Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Henry B. Wessel"'
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
Publikováno v:
American Journal of Medical Genetics. 66:60-63
Myotonic dystrophy (DM) is a trinucleotide repeat syndrome which can contain 50 to over 2,000 CTG repeats in affected individuals, but does not express a fragile site. Although one prior study [Jalal et al., Am J Med Genet 46:441-443, 1993] did not f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f30d5f35d9d6e6ab75255f4be28068c7
https://doi.org/10.1002/(sici)1096-8628(19961202)66:1<60::aid-ajmg13>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19961202)66:1<60::aid-ajmg13>3.0.co
Publikováno v:
The Journal of Pediatrics. 121:983-985
Tardive dyskinesia is a chronic, often permanent, movement disorder that has been reported in elderly patients receiving metoclopramide. We describe an 8-year-old boy with tardive dyskinesia that developed when he received metoclopramide as part of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c4a9f8a8c7a727de58366be7056241a
https://doi.org/10.1016/s0022-3476(05)80357-9
https://doi.org/10.1016/s0022-3476(05)80357-9
Autor:
D. Daentl, Corrado Angelini, F. L. Chou, Henry B. Wessel, Anna Fidziańska, Eric P. Hoffman, Claudia M. Greco, C. Garcia, Irena Hausmanowa-Petrusewicz
Publikováno v:
Scopus-Elsevier
Objective: To determine the frequency of calpain III mutations in a heterogeneous limb–girdle muscular dystrophy (LGMD) population. Background: Mutations of the calpain III gene have been shown to cause a subset of autosomal recessive LGMDs. Patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e47c7c97af96ca5e288d81f1fb4c37e2
http://hdl.handle.net/11577/3353389
http://hdl.handle.net/11577/3353389
Publikováno v:
American journal of medical genetics. 43(6)
A 4-year-old girl was identified with high creatine kinase (CK) values, and mild muscle weakness in a limb-girdle distribution. Results of dystrophin analysis of the muscle biopsy were consistent with a manifesting heterozygote for Duchenne muscular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32d747e4b475d1b53294d94c34cadeb2
https://pubmed.ncbi.nlm.nih.gov/1415326
https://pubmed.ncbi.nlm.nih.gov/1415326
Publikováno v:
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery. 104(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc2e9064cbb6e24969a00277e07dc0b6
https://pubmed.ncbi.nlm.nih.gov/1903867
https://pubmed.ncbi.nlm.nih.gov/1903867
Autor:
Henry B Wessel
Publikováno v:
Pediatric neurology. 6(1)
Dystrophin, the protein product of the gene related to Duchenne and Becker muscular dystrophies, is a large cytoskeletal protein associated with the muscle fiber membrane. Recently identified dystrophin-related myopathies affecting animals can serve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67ed98240fcc120b3e59ea5e64748096
https://pubmed.ncbi.nlm.nih.gov/2178617
https://pubmed.ncbi.nlm.nih.gov/2178617
Autor:
Henry B. Wessel, Dachling Pang
Publikováno v:
Neurosurgery. 22:105-21
Much controversy exists regarding the pathogenesis, diagnosis, and management of thoracic outlet syndrome. The authors review the embryology of several fibroosseous anomalies at the superior thoracic aperture and relate normal and morbid anatomy of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c79603307904cb7e62c86df937a0619
https://doi.org/10.1227/00006123-198801010-00018
https://doi.org/10.1227/00006123-198801010-00018
Autor:
W. A. Kofke, Peter L. Davis, David S. Warner, Jeff Gibson, Lenore Gray, Dean Johnson, Susan K. Woelfel, Rodney I. Meeke, Kent S. Pearson, Henry B. Wessel, Richard V. Young, Adrian W. Gelb, John Koncelik
Publikováno v:
Anesthesiology. 71:653-659
General anesthesia has been recommended to control convulsive status epilepticus that is refractory to conventional anticonvulsant therapy. Halothane has been the recommended agent, but without experimental justification. Isoflurane, which has no rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebe625494ea0d27a8092f3ea1b5d6f63
https://doi.org/10.1097/00000542-198911000-00005
https://doi.org/10.1097/00000542-198911000-00005
Autor:
Basil J. Zitelli, Henry B. Wessel
Publikováno v:
Pediatric neurology. 3(4)
A 15-year-old boy is described with myasthenia gravis, hemophilia A, positive HTLV-III serology, anti-thyroglobulin and antimicrosomal antibodies, and laboratory evidence of altered cell-mediated immunity. Treatment with pyridostigmine produced drama
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b62ea89a07291fc950fc01556814b799
https://pubmed.ncbi.nlm.nih.gov/3508072
https://pubmed.ncbi.nlm.nih.gov/3508072