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pro vyhledávání: '"N. Gadoth"'
Autor:
N. Gadoth
Publikováno v:
Medical Research Archives. 8
Attention Deficit Hyperactivity Disorder (ADHD) is a quite common neuropsychiatric ailment affecting all ages. The diagnosis is based on clinical judgement without a biological diagnostic marker. Thus, both over – and – underdiagnoses are not a r
Autor:
N. Gadoth
Publikováno v:
Unexplained Fever ISBN: 9780367811037
Unexplained Fever
Unexplained Fever
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac804486db12936c93ee4838546d3b9c
https://doi.org/10.1201/9780367811037-3
https://doi.org/10.1201/9780367811037-3
Autor:
N. Gadoth
Publikováno v:
Unexplained Fever ISBN: 9780367811037
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f16aef3669792650b7f54699edf8983d
https://doi.org/10.1201/9780367811037-12
https://doi.org/10.1201/9780367811037-12
Long-term glutamate supplementation failed to protect against peripheral neurotoxicity of paclitaxel
Autor:
D. Loven, Y. Karmon, H. Levavi, M. Andras, A. Fishman, N. Gadoth, G. Sabach, R. Zart, T. Levi, R. Dabby
Publikováno v:
European Journal of Cancer Care. 18:78-83
Toxic peripheral neuropathy is still a significant limiting factor for chemotherapy with paclitaxel (PAC), although glutamate and its closely related amino acid glutamine were claimed to ameliorate PAC neurotoxicity. This pilot trial aimed to evaluat
Publikováno v:
Clinical Genetics. 50:498-501
Pachygyria is a rare development disorder resulting from impaired neuronal migration. Usually, it is a sporadic phenomenon, but rare dominant or autosomal recessive syndromes are known. This report describes a family in which the parents are first co
Autor:
Emmanuel Mignot, Betty Lo, N. Gadoth, Juliette Faraco, Patricia Franco, Jamie M. Zeitzer, Jennifer File, Michel Lecendreux, Isabelle Arnulf, Ling Lin
Publikováno v:
Annals of Neurology. 63:482-493
Objective: Kleine–Levin syndrome is a rare disorder characterized by relapsing-remitting episodes of hypersomnia, cognitive disturbances, and behavioral disturbances, such as hyperphagia and hypersexuality. Methods: We collected detailed clinical d
Autor:
N Gadoth, Haim Sohmer
Publikováno v:
Clinical Neurophysiology. 113:171-174
Publikováno v:
Acta Neurologica Scandinavica. 102:299-302
Objective - To evaluate the prevalence of neurological abnormalities in patients with ET and attempt to identify risk factors for neurological complications. Method - Ninety-five patient charts were reviewed from January 1983-July 1999. Seventy patie
Publikováno v:
American Journal of Medical Genetics. 71:156-159
Myotonic dystrophy (DM) is associated with an increased number of CTG repeats in the 3' untranslated region of the myotonin gene. Because DM has been observed less frequently in Ashkenazic Jews and non-Jews than in North African and Yemenite Jews in