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A Vallo

Showing results (61-70 of 73) with videos related to

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Anales Espanoles De Pediatria|May 1, 1993
[Use of metronidazole in four cases of methyl-malonic acidemia]P Sanjurjo Crespo, M Labayru Echeverría, N Ingunza Aguirre, et al.
The Journal of Pediatrics|August 1, 1983
Biochemical features of dietary chloride deficiency syndrome: a comparative study of 30 casesJ Rodriguez-Soriano, A Vallo, G Castillo, et al.
Anales Espanoles De Pediatria|March 14, 1998
[Treatment of idiopathic nephrotic syndrome with cyclosporin A]G Ariceta Iraola, J Rodríguez Soriano, A Vallo Boado, et al.
Transplantation Proceedings|September 10, 2003
Immunoprophylaxis with Simulect (basiliximab) in pediatric kidney transplant recipients: results from routine clinical practice at 5 kidney transplant unitsC García Meseguer, A Vila López, A Luque de Pablos, et al.
Anales Espanoles De Pediatria|December 1, 1991
[Ornithine-transcarbamylase deficiency: prognostic difficulties]P Sanjurjo Crespo, M Sasieta Altuna, V Rubio Zamora, et al.
Lancet (London, England)|May 14, 1988
IgA antigliadin antibodies in children with IgA mesangial glomerulonephritisJ Rodriguez-Soriano, A Arrieta, A Vallo, et al.
Anales Espanoles De Pediatria|October 1, 1982
[Combined exchange transfusion and peritoneal dialysis treatment in a neonatal case of methylmalonic acidemia with severe hyperammonemia]P Sanjurjo, C Jaquotot, A Vallo, et al.
Pediatric Nephrology (Berlin, Germany)|August 21, 2001
Familial hypercalcemia and hypercalciuria: no mutations in the Ca2+-sensing receptor geneJ Rodríguez-Soriano, A Vallo, M J Quintela, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 30, 2002
Molecular analysis of Frasier syndrome: mutation in the WT1 gene in a girl with gonadal dysgenesis and nephronophthisisG Pérez de Nanclares, L Castaño, J R Bilbao, et al.
Anales Espanoles De Pediatria|October 15, 1985
[Echography in the diagnosis on childhood nephrocalcinosis. Apropos of 5 cases]J A López, A Martínez, F Sáez, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
Anales Espanoles De Pediatria|May 1, 1993
[Use of metronidazole in four cases of methyl-malonic acidemia]P Sanjurjo Crespo, M Labayru Echeverría, N Ingunza Aguirre, et al.
The Journal of Pediatrics|August 1, 1983
Biochemical features of dietary chloride deficiency syndrome: a comparative study of 30 casesJ Rodriguez-Soriano, A Vallo, G Castillo, et al.
Anales Espanoles De Pediatria|March 14, 1998
[Treatment of idiopathic nephrotic syndrome with cyclosporin A]G Ariceta Iraola, J Rodríguez Soriano, A Vallo Boado, et al.
Transplantation Proceedings|September 10, 2003
Immunoprophylaxis with Simulect (basiliximab) in pediatric kidney transplant recipients: results from routine clinical practice at 5 kidney transplant unitsC García Meseguer, A Vila López, A Luque de Pablos, et al.
Anales Espanoles De Pediatria|December 1, 1991
[Ornithine-transcarbamylase deficiency: prognostic difficulties]P Sanjurjo Crespo, M Sasieta Altuna, V Rubio Zamora, et al.
Lancet (London, England)|May 14, 1988
IgA antigliadin antibodies in children with IgA mesangial glomerulonephritisJ Rodriguez-Soriano, A Arrieta, A Vallo, et al.
Anales Espanoles De Pediatria|October 1, 1982
[Combined exchange transfusion and peritoneal dialysis treatment in a neonatal case of methylmalonic acidemia with severe hyperammonemia]P Sanjurjo, C Jaquotot, A Vallo, et al.
Pediatric Nephrology (Berlin, Germany)|August 21, 2001
Familial hypercalcemia and hypercalciuria: no mutations in the Ca2+-sensing receptor geneJ Rodríguez-Soriano, A Vallo, M J Quintela, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 30, 2002
Molecular analysis of Frasier syndrome: mutation in the WT1 gene in a girl with gonadal dysgenesis and nephronophthisisG Pérez de Nanclares, L Castaño, J R Bilbao, et al.
Anales Espanoles De Pediatria|October 15, 1985
[Echography in the diagnosis on childhood nephrocalcinosis. Apropos of 5 cases]J A López, A Martínez, F Sáez, et al.
Pageof 8