Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Fatih Bayrakli"'
Autor:
Fatih Bayrakli, Mehmet Canpolat, Huseyin Per, Hakan Gumus, Sefer Kumandas, Ugur Kartal, Hatice Balaban
Publikováno v:
Case Reports in Neurology, Vol 6, Iss 1, Pp 18-22 (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 of the autosomal recessive c
Externí odkaz:
https://doaj.org/article/33b61200e3bd40dca72ce2ea1fc92629
Autor:
Busra Aydin, Esra Yildirim, Onur Erdogan, Kazim Yalcin Arga, Betul Karademir Yilmaz, Suheyla Uyar Bozkurt, Fatih Bayrakli, Beste Turanli
Publikováno v:
OMICS: A Journal of Integrative Biology. 26:115-129
Innovation roadmaps are important, because they encourage the actors in an innovation ecosystem to creatively imagine multiple possible science future(s), while anticipating the prospects and challenges on the innovation trajectory. In this overarchi
Autor:
Ali Ozen, Onur Erdogan, Can Erzik, Süheyla Uyar Bozkurt, İrem Peker Eyüboğlu, Ozcan Sonmez, Mustafa Cengiz Yakicier, Fatih Bayrakli
Publikováno v:
Turkish neurosurgery. 30(3)
AIM: To identify the copy number variations that are specific to myxopapillary ependymomas (MPEs) of the cauda equina. MATERIAL and METHODS: The patient cohort included five patients who underwent resection of histologically confirmed MPEs. Tumor sam
Publikováno v:
British Journal of Neurosurgery. :1-3
We report a 45 years old female patient with a left temporal grade II oligodendroglioma that recurred on the wall of the fourth ventricle at grade II oligodendroglioma.
Autor:
Ozen Kardag, Ibrahim M. Ziyal, Adnan Dagcinar, Mustafa Sakar, Fatih Bayrakli, Şirin Yüksel, Askin Seker, Burcak Soylemez, Olcay Ünver, Yasar Bayri, Bahattin Tanrıkulu, Cagrı Canbolat, Cengiz Yakicier
Publikováno v:
Child's Nervous System. 31:1367-1370
WOS: 000358382400025
PubMed ID: 26005079
Meningomyelocele is one of the most common and socioeconomically, psychologically, and physically debilitating neurodevelopmental diseases. A few chromosomal locus and genes have been identified as r
PubMed ID: 26005079
Meningomyelocele is one of the most common and socioeconomically, psychologically, and physically debilitating neurodevelopmental diseases. A few chromosomal locus and genes have been identified as r
Autor:
Ergun Pinarbasi, Ugur Kartal, Hatice Balaban, Suat Topaktaş, Hamit Zafer Kars, Fatih Bayrakli
Publikováno v:
European Neurology. 68:111-116
WOS: 000306664500011
PubMed ID: 22797413
Background: Restless legs syndrome (RLS) is a sensorimotor disorder in which affected individuals suffer from uncomfortable sensations and an urge to move their lower limbs; it occurs mainly in resti
PubMed ID: 22797413
Background: Restless legs syndrome (RLS) is a sensorimotor disorder in which affected individuals suffer from uncomfortable sensations and an urge to move their lower limbs; it occurs mainly in resti
Autor:
Sengul Kavak Bayrakli, Adife Gulhan Ercan-Sencicek, Murat Gunel, İlter Güney, Tufan Cankaya, Kaya Bilguvar, Fatih Bayrakli, D Ceyhan, Matthew W. State, Shrikant Mane
Publikováno v:
Clinical Genetics. 77:499-502
Autor:
Ali K. Ozturk, Matthew W. State, Fatih Bayrakli, Murat Gunel, Zulfikar Arlier, Ozdem Erturk, Baris Korkmaz, Cengiz Yalcinkaya, Kaya Bilguvar, Yasar Bayri, Beyhan Tüysüz
Publikováno v:
American Journal of Medical Genetics Part A. :1039-1042
A Patient With Duchenne Muscular Dystrophy and Autism Demonstrates a Hemizygous Deletion Affecting Dystrophin Ozdem Erturk, Kaya Bilguvar, Baris Korkmaz, Yasar Bayri, Fatih Bayrakli, Zulfikar Arlier, Ali K. Ozturk, Cengiz Yalcinkaya, Beyhan Tuysuz, M
Publikováno v:
Journal of Neurosurgery: Pediatrics. 1:325-329
✓ Primary meningeal osteosarcomas are rare tumors, with only 19 reported cases in the literature; only 4 of these, including the present case, are in pediatric patients. In this report, the authors present the case of an 8-year-old boy with a histo
Autor:
Richard P. Lifton, Matthew W. State, Christopher E. Mason, Yasar Bayri, Fatih Bayrakli, Ali K. Ozturk, Murat Gunel, Cengiz Yalcinkaya, Baris Korkmaz, Kaya Bilguvar, Elif Ozdamar, Michael L. DiLuna, Beyhan Tüysüz, Aysegul Bursali
Publikováno v:
Neurogenetics. 9:119-125
Hereditary sensory and autonomic neuropathy type IV (HSAN IV), or congenital insensitivity to pain with anhidrosis, is an autosomal recessive disorder characterized by insensitivity to noxious stimuli, anhidrosis from deinnervated sweat glands, and d