Zobrazeno 1 - 10
of 267
pro vyhledávání: '"E Kararizou"'
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 2-4 (2014)
Background/aims: Pompe disease is a rare metabolic disorder caused by deficiency of the lysosomal enzyme acid alpha-glycosidase (GAA). The late onset form of the disease is characterized by muscle weakness and respiratory involvement of variable seve
Externí odkaz:
https://doaj.org/article/a8f4b0a673034764af6ea10f8fda2072
Background: Primary headaches, and particularly migraine and tension-type headache (TTH) as well as hypothyroidism are common medical conditions. To date, numerous studies have suggested a possible bidirectional relationship between migraine and hypo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::e3208cfffef3591810fbc7b29ef8da97
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997414
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997414
Despite recent advances in genetics, in most cases of Amyotrophic Lateral Sclerosis (ALS) no etiological factor can be identified. Cerebral Arteriovenous Malformations (AVMs) have been associated with ALS development in a few studies, but the nature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::3a32d515c21084bfb3a39e4a9d7b57f5
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2998008
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2998008
Verbal and Figural Fluency in Temporal Lobe Epilepsy: Does Hippocampal Sclerosis Affect Performance?
Background and Objectives: Clinicians commonly use verbal and nonverbal measures to test fluency in patients with epilepsy, either during routine cognitive assessment or as part of pre- A nd postsurgical evaluation. We hypothesized that patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::a3ed129216d253e5a348e43ace62d9e4
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2983399
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2983399
Autor:
Bougea, A. Velonakis, G. Spantideas, N. Anagnostou, E. Paraskevas, G. Kapaki, E. Kararizou, E.
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) was previously considered a rare, early-onset recessive form of small-vessel disease (SVD) caused by biallelic mutations in the serine protease gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::194bc5e865e8937d33b3a5f234166c96
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3108107
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3108107
Ocular motor cranial nerve palsies of viral etiology are uncommon and, when accompanied by skin lesions, zoster ophthalmicus is the most frequent diagnosis. We describe the case of a 68-year-old woman who developed fourth and sixth nerve palsies 3 da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::d964854b5ce0cddc729d399568bdef1c
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3125250
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3125250
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