Browsing by Author "Balaban H."
Now showing items 1-6 of 6
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Anti-aquaporin-4 antibody positive relapsing neuromyelitis optica in a patient with systemic lupus erythematosus [Sistemik lupus eritematozuslu bir olguda anti-aquaporin-4 antikor pozitifli?i ile seyreden relapsing nöromiyelitis optika]
Kayim Yildiz Ö.; Balaban H.; Şenel S. (2011)Neuromyelitis optica (NMO) is a rare inflammatory disorder of the central nervous system characterized by optic neuritis and myelitis. NMO may rarely be accompanied by systemic autoimmune disease including systemic lupus ... -
A database for screening and registering late onset Pompe disease in Turkey
Gokyigit M.C.; Ekmekci H.; Durmus H.; Karlı N.; Koseoglu E.; Aysal F.; Kotan D.; Ali A.; Koytak P.K.; Karasoy H.; Yaman A.; Sengun İ.S.; Sayin R.; Tiftikcioglu B.I.; Soysal A.; Tutkavul K.; Bayrak A.O.; Kısabay A.; Elci M.A.; Yayla V.; Yılmaz İ.A.; Ozdamar S.E.; Erdogan C.; Tasdemir N.; Serdaroglu Oflazer P.; Deymeer F.; Parman Y.; Kendirci M.; Sayan S.; Celebi L.G.; Uluç K.; Tanrıdağ T.; Yuceyar N.; Ekmekci O.; Colakoglu B.D.; Ozturk S.; Tireli H.; Selcuki D.; Neyal A.M.; Kayran Y.; Aluclu M.U.; Koyuncuoglu H.R.; Tokucoglu F.; Secil Y.; Guney F.; Gozke E.; Balaban H.; Akalın M.A.; Koc A.F.; Mulayim S.; Turgut N.; Turkish Study Group for Late Onset Pompe Disease (Elsevier Ltd, 2018)The aim of this study was to search for the frequency of late onset Pompe disease (LOPD) among patients who had a myopathy with unknown diagnosis registered in the pre-diagnostic part of a novel registry for LOPD within a ... -
The effect of pentoxiphylline, a nonspecific phospodiesterase inhibitor, on angiogenesis in chicken chorioallantoic membrane (CAM) model
Altuntaş E.E.; Balaban H.; Uysal I.O.; Akin P.Z. (2011)Objectives: Based on a neovascularization study conducted using specific phosphodiesterase inhibitors in the literature, the aim of the present study was to answer the question "As specific phosphodiesterase inhibitors ... -
A family with mental retardation, epilepsy and cerebellar hypoplasia showing linkage to chromosome 20p11.21-q11.23
Bayrakli F.; Canpolat M.; Per H.; Gumus H.; Kumandas S.; Kartal U.; Balaban H. (2014)Background: Cerebellar hypoplasia (CH) is a rare malformation caused by various etiologies, usually manifesting clinically as nonprogressive cerebellar ataxia with or without mental retardation. The molecular pathogenesis ... -
Presentation of the cerebellar abscess and sigmoid sinus septic thrombosis secondary to chronic otitis media: Case presentation and literature review
Polat K.; Altuntaş E.E.; Durmuş K.; Özüm Ü.; Balaban H.; Müderris S. (2011)Cerebellar abscess is a serious complication of ear disease. In the present report, a case of cerebellar abscess and thrombosis of the sigmoid sinus, secondary to chronic otitis media is described. A 25-year-old male ... -
Vocal cord paralysis in multifocal motor neuropathy: A case report [Multifokal motor nöropatide vokal kord paralizisi: Olgu sunumu]
Multifocal motor neuropathy is characterized by a slow, progressive, asymmetrical weakness of the extremities without sensory loss. The disease can also cause vocal cord paralysis as it runs its course. A 34-year-old man ...