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Sonia Clavero

Showing results (1-10 of 12) with videos related to

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Molecular Medicine (Cambridge, Mass.)|March 3, 2011
Congenital erythropoietic porphyria: characterization of murine models of the severe common (C73R/C73R) and later-onset genotypesDavid F Bishop, Sonia Clavero, Narla Mohandas, et al.
Human Genetics|July 6, 2004
Qualitative and quantitative analysis of the effect of splicing mutations in propionic acidemia underlying non-severe phenotypesSonia Clavero, Belén Pérez, Ana Rincón, et al.
Molecular Medicine (Cambridge, Mass.)|May 21, 2010
Feline congenital erythropoietic porphyria: two homozygous UROS missense mutations cause the enzyme deficiency and porphyrin accumulationSonia Clavero, David F Bishop, Urs Giger, et al.
Journal of Human Genetics|October 20, 2006
New splicing mutations in propionic acidemiaLourdes R Desviat, Sonia Clavero, Celia Perez-Cerdá, et al.
Biochimica Et Biophysica Acta|October 19, 2002
Functional characterization of PCCA mutations causing propionic acidemiaSonia Clavero, Maria Angeles Martínez, Belén Pérez, et al.
Human Molecular Genetics|November 26, 2009
Feline acute intermittent porphyria: a phenocopy masquerading as an erythropoietic porphyria due to dominant and recessive hydroxymethylbilane synthase mutationsSonia Clavero, David F Bishop, Mark E Haskins, et al.
Veterinary Journal (London, England : 1997)|November 19, 2013
Diagnosis of feline acute intermittent porphyria presenting with erythrodontia requires molecular analysesSonia Clavero, Yuri Ahuja, David F Bishop, et al.
Blood|December 8, 2009
Congenital erythropoietic porphyria: a novel uroporphyrinogen III synthase branchpoint mutation reveals underlying wild-type alternatively spliced transcriptsDavid F Bishop, Xiaoye Schneider-Yin, Sonia Clavero, et al.
Anales De Pediatria|March 19, 2026
Non-epileptic paroxismal episodes in pediatrics: experience in a pediatric emergency departmentSonia Clavero Sánchez, Juan Manuel Guijarro Núñez, Caridad Jun García García, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 24, 2024
Unusual presentations of acute mastoiditis should be considered when young children present with neurological symptomsMaría Suárez-Bustamante Huélamo, Jose Antonio Alonso-Cadenas, Maria Pérez Moreno, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Molecular Medicine (Cambridge, Mass.)|March 3, 2011
Congenital erythropoietic porphyria: characterization of murine models of the severe common (C73R/C73R) and later-onset genotypesDavid F Bishop, Sonia Clavero, Narla Mohandas, et al.
Human Genetics|July 6, 2004
Qualitative and quantitative analysis of the effect of splicing mutations in propionic acidemia underlying non-severe phenotypesSonia Clavero, Belén Pérez, Ana Rincón, et al.
Molecular Medicine (Cambridge, Mass.)|May 21, 2010
Feline congenital erythropoietic porphyria: two homozygous UROS missense mutations cause the enzyme deficiency and porphyrin accumulationSonia Clavero, David F Bishop, Urs Giger, et al.
Journal of Human Genetics|October 20, 2006
New splicing mutations in propionic acidemiaLourdes R Desviat, Sonia Clavero, Celia Perez-Cerdá, et al.
Biochimica Et Biophysica Acta|October 19, 2002
Functional characterization of PCCA mutations causing propionic acidemiaSonia Clavero, Maria Angeles Martínez, Belén Pérez, et al.
Human Molecular Genetics|November 26, 2009
Feline acute intermittent porphyria: a phenocopy masquerading as an erythropoietic porphyria due to dominant and recessive hydroxymethylbilane synthase mutationsSonia Clavero, David F Bishop, Mark E Haskins, et al.
Veterinary Journal (London, England : 1997)|November 19, 2013
Diagnosis of feline acute intermittent porphyria presenting with erythrodontia requires molecular analysesSonia Clavero, Yuri Ahuja, David F Bishop, et al.
Blood|December 8, 2009
Congenital erythropoietic porphyria: a novel uroporphyrinogen III synthase branchpoint mutation reveals underlying wild-type alternatively spliced transcriptsDavid F Bishop, Xiaoye Schneider-Yin, Sonia Clavero, et al.
Anales De Pediatria|March 19, 2026
Non-epileptic paroxismal episodes in pediatrics: experience in a pediatric emergency departmentSonia Clavero Sánchez, Juan Manuel Guijarro Núñez, Caridad Jun García García, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 24, 2024
Unusual presentations of acute mastoiditis should be considered when young children present with neurological symptomsMaría Suárez-Bustamante Huélamo, Jose Antonio Alonso-Cadenas, Maria Pérez Moreno, et al.
Pageof 2