Howard Feit

Albert Einstein College of Medicine, New York, New York, United States 
"Howard Feit"
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Johnson JO, Pioro EP, Boehringer A, et al. (2014) Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis. Nature Neuroscience. 17: 664-6
Piotrowski A, Xie J, Liu YF, et al. (2014) Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas. Nature Genetics. 46: 182-7
Nagel MA, Russman AN, Feit H, et al. (2013) VZV ischemic optic neuropathy and subclinical temporal artery infection without rash. Neurology. 80: 220-2
Senderek J, Garvey SM, Krieger M, et al. (2009) 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
Silbergleit AK, Feit H, Silbergleit R. (2009) Neurogenic stuttering in corticobasal ganglionic degeneration: A case report Journal of Neurolinguistics. 22: 83-90
Marsh DJ, Kum JB, Lunetta KL, et al. (1999) 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
Koffman B, Junck L, Elias SB, et al. (1999) Polyradiculopathy in sarcoidosis. Muscle & Nerve. 22: 608-13
Feit H, Silbergleit A, Schneider LB, et al. (1998) 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
Jiang N, Chopp M, Stein D, et al. (1996) Progesterone is neuroprotective after transient middle cerebral artery occlusion in male rats. Brain Research. 735: 101-7
Feit H, Kawai M, Mostafapour AS. (1989) The role of collagen crosslinking in the increased stiffness of avian dystrophic muscle. Muscle & Nerve. 12: 486-92
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