Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mehmet Akif Büyükavcı"'
Autor:
Şenay Güven Baysal, Nurdan Çiftci, İsmail Dündar, Mehmet Akif Büyükavcı, Fatma Hilal Yağın, Emine Çamtosun, Derya Doğan, Ayşehan Akıncı
Publikováno v:
JCRPE, Vol 15, Iss 2, Pp 172-181 (2023)
INTRODUCTION: With the diagnosis of chronic illness in children, a stressful period is likely to begin for both the affected child and their families. The aim of this study was to investigate the factors affecting chronic disease management by the pa
Externí odkaz:
https://doaj.org/article/249bbeb0793d4150b254bdae9fb11b1a
Autor:
Mehmet Akif Büyükavcı, Ismail Dundar
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism.
Objectives Congenital hypothyroidism (CH) is still one of the most common causes of preventable cognitive impairment in children, and its early detection and treatment prevent irreversible neurodevelopmental delay. Depending on the underlying cause,
Autor:
Tuğba, Karaca Ahat, Tuğba, Yılmaz Gençer, Şenay, Güven Baysal, Halise, Metin Baz, Umut, Durak, Sinem, Kortay Canaloğlu, Mehmet Akif, Büyükavcı, Derya, Gümüş Doğan
Publikováno v:
Turkish archives of pediatrics. 58(1)
The aim of this study was to analyze the impact of coronavirus disease 2019 pandemic on the number and diagnosis of patients admitted to the Developmental Pediatrics Unit. Materilas and Methods: We compared the number and the diagnosis of patients ad
Publikováno v:
Kahramanmaraş Sütçü İmam Üniversitesi Tıp Fakültesi Dergisi. 16:397-400
Vitamin D is a fat-soluble secosteroid prohormone that is produced on the skin by contact with sunlight. Through various metabolic changes in the body, it transforms into a hormone known as calcitriol, with a key role in the calcium and phosphate met
Publikováno v:
Acta Neurologica Belgica. 118:429-433
The aim of this study was to detect effects of ultrasound-guided botulinum toxin type-A (US-guided BoNT-A) injections prepared according to lower extremity innervation zones on spasticity and motor function in 3–16 years children with diplegic and
Publikováno v:
Archivos argentinos de pediatría, Volume: 117, Issue: 2, Pages: 114-119, Published: 01 APR 2019
Introducción. El síndrome de Down (SD) es un trastorno genético frecuente. Las familias de los niños con SD en general no reciben suficiente información al momento del diagnóstico. El objetivo de este estudio fue evaluar las experiencias de las
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a9d1ffcb98e5b35ffa97929a7ac49e4
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0325-00752019000200009&lng=en&tlng=en
http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0325-00752019000200009&lng=en&tlng=en
Autor:
Mehmet Akif Büyükavcı, Raikan Buyukavci, Feyzullah Necati Arslan, Derya Gumus Dogan, Semra Aktürk, Sinem Kortay Canaloglu
Publikováno v:
Acta neurologica Belgica. 121(2)
Down syndrome (DS) is a genetic disorder associated with mental and motor developmental delays in childhood. The aim of this study was to investigate the relationship of the femoral cartilage thickness with motor performance in children with Down syn
Publikováno v:
Annals of Medical Research. 28:1986