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Lancet (London, England)
|
January 21, 1989
Cystic fibrosis with and without meconium ileus
M Auvinet, Y Morel, V Chambon, et al.
La Revue De Medecine Interne
|
September 15, 2004
[Haemochromatosis screening in 120 patients complaining with persistant fatigue]
D Vital Durand, S François, R Nové-Josserand, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 7, 2001
Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
C Deneux, V Tardy, A Dib, et al.
La Revue De Medecine Interne
|
January 1, 1997
[Male infertility caused by bilateral agenesis of the vas deferens: a new clinical form of cystic fibrosis?]
I Durieu, F Bey-Omar, J Rollet, et al.
Endocrine Research
|
February 24, 2001
A new insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency
J Simard, M L Ricketts, A M Moisan, et al.
Annales De Pediatrie
|
September 1, 1993
[Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 9 treated pregnancies]
J L Nivelon, M Chouchane, M G Forest, et al.
Andrology
|
February 5, 2016
Endocrine and molecular investigations in a cohort of 25 adolescent males with prominent/persistent pubertal gynecomastia
F Paris, L Gaspari, F Mbou, et al.
Patient Education and Counseling
|
June 1, 1997
Personalities and alimentary behaviors in obese patients
A Golay, I Hagon, D Painot, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 19, 2010
Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier
V Tardy, R Menassa, V Sulmont, et al.
Bulletin De L'Academie Nationale De Medecine
|
February 1, 1994
[Therapeutic hopes in excretory azoospermia and genetic risks in congenital aplasia of the vas deferens]
M Cognat, I Durieu, F Bey-Omar, et al.
Page
of 14
Search research articles
Search
Showing results (91-100 of 138) with videos related to
Sort By:
Page
of 14
Lancet (London, England)
|
January 21, 1989
Cystic fibrosis with and without meconium ileus
M Auvinet, Y Morel, V Chambon, et al.
La Revue De Medecine Interne
|
September 15, 2004
[Haemochromatosis screening in 120 patients complaining with persistant fatigue]
D Vital Durand, S François, R Nové-Josserand, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 7, 2001
Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
C Deneux, V Tardy, A Dib, et al.
La Revue De Medecine Interne
|
January 1, 1997
[Male infertility caused by bilateral agenesis of the vas deferens: a new clinical form of cystic fibrosis?]
I Durieu, F Bey-Omar, J Rollet, et al.
Endocrine Research
|
February 24, 2001
A new insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency
J Simard, M L Ricketts, A M Moisan, et al.
Annales De Pediatrie
|
September 1, 1993
[Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 9 treated pregnancies]
J L Nivelon, M Chouchane, M G Forest, et al.
Andrology
|
February 5, 2016
Endocrine and molecular investigations in a cohort of 25 adolescent males with prominent/persistent pubertal gynecomastia
F Paris, L Gaspari, F Mbou, et al.
Patient Education and Counseling
|
June 1, 1997
Personalities and alimentary behaviors in obese patients
A Golay, I Hagon, D Painot, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 19, 2010
Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier
V Tardy, R Menassa, V Sulmont, et al.
Bulletin De L'Academie Nationale De Medecine
|
February 1, 1994
[Therapeutic hopes in excretory azoospermia and genetic risks in congenital aplasia of the vas deferens]
M Cognat, I Durieu, F Bey-Omar, et al.
Page
of 14