Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Muharrem, Ak"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-14 (2024)
Abstract Background/aims We aimed to develop a validated patient-reported Gastrointestinal Health Scale (GHS) specific to MECP2 Duplication Syndrome (MDS) to be used in clinical trials. Methods MDS parents completed a Gastrointestinal Health Question
Externí odkaz:
https://doaj.org/article/303cf64c7d374e0e8a60e2b909546447
Autor:
Muharrem Ak, Bernhard Suter, Zekeriya Akturk, Holly Harris, Kristina Bowyer, Laurence Mignon, Sasidhar Pasupuleti, Daniel G. Glaze, Davut Pehlivan
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Background MECP2 Duplication Syndrome (MDS), resulting from the duplication of Xq28 region, including MECP2, is a rare disorder with a nascent understanding in clinical features and severity. Studies using antisense oligonucleotides revealed
Externí odkaz:
https://doaj.org/article/cfd3a8b86f9c45929b4b5d4d74d11ba2
Publikováno v:
Neurogastroenterology & Motility.
Autor:
Mehmet Karatas, Muharrem Ak, Mehmet Fatih Korkmaz, Engin Burak Selcuk, Turgay Karatas, Murat Yalcinsoy, Burcu Kayhan Tetik
Publikováno v:
Medicine Science, Vol 5, Iss 2, Pp 505-18 (2016)
This study may provide insights into the positive and negative perceptions of physicians and citizens in Turkey regarding the Transformation in Health Project.We aimed to evaluate the views of physicians and citizens regarding the changing healthcare
Externí odkaz:
https://doaj.org/article/e8a5c351fa0b4faa98bd0f751889fb85
Autor:
Muharrem Ak, Bernhard Suter, Zekeriya Akturk, Holly Harris, Kristina Bowyer, Laurence Mignon, Sasidhar Pasupuleti, Daniel G. Glaze, Davut Pehlivan
Publikováno v:
Molecular Genetics & Genomic Medicine. 10
MECP2 Duplication Syndrome (MDS), resulting from the duplication of Xq28 region, including MECP2, is a rare disorder with a nascent understanding in clinical features and severity. Studies using antisense oligonucleotides revealed a broad phenotypic
Autor:
Muharrem Ak, Zekeriya Akturk, Kristina Bowyer, Laurence Mignon, Sasidhar Pasupuleti, Daniel G. Glaze, Bernhard Suter, Davut Pehlivan
Publikováno v:
Pediatric neurology. 133
MECP2 duplication syndrome (MDS) is a rare neurogenetic disorder characterized by severe neurodevelopmental disorder, refractory epilepsy, recurrent infections, and functional gastrointestinal problems. Because of the significant clinical problems an
Publikováno v:
Volume: 45, Issue: 2 409-415
Turkish Journal of Medical Sciences
Turkish Journal of Medical Sciences
Background/aim: A significant number of patients with type 2 diabetes mellitus require insulin and little is known about the possible physician-related factors that could cause a delay in the initiation of insulin treatment in patients with type 2 di
Publikováno v:
Journal of Perinatology. 35:137-141
The present study aims to determine the knowledge, attitudes and views of the Muslim religious officers regarding infant feeding, breast milk, wet nursing, milk kinship and human milk banks (HMBs).A total of 401 religious officers were included in th
Publikováno v:
Dicle Medical Journal, Vol 41, Iss 2, Pp 319-325 (2014)
Volume: 41, Issue: 2 319-325
Dicle Tıp Dergisi
Volume: 41, Issue: 2 319-325
Dicle Tıp Dergisi
Purpose: We aimed to examine, mothers' level of knowledge about complications of cesarean section and the factors that influence preference for cesarean section in this study Methods: The universe of the study consisted of the women who admitted to t
Autor:
Yusuf Kenan Coban, Muharrem Ak, Muhammed Gokhan Turtay, Emine Samdanci, Cemal Firat, Ahmet Hamdi Aytekin, Serkan Erbatur
Publikováno v:
Burns. 39:105-112
Saving the zone of stasis is one of the major goals of burn specialists. Increasing the tissue tolerance to ischaemia and inhibiting inflammation have been proposed to enable salvage of this zone. After a burn, excessive inflammation, including incre