Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Reem Alhammad"'
Publikováno v:
Neurology. 95:933-938
A 40-year-old man presented with slowly progressive weakness and eyelid droopiness. His symptoms began in his early 30s as increased fatigue with exertion. In his mid 30s, he developed droopy eyelids without double vision. About 3 years before presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8058bb8c5eae524dc66118c6c35b196
https://doi.org/10.1212/wnl.0000000000010613
https://doi.org/10.1212/wnl.0000000000010613
Autor:
Reem Alhammad, William J. Litchy, Jenny L. Davies, Peter J. Dyck, P. James B. Dyck, Rickey E. Carter
Publikováno v:
MusclenerveREFERENCES. 65(2)
Variable differences of nerve conduction amplitudes vs velocities and distal latencies (DLs) of healthy subjects assessed in ethnic cohorts. Introduction/aims The variables affecting reference compound muscle (CMAP) and sensory nerve action potential
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::298ca96f5c50aebe50412a080e37dac5
https://pubmed.ncbi.nlm.nih.gov/34766354
https://pubmed.ncbi.nlm.nih.gov/34766354
Autor:
Reem Alhammad, Teerin Liewluck
Publikováno v:
Neuromuscular Disorders. 29:39-47
Granulomatous myopathies are etiologically heterogeneous myopathies, pathologically characterized by the presence of intramuscular granulomas. Treatment outcomes are variable. We aimed to identify prognostic factors of treatment outcomes in myopathie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::475006a3b779df17a4494d2454343de9
https://doi.org/10.1016/j.nmd.2018.10.007
https://doi.org/10.1016/j.nmd.2018.10.007
Autor:
Heidi J. Turner, Roxanna S. Dronca, Michelle L. Mauermann, Jennifer A. Tracy, Christopher J. Klein, Nathan P. Staff, Lisa A. Kottschade, Reem Alhammad
Publikováno v:
Mayo Clinic Proceedings: Innovations, Quality & Outcomes, Vol 1, Iss 2, Pp 192-197 (2017)
Recently, guidelines have been outlined for management of immune-related adverse events occurring with immune checkpoint inhibitors in cancer, irrespective of affected organ systems. Increasingly, these complications have been recognized as including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e838ce42f4601df5e1262c04aa95c65
https://doi.org/10.1016/j.mayocpiqo.2017.07.004
https://doi.org/10.1016/j.mayocpiqo.2017.07.004
Autor:
Ellen D. McPhail, Michelle L. Mauermann, Reem Alhammad, Teerin Liewluck, Marcus V. Pinto, P. James B. Dyck, Martha Grogan, Margherita Milone
Publikováno v:
MusclenerveREFERENCES. 61(1)
Introduction Although peripheral neuropathy and cardiomyopathy are well-recognized manifestations of transthyretin (ATTR) amyloidosis, myopathy has been rarely reported. Methods In this study we reviewed our muscle biopsy database (January 1998 to Ju
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a56a1bb68a6cfe13e2b0dd514c422274
https://pubmed.ncbi.nlm.nih.gov/31639223
https://pubmed.ncbi.nlm.nih.gov/31639223
Autor:
Teerin Liewluck, Reem Alhammad
Publikováno v:
Neurology. 95:1023.2-1024
We read with great interest the recent article by Dr. Dieudonne et al.1 The authors reported the high prevalence of sporadic inclusion body myositis (SIBM) in patients with granulomatous myositis, and a significant proportion of these SIBM patients a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fd04904896c5eb1334da9655f89c770
https://doi.org/10.1212/wnl.0000000000011068
https://doi.org/10.1212/wnl.0000000000011068
Autor:
Elie Naddaf, Reem Alhammad
Publikováno v:
Journal of the Neurological Sciences. 405:36
Dropped head syndrome can be the presenting feature of a wide spectrum of neurological conditions. In this study, we aimed to define the clinical characteristics and treatment outcomes of 107 patients, where head drop was the presenting or predominan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c73f6378f9e530b6171d2ba4424ac75b
https://doi.org/10.1016/j.jns.2019.10.280
https://doi.org/10.1016/j.jns.2019.10.280