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Juliane Leger

Showing results (1-10 of 34) with videos related to

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European Journal of Pediatrics|November 29, 2018
Refeeding in anorexia nervosaAnne Bargiacchi, Julia Clarke, Anne Paulsen, et al.
Current Diabetes Reports|March 20, 2003
The effect of in-utero undernutrition on the insulin resistance syndromeDelphine Jaquet, Juliane Leger, Paul Czernichow, et al.
European Journal of Pediatrics|February 12, 2019
Growth impairment and limited range of joint motion in children should raise suspicion of an attenuated form of mucopolysaccharidosis: expert opinionNathalie Guffon, Pierre Journeau, Anaïs Brassier, et al.
Seminars in Nuclear Medicine|February 27, 2017
Congenital Hypothyroidism: Role of Nuclear MedicineIsabelle Keller-Petrot, Juliane Leger, Aline Sergent-Alaoui, et al.
International Journal of Paediatric Dentistry|June 12, 2010
Dental agenesis in Kallmann syndrome individuals with FGFR1 mutationsIsabelle Bailleul-Forestier, Catherine Gros, Delphine Zenaty, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 18, 2018
Dysregulated glucose homeostasis in congenital central hypoventilation syndromeYassmin Mansela Musthaffa, Vikas Goyal, Margaret-Anne Harris, et al.
Endocrine Connections|February 1, 2023
Gonadotropin administration to mimic mini-puberty in hypogonadotropic males: pump or injections?Tristan Avril, Quentin Hennocq, Anne-Sophie Lambert, et al.
Endocrinology|October 18, 2008
An inactivating mutation within the first extracellular loop of the thyrotropin receptor impedes normal posttranslational maturation of the extracellular domainSylvia Sura-Trueba, Chantal Aumas, Aurore Carre, et al.
Biochemical and Biophysical Research Communications|August 17, 2011
Deletion of P399_E401 in NADPH cytochrome P450 oxidoreductase results in partial mixed oxidase deficiencyChrista E Flück, Delphine Mallet, Gaby Hofer, et al.
The Journal of Clinical Endocrinology and Metabolism|September 4, 2008
Unexpected endocrine features and normal pigmentation in a young adult patient carrying a novel homozygous mutation in the POMC geneKarine Clément, Béatrice Dubern, Monica Mencarelli, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
European Journal of Pediatrics|November 29, 2018
Refeeding in anorexia nervosaAnne Bargiacchi, Julia Clarke, Anne Paulsen, et al.
Current Diabetes Reports|March 20, 2003
The effect of in-utero undernutrition on the insulin resistance syndromeDelphine Jaquet, Juliane Leger, Paul Czernichow, et al.
European Journal of Pediatrics|February 12, 2019
Growth impairment and limited range of joint motion in children should raise suspicion of an attenuated form of mucopolysaccharidosis: expert opinionNathalie Guffon, Pierre Journeau, Anaïs Brassier, et al.
Seminars in Nuclear Medicine|February 27, 2017
Congenital Hypothyroidism: Role of Nuclear MedicineIsabelle Keller-Petrot, Juliane Leger, Aline Sergent-Alaoui, et al.
International Journal of Paediatric Dentistry|June 12, 2010
Dental agenesis in Kallmann syndrome individuals with FGFR1 mutationsIsabelle Bailleul-Forestier, Catherine Gros, Delphine Zenaty, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 18, 2018
Dysregulated glucose homeostasis in congenital central hypoventilation syndromeYassmin Mansela Musthaffa, Vikas Goyal, Margaret-Anne Harris, et al.
Endocrine Connections|February 1, 2023
Gonadotropin administration to mimic mini-puberty in hypogonadotropic males: pump or injections?Tristan Avril, Quentin Hennocq, Anne-Sophie Lambert, et al.
Endocrinology|October 18, 2008
An inactivating mutation within the first extracellular loop of the thyrotropin receptor impedes normal posttranslational maturation of the extracellular domainSylvia Sura-Trueba, Chantal Aumas, Aurore Carre, et al.
Biochemical and Biophysical Research Communications|August 17, 2011
Deletion of P399_E401 in NADPH cytochrome P450 oxidoreductase results in partial mixed oxidase deficiencyChrista E Flück, Delphine Mallet, Gaby Hofer, et al.
The Journal of Clinical Endocrinology and Metabolism|September 4, 2008
Unexpected endocrine features and normal pigmentation in a young adult patient carrying a novel homozygous mutation in the POMC geneKarine Clément, Béatrice Dubern, Monica Mencarelli, et al.
Pageof 4