Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Hanife Gülden Düzkalir"'
Autor:
Hanife Gülden Düzkalır, Rasim Yılmazer
Publikováno v:
Turkish Archives of Otorhinolaryngology, Vol 61, Iss 3, Pp 142-145 (2023)
Congenital agenesis of the stapes and the oval window is rare. Congenital stapedial agenesis (CSA) may be recognized preoperatively in the presence of conductive hearing loss. The principal radiological imaging approach of the temporal bone, computed
Externí odkaz:
https://doaj.org/article/f4b5d03cc3a94fc6a1283e3b3414505c
Publikováno v:
Romanian Neurosurgery, Vol 33, Iss 4 (2019)
The systemic vasculitis of the small-medium arteries, arterioles, venules and rarely large arteries that involves respiratory system and kidneys was defined as Granulomatosis with Polyangiitis (GPA) disease by Wegener in 1936. Intracranial aneurysms
Externí odkaz:
https://doaj.org/article/720f83363a944858bb76289f44cef548
Autor:
Hanife Gülden Düzkalır, Emine Çalışkan
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 14, Iss 2, Pp 110-117 (2024)
Objective: We aimed to investigate whether idiopathic cuneate gyrus herniation (ICH) is an anomaly or a normal variant, its prevalence, whether there is a coexisting finding or pathology, as well as to characterize it with magnetic resonance imaging
Externí odkaz:
https://doaj.org/article/03a9e4bb19c44d29b727cf8021d0e772
Publikováno v:
Romanian Neurosurgery. :438-442
The systemic vasculitis of the small-medium arteries, arterioles, venules and rarely large arteries that involves respiratory system and kidneys was defined as Granulomatosis with Polyangiitis (GPA) disease by Wegener in 1936. Intracranial aneurysms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34271341727b7a9120a22cdb2a110d60
https://doi.org/10.33962/roneuro-2019-069
https://doi.org/10.33962/roneuro-2019-069
Publikováno v:
İstanbul Medical Journal, Vol 25, Iss 2, Pp 137-142 (2024)
Introduction: The prevalence and association of type 1 diabetes mellitus (T1D) and non-alcoholic fatty liver disease (NAFLD) have been explored; however, no study has examined liver parenchyma elasticity in pediatric T1D patients without NAFLD. Two-d
Externí odkaz:
https://doaj.org/article/02e40a847e6848ad9305b781817dc61a
Autor:
Nail Demirel, Ceyhun Saymaz, Mustafa Kaya, Hanife Gülden Düzkalir, Berrin Aktekin, Selcuk Ozdogan, Basar Sarikaya, Ali Haluk Duzkalir, Cumhur Kaan Yaltirik
Publikováno v:
The American Journal of Case Reports
WOS: 000417191500001
PubMed: 29192135
Patient: Male, 11 Final Diagnosis: Haberland syndrome Symptoms: Seizure Medication: - Clinical Procedure: Medical treatment Specialty: Neurosurgery Objective: Rare disease Background: Encephalocraniocut
PubMed: 29192135
Patient: Male, 11 Final Diagnosis: Haberland syndrome Symptoms: Seizure Medication: - Clinical Procedure: Medical treatment Specialty: Neurosurgery Objective: Rare disease Background: Encephalocraniocut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec310c3d62ef55143b72c0fe1db22047
https://doi.org/10.12659/ajcr.907685
https://doi.org/10.12659/ajcr.907685
Publikováno v:
World neurosurgery. 115
Kotil, Kadir (Arel Author)
BACKGROUND: The treatment options for patients with Chiarimalformation type 1 (CM1) and Chiarimalformation type 1.5 (CM1.5) have not yet been standardized. In these malformations, the main factors include obstruction a
BACKGROUND: The treatment options for patients with Chiarimalformation type 1 (CM1) and Chiarimalformation type 1.5 (CM1.5) have not yet been standardized. In these malformations, the main factors include obstruction a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6908aadeeca006a311786869859cf639
https://pubmed.ncbi.nlm.nih.gov/29698796
https://pubmed.ncbi.nlm.nih.gov/29698796