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C Badenas

Showing results (11-20 of 62) with videos related to

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Medicina Clinica|June 5, 1998
[Clinical, genetic and molecular studies on autosomal dominant polycystic kidney disease]R Torra, C Badenas, A Darnell, et al.
Journal of the American Society of Nephrology : JASN|November 1, 1996
Abdominal aortic aneurysms and autosomal dominant polycystic kidney diseaseR Torra, C Nicolau, C Badenas, et al.
Clinical Nephrology|January 1, 1997
Ultrasonographic study of pancreatic cysts in autosomal dominant polycystic kidney diseaseR Torra, C Nicolau, C Badenas, et al.
Journal of the American Society of Nephrology : JASN|October 1, 1996
Linkage, clinical features, and prognosis of autosomal dominant polycystic kidney disease types 1 and 2R Torra, C Badenas, A Darnell, et al.
Clinical Genetics|May 8, 2009
Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relativesC Badenas, J To-Figueras, J D Phillips, et al.
Molecular and Cellular Probes|May 9, 2000
Rare variants in the promoter of the fragile X syndrome gene (FMR1)M Milà, S Castellví-Bel, A Sánchez, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 9, 2000
Sonographic pattern of recessive polycystic kidney disease in young adults. Differences from the dominant formC Nicolau, R Torra, C Badenas, et al.
Journal of Inherited Metabolic Disease|July 4, 2006
Genetic and biochemical characterization of 16 acute intermittent porphyria cases with a high prevalence of the R173W mutationJ To-Figueras, C Badenas, C Carrera, et al.
American Journal of Human Genetics|July 27, 1999
A loss-of-function model for cystogenesis in human autosomal dominant polycystic kidney disease type 2R Torra, C Badenas, J L San Millán, et al.
American Journal of Medical Genetics|February 15, 2001
Linkage analysis in Spanish families with nonspecific X-linked mental retardation: Significant linkage at Xq13-q21C Badenas, S Castellví-Bel, V Volpini, et al.
Pageof 7

Showing results (11-20 of 62) with videos related to

Sort By:
Pageof 7
Medicina Clinica|June 5, 1998
[Clinical, genetic and molecular studies on autosomal dominant polycystic kidney disease]R Torra, C Badenas, A Darnell, et al.
Journal of the American Society of Nephrology : JASN|November 1, 1996
Abdominal aortic aneurysms and autosomal dominant polycystic kidney diseaseR Torra, C Nicolau, C Badenas, et al.
Clinical Nephrology|January 1, 1997
Ultrasonographic study of pancreatic cysts in autosomal dominant polycystic kidney diseaseR Torra, C Nicolau, C Badenas, et al.
Journal of the American Society of Nephrology : JASN|October 1, 1996
Linkage, clinical features, and prognosis of autosomal dominant polycystic kidney disease types 1 and 2R Torra, C Badenas, A Darnell, et al.
Clinical Genetics|May 8, 2009
Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relativesC Badenas, J To-Figueras, J D Phillips, et al.
Molecular and Cellular Probes|May 9, 2000
Rare variants in the promoter of the fragile X syndrome gene (FMR1)M Milà, S Castellví-Bel, A Sánchez, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 9, 2000
Sonographic pattern of recessive polycystic kidney disease in young adults. Differences from the dominant formC Nicolau, R Torra, C Badenas, et al.
Journal of Inherited Metabolic Disease|July 4, 2006
Genetic and biochemical characterization of 16 acute intermittent porphyria cases with a high prevalence of the R173W mutationJ To-Figueras, C Badenas, C Carrera, et al.
American Journal of Human Genetics|July 27, 1999
A loss-of-function model for cystogenesis in human autosomal dominant polycystic kidney disease type 2R Torra, C Badenas, J L San Millán, et al.
American Journal of Medical Genetics|February 15, 2001
Linkage analysis in Spanish families with nonspecific X-linked mental retardation: Significant linkage at Xq13-q21C Badenas, S Castellví-Bel, V Volpini, et al.
Pageof 7