Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Merve Şakar"'
Autor:
Ceren Güleryüz, Ece Eker, Gülin Karacan Küçükali, Merve Şakar, Fatma Nur Genç, Nursel Muratoğlu Şahin, Selin Elmaoğulları, Semra Çetinkaya, Şenay Savaş Erdeve
Publikováno v:
JCRPE, Vol 15, Iss 4, Pp 444-448 (2023)
A balanced and healthy diet is very important in type 1 diabetes mellitus (T1DM) in childhood. In addition to regulating blood glucose with diet, diet should also support optimal growth. Low-carbohydrate diet aims to provide daily energy from fats an
Externí odkaz:
https://doaj.org/article/3fe1053121774271b8228acf33ee8122
Autor:
Merve Şakar, Murat Ayanoğlu
Publikováno v:
İşletme Bilimi Dergisi, Vol 3, Iss 2, Pp 19-38 (2016)
Bayram, yılbaşı ve diğer tatil sezonları öncesinde kargo firmalarına olan taleplerde artış olduğu gözlenmektedir. Mevcut personel ve ekipmanlarla bu taleplere cevap verilmekte zorluk yaşandığından kısıtlar kuramı yaklaşımı ile ge
Externí odkaz:
https://doaj.org/article/b5bd31790991459fb76d36b44a4d2a57
Publikováno v:
Archives de Pédiatrie. 28:626-631
Background Personality traits of adolescents with type 1 diabetes mellitus (T1DM) and those of their mothers may lead to poor glycemic control through psychiatric comorbidity. However, it is not yet known how the personality traits of adolescents wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::029d60056f4e9483314bef7832d60b57
https://doi.org/10.1016/j.arcped.2021.10.002
https://doi.org/10.1016/j.arcped.2021.10.002
Autor:
Zeynep Donbaloğlu, Semra Çetinkaya, Zehra Aycan, Gülin Karacan Küçükali, Merve Şakar, Şenay Savaş‐Erdeve
Publikováno v:
Journal of paediatrics and child healthReferences. 58(8)
The incidence of congenital hypothyroidism (CH) has increased world-wide. Lowering cut-off in screening programs has led to an increase in the rate of transient CH. We aimed to evaluate the rates of permanent and transient CH in cases referred from t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::688bf12c3be9c0e239142f6e40d3bbe7
https://pubmed.ncbi.nlm.nih.gov/35686887
https://pubmed.ncbi.nlm.nih.gov/35686887
Autor:
Ceren Güleryüz, Ece Eker, Gülin Karacan Küçükali, Merve Şakar, Fatma Nur Genç, Nursel Muratoğlu Şahin, Selin Elmaoğulları, Semra Çetinkaya, Şenay Savaş Erdeve
Publikováno v:
Journal of clinical research in pediatric endocrinology.
A balanced and healthy diet is very important in type 1 diabetes mellitus in childhood. In addition to regulating blood glucose with diet, it should be aimed to support adequate growth. Low-carbohydrate diet aims to provide daily energy from fats and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8085c97e24eb1a153b753b59beeffb7b
https://pubmed.ncbi.nlm.nih.gov/35014244
https://pubmed.ncbi.nlm.nih.gov/35014244
Autor:
Semra Cetinkaya, Behiye Sarıkaya Özdemir, Merve Şakar, Naz Güleray Lafcı, Gülin Karacan Küçükali, Selin Elmaogullari, Şenay Savaş Erdeve
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 34(10)
Objectives Laron syndrome (LS) is a disease caused by growth hormone receptor (GHR) defects. It is characterized by severe postnatal growth retardation and distinctive facial features. Case presentation In this case report, we describe the clinical a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81cc0263828be7c6c09e1db58c64c169
https://pubmed.ncbi.nlm.nih.gov/34218547
https://pubmed.ncbi.nlm.nih.gov/34218547
Autor:
İlter Arifoğlu Barış, Şenay Savşa Erdeve, Ayşegül Zenciroğlu, Merve Şakar, Semra Cetinkaya, Akmet Öktem, Rüveyde Bundak
Publikováno v:
Trends in Pediatrics.
Primary hypoaldosteronism is a rare autosomal recessive disorder that causes defects in aldosterone synthase enzyme activity due to an inactivating mutation in the CYP11B2 gene. Patients with primary hypoaldosteronism exhibit symptoms such as vomitin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::792d404cd01f8cd71b4fdc7fd680c757
https://doi.org/10.5222/tp.2021.19483
https://doi.org/10.5222/tp.2021.19483
Autor:
Merve Şakar, Semra Çetinkaya, Gulseren Sahin, Naz Güleray Lafcı, Fatma Kurt Colak, Şenay Savaş-Erdeve
Publikováno v:
Hormones.
Transaldolase (TALDO) deficiency (OMIM #606003) is a rare autosomal recessive multi-systemic disorder of carbohydrate metabolism. It has a vast phenotypic spectrum ranging from neonatal liver failure to slowly progressive liver cirrhosis and is chara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01840f85b4e75256e61167d5b7fd545e
https://doi.org/10.1007/s42000-020-00252-4
https://doi.org/10.1007/s42000-020-00252-4