
2017 Shimojima Y, Kishida D, Hineno A, Yazaki M, Sekijima Y, Ikeda SI. Hypertrophic pachymeningitis is a characteristic manifestation of granulomatosis with polyangiitis: A retrospective study of anti-neutrophil cytoplasmic antibody-associated vasculitis. International Journal of Rheumatic Diseases. PMID 28217942 DOI: 10.1111/1756-185X.13046  0.6
2017 Doden T, Sekijima Y, Ikeda J, Ozawa K, Ohashi N, Kodaira M, Hineno A, Tachibana N, Ikeda SI. Postpartum Anti-N-methyl-D-aspartate Receptor Encephalitis: A Case Report and Literature Review. Internal Medicine (Tokyo, Japan). 56: 357-362. PMID 28154283 DOI: 10.2169/internalmedicine.56.7442  0.6
2017 Yoshinaga T, Yazaki M, Kametani F, Sekijima Y, Iesato Y, Miyahara T, Tsuchiya-Suzuki A, Sano K, Higuchi K, Ikeda SI. Marked biochemical difference in amyloid proportion between intra- and extraocular tissues in a liver-transplanted patient with hereditary ATTR amyloidosis. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 1-7. PMID 28081655 DOI: 10.1080/13506129.2016.1276055  0.6
2016 Ushiyama S, Kinoshita T, Shimojima Y, Ohashi N, Kishida D, Miyazaki D, Nakamura K, Sekijima Y, Ikeda SI. Hypertrophic Pachymeningitis as an Early Manifestation of Relapsing Polychondritis: Case Report and Review of the Literature. Case Reports in Neurology. 8: 211-217. PMID 27920712 DOI: 10.1159/000450850  0.6
2016 Katoh N, Ueno A, Yoshida T, Tazawa KI, Shimojima Y, Gono T, Sekijima Y, Matsuda M, Ikeda SI. Bortezomib-dexamethasone versus high-dose melphalan for Japanese patients with systemic light-chain (AL) amyloidosis: a retrospective single-center study. International Journal of Hematology. PMID 27832515 DOI: 10.1007/s12185-016-2128-6  0.6
2016 Sekijima Y, Yazaki M, Oguchi K, Ezawa N, Yoshinaga T, Yamada M, Yahikozawa H, Watanabe M, Kametani F, Ikeda SI. Cerebral amyloid angiopathy in posttransplant patients with hereditary ATTR amyloidosis. Neurology. PMID 27466465 DOI: 10.1212/WNL.0000000000003001  1
2016 Ueno KI, Shimojima Y, Kishida D, Sekijima Y, Ikeda SI. Advantage of administering tacrolimus for improving prognosis of patients with polymyositis and dermatomyositis. International Journal of Rheumatic Diseases. PMID 27457756 DOI: 10.1111/1756-185X.12931  0.6
2016 Miyazaki D, Fukushima K, Nakahara A, Kodaira M, Mochizuki K, Kaneko K, Kaneko T, Sekijima Y, Ikeda S. Crossed Cerebellar Diaschisis in Status Epilepticus. Internal Medicine (Tokyo, Japan). 55: 1649-51. PMID 27301522 DOI: 10.2169/internalmedicine.55.6689  0.6
2016 Kobayashi Y, Sekijima Y, Ogawa Y, Kondo Y, Miyazaki D, Ikeda SI. Extremely early onset hereditary ATTR amyloidosis with G47R (p.G67R) mutation. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 1-2. PMID 27206384 DOI: 10.1080/13506129.2016.1185410  1
2016 Minamisawa M, Koyama J, Sekijima Y, Ikeda SI, Kozuka A, Ebisawa S, Miura T, Motoki H, Okada A, Izawa A, Ikeda U. Comparison of the standard and speckle tracking echocardiographic features of wild-type and mutated transthyretin cardiac amyloidoses. European Heart Journal Cardiovascular Imaging. PMID 26873458 DOI: 10.1093/ehjci/jew003  0.6
2016 Nakagawa M, Sekijima Y, Yazaki M, Tojo K, Yoshinaga T, Doden T, Koyama J, Yanagisawa S, Ikeda SI. Carpal tunnel syndrome: a common initial symptom of systemic wild-type ATTR (ATTRwt) amyloidosis. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 1-6. PMID 26852880 DOI: 10.3109/13506129.2015.1135792  1
2015 Koyama J, Minamisawa M, Sekijima Y, Ikeda SI, Kozuka A, Ebisawa S, Miura T, Motoki H, Okada A, Izawa A, Ikeda U. Left ventricular deformation and torsion assessed by speckle-tracking echocardiography in patients with mutated transthyretin-associated cardiac amyloidosis and the effect of diflunisal on myocardial function. International Journal of Cardiology. Heart & Vasculature. 9: 1-10. PMID 28785698 DOI: 10.1016/j.ijcha.2015.07.010  0.6
2015 Ikeda J, Katoh N, Sekijima Y, Ikeda SI. Regression of localized ureter amyloidosis after treatment with steroids suggested by Tc-99 m pyrophosphate scintigraphy. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 1-2. PMID 26471431 DOI: 10.3109/13506129.2015.1089860  0.6
2015 Sekijima Y, Campos RI, Hammarström P, Nilsson KP, Yoshinaga T, Nagamatsu K, Yazaki M, Kametani F, Ikeda SI. Pathological, biochemical, and biophysical characteristics of the transthyretin variant Y114H (p.Y134H) explain its very mild clinical phenotype. Journal of the Peripheral Nervous System : Jpns. PMID 26306725 DOI: 10.1111/jns.12143  1
2015 Yazaki M, Yoshinaga T, Sekijima Y, Nishio S, Kanizawa Y, Kametani F, Miyashita K, Hachiya N, Higuchi K, Ikeda SI. The first pure form of Ostertag-type amyloidosis in Japan: a sporadic case of hereditary fibrinogen Aα-chain amyloidosis associated with a novel frameshift variant. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 1-3. PMID 26017329 DOI: 10.3109/13506129.2015.1037389  1
2015 Sekijima Y, Tojo K, Morita H, Koyama J, Ikeda SI. Safety and efficacy of long-term diflunisal administration in hereditary transthyretin (ATTR) amyloidosis. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 1-5. PMID 26017328 DOI: 10.3109/13506129.2014.997872  1
2015 Abe R, Sekijima Y, Kinoshita T, Yoshinaga T, Koyama S, Kato T, Ikeda SI. Spinal form cerebrotendinous xanthomatosis patient with long spinal cord lesion. The Journal of Spinal Cord Medicine. PMID 25941960 DOI: 10.1179/1079026815Z.000000000409  0.6
2015 Sekijima Y. Transthyretin (ATTR) amyloidosis: clinical spectrum, molecular pathogenesis and disease-modifying treatments. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 25604431 DOI: 10.1136/jnnp-2014-308724  1
2015 Sekijima Y. Transthyretin-type cerebral amyloid angiopathy: a serious complication in post-transplant patients with familial amyloid polyneuropathy. Journal of Neurology, Neurosurgery, and Psychiatry. 86: 124. PMID 25112309 DOI: 10.1136/jnnp-2014-308576  1
2015 Koyama J, Minamisawa M, Sekijima Y, Ikeda Si, Kozuka A, Ebisawa S, Miura T, Motoki H, Okada A, Izawa A, Ikeda U. Left ventricular deformation and torsion assessed by speckle-tracking echocardiography in patients with mutated transthyretin-associated cardiac amyloidosis and the effect of diflunisal on myocardial function Ijc Heart and Vasculature. 9: 1-10. DOI: 10.1016/j.ijcha.2015.07.010  0.6
2014 Sekijima Y. [Clinical diversity, diagnosis and treatment of hereditary amyloid neuropathy]. Rinshō Shinkeigaku = Clinical Neurology. 54: 953-6. PMID 25672679 DOI: DN/JST.JSTAGE/clinicalneurol/54.953  1
2014 Yoshinaga T, Sekijima Y, Koyama S, Maruyama K, Yoshida T, Kato T, Ikeda S. Clinical and radiological findings of a cerebrotendinous xanthomatosis patient with a novel p.A335V mutation in the CYP27A1 gene. Internal Medicine (Tokyo, Japan). 53: 2725-9. PMID 25447658 DOI: DN/JST.JSTAGE/internalmedicine/53.2996  1
2014 Uchiyama S, Sekijima Y, Tojo K, Sano K, Imaeda T, Moriizumi T, Ikeda S, Kato H. Effect of synovial transthyretin amyloid deposition on preoperative symptoms and postoperative recovery of median nerve function among patients with idiopathic carpal tunnel syndrome. Journal of Orthopaedic Science : Official Journal of the Japanese Orthopaedic Association. 19: 913-9. PMID 25146002 DOI: 10.1007/s00776-014-0635-y  1
2014 Nakamura K, Sekijima Y. Response to Satomura et al. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 21: e63. PMID 25039767 DOI: 10.1111/ene.12456  1
2014 Sekijima Y. [Newly developed drug therapies for familial amyloid polyneuropathy: diflunisal and tafamidis]. Brain and Nerve = Shinkei Kenkyū No Shinpo. 66: 773-81. PMID 24998822  1
2014 Sekijima Y. Recent progress in the understanding and treatment of transthyretin amyloidosis. Journal of Clinical Pharmacy and Therapeutics. 39: 225-33. PMID 24749898 DOI: 10.1111/jcpt.12145  1
2014 Nakamura K, Sekijima Y, Nakamura K, Hattori K, Nagamatsu K, Shimizu Y, Yazaki M, Sakurai A, Endo F, Fukushima Y, Ikeda SI. p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese males. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 21: 49-56. PMID 23724928 DOI: 10.1111/ene.12214  1
2013 Berk JL, Suhr OB, Obici L, Sekijima Y, Zeldenrust SR, Yamashita T, Heneghan MA, Gorevic PD, Litchy WJ, Wiesman JF, Nordh E, Corato M, Lozza A, Cortese A, Robinson-Papp J, et al. Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial. Jama. 310: 2658-67. PMID 24368466 DOI: 10.1001/jama.2013.283815  1
2013 Kobayashi A, Uhara H, Kido K, Sekijima Y, Tojo K, Ikeda S, Okuyama R. Bullous formation in a patient with familial amyloid polyneuropathy type I. International Journal of Dermatology. 52: 1398-400. PMID 24164154 DOI: 10.1111/j.1365-4632.2011.05146.x  1
2013 Tsuchiya-Suzuki A, Yazaki M, Sekijima Y, Kametani F, Ikeda S. Steady turnover of amyloid fibril proteins in gastric mucosa after liver transplantation in familial amyloid polyneuropathy. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 20: 156-63. PMID 23826783 DOI: 10.3109/13506129.2013.807790  1
2013 Nakagawa M, Sekijima Y, Tojo K, Ikeda S. High prevalence of ATTR amyloidosis in endomyocardial biopsy-proven cardiac amyloidosis patients. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 20: 138-40. PMID 23638696 DOI: 10.3109/13506129.2013.790809  1
2013 Tanaka K, Sekijima Y, Yoshida K, Tamai M, Kosho T, Sakurai A, Wakui K, Ikeda S, Fukushima Y. Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in Japan. Journal of Human Genetics. 58: 560-3. PMID 23635952 DOI: 10.1038/jhg.2013.34  1
2013 Tanaka K, Sekijima Y, Yoshida K, Mizuuchi A, Yamashita H, Tamai M, Ikeda S, Fukushima Y. [Current status of the predictive genetic testing for hereditary neurological diseases in Shinshu University Hospital]. Rinshō Shinkeigaku = Clinical Neurology. 53: 196-204. PMID 23524599 DOI: DN/JST.JSTAGE/clinicalneurol/53.196  1
2013 Sekijima Y, Nakamura K, Kishida D, Narita A, Adachi K, Ohno K, Nanba E, Ikeda S. Clinical and serial MRI findings of a sialidosis type I patient with a novel missense mutation in the NEU1 gene. Internal Medicine (Tokyo, Japan). 52: 119-24. PMID 23291686 DOI: DN/JST.JSTAGE/internalmedicine/52.8901  1
2012 Nakagawa M, Tojo K, Sekijima Y, Yamazaki KH, Ikeda S. Arterial thromboembolism in senile systemic amyloidosis: report of two cases. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 19: 118-21. PMID 22583098 DOI: 10.3109/13506129.2012.685131  1
2012 Berk JL, Suhr OB, Sekijima Y, Yamashita T, Heneghan M, Zeldenrust SR, Ando Y, Ikeda S, Gorevic P, Merlini G, Kelly JW, Skinner M, Bisbee AB, Dyck PJ, Obici L, et al. The Diflunisal Trial: study accrual and drug tolerance. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 19: 37-8. PMID 22551208 DOI: 10.3109/13506129.2012.678509  1
2012 Shimojima Y, Ishii W, Matsuda M, Katoh N, Tazawa K, Sekijima Y, Ikeda S. Coadministration of cyclosporin a with prednisolone in acute interstitial pneumonia complicating polymyositis/dermatomyositis. Clinical Medicine Insights. Arthritis and Musculoskeletal Disorders. 5: 43-52. PMID 22442637 DOI: 10.4137/CMAMD.S9398  1
2012 Nakamura A, Hineno A, Yoshida K, Sekijima Y, Hanaoka-Tachibana N, Takei Y, Ohara S, Ikeda S. Marked intrafamilial phenotypic variation in a family with SOD1 C111Y mutation. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 13: 479-86. PMID 22409359 DOI: 10.3109/17482968.2011.656311  1
2012 Miyamura M, Terasaki F, Ishibashi K, Shimazaki C, Kimura F, Kuwabara H, Tsuji M, Shibayama Y, Sekijima Y, Tojo K, Ishizaka N. Two siblings diagnosed to have transthyretin-related familial amyloid cardiomyopathy around the same time at different hospitals. Internal Medicine (Tokyo, Japan). 51: 465-9. PMID 22382560 DOI: JST.JSTAGE/internalmedicine/51.6369  1
2012 Nakamura K, Sekijima Y, Nagamatsu K, Yoshida K, Ikeda S. A novel nonsense mutation in the TITF-1 gene in a Japanese family with benign hereditary chorea. Journal of the Neurological Sciences. 313: 189-92. PMID 21982616 DOI: 10.1016/j.jns.2011.09.013  1
2011 Sekijima Y. [Epidemiological and clinical aspects of non-hereditary systemic amyloidosis]. Rinshō Shinkeigaku = Clinical Neurology. 51: 1130-3. PMID 22277508 DOI: JST.JSTAGE/clinicalneurol/51.1130  1
2011 Ikeda S, Sekijima Y, Tojo K, Koyama J. Diagnostic value of abdominal wall fat pad biopsy in senile systemic amyloidosis. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 18: 211-5. PMID 22004460 DOI: 10.3109/13506129.2011.623199  1
2011 Berk JL, Dyck PJ, Obici L, Zeldenrust SR, Sekijima Y, Yamashita T, Ando Y, Ikeda SI, Gorevic P, Merlini G, Kelly JW, Skinner M, Bisbee AB, Suhr OB. The diflunisal trial: update on study drug tolerance and disease progression. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 18: 196-7. PMID 21838485 DOI: 10.3109/13506129.2011.574354073  1
2011 Sekijima Y, Uchiyama S, Tojo K, Sano K, Shimizu Y, Imaeda T, Hoshii Y, Kato H, Ikeda S. High prevalence of wild-type transthyretin deposition in patients with idiopathic carpal tunnel syndrome: a common cause of carpal tunnel syndrome in the elderly. Human Pathology. 42: 1785-91. PMID 21733562 DOI: 10.1016/j.humpath.2011.03.004  1
2011 Yokoseki A, Ishihara T, Koyama A, Shiga A, Yamada M, Suzuki C, Sekijima Y, Maruta K, Tsuchiya M, Date H, Sato T, Tada M, Ikeuchi T, Tsuji S, Nishizawa M, et al. Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia. Brain : a Journal of Neurology. 134: 1387-99. PMID 21486904 DOI: 10.1093/brain/awr069  1
2011 Tojo K, Nitta K, Ishii W, Sekijima Y, Morita H, Takahashi Y, Tanaka K, Ikeda S. A Young Man with Anti-NMDAR Encephalitis following Guillain-Barré Syndrome. Case Reports in Neurology. 3: 7-13. PMID 21327179 DOI: 10.1159/000323751  0.4
2011 Tsuchiya-Suzuki A, Yazaki M, Kametani F, Sekijima Y, Ikeda S. Wild-type transthyretin significantly contributes to the formation of amyloid fibrils in familial amyloid polyneuropathy patients with amyloidogenic transthyretin Val30Met. Human Pathology. 42: 236-43. PMID 21056899 DOI: 10.1016/j.humpath.2010.06.014  1
2010 Sekijima Y. Familial amyloid polyneuropathy: diflunisal. Rinshō Shinkeigaku = Clinical Neurology. 50: 836. PMID 21921462 DOI: 10.5692/clinicalneurol.50.836  1
2010 Sekijima Y, Ohashi T, Ohira S, Kosho T, Fukushima Y. Successful pregnancy and lactation outcome in a patient with Gaucher disease receiving enzyme replacement therapy, and the subsequent distribution and excretion of imiglucerase in human breast milk. Clinical Therapeutics. 32: 2048-52. PMID 21118740 DOI: 10.1016/j.clinthera.2010.11.008  1
2010 Sekijima Y. [Molecular genetic understanding of hereditary disorders]. Nihon Rinsho. Japanese Journal of Clinical Medicine. 68: 52-7. PMID 20976884  1
2010 Sekijima Y, Yoshida T, Ikeda S. CPPD crystal deposition disease of the cervical spine: a common cause of acute neck pain encountered in the neurology department. Journal of the Neurological Sciences. 296: 79-82. PMID 20646716 DOI: 10.1016/j.jns.2010.05.028  1
2010 Nakamura K, Sekijima Y, Nakamura K, Hattori K, Nagamatsu K, Shimizu Y, Yasude T, Ushiyama M, Endo F, Fukushima Y, Ikeda S. Cerebral hemorrhage in Fabry's disease. Journal of Human Genetics. 55: 259-61. PMID 20300124 DOI: 10.1038/jhg.2010.18  1
2010 Tojo K, Tsuchiya-Suzuki A, Sekijima Y, Morita H, Sumita N, Ikeda S. Upper limb neuropathy such as carpal tunnel syndrome as an initial manifestation of ATTR Val30Met familial amyloid polyneuropathy. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 17: 32-5. PMID 20132088 DOI: 10.3109/13506121003619369  1
2009 Ueda M, Misumi Y, Mizuguchi M, Nakamura M, Yamashita T, Sekijima Y, Ota K, Shinriki S, Jono H, Ikeda S, Suhr OB, Ando Y. SELDI-TOF mass spectrometry evaluation of variant transthyretins for diagnosis and pathogenesis of familial amyloidotic polyneuropathy. Clinical Chemistry. 55: 1223-7. PMID 19372189 DOI: 10.1373/clinchem.2008.118505  1
2008 Sekijima Y, Kelly JW, Ikeda S. Pathogenesis of and therapeutic strategies to ameliorate the transthyretin amyloidoses. Current Pharmaceutical Design. 14: 3219-30. PMID 19075702 DOI: 10.2174/138161208786404155  1
2008 Naito KS, Sekijima Y, Ikeda S. Cerebral amyloid angiopathy-related hemorrhage in a middle-aged patient with Down's syndrome. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 15: 275-7. PMID 19065301 DOI: 10.1080/13506120802524981  1
2008 Kodaira M, Sekijima Y, Tojo K, Tsuchiya A, Yazaki M, Ikeda S, Sekijima Y, Hoshii Y, Tachibana S. Non-senile wild-type transthyretin systemic amyloidosis presenting as bilateral carpal tunnel syndrome. Journal of the Peripheral Nervous System : Jpns. 13: 148-50. PMID 18601659 DOI: 10.1111/j.1529-8027.2008.00170.x  1
2008 Tojo K, Sekijima Y, Machida K, Tsuchiya A, Yazaki M, Ikeda S. Amyloidogenic transthyretin Val30Met homozygote showing unusually early-onset familial amyloid polyneuropathy. Muscle & Nerve. 37: 796-803. PMID 18506713 DOI: 10.1002/mus.21028  1
2007 Yasude T, Sekijima Y, Mitsuhashi S, Gono T, Matsuda M, Ikeda S. Benign intracranial hypertension and leukoencephalopathy due to venous sinus stenosis in an SLE patient. Lupus. 16: 839-40. PMID 17895310 DOI: 10.1177/0961203307081119  1
2006 Sekijima Y, Dendle MA, Kelly JW. Orally administered diflunisal stabilizes transthyretin against dissociation required for amyloidogenesis. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 13: 236-49. PMID 17107884 DOI: 10.1080/13506120600960882  1
2006 Tojo K, Sekijima Y, Kelly JW, Ikeda S. Diflunisal stabilizes familial amyloid polyneuropathy-associated transthyretin variant tetramers in serum against dissociation required for amyloidogenesis. Neuroscience Research. 56: 441-9. PMID 17028027 DOI: 10.1016/j.neures.2006.08.014  1
2006 Sekijima Y, Dendle MT, Wiseman RL, White JT, D'Haeze W, Kelly JW. R104H may suppress transthyretin amyloidogenesis by thermodynamic stabilization, but not by the kinetic mechanism characterizing T119 interallelic trans-suppression. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 13: 57-66. PMID 16911959 DOI: 10.1080/13506120600722449  1
2006 Tojo K, Sekijima Y, Suzuki T, Suzuki N, Tomita Y, Yoshida K, Hashimoto T, Ikeda S. Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation. Movement Disorders : Official Journal of the Movement Disorder Society. 21: 1510-3. PMID 16817193 DOI: 10.1002/mds.21011  1
2005 Sekijima Y, Hashimoto T, Koshihara H, Kawachi Y, Otsuka F, Ikeda S. Massive mesenteric edema in a patient with type I hereditary angioedema. Modern Rheumatology / the Japan Rheumatism Association. 15: 361-3. PMID 17029094 DOI: 10.1007/s10165-005-0416-8  1
2005 Mitsuhashi S, Yazaki M, Tokuda T, Sekijima Y, Washimi Y, Shimizu Y, Ando Y, Benson MD, Ikeda S. Biochemical characteristics of variant transthyretins causing hereditary leptomeningeal amyloidosis. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 12: 216-25. PMID 16399646 DOI: 10.1080/13506120500352404  1
2005 Johnson SM, Wiseman RL, Sekijima Y, Green NS, Adamski-Werner SL, Kelly JW. Native state kinetic stabilization as a strategy to ameliorate protein misfolding diseases: a focus on the transthyretin amyloidoses. Accounts of Chemical Research. 38: 911-21. PMID 16359163 DOI: 10.1021/ar020073i  1
2005 Matsuda M, Dohi-Iijima N, Nakamura A, Sekijima Y, Morita H, Matsuzawa S, Sato S, Yahikozawa H, Tabata K, Yanagawa S, Ikeda S. Increase in incidence of elderly-onset patients with myasthenia gravis in Nagano Prefecture, Japan. Internal Medicine (Tokyo, Japan). 44: 572-7. PMID 16020882 DOI: JST.JSTAGE/internalmedicine/44.572  1
2005 Sekijima Y, Wiseman RL, Matteson J, Hammarström P, Miller SR, Sawkar AR, Balch WE, Kelly JW. The biological and chemical basis for tissue-selective amyloid disease. Cell. 121: 73-85. PMID 15820680 DOI: 10.1016/j.cell.2005.01.018  1
2005 Kaneko K, Matsuda M, Sekijima Y, Hosoda W, Gono T, Hoshi K, Shimojo H, Ikeda S. Acute respiratory distress syndrome due to systemic lupus erythematosus with hemophagocytic syndrome: an autopsy report. Clinical Rheumatology. 24: 158-61. PMID 15338452 DOI: 10.1007/s10067-004-0985-5  1
2004 Matsubara E, Sekijima Y, Tokuda T, Urakami K, Amari M, Shizuka-Ikeda M, Tomidokoro Y, Ikeda M, Kawarabayashi T, Harigaya Y, Ikeda S, Murakami T, Abe K, Otomo E, Hirai S, et al. Soluble Abeta homeostasis in AD and DS: impairment of anti-amyloidogenic protection by lipoproteins. Neurobiology of Aging. 25: 833-41. PMID 15212837 DOI: 10.1016/j.neurobiolaging.2003.10.004  1
2004 Sekijima Y, Hashimoto T, Kawachi Y, Koshihara H, Otsuka F, Ikeda S. A novel RNA splice site mutation in the C1 inhibitor gene of a patient with type I hereditary angioedema. Internal Medicine (Tokyo, Japan). 43: 253-5. PMID 15098611 DOI: 10.2169/internalmedicine.43.253  1
2004 Dohi-Iijima N, Sekijima Y, Nakamura A, Morita H, Matsuda M, Haniuda M, Hashimoto T, Ikeda S. Retrospective analyses of clinical features and therapeutic outcomes in thymectomized patients with myasthenia gravis at Shinshu University. Internal Medicine (Tokyo, Japan). 43: 189-93. PMID 15098598 DOI: 10.2169/internalmedicine.43.189  1
2004 Oide T, Ohara S, Oguchi K, Maruyama M, Yazawa M, Inoue K, Sekijima Y, Tokuda T, Ikeda S. Remitting seronegative symmetrical synovitis with pitting edema (RS3PE) syndrome in Nagano, Japan: clinical, radiological, and cytokine studies of 13 patients. Clinical and Experimental Rheumatology. 22: 91-8. PMID 15005010  1
2004 Miller SR, Sekijima Y, Kelly JW. Native state stabilization by NSAIDs inhibits transthyretin amyloidogenesis from the most common familial disease variants. Laboratory Investigation; a Journal of Technical Methods and Pathology. 84: 545-52. PMID 14968122 DOI: 10.1038/labinvest.3700059  1
2003 Ishii W, Sekijima Y, Hattori T, Tsuyuzaki J, Ikeda S. [A case of Guillain-Barré syndrome starting from severe upper back pain]. Nō to Shinkei = Brain and Nerve. 55: 963-6. PMID 14727536  1
2003 Kato T, Hoshi K, Sekijima Y, Matsuda M, Hashimoto T, Otani M, Suzuki A, Ikeda S. Rheumatoid meningitis: an autopsy report and review of the literature. Clinical Rheumatology. 22: 475-80. PMID 14677033 DOI: 10.1007/s10067-003-0788-0  1
2003 Matsuda M, Hosoda W, Sekijima Y, Hoshi K, Hashimoto T, Itoh S, Ikeda S. Neutropenia as a complication of high-dose intravenous immunoglobulin therapy in adult patients with neuroimmunologic disorders. Clinical Neuropharmacology. 26: 306-11. PMID 14646610 DOI: 10.1097/00002826-200311000-00009  1
2003 Hagiwara N, Sekijima Y, Takei Y, Ikeda S, Kawasaki S, Kobayashi K, Saheki T. Hepatocellular carcinoma in a case of adult-onset type II citrullinemia. Internal Medicine (Tokyo, Japan). 42: 978-82. PMID 14606711  1
2003 Sekijima Y, Hashimoto T, Onodera O, Date H, Okano T, Naito K, Tsuji S, Ikeda S. Severe generalized dystonia as a presentation of a patient with aprataxin gene mutation. Movement Disorders : Official Journal of the Movement Disorder Society. 18: 1198-200. PMID 14534929 DOI: 10.1002/mds.10526  1
2003 Hagiwara N, Sekijima Y, Hattori T, Hashimoto T, Ikeda S. [Two patients with different types of vasculitic neuropathy--a comparison between cutaneous polyarteritis nodosa and nonsystemic vasculitic neuropathy]. Rinshō Shinkeigaku = Clinical Neurology. 43: 102-8. PMID 12820558  1
2003 Kume H, Sekijima Y, Maruyama K, Kametani F. gamma-Secretase can cleave amyloid precursor protein fragments independent of alpha- and beta-secretase pre-cutting. International Journal of Molecular Medicine. 12: 57-60. PMID 12792809  1
2003 Hammarström P, Sekijima Y, White JT, Wiseman RL, Lim A, Costello CE, Altland K, Garzuly F, Budka H, Kelly JW. D18G transthyretin is monomeric, aggregation prone, and not detectable in plasma and cerebrospinal fluid: a prescription for central nervous system amyloidosis? Biochemistry. 42: 6656-63. PMID 12779320 DOI: 10.1021/bi027319b  1
2003 Sekijima Y, Hammarström P, Matsumura M, Shimizu Y, Iwata M, Tokuda T, Ikeda S, Kelly JW. Energetic characteristics of the new transthyretin variant A25T may explain its atypical central nervous system pathology. Laboratory Investigation; a Journal of Technical Methods and Pathology. 83: 409-17. PMID 12649341  1
2002 Yoshida T, Sekijima Y, Hoshi K, Kaneko K, Hashimoto T, Ikeda S. [Two patients with pseudogout manifested by severe neck pain]. Rinshō Shinkeigaku = Clinical Neurology. 42: 308-12. PMID 12561086  1
2002 Gono T, Matsuda M, Dohi N, Sekijima Y, Tada T, Sakashita K, Koike K, Kadosaka S, Ikeda S. Gastroduodenal lesions in primary AL amyloidosis. Gastrointestinal Endoscopy. 56: 563. PMID 12297775  1
2002 Sekijima Y, Ikeda S. [May-white syndrome (myoclonus, ataxia, deafness)]. Nihon Rinsho. Japanese Journal of Clinical Medicine. 60: 392-7. PMID 12013895  1
2001 Tojyo K, Sekijima Y, Hattori T, Tsuyuzaki J, Nakamura A, Kita N, Ikeda S. [A patient who developed dermatomyositis during the 1st trimester of gestation and improved after abortion]. Rinshō Shinkeigaku = Clinical Neurology. 41: 635-8. PMID 11968753  1
2001 Sekijima Y, Tokuda T, Kametani F, Tanaka K, Maruyama K, Ikeda S. Serum transthyretin monomer in patients with familial amyloid polyneuropathy. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 8: 257-62. PMID 11791618  1
2001 Tojyo K, Hattori T, Sekijima Y, Yoshida K, Ikeda S. [A case of idiopathic brain calcification associated with dyschromatosis symmetrica hereditaria, aplasia of dental root, and aortic valve sclerosis]. Rinshō Shinkeigaku = Clinical Neurology. 41: 299-305. PMID 11771159  1
2001 Date H, Onodera O, Tanaka H, Iwabuchi K, Uekawa K, Igarashi S, Koike R, Hiroi T, Yuasa T, Awaya Y, Sakai T, Takahashi T, Nagatomo H, Sekijima Y, Kawachi I, et al. Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene. Nature Genetics. 29: 184-8. PMID 11586299 DOI: 10.1038/ng1001-184  1
2001 Sekijima Y, Hoshi KI, Kasai H, Okada M, Namiki S, Ohta K, Nakano T, Hirayama J, Ikeda SI. Three patients with isolated adrenocorticotropin deficiency presenting with neuroleptic malignant syndrome-like symptoms. Internal Medicine (Tokyo, Japan). 40: 510-4. PMID 11446676  1
2000 Ishikawa S, Ishikawa M, Tokuda T, Yoshida K, Wakui K, Matsuura S, Ohara S, Sekijima Y, Hidaka E, Fukushima Y, Shigeta H, Komatsu K, Ikeda S. Japanese family with an autosomal dominant chromosome instability syndrome: a new neurodegenerative disease? American Journal of Medical Genetics. 94: 265-70. PMID 11038437 DOI: 10.1002/1096-8628(20001002)94:4<265::AID-AJMG1>3.0.CO;2-#  1
1999 Tamaoka A, Sekijima Y, Matsuno S, Tokuda T, Shoji S, Ikeda SI. Amyloid beta protein species in cerebrospinal fluid and in brain from patients with Down's syndrome. Annals of Neurology. 46: 933. PMID 10589550 DOI: 10.1002/1531-8249(199912)46:6<933::AID-ANA20>3.0.CO;2-4  1
1999 Sekijima Y. [Sarin poisoning]. RyōIkibetsu ShōKōGun ShirīZu. 646-9. PMID 10434739  1
1999 Sekijima Y, Kametani F, Tanaka K, Okochi M, Usami M, Mori H, Tokuda T, Ikeda S. Presenilin-1 exists in the axoplasm fraction in the brains of aged Down's syndrome subjects and non-demented individuals. Neuroscience Letters. 267: 121-4. PMID 10400227 DOI: 10.1016/S0304-3940(99)00348-1  1
1999 Ishikawa S, Kato M, Tokuda T, Momoi H, Sekijima Y, Higuchi M, Yanagisawa N. Licorice-induced hypokalemic myopathy and hypokalemic renal tubular damage in anorexia nervosa. The International Journal of Eating Disorders. 26: 111-4. PMID 10349593 DOI: 10.1002/(SICI)1098-108X(199907)26:1<111::AID-EAT16>3.0.CO;2-U  1
1999 Nohara M, Sekijima Y, Nakajima T, Mimura S. Ocular manifestations in the follow-up of victims after sarin poisoning in Matsumoto area Japanese Journal of Clinical Ophthalmology. 53: 659-663.  1
1998 Sekijima Y, Morita H, Hashimoto T, Yamazaki M, Yanagisawa N. Sleep apnoea of central origin in a case of myotonic dystrophy. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 5: 112-5. PMID 18644306  1
1998 Kurogouchi F, Oguchi T, Mawatari E, Yamaura S, Hora K, Takei M, Sekijima Y, Ikeda Si, Kiyosawa K. A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation. American Journal of Nephrology. 18: 551-6. PMID 9845835  1
1998 Nakajima T, Sasaki K, Ozawa H, Sekijima Y, Morita H, Fukushima Y, Yanagisawa N. Urinary metabolites of sarin in a patient of the Matsumoto sarin incident Archives of Toxicology. 72: 601-603. PMID 9806433 DOI: 10.1007/s002040050549  1
1998 Akanuma H, Sekijima Y, Tokuda T, Takematsu H, Yanagisawa N. [A case of severe status epilepticus of frontal lobe origin successfully treated with corticosteroids]. Rinshō Shinkeigaku = Clinical Neurology. 38: 461-4. PMID 9805996  1
1998 Sekijima Y, Ohara S, Nakagawa S, Tabata K, Yoshida K, Ishigame H, Shimizu Y, Yanagisawa N. Hereditary motor and sensory neuropathy associated with cerebellar atrophy (HMSNCA): clinical and neuropathological features of a Japanese family. Journal of the Neurological Sciences. 158: 30-7. PMID 9667774 DOI: 10.1016/S0022-510X(98)00103-8  1
1998 Sekijima Y, Ikeda S, Tokuda T, Satoh S, Hidaka H, Hidaka E, Ishikawa M, Yanagisawa N. Prevalence of dementia of Alzheimer type and apolipoprotein E phenotypes in aged patients with Down's syndrome. European Neurology. 39: 234-7. PMID 9635475 DOI: 10.1159/000007940  1
1998 Kawakami T, Sekijima Y, Tokuda T, Yamazaki M, Yanagisawa N. [A case of chronic inflammatory demyelinating polyradiculoneuropathy complicated by phrenic nerve palsy]. Rinshō Shinkeigaku = Clinical Neurology. 38: 118-21. PMID 9619073  1
1997 Sekijima Y, Morita H, Yanagisawa N. Follow-up of sarin poisoning in Matsumoto. Annals of Internal Medicine. 127: 1042. PMID 9412293  1
1997 Sekijima Y, Tokuda T, Hashimoto T, Koh CS, Shoji S, Yanagisawa N. Serial magnetic resonance imaging (MRI) study of a patient with Balo's concentric sclerosis treated with immunoadsorption plasmapheresis. Multiple Sclerosis (Houndmills, Basingstoke, England). 2: 291-4. PMID 9065920 DOI: 10.1177/135245859700200605  1
1997 Tokuda T, Fukushima T, Ikeda S, Sekijima Y, Shoji S, Yanagisawa N, Tamaoka A. Plasma levels of amyloid beta proteins Abeta1-40 and Abeta1-42(43) are elevated in Down's syndrome. Annals of Neurology. 41: 271-3. PMID 9029078 DOI: 10.1002/ana.410410220  1
1996 Satoh S, Tokuda T, Ikeda S, Sekijima Y, Yanagisawa N, Hidaka H, Kametani F. No association between apolipoprotein E epsilon4 allele and the age of onset in type I familial amyloid polyneuropathy. Neuroscience Letters. 204: 209-11. PMID 8938267 DOI: 10.1016/0304-3940(96)12344-2  1
1995 Sekijima Y, Morita H, Shindo M, Okudera H, Shibata T. [A case of severe sarin poisoning in the sarin attack in Matsumoto--one-year follow-up of clinical findings, and laboratory data]. Rinshō Shinkeigaku = Clinical Neurology. 35: 1241-5. PMID 8720336  1
1995 Sekijima Y, Ikeda S, Katai S, Matsuda M, Hashimoto T, Haruta S, Owa M, Sakai T, Takeda S, Yanagisawa N. Cytoplasmic body myopathy with hypertrophic cardiomyopathy. Internal Medicine (Tokyo, Japan). 34: 166-70. PMID 7787321  1
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