Zobrazeno 1 - 10
of 92
pro vyhledávání: '"H. Karasoy"'
Autor:
Elçin Bora, Koray Koçoğlu, Gülden Akdal, H. Karasoy, İhsan Şükrü Şengün, Ayşe Nur Yüceyar, Özgül Ekmekci, Tural Tanriverdizade, Fikret Bademkiran
Publikováno v:
Journal of Neurology. 268:526-531
Objective: To find out if Charcot–Marie–Tooth (CMT) patients, who have peripheral vestibular as well as peripheral somatosensory impairment, have worse postural balance than those who do not. Methods: We studied 32 patients with various CMT pheno
Autor:
Ibrahim Aydoğdu, H. Karasoy, Aycin Yıldız Tabakoglu, Şeyma Çiftçi, Ayşe Güler, Fikret Bademkiran, Ayşen Süzen Ekinci
Publikováno v:
Neurological Sciences and Neurophysiology. 35:189-192
WOS: 000458116700006
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a syndrome which is characterized as mitochondrial myopathy, encephalopathy, lactic acidosis and recurrent stroke-like episodes. Re
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a syndrome which is characterized as mitochondrial myopathy, encephalopathy, lactic acidosis and recurrent stroke-like episodes. Re
Autor:
Eser Yıldırım Sözmen, Mahmut Çoker, Ayşe Nur Yüceyar, H. Karasoy, Melisa Vural, Erhan Canbay, Sema Kalkan Uçar, Ebru Sezer
Background Recently, urinary excretion of the tetrasaccharide 6-α-D-glucopyranosyl-maltotriose (Glc4) has been proposed as a marker for the diagnosis and monitoring of Pompe disease (PD). We aimed to determine the reference intervals and reliable de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb83fb977cb5883563ab0acb7464a0ae
https://hdl.handle.net/11454/62636
https://hdl.handle.net/11454/62636
Autor:
Gökhan Uyanik, Kerstin Becker, Peter Nürnberg, Hülya-Sevcan Daimagüler, Akgun Olmez, Rosanne Sprute, Francesco Muntoni, Salem Alawbathani, Haluk Topaloglu, Hannah Jergas, Hormos Salimi Dafsari, Sebahattin Cirak, H. Karasoy
Autosomal-recessive mutations in the Alsin Rho guanine nucleotide exchange factor (ALS2) gene may cause specific subtypes of childhood-onset progressive neurodegenerative motor neuron diseases (MND). These diseases can manifest with a clinical contin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ab331791c0518b28091e839c1ea78b4
https://hdl.handle.net/11454/61782
https://hdl.handle.net/11454/61782
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Neuromuscular Disorders. 29:S198-S199
Publikováno v:
Neuromuscular Disorders. 25:340-344
Myosin storage myopathy (MSM) is a protein aggregate myopathy caused by the accumulation of myosin in muscle fibres and results from MYH7 mutation. Although MYH7 mutation is also an established cause of variable cardiomyopathy with or without skeleta
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Fikret Bademkiran, Tural Tanriverdizade, Ayşe Nur Yüceyar, İhsan Şükrü Şengün, Özgül Ekmekci, Gülden Akdal, Koray Koçoğlu, Gabor Michael Halmagyi, H. Karasoy
Publikováno v:
Journal of neurology. 265(2)
Chronic inflammatory demyelinating polyneuropathy (CIDP) is a common, treatable, autoimmune peripheral neuropathy considered to produce imbalance by weakness and proprioceptive impairment rather than vestibular impairment. We measured semicircular ca
Autor:
Ayşe Güler, Ibrahim Aydogdu, H. Karasoy, Ayşen Süzen Ekinci, Fikret Bademkiran, Şeyma Çiftçi, Aycin Yıldız Tabakoglu
Publikováno v:
Journal of Neurological Sciences (Turkish).