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Showing page 1 of results 1 - 10 of about 19 pages

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Typical Phenotype of Isolated Aldosterone Synthetase (AS) Deficiency in two Infants with Heterozygous AS Gene Mutation: Dilemma for Diagnosis | ESPE2019
Elif Ozsu; Aysegul Ceran; Rukiye Uyanik; Esra Bilici; Tugba Cetin; Zeynep Siklar; Zehra Aycan; Merih Berberoglu
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-8
Published: 2019-08-22

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Clinical Characteristics and Response to Growth Hormone Treatment in Patients with Prader-Willi Syndrome | ESPE2019
Olcay Evliyaoglu; Cakir Aydilek Dagdeviren; Firdevs Bas; Onur Akin; Zeynep Siklar; Bahar Özcabi; Merih Berberoglu; Asli Derya K
http://abstracts.eurospe.org/hrp/0092/hrp0092P2-137
Published: 2019-08-22

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Metabolically Unhealthy Obese Children and Adolescents Have Higher Bone Mineral Density Than Normal Weighted Controls but Lower than Metabolically Healthy Obeses: No Effect of FGF21 Levels | ESPE2019
Filiz Akduman; Zeynep Siklar; Elif Ozsu; Ozlem Doğan; Metin Kir; Merih Berberoglu
http://abstracts.eurospe.org/hrp/0092/hrp0092FC6.4
Published: 2019-08-22

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Typical Phenotype of Isolated Aldosterone Synthetase (AS) Deficiency in two Infants with Heterozygous AS Gene Mutation: Dilemma for Diagnosis | ESPE2019
Elif Ozsu; Aysegul Ceran; Rukiye Uyanik; Esra Bilici; Tugba Cetin; Zeynep Siklar; Zehra Aycan; Merih Berberoglu
http://abstracts.eurospe.org/hrp/0092/hrp0092p3-8.html
Published: 2019-08-22

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Clinical Characteristics and Response to Growth Hormone Treatment in Patients with Prader-Willi Syndrome | ESPE2019
Olcay Evliyaoglu; Cakir Aydilek Dagdeviren; Firdevs Bas; Onur Akin; Zeynep Siklar; Bahar Özcabi; Merih Berberoglu; Asli Derya K
http://abstracts.eurospe.org/hrp/0092/hrp0092p2-137.html
Published: 2019-08-22

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Metabolically Unhealthy Obese Children and Adolescents Have Higher Bone Mineral Density Than Normal Weighted Controls but Lower than Metabolically Healthy Obeses: No Effect of FGF21 Levels | ESPE2019
Filiz Akduman; Zeynep Siklar; Elif Ozsu; Ozlem Doğan; Metin Kir; Merih Berberoglu
http://abstracts.eurospe.org/hrp/0092/hrp0092fc6.4.html
Published: 2019-08-22

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Central Precocious Puberty Appeared in Infancy Period in a Patient of Sotos Syndrome | ESPE2018
Tuğba Cetin; Serdar Ceylaner; Zeynep Şıklar; Merih Berberoğlu
http://abstracts.eurospe.org/hrp/0089/hrp0089p3-p320.htm
Published: 2018-08-28

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Syndromic Patients with Negative Islet Autoantibodies should be Tested for Mongenic Diabetes: Lessons from Patient with Trmt10a Mutation | ESPE2018
Zeynep Siklar; Kevin Colclough; Kashyap A Patel; Tuğba Cetin; Merih Berberoğlu
http://abstracts.eurospe.org/hrp/0089/hrp0089p2-p072.htm
Published: 2018-08-28

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Comprehensive Genetic Testing Shows One in Five Children with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology | ESPE2018
Kashyap A Patel; Kevin Colclough; Ozbek Mehmet Nuri; Melek Yildiz; Tulay Guran; Cemil Kocyigit; Sezer Acar; Zeynep Siklar; Muge
http://abstracts.eurospe.org/hrp/0089/hrp0089p1-p058.htm
Published: 2018-08-28

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Contribution of Functionally Assessed GHRHR Mutations to Idiopathic Isolated Growth Hormone Deficiency in a Cohort of 312 Unrelated Patients | ESPE2018
Enzo Cohen; Sabrina Belkacem; Soumeya Fedala; Nathalie Collot; Eliane Khallouf; Florence Dastot; Michel Polak; Philippe Duquesno
http://abstracts.eurospe.org/hrp/0089/hrp0089fc9.2.htm
Published: 2018-08-28

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