Stephane Mathis - Publications

Affiliations: 
Observatoire de Meudon 

102 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 Deschamps N, Mathis S, Duchesne M, Ghorab K, Gallouedec G, Richard L, Boulesteix JM, Corcia P, Magy L, Vallat JM. CIDP and hemopathies, an underestimated association. Journal of the Neurological Sciences. 429: 118055. PMID 34455207 DOI: 10.1016/j.jns.2021.118055  1
2021 Uncini A, Mathis S, Vallat JM. New classification of autoimmune neuropathies based on target antigens and involved domains of myelinated fibres. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 34373238 DOI: 10.1136/jnnp-2021-326889  1
2021 Vallat JM, Mathis S, Magy L. Diagnosis and treatment of chronic inflammatory demyelinating polyneuropathy: A "grand cru" of updated data. European Journal of Neurology. PMID 34152068 DOI: 10.1111/ene.14989  1
2021 Mathis S, Le Masson G, Soulages A, Duval F, Carla L, Vallat JM, Solé G. Olfaction and anosmia: From ancient times to COVID-19. Journal of the Neurological Sciences. 425: 117433. PMID 33848701 DOI: 10.1016/j.jns.2021.117433  1
2021 Solé G, Mathis S, Friedman D, Salort-Campana E, Tard C, Bouhour F, Magot A, Annane D, Clair B, Le Masson G, Soulages A, Duval F, Carla L, Violleau MH, Saulnier T, et al. Impact of Coronavirus Disease 2019 in a French Cohort of Myasthenia Gravis. Neurology. PMID 33568541 DOI: 10.1212/WNL.0000000000011669  1
2021 Mathis S, Soulages A, Le Masson G, Vallat JM. Correction to: Epidemics and outbreaks of peripheral nervous system disorders: I. infectious and immune-mediated causes. Journal of Neurology. PMID 33399969 DOI: 10.1007/s00415-020-10280-0  1
2020 Vallat JM, Duchesne M, Corcia P, Richard L, Ghorab K, Magy L, Mathis S. The Wide Spectrum of Pathophysiological Mechanisms of Paraproteinemic Neuropathy. Neurology. PMID 33277411 DOI: 10.1212/WNL.0000000000011324  1
2020 Mathis S, Soulages A, Vallat JM, Le Masson G. Epidemics and outbreaks of peripheral nervous system disorders: II. Toxic and nutritional causes. Journal of Neurology. PMID 32915310 DOI: 10.1007/s00415-020-10216-8  1
2020 Mathis S, Soulages A, Le Masson G, Vallat JM. Epidemics and outbreaks of peripheral nervous system disorders: I. infectious and immune-mediated causes. Journal of Neurology. PMID 32914207 DOI: 10.1007/s00415-020-10215-9  1
2020 Mathis S, Vallat JM, Weis J. When botany inspired pathology of the peripheral nervous system. Neurology. 95: 532-536. PMID 32759198 DOI: 10.1212/WNL.0000000000010588  1
2020 Mathis S, Duval F, Soulages A, Solé G, Le Masson G. The ataxic neuropathies. Journal of Neurology. PMID 32556571 DOI: 10.1007/s00415-020-09994-y  1
2020 Matharan M, Mathis S, Bonabaud S, Carla L, Soulages A, Le Masson G. Minimizing the Diagnostic Delay in Amyotrophic Lateral Sclerosis: The Role of Nonneurologist Practitioners. Neurology Research International. 2020: 1473981. PMID 32455015 DOI: 10.1155/2020/1473981  1
2020 Mathis S, Soulages A, Vallat JM, Le Masson G. History of acute polyradiculoneuropathy (part 1): The prehistory of Guillain-Barré syndrome. Neurology. PMID 32345732 DOI: 10.1212/WNL.0000000000009401  1
2020 Mathis S, Soulages A, Le Masson G, Vallat JM. History of acute polyradiculoneuropathy (part 2): From 1916 to 2019. Neurology. PMID 32345731 DOI: 10.1212/WNL.0000000000009402  1
2020 Mathis S, Vallat JM. The mysterious death of Georges Cuvier (1832): An early case of severe Guillain-Barré syndrome? Neuromuscular Disorders : Nmd. 30: 250-253. PMID 32165107 DOI: 10.1016/j.nmd.2020.01.007  1
2020 Gacem N, Kavo A, Zerad L, Richard L, Mathis S, Kapur RP, Parisot M, Amiel J, Dufour S, de la Grange P, Pingault V, Vallat JM, Bondurand N. ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell development. Nature Communications. 11: 198. PMID 31924792 DOI: 10.1038/s41467-019-14090-5  1
2019 Vallat JM, Magy L, Corcia P, Boulesteix JM, Uncini A, Mathis S. Ultrastructural Lesions of Nodo-Paranodopathies in Peripheral Neuropathies. Journal of Neuropathology and Experimental Neurology. PMID 31923310 DOI: 10.1093/jnen/nlz134  1
2019 Vallat JM, Mathis S, Vegezzi E, Richard L, Duchesne M, Gallouedec G, Corcia P, Magy L, Uncini A, Devaux J. Antibody- and macrophage-mediated segmental demyelination in chronic inflammatory demyelinating polyneuropathy: clinical, electrophysiological, immunological and pathological correlates. European Journal of Neurology. PMID 31769579 DOI: 10.1111/ene.14133  1
2019 Tang MH, Mathis S, Duffau P, Cazenave P, Solé G, Duval F, Soulages A, Le Masson G. Prognostic factor of poor outcome in anti-MAG neuropathy: clinical and electrophysiological analysis of a French Cohort. Journal of Neurology. PMID 31705291 DOI: 10.1007/s00415-019-09618-0  1
2019 Mathis S, Le Masson G, Soulages A, Duval F, Solé G, Boissonnot M, Lathière T, Bonduelle T, Carla L, Nadal L, Baron C, Balaboi I, Ciron J, Vallat JM. Papilledema and Peripheral Neuropathies. The Neurologist. 24: 185-193. PMID 31688711 DOI: 10.1097/NRL.0000000000000250  1
2019 Mathis S, Le Masson G, Vallat JM. Early clinicopathologic description of nodoparanodopathy in the 19th century. Neurology. 93: 788-792. PMID 31659130 DOI: 10.1212/WNL.0000000000008399  1
2019 Mathis S, Vallat JM. The journal behind the nodes of Ranvier? The Lancet. Neurology. 18: 628. PMID 31202467 DOI: 10.1016/S1474-4422(19)30203-0  1
2019 Soulages A, Tang HM, Pham-Ledard A, Négrier-Leibreich ML, Cosnard A, Duval F, Solé G, Carla L, Le Masson G, Mathis S. Myopathy and scleromyxedema. Journal of Neurology. PMID 31115676 DOI: 10.1007/s00415-019-09379-w  1
2019 Correard S, Plassais J, Lagoutte L, Botherel N, Thibaud JL, Hédan B, Richard L, Lia AS, Delague V, Mège C, Mathis S, Guaguère E, Paradis M, Vallat JM, Quignon P, et al. Canine neuropathies: powerful spontaneous models for human hereditary sensory neuropathies. Human Genetics. PMID 30955094 DOI: 10.1007/S00439-019-02003-X  1
2019 Franques J, Chiche L, De Paula AM, Grapperon AM, Attarian S, Pouget J, Mathis S. Characteristics of patients with vitamin B12-responsive neuropathy: a case series with systematic repeated electrophysiological assessment. Neurological Research. 41: 569-576. PMID 30887907 DOI: 10.1080/01616412.2019.1588490  1
2019 Mathis S, Goizet C, Soulages A, Vallat JM, Masson GL. Genetics of amyotrophic lateral sclerosis: A review. Journal of the Neurological Sciences. 399: 217-226. PMID 30870681 DOI: 10.1016/j.jns.2019.02.030  1
2019 Jouaud M, Mathis S, Richard L, Lia AS, Magy L, Vallat JM. Rodent models with expression of PMP22: Relevance to dysmyelinating CMT and HNPP. Journal of the Neurological Sciences. 398: 79-90. PMID 30685714 DOI: 10.1016/j.jns.2019.01.030  1
2018 Šinkūnaitė L, Burbaud P, Soulages A, Vergnet S, Duval F, Solé G, Tang HM, Le Masson G, Mathis S. Focal neurogenic muscle hypertrophy and fasciculations in multifocal motor neuropathy. Muscle & Nerve. PMID 30152094 DOI: 10.1002/mus.26185  1
2018 Mathis S, Tazir M, Solé G, Magy L, Le Masson G, Couratier P, Ghorab K, Duval F, Lacoste I, Goizet C, Vallat JM. Some new proposals for the classification of inherited myopathies. Journal of the Neurological Sciences. 391: 118-119. PMID 30103959 DOI: 10.1016/j.jns.2018.06.014  1
2018 Mathis S, Magy L, Le Masson G, Richard L, Soulages A, Solé G, Duval F, Ghorab K, Vallat JM, Duchesne M. Value of nerve biopsy in the management of peripheral neuropathies. Expert Review of Neurotherapeutics. PMID 29923431 DOI: 10.1080/14737175.2018.1489240  1
2018 Vallat JM, Mathis S, Magy L, Bounolleau P, Skarzynski M, Heitzmann A, Manso C, Devaux J, Uncini A. Subacute nodopathy with conduction blocks and anti-neurofascin 140/186 antibodies: an ultrastructural study. Brain : a Journal of Neurology. 141: e56. PMID 29800077 DOI: 10.1093/brain/awy134  1
2018 Hachulla E, Le Masson G, Solé G, Hamidou M, Desnuelle C, Azulay JP, Besson G, Swiader L, Abad S, Antoine JC, Bouhour F, Créange A, Grenouillet M, Magy L, Marcel S, ... ... Mathis S, et al. Safety of Intravenous Immunoglobulin (Tegeline®), Administered at Home in Patients with Autoimmune Disease: Results of a French Study. Biomed Research International. 2018: 8147251. PMID 29736397 DOI: 10.1155/2018/8147251  1
2018 Ciron J, Baron C, Boissonnot M, Neau JP, Magdelaine C, Vallat JM, Mathis S. Peripheral nervous system involvement in Leber's hereditary optic neuropathy. Journal of the Neurological Sciences. 388: 94-96. PMID 29627039 DOI: 10.1016/j.jns.2018.03.002  1
2018 Magy L, Mathis S, Le Masson G, Goizet C, Tazir M, Vallat JM. Updating the classification of inherited neuropathies: Results of an international survey. Neurology. PMID 29429969 DOI: 10.1212/WNL.0000000000005074  1
2018 Trimouille A, Obre É, Banneau G, Durr A, Stevanin G, Clot F, Pennamen P, Perez JT, Bailly-Scappaticci C, Rouanet M, Delleci C, Sole G, Mathis S, Goizet C. An in-frame deletion in BICD2 associated with a non-progressive form of SMALED. Clinical Neurology and Neurosurgery. 166: 1-3. PMID 29353221 DOI: 10.1016/j.clineuro.2018.01.013  1
2018 Mathis S, Le Masson G. RNA-Targeted Therapies and Amyotrophic Lateral Sclerosis. Biomedicines. 6. PMID 29342921 DOI: 10.3390/biomedicines6010009  1
2018 Duval F, Lacoste I, Galli G, Chaumont H, Solé G, Léger F, Damon-Perrière N, Rouanet M, Le Masson G, Mathis S. Acute Brachial Radiculoplexopathy and Giant Cell Arteritis. The Neurologist. 23: 23-28. PMID 29266041 DOI: 10.1097/NRL.0000000000000162  1
2018 Mathis S, Tazir M, Magy L, Duval F, Le Masson G, Duchesne M, Couratier P, Ghorab K, Solé G, Lacoste I, Goizet C, Vallat JM. History and current difficulties in classifying inherited myopathies and muscular dystrophies. Journal of the Neurological Sciences. 384: 50-54. PMID 29249377 DOI: 10.1016/j.jns.2017.10.051  1
2017 Duchesne M, Mathis S, Richard L, Magdelaine C, Corcia P, Nouioua S, Tazir M, Magy L, Vallat JM. Nerve Biopsy Is Still Useful in Some Inherited Neuropathies. Journal of Neuropathology and Experimental Neurology. PMID 29300988 DOI: 10.1093/jnen/nlx111  1
2017 Mathis S, Magy L, Le Masson G, Vallat JM. Did Jules Dejerine describe AMAN at the end of the 19th century? Neurology. 89: 1749-1753. PMID 29038133 DOI: 10.1212/WNL.0000000000004527  1
2017 Mathis S, Duval F, Solé G, Tourdias T, Le Masson G. Chronic Inflammatory Demyelinating Polyradiculoneuropathy Causing Myelopathy. Muscle & Nerve. PMID 28786217 DOI: 10.1002/mus.25756  1
2017 Mathis S, Vallat JM. Jules Dejerine and the peripheral nervous system. Neurology. 89: 611-615. PMID 28784633 DOI: 10.1212/WNL.0000000000004217  1
2017 Mathis S, Chapon F, Franques J. MRI and surgical lumbosacral trunk positioning palsy. Muscle & Nerve. 56: E36-E37. PMID 28556281 DOI: 10.1002/mus.25703  1
2017 Mathis S, Couratier P, Julian A, Corcia P, Le Masson G. Current view and perspectives in amyotrophic lateral sclerosis. Neural Regeneration Research. 12: 181-184. PMID 28400790 DOI: 10.4103/1673-5374.200794  1
2017 Franques J, Chiche L, Mathis S. Sensory Neuronopathy Revealing Severe Vitamin B12 Deficiency in a Patient with Anorexia Nervosa: An Often-Forgotten Reversible Cause. Nutrients. 9. PMID 28294987 DOI: 10.3390/nu9030281  1
2017 Franques J, Chapon F, Devaux J, Mathis S. Teaching Neuro: Cranial nerve hypertrophy in IgG4 anti-neurofascin 155 antibody-positive polyneuropathy. Neurology. 88: e52. PMID 28193760 DOI: 10.1212/WNL.0000000000003616  1
2016 Mathis S, Magy L, Corcia P, Ghorab K, Richard L, Ciron J, Duchesne M, Vallat JM. Simultaneous Combined Myositis, Inflammatory Polyneuropathy, and Overlap Myasthenic Syndrome. Case Reports in Neurological Medicine. 2016: 6108234. PMID 28044116 DOI: 10.1155/2016/6108234  1
2016 Vallat JM, Yuki N, Sekiguchi K, Kokubun N, Oka N, Mathis S, Magy L, Sherman DL, Brophy PJ, Devaux JJ. Paranodal lesions in chronic inflammatory demyelinating polyneuropathy associated with anti-Neurofascin 155 antibodies. Neuromuscular Disorders : Nmd. PMID 27986399 DOI: 10.1016/j.nmd.2016.10.008  1
2016 Vallat JM, Nizon M, Magee A, Isidor B, Magy L, Péréon Y, Richard L, Ouvrier R, Cogné B, Devaux J, Zuchner S, Mathis S. Contactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal Region. Journal of Neuropathology and Experimental Neurology. PMID 27818385 DOI: 10.1093/jnen/nlw093  1
2016 Mathis S, Couratier P, Julian A, Vallat JM, Corcia P, Le Masson G. Management and therapeutic perspectives in amyotrophic lateral sclerosis. Expert Review of Neurotherapeutics. 1-14. PMID 27644548 DOI: 10.1080/14737175.2016.1227705  1
2016 Avila-Smirnow D, Gueneau L, Batonnet-Pichon S, Delort F, Bécane HM, Claeys K, Beuvin M, Goudeau B, Jais JP, Nelson I, Richard P, Ben Yaou R, Romero NB, Wahbi K, Mathis S, et al. Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC. Revue Neurologique. PMID 27633507 DOI: 10.1016/j.neurol.2016.07.017  1
2016 Mathis S, Godenèche G, Haroche J, Milin S, Julian A, Berthomet A, Baron C, Palazzo P, Neau JP. Long-term outcome of basilar stenosis in Erdheim-Chester disease: A case report. Medicine. 95: e4813. PMID 27603396 DOI: 10.1097/MD.0000000000004813  1
2016 Mathis S, Franques J, Richard L, Vallat JM. Monoclonal gammopathy of undeterminated significance and endoneurial IgG deposition: A case report. Medicine. 95: e4807. PMID 27603395 DOI: 10.1097/MD.0000000000004807  1
2016 Schäfer MK, Bellouze S, Jacquier A, Schaller S, Richard L, Mathis S, Vallat JM, Haase G. Sensory neuropathy in progressive motor neuronopathy (pmn) mice is associated with defects in microtubule polymerization and axonal transport. Brain Pathology (Zurich, Switzerland). PMID 27488538 DOI: 10.1111/bpa.12422  1
2016 Mathis S, Goizet C, Tazir M, Magy L, Vallat JM. Reasons Charcot-Marie-Tooth disease due to mutations in the MME gene should not be named AR-CMT2T. Annals of Neurology. 80: 477. PMID 27458975 DOI: 10.1002/ana.24741  1
2016 Vallat JM, Magy L, Ciron J, Corcia P, Le Masson G, Mathis S. Therapeutic options and management of polyneuropathy associated with anti-MAG antibodies. Expert Review of Neurotherapeutics. PMID 27267749 DOI: 10.1080/14737175.2016.1198257  1
2016 Jouaud M, Gonnaud PM, Richard L, Latour P, Ollagnon-Roman E, Sturtz F, Mathis S, Magy L, Vallat JM. Congenital hypomyelinating neuropathy due to the association of a truncating mutation in PMP22 with the classical HNPP deletion. Neuromuscular Disorders : Nmd. 26: 316-21. PMID 27067623 DOI: 10.1016/j.nmd.2016.01.004  1
2016 Watrin L, Ghawché F, Larre P, Neau JP, Mathis S, Fournier E. Guillain-Barré Syndrome (42 Cases) Occurring During a Zika Virus Outbreak in French Polynesia. Medicine. 95: e3257. PMID 27057874 DOI: 10.1097/MD.0000000000003257  1
2016 Mathis S, Palazzo P, Lamy M, Ragot S, Lapeyrie S, Ricco JB, Neau JP. Posterior reversible encephalopathy syndrome and reversible cerebral vasoconstriction syndrome after bilateral carotid paraganglioma resection: A case report. Cephalalgia : An International Journal of Headache. PMID 26873258 DOI: 10.1177/0333102416629235  1
2016 Antoine JC, Robert-Varvat F, Maisonobe T, Créange A, Franques J, Mathis S, Delmont E, Kuntzer T, Lefaucheur JP, Pouget J, Viala K, Desnuelle C, Echaniz-Laguna A, Rotolo F, Camdessanché JP, et al. Identifying a therapeutic window in acute and subacute inflammatory sensory neuronopathies. Journal of the Neurological Sciences. 361: 187-91. PMID 26810539 DOI: 10.1016/j.jns.2015.12.044  1
2016 Mathis S, Vallat JM, Magy L. Novel immunotherapeutic strategies in chronic inflammatory demyelinating polyneuropathy. Immunotherapy. 8: 165-78. PMID 26809024 DOI: 10.2217/imt.15.107  1
2016 Mathis S, Boissonnot M, Tasu JP, Simonet C, Ciron J, Neau JP. Intraventricular Silicone Oil: A Case Report. Medicine. 95: e2359. PMID 26735537 DOI: 10.1097/MD.0000000000002359  1
2016 Duchesne M, Magy L, Richard L, Ingrand P, Neau JP, Mathis S, Vallat JM. Simultaneous Quantification of Unmyelinated Nerve Fibers in Sural Nerve and in Skin. Journal of Neuropathology and Experimental Neurology. 75: 53-60. PMID 26705410 DOI: 10.1093/jnen/nlv005  1
2016 Vallat JM, Goizet C, Magy L, Mathis S. Too many numbers and complexity: time to update the classifications of neurogenetic disorders? Journal of Medical Genetics. 53: 647-50. PMID 26518709 DOI: 10.1136/jmedgenet-2015-103477  1
2016 Duchesne M, Magy L, Richard L, Ingrand P, Neau JP, Mathis S, Vallat JM. Simultaneous quantification of unmyelinated nerve fibers in sural nerve and in skin Journal of Neuropathology and Experimental Neurology. 75: 53-60. DOI: 10.1093/jnen/nlv005  1
2015 Mathis S, Goizet C, Tazir M, Magdelaine C, Lia AS, Magy L, Vallat JM. Charcot-Marie-Tooth diseases: an update and some new proposals for the classification. Journal of Medical Genetics. 52: 681-90. PMID 26246519 DOI: 10.1136/jmedgenet-2015-103272  1
2015 Vix J, Mathis S, Lacoste M, Guillevin R, Neau JP. Neurological Manifestations in Parry-Romberg Syndrome: 2 Case Reports. Medicine. 94: e1147. PMID 26181554 DOI: 10.1097/MD.0000000000001147  1
2015 Mathis S, Pin JC, Pierre F, Ciron J, Iljicsov A, Lamy M, Neau JP. Anti-NMDA Receptor Encephalitis During Pregnancy: A Case Report. Medicine. 94: e1034. PMID 26131809 DOI: 10.1097/MD.0000000000001034  1
2015 Magy L, Kaboré R, Mathis S, Lebeau P, Ghorab K, Caudie C, Vallat JM. Heterogeneity of Polyneuropathy Associated with Anti-MAG Antibodies. Journal of Immunology Research. 2015: 450391. PMID 26065001 DOI: 10.1155/2015/450391  1
2015 Vallat JM, Mathis S, Ghorab K, Milor MA, Richard L, Magy L. Natalizumab as a disease-modifying therapy in chronic inflammatory demyelinating polyneuropathy - A report of three cases European Neurology. 73: 294-302. PMID 25925430 DOI: 10.1159/000381767  1
2015 Mathis S, Magy L, Vallat JM. Therapeutic options in Charcot-Marie-Tooth diseases. Expert Review of Neurotherapeutics. 15: 355-66. PMID 25703094 DOI: 10.1586/14737175.2015.1017471  1
2015 Duchesne M, Mathis S, Corcia P, Richard L, Ghorab K, Jaccard A, Magy L, Vallat JM. Value of nerve biopsy in patients with latent malignant hemopathy and peripheral neuropathy: A case series Medicine (United States). 94: e394. PMID 25621682 DOI: 10.1097/MD.0000000000000394  1
2015 Ayrignac X, Carra-Dalliere C, Menjot de Champfleur N, Denier C, Aubourg P, Bellesme C, Castelnovo G, Pelletier J, Audoin B, Kaphan E, de Seze J, Collongues N, Blanc F, Chanson JB, Magnin E, ... ... Mathis S, et al. Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients. Brain : a Journal of Neurology. 138: 284-92. PMID 25527826 DOI: 10.1093/Brain/Awu353  1
2015 Ciron J, Mathis S, Iljicsov A, Boucebci S, Neau JP. Multiple simultaneous intracranial hemorrhages due to hornet stings. Clinical Neurology and Neurosurgery. 128: 53-5. PMID 25462096 DOI: 10.1016/j.clineuro.2014.10.014  1
2015 Jhunjhunwala K, Lenka A, Pal PK, Acharya UR, Adeli H, Sudarshan VK, Santhosh J, Koh JEW, Adeli A, Mugikura S, Fujimura M, Takahashi S, Zangemeister WH, Buhmann C, Gerloff C, ... ... Mathis S, et al. Contents Vol. 73, 2015 European Neurology. 73. DOI: 10.1159/000433495  1
2014 Tazir M, Hamadouche T, Nouioua S, Mathis S, Vallat JM. Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update. Journal of the Neurological Sciences. 347: 14-22. PMID 25454638 DOI: 10.1016/j.jns.2014.10.013  1
2014 Antoine JC, Robert-Varvat F, Maisonobe T, Créange A, Franques J, Mathis S, Delmont E, Kuntzer T, Lefaucheur JP, Pouget J, Viala K, Desnuelle C, Echaniz-Laguna A, Rotolo F, Camdessanché JP, et al. Testing the validity of a set of diagnostic criteria for sensory neuronopathies: a francophone collaborative study. Journal of Neurology. 261: 2093-100. PMID 25108558 DOI: 10.1007/s00415-014-7423-7  1
2014 Mathis S, Lamy M, Ciron J, Iljicsov A, Arjmand R, Agius P, Neau JP. Paroxysmal sneezing at the onset of syncopes and transient ischemic attack revealing a papillary cardiac fibroelastoma. Case Reports in Neurological Medicine. 2014: 734849. PMID 25045556 DOI: 10.1155/2014/734849  1
2014 Romero NB, Xie T, Malfatti E, Schaeffer U, Böhm J, Wu B, Xu F, Boucebci S, Mathis S, Neau JP, Monnier N, Fardeau M, Laporte J. Autosomal dominant eccentric core disease caused by a heterozygous mutation in the MYH7 gene. Journal of Neurology, Neurosurgery, and Psychiatry. 85: 1149-52. PMID 24828896 DOI: 10.1136/jnnp-2013-306754  1
2014 Mathis S, Neau JP, Pluchon C, Fargeau MN, Karolewicz S, Iljicsov A, Gil R. Apathy in Parkinson's disease: an electrophysiological study. Neurology Research International. 2014: 290513. PMID 24804097 DOI: 10.1155/2014/290513  1
2014 Mathis S, Corcia P, Tazir M, Camu W, Magdelaine C, Latour P, Biberon J, Guennoc AM, Richard L, Magy L, Funalot B, Vallat JM. Peripheral Myelin Protein 22 gene duplication with atypical presentations: A new example of the wide spectrum of Charcot-Marie-Tooth 1A disease Neuromuscular Disorders. 24: 524-528. PMID 24792522 DOI: 10.1016/j.nmd.2014.03.014  1
2014 Mathis S, Funalot B, Boyer O, Lacroix C, Marcorelles P, Magy L, Richard L, Antignac C, Vallat JM. Neuropathologic characterization of INF2-related Charcot-Marie-Tooth disease: Evidence for a Schwann cell actinopathy Journal of Neuropathology and Experimental Neurology. 73: 223-233. PMID 24487800 DOI: 10.1097/NEN.0000000000000047  1
2014 Neau JP, Godeneche G, Mathis S, Guillet G. Neurodermatology. Handbook of Clinical Neurology. 121: 1561-94. PMID 24365436 DOI: 10.1016/B978-0-7020-4088-7.00104-8  1
2013 Mathis S, Bataille B, Boucebci S, Jeantet M, Ciron J, Vandamme L, Neau JP. A rare cause of stroke in young adults: occlusion of the middle cerebral artery by a meningioma postpartum. Case Reports in Neurological Medicine. 2013: 652538. PMID 24198989 DOI: 10.1155/2013/652538  1
2013 Ricard E, Mathis S, Magdelaine C, Delisle MB, Magy L, Funalot B, Vallat JM. CMT4D (NDRG1 mutation): genotype-phenotype correlations. Journal of the Peripheral Nervous System : Jpns. 18: 261-5. PMID 24028195 DOI: 10.1111/jns5.12039  1
2013 Vallat JM, Mathis S, Funalot B. The various Charcot-Marie-Tooth diseases. Current Opinion in Neurology. 26: 473-80. PMID 23945280 DOI: 10.1097/WCO.0b013e328364c04b  1
2013 Ciron J, Godenèche G, Vandamme X, Rosier MP, Sharov I, Mathis S, Larrieu D, Neau JP. Obstetrical outcome of young women with a past history of cerebral venous thrombosis. Cerebrovascular Diseases (Basel, Switzerland). 36: 55-61. PMID 23921093 DOI: 10.1159/000351507  1
2013 Gizon L, Ballot J, Michel E, Stahn T, Vauclair G, Bruntt H, Quirion PO, Benomar O, Vauclair S, Appourchaux T, Auvergne M, Baglin A, Barban C, Baudin F, Bazot M, ... ... Mathis S, et al. Seismic constraints on rotation of Sun-like star and mass of exoplanet. Proceedings of the National Academy of Sciences of the United States of America. 110: 13267-71. PMID 23898183 DOI: 10.1073/Pnas.1303291110  1
2012 Ciron J, Colin O, Larrieu D, Benatru I, Mathis S, Vandermarcq P, Neau JP. Oculomotor and gait disturbance during pregnancy. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 19: 1426; answer 1468. PMID 23139937 DOI: 10.1016/j.jocn.2011.12.020  1
2012 Ciron J, Blanc JL, Bouamama N, Mathis S, Neau JP. Syrinx exceptionally revealed by isolated bilateral Horner's syndrome. European Neurology. 68: 259. PMID 23006676 DOI: 10.1159/000340042  1
2012 Neau JP, Paquereau J, Auche V, Mathis S, Godeneche G, Ciron J, Moinot N, Bouche G. Sleep disorders and multiple sclerosis: a clinical and polysomnography study. European Neurology. 68: 8-15. PMID 22627080 DOI: 10.1159/000335076  1
2012 Mathis S, du Boisguéheneuc F, Godenèche G, Ansquer S, Neau JP. Bilateral femoral neuropathy after massive toxic ingestion in a suicide attempt. The Neurologist. 18: 70-2. PMID 22367832 DOI: 10.1097/NRL.0b013e318247b9bf  1
2012 Mathis S, Magy L, Diallo L, Boukhris S, Vallat JM. Amyloid neuropathy mimicking chronic inflammatory demyelinating polyneuropathy. Muscle & Nerve. 45: 26-31. PMID 22190302 DOI: 10.1002/mus.22229  1
2012 Mathis S, Dupuis-Girod S, Plauchu H, Giroud M, Barroso B, Ly KH, Ingrand P, Gilbert B, Godenèche G, Neau JP. Cerebral abscesses in hereditary haemorrhagic telangiectasia: a clinical and microbiological evaluation. Clinical Neurology and Neurosurgery. 114: 235-40. PMID 22093524 DOI: 10.1016/j.clineuro.2011.10.036  1
2011 Magy L, Mathis S, Vallat JM. Diagnostic and therapeutic challenges in chronic inflammatory demyelinating polyneuropathy and other immune-mediated neuropathies. Current Opinion in Critical Care. 17: 101-5. PMID 21157311 DOI: 10.1097/MCC.0b013e328342aded  1
2011 Mathis S, Maisonobe T, Neau JP. Neuropathy in Wolfram syndrome. European Journal of Medical Genetics. 54: 73-5. PMID 20888932 DOI: 10.1016/j.ejmg.2010.09.011  1
2010 Neau JP, Marion P, Mathis S, Julian A, Godeneche G, Larrieu D, Meurice JC, Paquereau J, Ingrand P. Restless legs syndrome and pregnancy: follow-up of pregnant women before and after delivery. European Neurology. 64: 361-6. PMID 21088424 DOI: 10.1159/000322124  1
2010 Neau JP, Porcheron A, Mathis S, Julian A, Meurice JC, Paquereau J, Godeneche G, Ciron J, Bouche G. Restless legs syndrome and pregnancy: a questionnaire study in the Poitiers District, France. European Neurology. 64: 268-74. PMID 20980760 DOI: 10.1159/000321413  1
2010 Mathis S, Balaboi I, Nocon C, Marsac E, Neau JP. Tibial ischemic neuropathy as an unusual complication of interventional radiology. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 17: 1353-4. PMID 20599385 DOI: 10.1016/j.jocn.2010.02.012  1
2010 Wang X, Zhang W, Huang H, Preter M, Sahraian MA, Khorramnia S, Ebrahim MM, Moinfar Z, Lotfi J, Pakdaman H, Staykov D, Huttner HB, Kollmar R, Ganslandt O, Doerfler A, ... ... Mathis S, et al. Contents Vol. 64, 2010 European Neurology. 64. DOI: 10.1159/000322711  1
2010 Wang X, Zhang W, Huang H, Preter M, Sahraian MA, Khorramnia S, Ebrahim MM, Moinfar Z, Lotfi J, Pakdaman H, Staykov D, Huttner HB, Kollmar R, Ganslandt O, Doerfler A, ... ... Mathis S, et al. Subject Index Vol. 64, 2010 European Neurology. 64: 369-370. DOI: 10.1159/000322710  1
2008 Mathis S, Scheper GC, Baumann N, Petit E, Gil R, van der Knaap MS, Neau JP. The ovarioleukodystrophy. Clinical Neurology and Neurosurgery. 110: 1035-7. PMID 18678442 DOI: 10.1016/j.clineuro.2008.06.002  1
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