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yves morel
yves morel
PU-PH faculté de médecine Lyon-Est
Email verificata su chu-lyon.fr
Titolo
Citata da
Citata da
Anno
Consensus statement on management of intersex disorders
PA Lee, CP Houk, SF Ahmed, IA Hughes, ...
Pediatrics 118 (2), e488-e500, 2006
14032006
Clinical features and prognostic factors of listeriosis: the MONALISA national prospective cohort study
C Charlier, É Perrodeau, A Leclercq, B Cazenave, B Pilmis, B Henry, ...
The Lancet Infectious Diseases 17 (5), 510-519, 2017
4822017
Evaluation of gonadal function in 107 intersex patients by means of serum antimullerian hormone measurement
RA Rey, C Belville, C Nihoul-Fékété, L Michel-Calemard, MG Forest, ...
The Journal of Clinical Endocrinology & Metabolism 84 (2), 627-631, 1999
3121999
Congenital adrenal hyperplasia due to point mutations in the type II 3β–hydroxysteroid dehydrogenase gene
E Rhéaume, J Simard, Y Morel, F Mebarki, M Zachmann, MG Forest, ...
Nature genetics 1 (4), 239-245, 1992
2781992
Fertility in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
M Bidet, C Bellanné-Chantelot, MB Galand-Portier, JL Golmard, V Tardy, ...
The Journal of Clinical Endocrinology & Metabolism 95 (3), 1182-1190, 2010
2402010
Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Y Morel, WL Miller
Advances in human genetics, 1-68, 1991
2401991
Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members
M Bidet, C Bellanné-Chantelot, MB Galand-Portier, V Tardy, L Billaud, ...
The Journal of Clinical Endocrinology & Metabolism 94 (5), 1570-1578, 2009
2382009
Aerosol administration of a recombinant adenovirus expressing CFTR to cystic fibrosis patients: a phase I clinical trial
G Bellon, L Michel-Calemard, D Thouvenot, V Jagneaux, F Poitevin, ...
Human gene therapy 8 (1), 15-25, 1997
2161997
Summary of consensus statement on intersex disorders and their management
CP Houk, IA Hughes, SF Ahmed, PA Lee, ...
Pediatrics 118 (2), 753-757, 2006
2092006
Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development
S Benko, CT Gordon, D Mallet, R Sreenivasan, C Thauvin-Robinet, ...
Journal of medical genetics 48 (12), 825-830, 2011
2082011
Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
C Deneux, V Tardy, A Dib, E Mornet, L Billaud, D Charron, Y Morel, ...
The Journal of Clinical Endocrinology & Metabolism 86 (1), 207-213, 2001
1992001
Prenatal diagnosis and treatment of 21-hydroxylase deficiency
MG Forest, M David, Y Morel
The Journal of steroid biochemistry and molecular biology 45 (1-3), 75-82, 1993
1911993
Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus.
Y Morel, J Bristow, SE Gitelman, WL Miller
Proceedings of the National Academy of Sciences 86 (17), 6582-6586, 1989
1901989
Postnatal changes of T, LH, and FSH in 46, XY infants with mutations in the AR gene
C Bouvattier, JC Carel, C Lecointre, A David, C Sultan, AM Bertrand, ...
The Journal of Clinical Endocrinology & Metabolism 87 (1), 29-32, 2002
1862002
Influence of SHBG Gene Pentanucleotide TAAAA Repeat and D327N Polymorphism on Serum Sex Hormone-Binding Globulin Concentration in Hirsute Women
P Cousin, L Calemard-Michel, H Lejeune, G Raverot, N Yessaad, ...
The Journal of Clinical Endocrinology & Metabolism 89 (2), 917-924, 2004
1712004
Molecular biology and genetics of the 3β-hydroxysteroid dehydrogenase/Δ5-Δ4 isomerase gene family.
J Simard, F Durocher, F Mebarki, C Turgeon, R Sanchez, Y Labrie, ...
1691996
Aetiological diagnosis of male sex ambiguity: a collaborative study
Y Morel, R Rey, C Teinturier, M Nicolino, L Michel-Calemard, ...
European journal of pediatrics 161, 49-59, 2002
1612002
Anti-müllerian hormone in children with androgen insensitivity
R Rey, F Mebarki, MG Forest, I Mowszowicz, RL Cate, Y Morel, ...
The Journal of Clinical Endocrinology & Metabolism 79 (4), 960-964, 1994
1561994
The molecular genetics of 21-hydroxylase deficiency
WL Miller, Y Morel
Annual review of genetics 23 (1), 371-393, 1989
1521989
Long Term Treatment of Male and Female Precocious Puberty by Periodic Administration of a Long-Acting Preparation of D-Trp6-Luteinizing Hormone-Releasing …
M Roger, JL Chaussain, P Berlier, M Bost, P CANLORBE, M Colle, ...
The Journal of Clinical Endocrinology & Metabolism 62 (4), 670-677, 1986
1501986
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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