Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Hülya Maraş Genç"'
Autor:
Bülent Kara, Filiz Mine Çizmecioğlu Jones, Emek Uyur Yalçın, Hülya Maraş Genç, Bengü Altınordu, Mesut Güngör
Publikováno v:
Journal of Contemporary Medicine, Vol 13, Iss 1, Pp 146-152 (2023)
Background: We aimed to investigate the short-term effects of adrenocorticotropic hormone (ACTH) treatment on the adrenal pathway and bone metabolism in patients with epileptic encephalopathy. Methods: Two groups with 16 patients and 16 controls were
Externí odkaz:
https://doaj.org/article/15b9cdd3b8af4733a57df157472cb2f9
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 7, Iss 1, Pp 36-38 (2020)
Atropa belladonna plant, also known as “beautiful woman herb” in our country, contains tropane alkaloids such as atropine, scopalamine and hyoshiamine in the fruits and leaves. When this plant is consumed it causes anticholinergic toxic syndrome.
Externí odkaz:
https://doaj.org/article/6c41e6644991422a90e885f757ce88b2
Autor:
Adalet Elçin Yıldız, Hülya Maraş Genç, Esra Gürkaş, Havva Akmaz Ünlü, İbrahim Halil Öncel, Alev Güven
Publikováno v:
Diagnostic and Interventional Radiology, Vol 24, Iss 2, Pp 108-112 (2018)
PURPOSE:We aimed to present clinical and radiologic characteristics of mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) in children.METHODS:Eight children (5 boys and 3 girls; median age, 5.9 years; age range, 8 months to 14.
Externí odkaz:
https://doaj.org/article/3fb0cca60c744a5db3485922f555db24
Publikováno v:
Journal of Pediatric Research, Vol 5, Iss 2, Pp 100-102 (2018)
Triple X syndrome (trisomy X) is a sex chromosomal anomaly caused by the presence of an extra X chromosome. The patients with Triple X syndrome have a wide range of phenotypic variability. Some individuals are only mildly affected or asymptomatic. Ep
Externí odkaz:
https://doaj.org/article/f7a1a1e483b047459c02bc7b0ce352cf
Autor:
Mesut GÜNGÖR, Bengü ALTINORDU, Hülya MARAŞ GENÇ, Emek UYUR YALÇIN, Filiz Mine ÇİZMECİOĞLU JONES, Bülent KARA
Publikováno v:
Journal of Contemporary Medicine. 13:146-152
Background: We aimed to investigate the short-term effects of adrenocorticotropic hormone (ACTH) treatment on the adrenal pathway and bone metabolism in patients with epileptic encephalopathy. Methods: Two groups with 16 patients and 16 controls were
Autor:
Hülya Maraş Genç, Gürler Akpınar, Murat Kasap, Emek Uyur Yalçın, Duran Üstek, Ayça Dilruba Aslanger, Bülent Kara
Publikováno v:
Molecular Syndromology. :1-13
Variation in the mitochondrial tRNALys gene at position 8296 was previously found to be associated with maternally inherited diabetes mellitus and deafness, hypertrophic cardiomyopathy, myoclonic epilepsy with ragged-red fibers and mitochondrial ence
Publikováno v:
Pediatric Nephrology. 37:333-336
Autor:
Gurler Akpinar, Yonca Anik, Emek Uyur Yalçın, Hülya Maraş Genç, Murat Kasap, Eylul Ece Islek, Güven Toksoy, Oya Uyguner, Bülent Kara, Duran Ustek
Publikováno v:
Molecular Syndromology. 13:12-22
Three siblings born to Turkish parents from the same village had normal brain development until acute neurological deterioration between 12 months and 8 years of age. Consequent loss of all acquired motor, social, and language functions following inf
Autor:
Sevinç Kalın, Funda Tekkeşin, Büşra Kutlubay, Burcu Karakayali, Gülhan Sözen, Betül Sözeri, Fikret Asarcikli, Hülya Maraş Genç
Publikováno v:
Turkish Journal of Pediatric Disease. :1-7
Autor:
Hülya Maraş Genç, Yasemin Kendir Demirkol, Hande Beklen, Özlem Akgün Doğan, Büşra Kutlubay, Hatice Gülhan Sözen
Publikováno v:
Çocuk Dergisi / Journal of Child.