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Yves Morel

Showing results (21-30 of 92) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|October 9, 2004
Gonadal dysgenesis without adrenal insufficiency in a 46, XY patient heterozygous for the nonsense C16X mutation: a case of SF1 haploinsufficiencyDelphine Mallet, Patricia Bretones, Laurence Michel-Calemard, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|January 12, 2010
Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriersFrançoise Paris, Véronique Tardy, Anne Chalançon, et al.
Prenatal Diagnosis|March 28, 2006
Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD) without DNA from an index patient in a current pregnancyHarald Gaspar, Laurence Michel-Calemard, Yves Morel, et al.
Gastroenterologie Clinique Et Biologique|July 18, 2002
[Non alcoholic steatohepatitis: a multifactorial, frequent, paucysymptomatic liver disease with a fibrotic outcome]Nadia Laroussi, Jean-François Mosnier, Yves Morel, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 8, 2009
Precocious puberty and unlicensed paediatric drugs for severe hyperparathyroidismJustine Bacchetta, Ingrid Plotton, Bruno Ranchin, et al.
Prenatal Diagnosis|August 10, 2004
Campomelic acampomelic dysplasia presenting with increased nuchal translucency in the first trimesterLaurence Michel-Calemard, Gaëtan Lesca, Yves Morel, et al.
Archives of Pediatrics & Adolescent Medicine|February 8, 2012
Efficiency of neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency in children born in mainland France between 1996 and 2003Bénédicte Coulm, Joel Coste, Véronique Tardy, et al.
SN Computer Science|May 31, 2021
Cross-Validation Comparison of COVID-19 Forecast ModelsMintodê Nicodème Atchadé, Yves Morel Sokadjo, Aliou Djibril Moussa, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 30, 2016
A novel morphological approach to gonads in disorders of sex developmentLaureline Lepais, Yves Morel, Pierre Mouriquand, et al.
Expert Review of Endocrinology & Metabolism|February 21, 2019
Complete androgen insensitivity syndrome: diagnosis and managementAlaa Cheikhelard, Elisabeth Thibaud, Yves Morel, et al.
Pageof 10

Showing results (21-30 of 92) with videos related to

Sort By:
Pageof 10
The Journal of Clinical Endocrinology and Metabolism|October 9, 2004
Gonadal dysgenesis without adrenal insufficiency in a 46, XY patient heterozygous for the nonsense C16X mutation: a case of SF1 haploinsufficiencyDelphine Mallet, Patricia Bretones, Laurence Michel-Calemard, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|January 12, 2010
Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriersFrançoise Paris, Véronique Tardy, Anne Chalançon, et al.
Prenatal Diagnosis|March 28, 2006
Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD) without DNA from an index patient in a current pregnancyHarald Gaspar, Laurence Michel-Calemard, Yves Morel, et al.
Gastroenterologie Clinique Et Biologique|July 18, 2002
[Non alcoholic steatohepatitis: a multifactorial, frequent, paucysymptomatic liver disease with a fibrotic outcome]Nadia Laroussi, Jean-François Mosnier, Yves Morel, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 8, 2009
Precocious puberty and unlicensed paediatric drugs for severe hyperparathyroidismJustine Bacchetta, Ingrid Plotton, Bruno Ranchin, et al.
Prenatal Diagnosis|August 10, 2004
Campomelic acampomelic dysplasia presenting with increased nuchal translucency in the first trimesterLaurence Michel-Calemard, Gaëtan Lesca, Yves Morel, et al.
Archives of Pediatrics & Adolescent Medicine|February 8, 2012
Efficiency of neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency in children born in mainland France between 1996 and 2003Bénédicte Coulm, Joel Coste, Véronique Tardy, et al.
SN Computer Science|May 31, 2021
Cross-Validation Comparison of COVID-19 Forecast ModelsMintodê Nicodème Atchadé, Yves Morel Sokadjo, Aliou Djibril Moussa, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 30, 2016
A novel morphological approach to gonads in disorders of sex developmentLaureline Lepais, Yves Morel, Pierre Mouriquand, et al.
Expert Review of Endocrinology & Metabolism|February 21, 2019
Complete androgen insensitivity syndrome: diagnosis and managementAlaa Cheikhelard, Elisabeth Thibaud, Yves Morel, et al.
Pageof 10