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J Vaquerizo

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Journal of Medical Genetics|February 12, 2002
Severe phenotype in Angelman syndrome resulting from paternal isochromosome 15D Poyatos, M Guitart, E Gabau, et al.
Revista De Neurologia|September 2, 2004
[Hair with a double crown and dilatation of Virchow-Robin spaces: a proposal for a new neurocutaneous association]J Vaquerizo-Madrid, J L Gamero-Telo, C Cáceres-Marzal, et al.
Anales Espanoles De Pediatria|May 9, 1998
[Congenital oculomotor apraxia and partial deficiency of pyruvate carboxylase]J Vaquerizo Madrid, J M Val Sánchez de León, J Sánchez Alarcón, et al.
Presse Medicale (Paris, France : 1983)|September 30, 1995
[Splenic hemangiopericytoma]C Gilsanz, J Garcia-Castaño, M V Villalba, et al.
Anales Espanoles De Pediatria|June 1, 1996
[The congenital bilateral perisylvian syndrome: a report of 2 new cases]J Vaquerizo Madrid, J M Catalá Rubio, H Gómez Martín, et al.
Revista De Neurologia|March 13, 2009
[Non-verbal learning disorders: a clinical study and pharmacological treatment]J Vaquerizo-Madrid, M Ramírez-Arenas, C Cáceres-Marzal, et al.
Anales Espanoles De Pediatria|January 1, 1997
[Cystathioninuria in two families: a clinical and biochemical follow-up]J M Val Sánchez de León, J Vaquerizo Madrid, J Sánchez Alarcón, et al.
Thorax|March 4, 2003
Effect of montelukast added to inhaled budesonide on control of mild to moderate asthmaM J Vaquerizo, P Casan, J Castillo, et al.
Pediatric Research|August 29, 2000
Glutaryl-CoA dehydrogenase deficiency in Spain: evidence of two groups of patients, genetically, and biochemically distinctC Busquets, B Merinero, E Christensen, et al.
Neuropsychiatric Disease and Treatment|February 23, 2013
Response to methylphenidate by adult and pediatric patients with attention-deficit/hyperactivity disorder: the Spanish multicenter DIHANA studyJ R Valdizán-Usón, A Cánovas-Martínez, M T De Lucas-Taracena, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Journal of Medical Genetics|February 12, 2002
Severe phenotype in Angelman syndrome resulting from paternal isochromosome 15D Poyatos, M Guitart, E Gabau, et al.
Revista De Neurologia|September 2, 2004
[Hair with a double crown and dilatation of Virchow-Robin spaces: a proposal for a new neurocutaneous association]J Vaquerizo-Madrid, J L Gamero-Telo, C Cáceres-Marzal, et al.
Anales Espanoles De Pediatria|May 9, 1998
[Congenital oculomotor apraxia and partial deficiency of pyruvate carboxylase]J Vaquerizo Madrid, J M Val Sánchez de León, J Sánchez Alarcón, et al.
Presse Medicale (Paris, France : 1983)|September 30, 1995
[Splenic hemangiopericytoma]C Gilsanz, J Garcia-Castaño, M V Villalba, et al.
Anales Espanoles De Pediatria|June 1, 1996
[The congenital bilateral perisylvian syndrome: a report of 2 new cases]J Vaquerizo Madrid, J M Catalá Rubio, H Gómez Martín, et al.
Revista De Neurologia|March 13, 2009
[Non-verbal learning disorders: a clinical study and pharmacological treatment]J Vaquerizo-Madrid, M Ramírez-Arenas, C Cáceres-Marzal, et al.
Anales Espanoles De Pediatria|January 1, 1997
[Cystathioninuria in two families: a clinical and biochemical follow-up]J M Val Sánchez de León, J Vaquerizo Madrid, J Sánchez Alarcón, et al.
Thorax|March 4, 2003
Effect of montelukast added to inhaled budesonide on control of mild to moderate asthmaM J Vaquerizo, P Casan, J Castillo, et al.
Pediatric Research|August 29, 2000
Glutaryl-CoA dehydrogenase deficiency in Spain: evidence of two groups of patients, genetically, and biochemically distinctC Busquets, B Merinero, E Christensen, et al.
Neuropsychiatric Disease and Treatment|February 23, 2013
Response to methylphenidate by adult and pediatric patients with attention-deficit/hyperactivity disorder: the Spanish multicenter DIHANA studyJ R Valdizán-Usón, A Cánovas-Martínez, M T De Lucas-Taracena, et al.
Pageof 3