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E Mayayo

Showing results (121-130 of 130) with videos related to

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Anales Espanoles De Pediatria|December 1, 1993
[Reduced erythrocyte glutathione and urinary thioethers in children undergoing treatment with paracetamol]M L Bernal Ruiz, B Sinues Porta, J Lanuza Giménez, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 1, 2003
Value of magnetic resonance imaging for the diagnosis and follow-up of haemophilic arthropathyM Dobón, J F Lucía, C Aguilar, et al.
Gastroenterologia Y Hepatologia|November 17, 2004
[Spontaneous aneurysmal portohepatic fistula: imaging diagnosis]E Mayayo Sinués, M C Lidón Lorente, J Fuentes Olmo, et al.
Anales Espanoles De Pediatria|October 1, 1988
[Patterns of growth in congenital adrenal hyperplasia. Correlation between glucocorticoid therapy and stature]J M Igea, L Lóridan, P Martul, 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.
American Journal of Nephrology|January 1, 1993
Minimal-change glomerulopathy and carcinoma. Report of two cases and review of the literatureA Martinez-Vea, J M Panisello, C García, 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 Espanoles De Pediatria|June 1, 1981
[Solitary unilocular hepatic cyst in the newborn infant]A Gómez Fraile, V Segarra Llido, R Segade Andrade, et al.
Revista Espanola De Enfermedades Digestivas|February 1, 1995
[Intraperitoneal hemorrhage caused by cavernous hemangioma of the small intestine]J M Castellote Caixal, R Luengo, L Ledesma, et al.
The Journal of Clinical Endocrinology and Metabolism|February 13, 2010
Novel (60%) and recurrent (40%) androgen receptor gene mutations in a series of 59 patients with a 46,XY disorder of sex developmentL Audi, M Fernández-Cancio, A Carrascosa, et al.
Pageof 13

Showing results (121-130 of 130) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 130 results.
Anales Espanoles De Pediatria|December 1, 1993
[Reduced erythrocyte glutathione and urinary thioethers in children undergoing treatment with paracetamol]M L Bernal Ruiz, B Sinues Porta, J Lanuza Giménez, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 1, 2003
Value of magnetic resonance imaging for the diagnosis and follow-up of haemophilic arthropathyM Dobón, J F Lucía, C Aguilar, et al.
Gastroenterologia Y Hepatologia|November 17, 2004
[Spontaneous aneurysmal portohepatic fistula: imaging diagnosis]E Mayayo Sinués, M C Lidón Lorente, J Fuentes Olmo, et al.
Anales Espanoles De Pediatria|October 1, 1988
[Patterns of growth in congenital adrenal hyperplasia. Correlation between glucocorticoid therapy and stature]J M Igea, L Lóridan, P Martul, 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.
American Journal of Nephrology|January 1, 1993
Minimal-change glomerulopathy and carcinoma. Report of two cases and review of the literatureA Martinez-Vea, J M Panisello, C García, 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 Espanoles De Pediatria|June 1, 1981
[Solitary unilocular hepatic cyst in the newborn infant]A Gómez Fraile, V Segarra Llido, R Segade Andrade, et al.
Revista Espanola De Enfermedades Digestivas|February 1, 1995
[Intraperitoneal hemorrhage caused by cavernous hemangioma of the small intestine]J M Castellote Caixal, R Luengo, L Ledesma, et al.
The Journal of Clinical Endocrinology and Metabolism|February 13, 2010
Novel (60%) and recurrent (40%) androgen receptor gene mutations in a series of 59 patients with a 46,XY disorder of sex developmentL Audi, M Fernández-Cancio, A Carrascosa, et al.
Pageof 13