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Showing page 1 of results 1 - 7 of about 7 pages

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Congenital Adrenal Hyperplasia due to 21 OH Deficiency: Final Height Before and After Newborn Screening Era in Emilia-Romagna Region, Italy | ESPE2015
Federico Baronio; Soara Menabo; Ilaria Bettocchi; Lilia Baldazzi; Federica Tamburrino; Francesca Montanari; Alessandra Cassio; L
http://abstracts.eurospe.org/hrp/0084/hrp0084fc1.4.htm
Published: 2015-08-26

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Relation between Levels of Atymullerian Hormone and Inhibin B and Spontaneous Puberty in Patients with Turner Syndrome – Preliminary Results | ESPE2019
Anna Ruszała; Małgorzata Wójcik; Jerzy B. Starzyk
http://abstracts.eurospe.org/hrp/0092/hrp0092P3-279
Published: 2019-08-22

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Relation between Levels of Atymullerian Hormone and Inhibin B and Spontaneous Puberty in Patients with Turner Syndrome – Preliminary Results | ESPE2019
Anna Ruszała; Małgorzata Wójcik; Jerzy B. Starzyk
http://abstracts.eurospe.org/hrp/0092/hrp0092p3-279.html
Published: 2019-08-22

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Genotype and Phenotype Characteristics in 22 Patients with Vitamin D Dependent Rickets Type I | ESPE2015
Sophia Tahir; Huseyin Demirbilek; Mehmet Nuri Ozbek; Riza Taner Baran; Sibel Tanriverdi; Khalid Hussain
http://abstracts.eurospe.org/hrp/0084/hrp0084p2-220.htm
Published: 2015-08-26

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Isolated GH Deficiency (IGHD) may be due to Several Different Causes: mutations in the GHRH Receptor Gene Are a Relatively Rare Cause of IGHD | ESPE2014
Huseyin Demirbilek; Sophia Tahir; Riza Taner Baran; Maha Sherif; Mehmet Nuri Ozbek; Khalid Hussain
http://abstracts.eurospe.org/hrp/0082/hrp0082p2-d1-448.htm
Published: 2014-08-28

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Two Novel Homozygous Mutations in <em>WFS1</em> Gene in Two Turkish Families with Mild Phenotypic Expression of Wolfram Syndrome | ESPE2014
Maha Sherif; Huseyin Demirbilek; Atilla Cayir; Mehmet Nuri Ozbek; Riza Taner Baran; Ayse Nurcan Cebeci; Sophia Tahir; Sofia Rahm
http://abstracts.eurospe.org/hrp/0082/hrp0082p2-d1-324.htm
Published: 2014-08-28

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Characterising the Immunohistochemical Expression of Dipeptidyl Peptidase-4 in Pancreatic Tissue from Patients with Diffuse and Focal Congenital Hyperinsulinism | ESPE2014
Sofia Rahman; Maha Sherif; Sophia Tahir; Khalid Hussain
http://abstracts.eurospe.org/hrp/0082/hrp0082fc9.2.htm
Published: 2014-08-28

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