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Advances in Experimental Medicine and Biology
|
June 22, 2011
Studies of a cohort of 46,XY with DSD including steroid biosynthesis deficiencies
Yves Morel, Ingrid Plotton, Delphine Mallet, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 27, 2005
Delayed diagnosis of congenital adrenal hyperplasia with salt wasting due to type II 3beta-hydroxysteroid dehydrogenase deficiency
Trine H Johannsen, Delphine Mallet, Harriet Dige-Petersen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 7, 2004
Influence of SHBG gene pentanucleotide TAAAA repeat and D327N polymorphism on serum sex hormone-binding globulin concentration in hirsute women
Patrice Cousin, Laurence Calemard-Michel, Hervé Lejeune, et al.
The British Journal of Nutrition
|
November 21, 2015
Effect of dietary protein on plasma insulin-like growth factor-1, growth, and body composition in healthy term infants: a randomised, double-blind, controlled trial (Early Protein and Obesity in Childhood (EPOCH) study)
Guy Putet, Jean-Marc Labaune, Katherine Mace, et al.
American Journal of Medical Genetics. Part A
|
May 19, 2009
Familial acampomelic form of campomelic dysplasia caused by a 960 kb deletion upstream of SOX9
Claire Lecointre, Olivier Pichon, Antoine Hamel, et al.
Clinical Endocrinology
|
April 4, 2012
Healthy birth after testicular extraction of sperm and ICSI from an azoospermic man with mild androgen insensitivity syndrome caused by an androgen receptor partial loss-of-function mutation
Nathalie Massin, Hélène Bry, Lavinia Vija, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 8, 2016
P450 Oxidoreductase Deficiency: Loss of Activity Caused by Protein Instability From a Novel L374H Mutation
Shaheena Parween, Florence Roucher-Boulez, Christa E Flück, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 17, 2007
We used to call them hermaphrodites
Eric Vilain, John C Achermann, Erica A Eugster, et al.
Biochemical and Biophysical Research Communications
|
August 17, 2011
Deletion of P399_E401 in NADPH cytochrome P450 oxidoreductase results in partial mixed oxidase deficiency
Christa E Flück, Delphine Mallet, Gaby Hofer, et al.
African Journal of Paediatric Surgery : AJPS
|
November 28, 2015
Laparoscopic-assisted vaginal pull-through: A new approach for congenital adrenal hyperplasia patients with high urogenital sinus
Jacques Birraux, Faustin Tambo Mouafo, Sophie Dahoun, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 92) with videos related to
Sort By:
Page
of 10
Advances in Experimental Medicine and Biology
|
June 22, 2011
Studies of a cohort of 46,XY with DSD including steroid biosynthesis deficiencies
Yves Morel, Ingrid Plotton, Delphine Mallet, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 27, 2005
Delayed diagnosis of congenital adrenal hyperplasia with salt wasting due to type II 3beta-hydroxysteroid dehydrogenase deficiency
Trine H Johannsen, Delphine Mallet, Harriet Dige-Petersen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 7, 2004
Influence of SHBG gene pentanucleotide TAAAA repeat and D327N polymorphism on serum sex hormone-binding globulin concentration in hirsute women
Patrice Cousin, Laurence Calemard-Michel, Hervé Lejeune, et al.
The British Journal of Nutrition
|
November 21, 2015
Effect of dietary protein on plasma insulin-like growth factor-1, growth, and body composition in healthy term infants: a randomised, double-blind, controlled trial (Early Protein and Obesity in Childhood (EPOCH) study)
Guy Putet, Jean-Marc Labaune, Katherine Mace, et al.
American Journal of Medical Genetics. Part A
|
May 19, 2009
Familial acampomelic form of campomelic dysplasia caused by a 960 kb deletion upstream of SOX9
Claire Lecointre, Olivier Pichon, Antoine Hamel, et al.
Clinical Endocrinology
|
April 4, 2012
Healthy birth after testicular extraction of sperm and ICSI from an azoospermic man with mild androgen insensitivity syndrome caused by an androgen receptor partial loss-of-function mutation
Nathalie Massin, Hélène Bry, Lavinia Vija, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 8, 2016
P450 Oxidoreductase Deficiency: Loss of Activity Caused by Protein Instability From a Novel L374H Mutation
Shaheena Parween, Florence Roucher-Boulez, Christa E Flück, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 17, 2007
We used to call them hermaphrodites
Eric Vilain, John C Achermann, Erica A Eugster, et al.
Biochemical and Biophysical Research Communications
|
August 17, 2011
Deletion of P399_E401 in NADPH cytochrome P450 oxidoreductase results in partial mixed oxidase deficiency
Christa E Flück, Delphine Mallet, Gaby Hofer, et al.
African Journal of Paediatric Surgery : AJPS
|
November 28, 2015
Laparoscopic-assisted vaginal pull-through: A new approach for congenital adrenal hyperplasia patients with high urogenital sinus
Jacques Birraux, Faustin Tambo Mouafo, Sophie Dahoun, et al.
Page
of 10