ISSN 1470-3947 (print) | ISSN 1479-6848 (online)
Searchable abstracts of presentations at key conferences in endocrinology
Showing page 1 of results 1 - 10 of about 12 matches for "bulstrode-neil"
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FGF21 causes GH resistance in human chondrocytes through activation of SOCS2 and inhibition of IGF1 expression Leonardo Guasti; Patrizia Ferretti; Neil Bulstrode; Leo Dunkel http://www.endocrine-abstracts.org/ea/0033/ea0033oc2.4.htm Published: 2013-11-01
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Biochemical and molecular modelling analyses explain the functional loss of HSD17B3 mutant G133R in three Tunisian patients Roger Engeli; Bochra Ben Rhouma; Christoph R Sager; Faiza Fakhfakh; Leila Keskes; Angelo Vedani; Neila Belguith; Alex Odermatt http://www.endocrine-abstracts.org/ea/0037/ea0037ep116.htm Published: 2015-05-01
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Primary Amenorrhea Revealing Leydig Cell Hypoplasia | ESPE2019 Imen Gargouri; Faten Hadjkacem; Wajdi Safi; Wafa Ben Othman; Mouna Mnif; Mongia Hachicha; Thouraya Kamoun; Bochra Ben Rhoum; Nei http://abstracts.eurospe.org/hrp/0092/hrp0092P3-229 Published: 2019-08-22
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Gonadal Dysgenesis, 46 XY About 5 Familial Cases | ESPE2019 Wajdi Safi; Kacem Faten Hadj; Mrad Fatma Ben; Imene Gargouri; Wafa Belabed; Nabila Rekik; Nadia Charfi; Bochra Ben Rhouma; Feki http://abstracts.eurospe.org/hrp/0092/hrp0092P3-221 Published: 2019-08-22
Familial Occurrence of Turner Syndrome in two Tunisian Families | ESPE2019 Imen Gargouri; Sana Kmiha; Fatma Abdelhedi; Faten Hadjkacem; Wajdi Safi; Fatma Loukil; Mouna Mnif; Mongia Hachicha; Thouraya Kam http://abstracts.eurospe.org/hrp/0092/hrp0092P1-94 Published: 2019-08-22
Primary Amenorrhea Revealing Leydig Cell Hypoplasia | ESPE2019 Imen Gargouri; Faten Hadjkacem; Wajdi Safi; Wafa Ben Othman; Mouna Mnif; Mongia Hachicha; Thouraya Kamoun; Bochra Ben Rhoum; Nei http://abstracts.eurospe.org/hrp/0092/hrp0092p3-229.html Published: 2019-08-22
Gonadal Dysgenesis, 46 XY About 5 Familial Cases | ESPE2019 Wajdi Safi; Kacem Faten Hadj; Mrad Fatma Ben; Imene Gargouri; Wafa Belabed; Nabila Rekik; Nadia Charfi; Bochra Ben Rhouma; Feki http://abstracts.eurospe.org/hrp/0092/hrp0092p3-221.html Published: 2019-08-22
Familial Occurrence of Turner Syndrome in two Tunisian Families | ESPE2019 Imen Gargouri; Sana Kmiha; Fatma Abdelhedi; Faten Hadjkacem; Wajdi Safi; Fatma Loukil; Mouna Mnif; Mongia Hachicha; Thouraya Kam http://abstracts.eurospe.org/hrp/0092/hrp0092p1-94.html Published: 2019-08-22
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Unusual association: turner syndrome and anterior pituitary insufficiency in 6 cases | ECE2018 Wajdi Safi; Faten Hadj Kacem; Mariem Moalla; Dorra Ghorbel; Fatma Mnif; Mouna Mnif Feki; Nabila Rekik; Neila Belghith; Fatma Abd http://www.endocrine-abstracts.org/ea/0056/ea0056ep103.htm Published: 2018-05-08
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Congenital hypothyroidism: genes involved in organogenesis disorders | ECE2018 Rim Chaabane; Imen Gargouri; Faten Hadjkacem; Houssem Mrabet; Mouna Elleuch; Dorra ghorbel; Mouna Mnif; Nadia Charfi; Neila Belg http://www.endocrine-abstracts.org/ea/0056/ea0056p1109.htm Published: 2018-05-08
Event series: --All Event Series-- European Congress of Endocrinology British Endocrine Societies (pre 2005) Society for Endocrinology Annual Meeting Society for Endocrinology BES BSPED Annual Meeting Hammersmith Hospital ESE Basic Endocrinology Course World Congress on Clinical Trials in Diabetes Androgens Biannual Meeting UKINETS Annual Conference Theranostics World Congress Endocrine Update Obesity Update Nuclear Receptors Belgian Endocrine Society Meeting EYES Meeting
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