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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

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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

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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.html
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.html
Published: 2019-08-22

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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

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