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The Journal of Pediatrics
|
October 21, 2009
Long-term growth hormone therapy in an adolescent boy with 45,X/46,XidicY(p11)
Frances M Guevarra, Saroj Nimkarn, Maria I New, et al.
European Journal of Pediatrics
|
November 16, 2011
Congenital lipoid adrenal hyperplasia (a rare form of adrenal insufficiency and ambiguous genitalia) caused by a novel mutation of the steroidogenic acute regulatory protein gene
Oksana Lekarev, Delphine Mallet, Tony Yuen, et al.
Trends in Endocrinology and Metabolism: TEM
|
April 6, 2005
Monogenic low renin hypertension
Maria I New, David S Geller, Francesco Fallo, et al.
Fertility and Sterility
|
December 21, 2013
Fertility in patients with congenital adrenal hyperplasia
David E Reichman, Perrin C White, Maria I New, et al.
Pediatrics
|
February 5, 2002
Bilateral laparoscopic adrenalectomy as a treatment for classic congenital adrenal hyperplasia attributable to 21-hydroxylase deficiency
Glenn A Gmyrek, Maria I New, R E Sosa, et al.
Hormone Research in Paediatrics
|
August 7, 2010
The clinical and molecular heterogeneity of 17βHSD-3 enzyme deficiency
Minu M George, Maria I New, Svetlana Ten, et al.
Archives of Sexual Behavior
|
December 25, 2007
Sexual orientation in women with classical or non-classical congenital adrenal hyperplasia as a function of degree of prenatal androgen excess
Heino F L Meyer-Bahlburg, Curtis Dolezal, Susan W Baker, et al.
International Journal of Endocrinology
|
July 3, 2014
Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian Families with 11 β -Hydroxylase Deficiency
Katja Dumic, Tony Yuen, Zorana Grubic, et al.
Journal of Pediatric Psychology
|
May 19, 2016
Stigma in Medical Settings As Reported Retrospectively by Women With Congenital Adrenal Hyperplasia (CAH) for Their Childhood and Adolescence
Heino F L Meyer-Bahlburg, Jananne Khuri, Jazmin Reyes-Portillo, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 20, 2009
Partial hypogonadotropic hypogonadism associated with the Leu266Arg and Gln106Arg mutation of the gonadotropin-releasing hormone receptor
J B Quintos, Stephan Krotz, Maria G Vogiatzi, et al.
Page
of 11
Search research articles
Search
Showing results (31-40 of 104) with videos related to
Sort By:
Page
of 11
The Journal of Pediatrics
|
October 21, 2009
Long-term growth hormone therapy in an adolescent boy with 45,X/46,XidicY(p11)
Frances M Guevarra, Saroj Nimkarn, Maria I New, et al.
European Journal of Pediatrics
|
November 16, 2011
Congenital lipoid adrenal hyperplasia (a rare form of adrenal insufficiency and ambiguous genitalia) caused by a novel mutation of the steroidogenic acute regulatory protein gene
Oksana Lekarev, Delphine Mallet, Tony Yuen, et al.
Trends in Endocrinology and Metabolism: TEM
|
April 6, 2005
Monogenic low renin hypertension
Maria I New, David S Geller, Francesco Fallo, et al.
Fertility and Sterility
|
December 21, 2013
Fertility in patients with congenital adrenal hyperplasia
David E Reichman, Perrin C White, Maria I New, et al.
Pediatrics
|
February 5, 2002
Bilateral laparoscopic adrenalectomy as a treatment for classic congenital adrenal hyperplasia attributable to 21-hydroxylase deficiency
Glenn A Gmyrek, Maria I New, R E Sosa, et al.
Hormone Research in Paediatrics
|
August 7, 2010
The clinical and molecular heterogeneity of 17βHSD-3 enzyme deficiency
Minu M George, Maria I New, Svetlana Ten, et al.
Archives of Sexual Behavior
|
December 25, 2007
Sexual orientation in women with classical or non-classical congenital adrenal hyperplasia as a function of degree of prenatal androgen excess
Heino F L Meyer-Bahlburg, Curtis Dolezal, Susan W Baker, et al.
International Journal of Endocrinology
|
July 3, 2014
Two Novel CYP11B1 Gene Mutations in Patients from Two Croatian Families with 11 β -Hydroxylase Deficiency
Katja Dumic, Tony Yuen, Zorana Grubic, et al.
Journal of Pediatric Psychology
|
May 19, 2016
Stigma in Medical Settings As Reported Retrospectively by Women With Congenital Adrenal Hyperplasia (CAH) for Their Childhood and Adolescence
Heino F L Meyer-Bahlburg, Jananne Khuri, Jazmin Reyes-Portillo, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 20, 2009
Partial hypogonadotropic hypogonadism associated with the Leu266Arg and Gln106Arg mutation of the gonadotropin-releasing hormone receptor
J B Quintos, Stephan Krotz, Maria G Vogiatzi, et al.
Page
of 11