Howard Feit - Publications

Affiliations: 
Albert Einstein College of Medicine, New York, New York, United States 

55 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
2014 Johnson JO, Pioro EP, Boehringer A, Chia R, Feit H, Renton AE, Pliner HA, Abramzon Y, Marangi G, Winborn BJ, Gibbs JR, Nalls MA, Morgan S, Shoai M, Hardy J, et al. Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis. Nature Neuroscience. 17: 664-6. PMID 24686783 DOI: 10.1038/Nn.3688  1
2014 Piotrowski A, Xie J, Liu YF, Poplawski AB, Gomes AR, Madanecki P, Fu C, Crowley MR, Crossman DK, Armstrong L, Babovic-Vuksanovic D, Bergner A, Blakeley JO, Blumenthal AL, Daniels MS, ... Feit H, et al. Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas. Nature Genetics. 46: 182-7. PMID 24362817 DOI: 10.1038/Ng.2855  1
2013 Nagel MA, Russman AN, Feit H, Traktinskiy I, Khmeleva N, Schmid DS, Skarf B, Gilden D. VZV ischemic optic neuropathy and subclinical temporal artery infection without rash. Neurology. 80: 220-2. PMID 23255829 DOI: 10.1212/Wnl.0B013E31827B92D1  1
2009 Senderek J, Garvey SM, Krieger M, Guergueltcheva V, Urtizberea A, Roos A, Elbracht M, Stendel C, Tournev I, Mihailova V, Feit H, Tramonte J, Hedera P, Crooks K, Bergmann C, et al. Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3. American Journal of Human Genetics. 84: 511-8. PMID 19344878 DOI: 10.1016/j.ajhg.2009.03.006  1
2009 Silbergleit AK, Feit H, Silbergleit R. Neurogenic stuttering in corticobasal ganglionic degeneration: A case report Journal of Neurolinguistics. 22: 83-90. DOI: 10.1016/j.jneuroling.2008.06.003  1
1999 Marsh DJ, Kum JB, Lunetta KL, Bennett MJ, Gorlin RJ, Ahmed SF, Bodurtha J, Crowe C, Curtis MA, Dasouki M, Dunn T, Feit H, Geraghty MT, Graham JM, Hodgson SV, et al. PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. Human Molecular Genetics. 8: 1461-72. PMID 10400993 DOI: 10.1093/Hmg/8.8.1461  1
1999 Koffman B, Junck L, Elias SB, Feit HW, Levine SR. Polyradiculopathy in sarcoidosis. Muscle & Nerve. 22: 608-13. PMID 10331360 DOI: 10.1002/(SICI)1097-4598(199905)22:5<608::AID-MUS9>3.0.CO;2-L  1
1998 Feit H, Silbergleit A, Schneider LB, Gutierrez JA, Fitoussi RP, Réyès C, Rouleau GA, Brais B, Jackson CE, Beckmann JS, Seboun E. Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31. American Journal of Human Genetics. 63: 1732-42. PMID 9837826 DOI: 10.1086/302166  1
1996 Jiang N, Chopp M, Stein D, Feit H. Progesterone is neuroprotective after transient middle cerebral artery occlusion in male rats. Brain Research. 735: 101-7. PMID 8905174 DOI: 10.1016/0006-8993(96)00605-1  1
1989 Feit H, Kawai M, Mostafapour AS. The role of collagen crosslinking in the increased stiffness of avian dystrophic muscle. Muscle & Nerve. 12: 486-92. PMID 2725576 DOI: 10.1002/mus.880120609  1
1989 Feit H. Muscular dystrophy in the chicken. Archives of Neurology. 46: 484. PMID 2712743 DOI: 10.1001/archneur.1989.00520410018014  1
1989 Feit H, Kawai M, Mostafapour AS. Increased resistance of the collagen in avian dystrophic muscle to collagenolytic attack: evidence for increased crosslinking. Muscle & Nerve. 12: 476-85. PMID 2542788 DOI: 10.1002/mus.880120608  1
1987 Levine SR, Washington JM, Jefferson MF, Kieran SN, Moen M, Feit H, Welch KM. "Crack" cocaine-associated stroke. Neurology. 37: 1849-53. PMID 3683875 DOI: 10.1212/WNL.37.12.1849  1
1987 Levine SR, Diaczok IM, Deegan MJ, Kieran SN, Feit H, Elias SB, Welch KM. Recurrent stroke associated with thymoma and anticardiolipin antibodies. Archives of Neurology. 44: 678-9. PMID 3579690 DOI: 10.1001/archneur.1987.00520180090026  1
1987 Levine SR, Kieran S, Puzio K, Feit H, Patel SC, Welch KM. Cerebral venous thrombosis with lupus anticoagulants. Report of two cases. Stroke; a Journal of Cerebral Circulation. 18: 801-4. PMID 3111017  1
1986 Feit H, Glasberg MR. Neurologic complications of gastric partitioning. Archives of Neurology. 43: 642. PMID 3015090 DOI: 10.1001/archneur.1986.00520070004003  1
1985 Feit H, Kawai M, Schulman MI. Stiffness and contractile properties of avian normal and dystrophic muscle bundles as measured by sinusoidal length perturbations. Muscle & Nerve. 8: 503-10. PMID 16758574 DOI: 10.1002/mus.880080605  1
1985 Feit H, Hammon K, Kawai M. Collagen in chemically skinned, extracted dystrophic myofibers. Muscle & Nerve. 8: 806-7. PMID 4079959 DOI: 10.1002/mus.880080910  1
1985 Feit H, Kawai M. Physiological and biochemical characterization of avian dystrophic muscle reveals alterations of collagen Annals of the New York Academy of Sciences. 431-433.  1
1985 Feit H. Reply from the Author: Acute subdural hematomas may appear isodense in anemia Neurology. 35: 141.  1
1984 Pettegrew J, Minshew N, Feit H. 31P-NMR studies of normal and dystrophic chicken muscle. Muscle & Nerve. 7: 442-6. PMID 6543898 DOI: 10.1002/Mus.880070605  1
1984 Feit H. Two-dimensional electrophoresis. Neurology. 34: 560-1. PMID 6538323 DOI: 10.1212/WNL.34.4.560  1
1984 Feit H, Domke R. Changes in turbidity during microtubule assembly in brain extracts from normal chickens and chickens with muscular dystrophy. Journal of Neurogenetics. 1: 141-52. PMID 6536723 DOI: 10.3109/01677068409107079  1
1984 Feit H, Frenkel EP, Dunn BR, Diehl J, Samson D. Acute subdural hematomas with lupus anticoagulant (procoagulant inhibitor). Neurology. 34: 519-21. PMID 6422324  1
1984 Feit H, Farrell C. The interaction of unregulated actin and myosin in avian muscular dystrophy. Muscle & Nerve. 7: 668-75. PMID 6242314 DOI: 10.1002/mus.880070813  1
1983 Feit H. Chromatin alterations in neurologic disease. Archives of Neurology. 40: 528. PMID 6870619 DOI: 10.1001/archneur.1983.04210070068023  1
1983 Feit H. Possible biochemical consequences of different subsets of contractile proteins in single dystrophic muscle fibers. Muscle & Nerve. 6: 171-2. PMID 6855801  1
1983 Feit H. ALS and parkinsonian syndromes among the Auyu and Jakai. Neurology. 33: 812. PMID 6682531  1
1983 Feit H, Cook JD, Domke R. Heterogeneity of tropomyosin and actin in normal and diseased muscle. Journal of Neurogenetics. 1: 91-103. PMID 6681443 DOI: 10.3109/01677068309107075  1
1983 Feit H, Fuseler J, Cook JD. Myofibrillar creatine kinase in Duchenne and avian muscular dystrophy. Biochemical Medicine. 29: 355-9. PMID 6615491 DOI: 10.1016/0006-2944(83)90070-4  1
1983 Feit H, Kirkpatrick J, Van Woert MH, Pandian G. Myoclonus, ataxia, and hypoventilation: response to L-5-hydroxytryptophan. Neurology. 33: 109-12. PMID 6600288 DOI: 10.1212/WNL.33.1.109  1
1983 Haller RG, Dempsey WB, Feit H, Cook JD, Knochel JP. Low muscle levels of pyridoxine in McArdle's syndrome. The American Journal of Medicine. 74: 217-20. PMID 6572033 DOI: 10.1016/0002-9343(83)90614-9  1
1982 Feit H, Domke R. Persistence of the expression of beta-tropomyosin in dystrophic avian pectoral muscle. Cell Motility. 2: 309-15. PMID 7172223  1
1982 Feit H. The contractile proteins in muscular dystrophy: an analytical review and a new hypothesis. Medical Hypotheses. 8: 319-24. PMID 7099056 DOI: 10.1016/0306-9877(82)90023-8  1
1982 Feit H. Further observations on the diagnosis and management of carotidynia. Headache. 22: 86-8. PMID 7085268  1
1982 Feit H, Stauver M, Domke R, Shay JW. Fragmentation analysis of normal and dystrophic avian muscle. Muscle & Nerve. 5: 373-81. PMID 6889679 DOI: 10.1002/Mus.880050507  1
1982 Feit H, Glasberg M, Ireton C, Rosenberg RN, Thal E. Peripheral neuropathy and starvation after gastric partitioning for morbid obesity. Annals of Internal Medicine. 96: 453-5. PMID 6279006  1
1982 Feit H, Tindall RS, Glasberg M. Sources of error in the diagnosis of Guillain-Barre syndrome. Muscle & Nerve. 5: 111-7. PMID 6122160 DOI: 10.1002/mus.880050206  1
1981 Pool KD, Feit H, Kirkpatrick J. Penicillamine-induced neuropathy in rheumatoid arthritis. Annals of Internal Medicine. 95: 457-8. PMID 7283299  1
1981 Feit H, Luby JP, Molenrich S. Brainstem encephalitis with serological evidence of St Louis encephalitis. Journal of Neurology, Neurosurgery, and Psychiatry. 44: 368. PMID 7241168  1
1980 Feit H, Shay JW. The assembly of tubulin into membranes. Biochemical and Biophysical Research Communications. 94: 324-31. PMID 7387698 DOI: 10.1016/S0006-291X(80)80224-5  1
1980 Shay JW, Feit H, Cook J. The effect of isaxonine on microtubule assembly in avian and human dystrophic cells. Transactions of the American Neurological Association. 105: 359-61. PMID 6897469  1
1980 Shay JW, Feit H. Avian muscular dystrophy: Microtubules, righting ability, CPK and muscle histology following isaxonine treatment European Journal of Cell Biology. 22: P1657.  1
1979 Shay JW, Cook J, Fuseler JW, Feit H, Thomas LE, Studt JL. Microtubules and Duchenne muscular dystrophy. Transactions of the American Neurological Association. 104: 12-5. PMID 553386  1
1979 Feit H. A form of chorea that responds to dantrolene sodium. Neurology. 29: 1631-2. PMID 159420  1
1979 Fuseler JW, Feit H, Shay JW. The effects of antimitotic agents on intermediate filaments of brain cells Journal of Cell Biology. 83: No. MT1874.  1
1977 Feit H, Neudeck U, Shay J. Anomalous electrophoretic properties of brain filament protein subunits. Brain Research. 133: 341-9. PMID 902097 DOI: 10.1016/0006-8993(77)90769-7  1
1977 Feit H, Neudeck U, Baskin F. Comparison of the isoelectric and molecular weight properties of tubulin subunits. Journal of Neurochemistry. 28: 697-706. PMID 894278  1
1977 Feit H, Kelly P, Cotman CW. Identification of a protein related to tubulin in the postsynaptic density. Proceedings of the National Academy of Sciences of the United States of America. 74: 1047-51. PMID 265548 DOI: 10.1073/Pnas.74.3.1047  1
1976 Feit H, Brooke MH. Myophosphorylase deficiency: two different molecular etiologies. Neurology. 26: 963-7. PMID 1066528 DOI: 10.1212/WNL.26.10.963  1
1975 Feit H, Shelanski ML. Is tubulin a glycoprotein? Biochemical and Biophysical Research Communications. 66: 920-7. PMID 1180946 DOI: 10.1016/0006-291X(75)90728-7  1
1972 Shelanski ML, Feit H, Berry RW, Daniels MP. Some biochemical aspects of neurotubule and neurofilament proteins. Advances in Experimental Medicine and Biology. 32: 55-67. PMID 4671991 DOI: 10.1007/978-1-4684-6979-0_6  1
1971 Feit H, Slusarek L, Shelanski ML. Heterogeneity of tubulin subunits. Proceedings of the National Academy of Sciences of the United States of America. 68: 2028-31. PMID 5289362 DOI: 10.1073/Pnas.68.9.2028  1
1971 Feit H, Dutton GR, Barondes SH, Shelanski ML. Microtubule protein. Identification in and transport to nerve endings. The Journal of Cell Biology. 51: 138-47. PMID 5111874 DOI: 10.1083/Jcb.51.1.138  1
1970 Feit H, Barondes SH. Colchicine-binding activity in particulate fractions of mouse brain. Journal of Neurochemistry. 17: 1355-64. PMID 5496387 DOI: 10.1111/J.1471-4159.1970.Tb06870.X  1
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