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Anales Espanoles De Pediatria
|
February 26, 2000
[Reference values for thyroid hormones, thyrotropin and thyroglobulin in healthy children of Zaragoza]
A Cortés-Blanco, E Mayayo Dehesa, A Ferrández Longás, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 12, 2004
Childhood-onset congenital adrenal hyperplasia: long-term outcome and optimization of therapy
J I Labarta, E Bello, M Ruiz-Echarri, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
May 6, 2005
[Study of bone mass in Turner syndrome]
E Cancer Gaspar, M Ruiz-Echarri Zelaya, J I Labarta Aizpún, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
October 13, 2005
[Study of bone mass in patients with growth hormone deficiency]
E Cancer Gaspar, M Ruiz-Echarri Zelaya, J I Labarta Aizpún, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 17, 1998
Insulin-like growth factor binding protein-I levels are strongly associated with insulin sensitivity and obesity in early pubertal children
S H Travers, J I Labarta, S E Gargosky, et al.
Clinical Endocrinology
|
March 14, 1998
Immunoblot studies of the acid-labile subunit (ALS) in biological fluids, normal human serum and in children with GH deficiency and GH receptor deficiency before and after long-term therapy with GH or IGF-I respectively
J I Labarta, S E Gargosky, D M Simpson, et al.
Journal of Endocrinological Investigation
|
November 18, 2021
Delphi consensus on the diagnosis and treatment of patients with short stature in Spain: GROW-SENS study
R Corripio-Collado, C Fernández-Ramos, I González-Casado, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
December 21, 2010
[Different expression of the Asn264LysfsX35 mutation of the GNAS gene in a family with pseudohypoparathyroidism.]
A de Arriba Muñoz, J I Labarta Aizpún, E Mayayo Dehesa, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
March 6, 2014
[Congenital adrenal hyperplasia due to lack of 17α-hydroxylase: a report of a new mutation in the gene CYP17A1]
J I Perales Martínez, B Pina Marqués, A de Arriba Muñoz, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
March 4, 2014
[Type 1 polyglandular autoimmune syndrome associated with C322fsx372 mutation]
P Roncalés-Samanes, A de Arriba Muñoz, G M Lou Francés, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Anales Espanoles De Pediatria
|
February 26, 2000
[Reference values for thyroid hormones, thyrotropin and thyroglobulin in healthy children of Zaragoza]
A Cortés-Blanco, E Mayayo Dehesa, A Ferrández Longás, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 12, 2004
Childhood-onset congenital adrenal hyperplasia: long-term outcome and optimization of therapy
J I Labarta, E Bello, M Ruiz-Echarri, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
May 6, 2005
[Study of bone mass in Turner syndrome]
E Cancer Gaspar, M Ruiz-Echarri Zelaya, J I Labarta Aizpún, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
October 13, 2005
[Study of bone mass in patients with growth hormone deficiency]
E Cancer Gaspar, M Ruiz-Echarri Zelaya, J I Labarta Aizpún, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 17, 1998
Insulin-like growth factor binding protein-I levels are strongly associated with insulin sensitivity and obesity in early pubertal children
S H Travers, J I Labarta, S E Gargosky, et al.
Clinical Endocrinology
|
March 14, 1998
Immunoblot studies of the acid-labile subunit (ALS) in biological fluids, normal human serum and in children with GH deficiency and GH receptor deficiency before and after long-term therapy with GH or IGF-I respectively
J I Labarta, S E Gargosky, D M Simpson, et al.
Journal of Endocrinological Investigation
|
November 18, 2021
Delphi consensus on the diagnosis and treatment of patients with short stature in Spain: GROW-SENS study
R Corripio-Collado, C Fernández-Ramos, I González-Casado, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
December 21, 2010
[Different expression of the Asn264LysfsX35 mutation of the GNAS gene in a family with pseudohypoparathyroidism.]
A de Arriba Muñoz, J I Labarta Aizpún, E Mayayo Dehesa, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
March 6, 2014
[Congenital adrenal hyperplasia due to lack of 17α-hydroxylase: a report of a new mutation in the gene CYP17A1]
J I Perales Martínez, B Pina Marqués, A de Arriba Muñoz, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
March 4, 2014
[Type 1 polyglandular autoimmune syndrome associated with C322fsx372 mutation]
P Roncalés-Samanes, A de Arriba Muñoz, G M Lou Francés, et al.
Page
of 3