Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Pınar Edem"'
Publikováno v:
Nutrients, Vol 16, Iss 9, p 1384 (2024)
Background: Research on the interaction of parenting style, parents’ mealtime behaviors, and children’s eating behavior in the presence of chronic disease is limited. This study aimed to investigate the impact of parenting style and parental meal
Externí odkaz:
https://doaj.org/article/383401cbe285453ab8df74aeff945a69
Autor:
Çağatay Günay, Cem Paketçi, Pınar Edem, Gamze Sarıkaya Uzan, Ayşe Semra Hız Kurul, Zümrüt Arslan Gülten, Pelin Teke Kısa, Nur Arslan, Uluç Yıs
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 12, Iss 1, Pp 27-36 (2022)
Objective: Due to the fact that mitochondrial diseases can involve different organ systems, neuromuscular involvement is frequently observed and has a substantial place in clinical practice. In this study, the clinical, radiological, electrophysiolog
Externí odkaz:
https://doaj.org/article/f2cf20a896a44f0f84ff2bb575993c9f
Autor:
Annabelle Arlt, Nicolai Kohlschmidt, Andreas Hentschel, Enrika Bartels, Claudia Groß, Ana Töpf, Pınar Edem, Nora Szabo, Albert Sickmann, Nancy Meyer, Ulrike Schara-Schmidt, Jarred Lau, Hanns Lochmüller, Rita Horvath, Yavuz Oktay, Andreas Roos, Semra Hiz
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-19 (2022)
Abstract Background Goltz syndrome (GS) is a X-linked disorder defined by defects of mesodermal- and ectodermal-derived structures and caused by PORCN mutations. Features include striated skin-pigmentation, ocular and skeletal malformations and super
Externí odkaz:
https://doaj.org/article/82ae0241ff1e44fc9314229249815e34
Publikováno v:
Journal of Pediatric Research, Vol 8, Iss 3, Pp 320-325 (2021)
Aim:Childhood absence epilepsy is common idiopathic epilepsy in childhood. This epilepsy, which has been shown to impair cognition, needs to be treated promptly and correctly. Therefore, determining its prognostic factors before treatment can provide
Externí odkaz:
https://doaj.org/article/e0396029e3fc44d9b1b61be10b6ffdda
Autor:
Gamze Sarıkaya Uzan, Cem Paketçi, Çağatay Günay, Pınar Edem, Özlem Özsoy, Semra Hız Kurul, Uluç Yiş
Publikováno v:
Neuropediatrics. 53:321-329
Introduction We evaluated the effect of nusinersen on clinical and laboratory parameters and presented its safety and effect on laboratory parameters. Methods Two groups were formed from among patients with spinal muscular atrophy (SMA) followed up b
Autor:
Çağatay Günay, Duygu Aykol, Özlem Özsoy, Ece Sönmezler, Yaren Sena Hanci, Bülent Kara, Deniz Akkoyunlu Sünnetçi, Naci Cine, Adnan Deniz, Tolgahan Özer, Cemile Büşra Ölçülü, Özlem Yilmaz, Seda Kanmaz, Sanem Yilmaz, Hasan Tekgül, Nihal Yildiz, Elif Acar Arslan, Ali Cansu, Nihal Olgaç Dündar, Fatma Kusgoz, Elif Didinmez, Pınar Gençpinar, Tuğçe Aksu Uzunhan, Biray Ertürk, Alper Gezdirici, Akif Ayaz, Akgün Ölmez, Müge Ayanoğlu, Ayşe Tosun, Yasemin Topçu, Betül Kiliç, Kürşad Aydin, Ezgi Çağlar, Özlem Ersoy Kosvali, Çetin Okuyaz, Şeyda Besen, Leman Tekin Orgun, İlknur Erol, Deniz Yüksel, Abdullah Sezer, Ergin Atasoy, Ülkühan Toprak, Serdal Güngör, Bilge Ozgor, Meral Karadağ, Cengiz Dilber, Bahtiyar Şahinoğlu, Emek Uyur Yalçin, Nilüfer Eldes Hacifazlioglu, Ahmet Yaramiş, Pınar Edem, Hande Gezici Tekin, Ünsal Yilmaz, Aycan Ünalp, Sevim Turay, Didem Biçer, Gülen Gül Mert, İpek Dokurel Çetin, Serkan Kirik, Gülten Öztürk, Yasemin Karal, Aslıhan Sanri, Ayşe Aksoy, Muzaffer Polat, Nezir Özgün, Didem Soydemir, Gamze Sarikaya Uzan, Döndü Ülker Üstebay, Ayşen Gök, Mehmet Can Yeşilmen, Uluç Yiş, Gökhan Karakülah, Ahmet Bursali, Yavuz Oktay, Semra Hiz Kurul
Publikováno v:
Neuropediatrics.
Background Although the underlying genetic causes of intellectual disability (ID) continue to be rapidly identified, the biological pathways and processes that could be targets for a potential molecular therapy are not yet known. This study aimed to
Autor:
Gamze Sarıkaya Uzan, Pınar Edem, Tolga Besci, Cem Paketçi, Gültaç Evren, Semra Hız Kurul, Murat Duman, Uluç Yiş
Background & Objective: We present 11-year data of patients with neuromuscular disease (NMD) thatwere treated in the pediatric intensive care unit of a tertiary children’s hospital. Methods: The data ofall cases followed-up in the pediatric intensi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7c7a9dc77f797299f570c5f7091dbb9
https://avesis.deu.edu.tr/publication/details/749e5d9d-6035-4027-ac99-d05c25eb05d3/oai
https://avesis.deu.edu.tr/publication/details/749e5d9d-6035-4027-ac99-d05c25eb05d3/oai
Autor:
Müge Ayanoğlu, Uluç Yiş, Hale Ünver Tuhan, Ayşe İpek Polat, Tuncay Derya Okur, Pınar Edem, Cem Paketçi, Erhan Bayram, Ayhan Abacı, Semra Hız
Objective: To evaluate the risk factors of subclinical neuropathy, and the nerve conduction study (NCS) results in children, and adolescents with type 1 diabetes mellitus (T1DM). Methods: A total of 81 patients without neuropathy symptoms were studie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7cebbaddd07fb5af3e4c8e6abf730fd
https://avesis.deu.edu.tr/publication/details/2d3b6d5c-5e98-41d5-8946-1fc3e2a7b688/oai
https://avesis.deu.edu.tr/publication/details/2d3b6d5c-5e98-41d5-8946-1fc3e2a7b688/oai
Publikováno v:
Journal of Pediatric Research, Vol 8, Iss 3, Pp 320-325 (2021)
Aim:Childhood absence epilepsy is common idiopathic epilepsy in childhood. This epilepsy, which has been shown to impair cognition, needs to be treated promptly and correctly. Therefore, determining its prognostic factors before treatment can provide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a550c3aeaeb8cacc911b77996ee182c
https://avesis.deu.edu.tr/publication/details/c4c1843c-af09-4655-bec8-52a3b687fba6/oai
https://avesis.deu.edu.tr/publication/details/c4c1843c-af09-4655-bec8-52a3b687fba6/oai
Publikováno v:
Güncel Pediatri. 12:107-111