Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mohammed Al-Lozi"'
Publikováno v:
Muscle & Nerve. 40:960-966
Ultrasound has been used for visualizing peripheral nerve pathology. Our goal was to use ultrasound to quantitate the sizes of upper extremity nerves along their length in control subjects and patients with neuropathy. We measured median and ulnar ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e1fca75a4010070e446ddf0bf22544e
https://doi.org/10.1002/mus.21431
https://doi.org/10.1002/mus.21431
Publikováno v:
Annals of Neurology. 37:41-46
We evaluated a 69-year-old man with Waldenström's macroglobulinemia (IgM-kappa M-protein) and progressive weakness over 2 to 3 years. The neurological examination showed symmetrical, predominantly proximal weakness. Electrophysiological testing reve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0ae7d8cdcd66a4da9514f8a164cdae9
https://doi.org/10.1002/ana.410370109
https://doi.org/10.1002/ana.410370109
Autor:
Sara E. Miller, Conrad C. Weihl, Mohammed Al-Lozi, Robert H. Baloh, Craig M. Zaidman, Alan Pestronk
Homozygous mutations in the UDP- N -acetylglucosamine 2-epimerase/ N -acetylmannosamine kinase ( GNE ) gene cause hereditary inclusion body myopathy type 2 (HIBM2). We describe two unrelated American patients with novel GNE mutations. While one patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9ed7e2210cc1cf78c1e0a0147c8bca5
https://europepmc.org/articles/PMC3030125/
https://europepmc.org/articles/PMC3030125/
Publikováno v:
Musclenerve. 40(6)
Ultrasound has been used for visualizing peripheral nerve pathology. Our goal was to use ultrasound to quantitate the sizes of upper extremity nerves along their length in control subjects and patients with neuropathy. We measured median and ulnar ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7f9b8be746103fe6307f6a43f7610987
https://pubmed.ncbi.nlm.nih.gov/19697380
https://pubmed.ncbi.nlm.nih.gov/19697380
Autor:
Anne M. Connolly, Alan Pestronk, Yoram Nevo, Mohammed Al-Lozi, Alexander Parsadanian, Jeffrey L. Elliott
Publikováno v:
Pediatric neurology. 21(1)
The purpose of this study was to search for STA gene defects in three families with clinically typical Emery-Dreifuss muscular dystrophy. Emery-Dreifuss is an X-linked muscular dystrophy with humeroperoneal weakness and life-threatening, but treatabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b12d5d23e0016bdfa3c4c9b976f42053
https://pubmed.ncbi.nlm.nih.gov/10428430
https://pubmed.ncbi.nlm.nih.gov/10428430