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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 18, 1999
[Neonatal screening of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Lille experience 1980-1996]
M Cartigny-Maciejewski, N Guilley, S Vanderbecken, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 27, 2010
[Autoimmune polyendocrine syndrome type 1]
E Proust-Lemoine, P Saugier-Veber, H Lefebvre, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1992
Screening for Y-derived sex determining gene SRY in 40 patients with Turner syndrome
R Medlej, J M Lobaccaro, P Berta, et al.
Neurology. Clinical Practice
|
November 16, 2022
Discordance Between Perceptions and Experience of Lumbar Puncture: A Prospective Study
Yoshie Umemura, Baber Khan, Benjamin J Weill, et al.
Diabetologia
|
January 20, 2007
Single nucleotide polymorphisms in the neuropeptide Y2 receptor (NPY2R) gene and association with severe obesity in French white subjects
A Siddiq, M Gueorguiev, C Samson, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 12, 2002
Mutation screening of the urocortin gene: identification of new single nucleotide polymorphisms and association studies with obesity in French Caucasians
J Delplanque, F Vasseur, E Durand, et al.
Annals of Human Genetics
|
October 24, 2008
A genetic study of the ghrelin and growth hormone secretagogue receptor (GHSR) genes and stature
M Gueorguiev, C Lecoeur, M Benzinou, et al.
Hormone Research in Paediatrics
|
May 11, 2010
Autoimmune polyendocrine syndrome type 1 in north-western France: AIRE gene mutation specificities and severe forms needing immunosuppressive therapies
E Proust-Lemoine, P Saugier-Véber, D Lefranc, et al.
International Journal of Obesity (2005)
|
October 24, 2012
Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French population
S Robiou-du-Pont, A Bonnefond, L Yengo, et al.
The Journal of Pediatrics
|
February 1, 1996
Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathy
J L Michaud, E Héon, F Guilbert, et al.
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of 13
Search research articles
Search
Showing results (111-120 of 123) with videos related to
Sort By:
Page
of 13
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 18, 1999
[Neonatal screening of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Lille experience 1980-1996]
M Cartigny-Maciejewski, N Guilley, S Vanderbecken, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 27, 2010
[Autoimmune polyendocrine syndrome type 1]
E Proust-Lemoine, P Saugier-Veber, H Lefebvre, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1992
Screening for Y-derived sex determining gene SRY in 40 patients with Turner syndrome
R Medlej, J M Lobaccaro, P Berta, et al.
Neurology. Clinical Practice
|
November 16, 2022
Discordance Between Perceptions and Experience of Lumbar Puncture: A Prospective Study
Yoshie Umemura, Baber Khan, Benjamin J Weill, et al.
Diabetologia
|
January 20, 2007
Single nucleotide polymorphisms in the neuropeptide Y2 receptor (NPY2R) gene and association with severe obesity in French white subjects
A Siddiq, M Gueorguiev, C Samson, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 12, 2002
Mutation screening of the urocortin gene: identification of new single nucleotide polymorphisms and association studies with obesity in French Caucasians
J Delplanque, F Vasseur, E Durand, et al.
Annals of Human Genetics
|
October 24, 2008
A genetic study of the ghrelin and growth hormone secretagogue receptor (GHSR) genes and stature
M Gueorguiev, C Lecoeur, M Benzinou, et al.
Hormone Research in Paediatrics
|
May 11, 2010
Autoimmune polyendocrine syndrome type 1 in north-western France: AIRE gene mutation specificities and severe forms needing immunosuppressive therapies
E Proust-Lemoine, P Saugier-Véber, D Lefranc, et al.
International Journal of Obesity (2005)
|
October 24, 2012
Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French population
S Robiou-du-Pont, A Bonnefond, L Yengo, et al.
The Journal of Pediatrics
|
February 1, 1996
Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathy
J L Michaud, E Héon, F Guilbert, et al.
Page
of 13