Erdal Kurnaz

Publication Activity (10 Years)

Years Active: 2017-2021
Publications (10 Years): 5

Top Topics

Gene Expression

Top Venues

Cardiology in the young

Journal of clinical research in pediatric endocrinology

European journal of pediatrics

This page only lists publications with an associated author ORCID identifier.

Publications

Atilla Cayir, Ali Akyigit, Ufuk Utku Gullu, Hasan Kahveci, Duran Yildiz, Erdal Kurnaz, Dogus Vuralli, Abdulkadir Kaya, Gonul Buyukyilmaz, Huseyin Demirbilek
Clinical, biochemical, and echocardiographic evaluation of neonates with vitamin D deficiency due to maternal vitamin D deficiency. Cardiology in the young (2021)
Erdal Kurnaz, Semra Cetinkaya, Selin Elmaoğulları, Aslıhan Araslı Yılmaz, Nursel Muratoğlu Şahin, Melikşah Keskin, Şenay Savaş Erdeve
A major health problem facing immigrant children: nutritional rickets. Journal of pediatric endocrinology & metabolism : JPEM (2021)
Enzo Cohen, Sabrina Belkacem, Soumeya Fedala, Nathalie Collot, Eliane Khallouf, Florence Dastot, Michel Polak, Philippe Duquesnoy, Frederic Brioude, Sophie Rose, Géraldine Viot, Aude Soleyan, Jean-Claude Carel, Marie-Laure Sobrier, Philippe Chanson, Frédérique Gatelais, Claudine Heinrichs, Noureddine Kaffel, Regis Coutant, Senay Savas Erdeve, Erdal Kurnaz, Zehra Aycan, Caroline Thalassinos, Stanislas Lyonnet, Zeynep Şıklar, Merih Berberoglu, Cécile Brachet, Serge Amselem, Marie Legendre
Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations. Human mutation 40 (11) (2019)
Nursel Muratoğlu Şahin, Elvan Bayramoğlu, H Nursun Ozcan, Erdal Kurnaz, Melikşah Keskin, Senay Savas Erdeve, Semra Cetinkaya, Zehra Aycan
Antimüllerian Hormone Levels of Infants with Premature Thelarche Journal of clinical research in pediatric endocrinology 11 (3) (2019)
Erdal Kurnaz, Paolo Duminuco, Zehra Aycan, Şenay Savaş-Erdeve, Nursel Muratoğlu Şahin, Melişah Keskin, Elvan Bayramoğlu, Marco Bonomi, Semra Çetinkaya
Clinical and genetic characterisation of a series of patients with triple A syndrome. European journal of pediatrics 177 (3) (2017)