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

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Age at Diagnosis and Mental Development in Children with Congenital Hypothyroidism in the Absence of Newborn Screening Programme | ESPE2016
Yasmine Ouarezki; Asmahane Ladjouze; Sakina Kherra; Adel Djermane; Abdennour Laraba
http://abstracts.eurospe.org/hrp/0086/hrp0086p2-p944.htm
Published: 2016-08-19

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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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A Novel Human CYP19A1 Deletion-Insertion Mutation Reveals that the C-terminus of the Aromatase Protein is Crucial for its Activity | ESPE2015
Asmahane Ladjouze; Kay-Sarah Sauter; Yasmine Ouarezki; Leila Kedji; Abdenour Laraba; Amit V Pandey; Christa E Fluck
http://abstracts.eurospe.org/hrp/0084/hrp0084p2-313.htm
Published: 2015-08-26

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Triple A Syndrome - the Second Most Common Cause of Chronic Adrenal Insufficiency in North Africa? | ESPE2015
Kahina Mohammedi; Asmahane Ladjouze; Ammar Tebaibia; Leila Kedji; Abdelmajid Maoudj; Karima Berkouk; Manoubia Bensmina; Souhila
http://abstracts.eurospe.org/hrp/0084/hrp0084p2-176.htm
Published: 2015-08-26

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Genotype-Phenotype Correlation in Turner Syndrome | ESPE2014
Adel Djermane; Asmahane Ladjouze; Yasmine Ouarezki; Belaid Ait-Abdelkader; Leila Kedji; Abdeljalil Maoudj; Karima Berkouk; Lakhd
http://abstracts.eurospe.org/hrp/0082/hrp0082p3-d3-869.htm
Published: 2014-08-28

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A New Mutation of MAMLD1 (CXorf6) Associated with NR5A1 (SF1) Variant in a Patient with 46,XY DSD | ESPE2014
Asmahane Ladjouze; Pascal Philibert; Yasmine Ouarezki; Adel Djermane; Leila Kedji; Abdeljalil Maoudj; Karima Berkouk; Charles Su
http://abstracts.eurospe.org/hrp/0082/hrp0082p2-d1-567.htm
Published: 2014-08-28

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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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