Zobrazeno 1 - 10
of 25
pro vyhledávání: '"V. V. Vedanarayanan"'
Publikováno v:
Current rheumatology reports. 20(8)
While sporadic inclusion body myositis (sIBM) is the most common acquired muscle disease after age 50, the pathogenesis of this disease is still poorly understood. In this review, we discuss our current state of knowledge in sIBM and provide an updat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4741be4e048dda471c65591b18e94e40
https://pubmed.ncbi.nlm.nih.gov/29955981
https://pubmed.ncbi.nlm.nih.gov/29955981
Publikováno v:
Journal of Clinical Neuromuscular Disease. 12:76-79
Familial occurrence of myasthenia gravis is uncommon and reports of maternal transmission of muscle-specific tyrosine kinase (MuSK) antibody myasthenia are rarer still. We report two families with maternal transmission of MuSK antibody myasthenia gra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b4ea3676ec4991107c1925ac7c27e53
https://doi.org/10.1097/cnd.0b013e3181f8a9aa
https://doi.org/10.1097/cnd.0b013e3181f8a9aa
Autor:
Anne M. Connolly, Jennifer Huang, Masanori Igarashi, V. V. Vedanarayanan, Erik K Henricson, Julaine Florence, Diana M. Escolar, Henry B. Wessel, Yoram Nevo, Robert McCarter, Paula R. Clemens, Thomas P. Mayhew, S. H. Subramony, Kantilal M. Patel, Nathalie Goemans, Ksenija Gorni, Carolina Tesi-Rocha, J. Mayhew, Alan Pestronk, Jose Carlo, Livia Pasquali, Susan T. Iannaccone, Tulio E. Bertorini, Gunnar Buyse, Robert T. Leshner
Publikováno v:
Annals of Neurology. 58:151-155
We tested the efficacy and safety of glutamine (0.6 gm/kg/day) and creatine (5 gm/day) in 50 ambulant boys with Duchenne muscular dystrophy in a 6-month, double-blind, placebo-controlled clinical trial. Drug efficacy was tested by measuring muscle st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a194e4f171e5e0bfd18e201b145ef85b
https://doi.org/10.1002/ana.20523
https://doi.org/10.1002/ana.20523
Autor:
C. Semino-Mora, S. H. Subramony, Mark R. Davis, Nigel G. Laing, Peter C. Scacheri, Eric P. Hoffman, A. Senchak, V. V. Vedanarayanan, Jonathan D. Fratkin
Publikováno v:
Neurology. 55:1689-1696
Background: Central core disease (CCD) and nemaline rod myopathy are generally considered two genetically and histologically distinct disorders. CCD is defined by the presence of well-demarcated round cores within most myofibers. Nemaline rod myopath
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38d3e31afb03aa2bcb45fbf8bedafd5d
https://doi.org/10.1212/wnl.55.11.1689
https://doi.org/10.1212/wnl.55.11.1689
Autor:
Mohamed Lehar, James A. Russell, Donald R. Johns, Ralph W. Kuncl, V. V. Vedanarayanan, Ricardo Fadic
Publikováno v:
Neurology. 49:239-245
Four unrelated patients presented with a severe sensory ataxic neuropathy in association with dysarthria and chronic progressive external ophthalmoplegia. Electrophysiologic and pathologic studies showed severe axonal loss disproportionately affectin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84d5e537541f3b63ac1c8dd910e8fc6b
https://doi.org/10.1212/wnl.49.1.239
https://doi.org/10.1212/wnl.49.1.239
Publikováno v:
Neuropediatrics. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0808db71cc032b62f7c735664552d2e4
https://doi.org/10.1055/s-2006-943666
https://doi.org/10.1055/s-2006-943666
Autor:
V. V. Vedanarayanan, Nimish J. Thakore, C. A. Crowe, Peter C. Scacheri, E. M. Gillanders, M. Bingler, Eric P. Hoffman, S. H. Subramony
Publikováno v:
Neurology. 58(4)
Objective: To investigate the molecular basis of autosomal dominant limb-girdle muscular dystrophy (AD-LGMD) in three large new families. Methods andResults: Genome-wide linkage was performed to show that the causative gene in all three families loca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a57ebee01feb5a6a0059e1d656267767
https://pubmed.ncbi.nlm.nih.gov/11865138
https://pubmed.ncbi.nlm.nih.gov/11865138
Publikováno v:
Musclenerve. 21(11)
Peripheral neuropathy is an uncommon cause of generalized hypotonia and weakness in infancy. It occurs as a part of the clinical syndrome in some neurodegenerative disorders of infancy, but seldom causes respiratory failure or swallowing difficulties
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::17a2840d0b731745930de4fa70f81fc9
https://pubmed.ncbi.nlm.nih.gov/9771672
https://pubmed.ncbi.nlm.nih.gov/9771672
Publikováno v:
Neurology. 41(6)
We treated four children with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) with high-dose intravenous immunoglobulin (IVIG). All patients received 400 mg/kg of IVIG a day for 5 days during relapses, and one patient received additi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11ead0877a6e8c908f1a75c46454f0c8
https://pubmed.ncbi.nlm.nih.gov/2046925
https://pubmed.ncbi.nlm.nih.gov/2046925
Publikováno v:
Journal of Pediatric Hematology/Oncology. 19:382
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce24dc55be49bebaf278a89a2a8749b4
https://doi.org/10.1097/00043426-199707000-00088
https://doi.org/10.1097/00043426-199707000-00088