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R Reynaud

Showing results (41-50 of 47) with videos related to

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European Journal of Endocrinology|January 29, 2011
Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative formsR Reynaud, F Albarel, A Saveanu, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 23, 2016
GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone DeficiencyF Castinetti, A F Daly, C A Stratakis, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarismF Castinetti, A Saveanu, R Reynaud, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 30, 2022
Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in FranceL Levaillant, F Huet, P Bretones, et al.
Primary Care Diabetes|November 24, 2023
Impact of continuous glucose monitoring on everyday life of young children with type 1 diabetes and their parents: An evaluation of 114 familiesK Aouchiche, D Bernoux, E Baechler Sadoul, et al.
Bone Marrow Transplantation|July 5, 2011
Growth hormone treatment impact on growth rate and final height of patients who received HSCT with TBI or/and cranial irradiation in childhood: a report from the French Leukaemia Long-Term Follow-Up Study (LEA)F Isfan, J Kanold, E Merlin, et al.
Journal of Pediatric Urology|October 28, 2011
Polymorphisms of MAMLD1 gene in hypospadiasN Kalfa, F Cassorla, F Audran, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
European Journal of Endocrinology|January 29, 2011
Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative formsR Reynaud, F Albarel, A Saveanu, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 23, 2016
GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone DeficiencyF Castinetti, A F Daly, C A Stratakis, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarismF Castinetti, A Saveanu, R Reynaud, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 30, 2022
Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in FranceL Levaillant, F Huet, P Bretones, et al.
Primary Care Diabetes|November 24, 2023
Impact of continuous glucose monitoring on everyday life of young children with type 1 diabetes and their parents: An evaluation of 114 familiesK Aouchiche, D Bernoux, E Baechler Sadoul, et al.
Bone Marrow Transplantation|July 5, 2011
Growth hormone treatment impact on growth rate and final height of patients who received HSCT with TBI or/and cranial irradiation in childhood: a report from the French Leukaemia Long-Term Follow-Up Study (LEA)F Isfan, J Kanold, E Merlin, et al.
Journal of Pediatric Urology|October 28, 2011
Polymorphisms of MAMLD1 gene in hypospadiasN Kalfa, F Cassorla, F Audran, et al.
Pageof 5