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M Oyarzábal

Showing results (1-10 of 15) with videos related to

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Anales Del Sistema Sanitario De Navarra|November 26, 2008
[Low height and rare diseases]Mj Chueca Guindulain, S Berrade, M Oyarzábal
Anales Del Sistema Sanitario De Navarra|August 2, 2003
[Neonatal screening of congenital Hypothyroidism: result of the Navarra program]M Oyarzábal, M Chueca, J Elso, et al.
Anales Espanoles De Pediatria|August 1, 1978
[Leopard syndrom. Four observations (author's transl)]M Oyarzábal, E Los Arcos, C Mendívil, et al.
Atencion Primaria|January 1, 1994
[The costs for a health center in relation to its activities]M Oyarzábal, P Albert, J Escamilla, et al.
Pediatric Endocrinology Reviews : PER|August 6, 2010
The effects of growth hormone deficiency and growth hormone replacement therapy on intellectual ability, personality and adjustment in childrenB Puga González, A Ferrández Longás, M Oyarzábal, et al.
Anales Espanoles De Pediatria|August 1, 1978
[Neurological alterations due to metoclopramide in children (author's transl)]A Delgado, J Molina, J Egüés, et al.
Anales Espanoles De Pediatria|January 1, 1983
[Precocious puberty associated with Von Recklinghausen's disease. Developmental follow-up under cyproterone acetate treatment]M Oyarzábal, M Puente, R Mayorga, et al.
Hormone Research|August 26, 1999
A novel frameshift mutation in the first exon of the 21-OH gene found in homozygosity in an apparently nonconsanguineous familyB Ezquieta, M Oyarzábal, C M Jariego, et al.
Anales Del Sistema Sanitario De Navarra|August 2, 2003
[Child obesity in Navarra: evolution, tendency and relation between child and adult obesity. Pecna study]F Repáraz, M Chueca, R Elcarte, et al.
Clinical Genetics|September 11, 2002
Gene conversion (655G splicing mutation) and the founder effect (Gln318Stop) contribute to the most frequent severe point mutations in congenital adrenal hyperplasia (21-hydroxylase deficiency) in the Spanish populationB Ezquieta, E Cueva, M Oyarzábal, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Anales Del Sistema Sanitario De Navarra|November 26, 2008
[Low height and rare diseases]Mj Chueca Guindulain, S Berrade, M Oyarzábal
Anales Del Sistema Sanitario De Navarra|August 2, 2003
[Neonatal screening of congenital Hypothyroidism: result of the Navarra program]M Oyarzábal, M Chueca, J Elso, et al.
Anales Espanoles De Pediatria|August 1, 1978
[Leopard syndrom. Four observations (author's transl)]M Oyarzábal, E Los Arcos, C Mendívil, et al.
Atencion Primaria|January 1, 1994
[The costs for a health center in relation to its activities]M Oyarzábal, P Albert, J Escamilla, et al.
Pediatric Endocrinology Reviews : PER|August 6, 2010
The effects of growth hormone deficiency and growth hormone replacement therapy on intellectual ability, personality and adjustment in childrenB Puga González, A Ferrández Longás, M Oyarzábal, et al.
Anales Espanoles De Pediatria|August 1, 1978
[Neurological alterations due to metoclopramide in children (author's transl)]A Delgado, J Molina, J Egüés, et al.
Anales Espanoles De Pediatria|January 1, 1983
[Precocious puberty associated with Von Recklinghausen's disease. Developmental follow-up under cyproterone acetate treatment]M Oyarzábal, M Puente, R Mayorga, et al.
Hormone Research|August 26, 1999
A novel frameshift mutation in the first exon of the 21-OH gene found in homozygosity in an apparently nonconsanguineous familyB Ezquieta, M Oyarzábal, C M Jariego, et al.
Anales Del Sistema Sanitario De Navarra|August 2, 2003
[Child obesity in Navarra: evolution, tendency and relation between child and adult obesity. Pecna study]F Repáraz, M Chueca, R Elcarte, et al.
Clinical Genetics|September 11, 2002
Gene conversion (655G splicing mutation) and the founder effect (Gln318Stop) contribute to the most frequent severe point mutations in congenital adrenal hyperplasia (21-hydroxylase deficiency) in the Spanish populationB Ezquieta, E Cueva, M Oyarzábal, et al.
Pageof 2