ESPE Abstracts

ESPE Abstracts

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

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Relationship Between Residual Endogenous Insulin Secretion and Glycemic Control in Japanese Children and Adolescents with Type 1 Diabetes | ESPE2018
Ikuma Musha; Hiroshi Kawana; Junya Akatsuka; Akira Ohtake; Shin Amemiya; Toru Kikuchi
http://abstracts.eurospe.org/hrp/0089/hrp0089p2-p088.htm
Published: 2018-08-28

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Age at Diagnosis and Outcome in Maghreb patients with 21-hydroxylase Deficient Congenital Adrenal Hyperplasia; Urgent need for Newborn Screening | ESPE2018
Asmahane Ladjouze; Imane Yala; Manel Yahiaoui; Dounia Zerguini; Veronique Tardy; Kahina Mohammedi; Ourida N Taleb; Soraya Kerkou
http://abstracts.eurospe.org/hrp/0089/hrp0089p3-p005.htm
Published: 2018-08-28

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Aetiology of 46,XY DSD in Algeria; Putative Modifier Role of pV89L Polymorphism in the SRD5A2 Gene in Androgen Receptor Mutation-Negative Subjects | ESPE2016
Asmahane Ladjouze; Pascal Philibert; Ourida Taleb; Lila Kedji; Abdeljalil Maoudj; Karima Berkouk; Nadjet Bouhafs; Nabila Dahmane
http://abstracts.eurospe.org/hrp/0086/hrp0086p2-p401.htm
Published: 2016-08-19

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High Prevalence of SGA in Patients with Disorders of Sexual Development, Especially Idiopathic 46,XY DSD | ESPE2016
Asmahane Ladjouze; Ourida Taleb; Lila Kedji; Abdeljalil Maoudj; Karima Berkouk; Manoubia Bensmina; Rawda Aboura; Yasmine Ouarezk
http://abstracts.eurospe.org/hrp/0086/hrp0086p2-p386.htm
Published: 2016-08-19

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Estrogen Insensitivity due to a Novel ESR1 Mutation in a Consanguineous Family from Algeria | ESPE2016
Sakina Kherra; Asmahane Ladjouze; Valerie Bernard; Tahar Anane; Abdenour Laraba; Sophie Christin-Maitre
http://abstracts.eurospe.org/hrp/0086/hrp0086fc7.3.htm
Published: 2016-08-19

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The Triptorelin Test Compares Favourably with the GnRH Test in the Diagnosis of Central Precocious Puberty | ESPE2014
Asmahane Ladjouze; Adel Djermane; Yasmine Ouarezki; Leila Kedji; Karima Berkouk; Maoudj Abdeljalil; Rawda Aboura; Minoubia Bensm
http://abstracts.eurospe.org/hrp/0082/hrp0082p2-d2-547.htm
Published: 2014-08-28

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A Very Rare Case of Rickets: Fanconi-Bickel Syndrome | ESPE2014
Adel Djermane; Asmahane Ladjouze; Yasmine Ouarezki; Sandrine Vuillaumier-Barrot; Benfetima Ali Khodja; Leila Kedji; Abdeljalil M
http://abstracts.eurospe.org/hrp/0082/hrp0082p2-d1-293.htm
Published: 2014-08-28

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