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Teresa Casals

Showing results (1-10 of 33) with videos related to

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Medicina Clinica|October 22, 2005
[Prevalence of diseases: estimation and relevance]Teresa Casals-Senent
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 15, 2010
Optimizing strategies for CFTR molecular testingJavier Gimenez, Maria D Ramos, Teresa Casals
American Journal of Human Genetics|November 20, 2001
Can a place of origin of the main cystic fibrosis mutations be identified?Eva Mateu, Francesc Calafell, Maria Dolors Ramos, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 25, 2012
GUSB and ATP2B4 are suitable reference genes for CFTR gene expression data normalization in nasal epithelium cellsLaia Masvidal, Antoni Alvarez, Laura Ruano, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|January 18, 2006
Patients' perceptions of health related quality of life in rheumatoid arthritis and chronic low back painMontserrat Núñez, Alex Sanchez, Esther Nuñez, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 30, 2005
Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutationsSatu Kinnunen, Sandra Bonache, Teresa Casals, et al.
Genetic Testing and Molecular Biomarkers|October 9, 2009
The p.Arg258Gly mutation in intracellular loop 2 of CFTR is associated with CFTR-related disordersLaia Masvidal, Javier Giménez, María D Ramos, et al.
Pharmaceutical Research|July 24, 2002
Quantitative assessment of chimeraplast stability in biological fluids by polyacrylamide gel electrophoresis and laser-assisted fluorescence analysisDavid de Semir, Anna Avinyó, Sara Larriba, et al.
Human Molecular Genetics|April 30, 2003
New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12Franco Pagani, Cristiana Stuani, Maria Tzetis, et al.
Clinical Chemistry|October 27, 2004
Multimutational analysis of eleven cystic fibrosis mutations common in the Mediterranean areasM Esther Farez-Vidal, Carolina Gómez-Llorente, Sonia Blanco, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Medicina Clinica|October 22, 2005
[Prevalence of diseases: estimation and relevance]Teresa Casals-Senent
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 15, 2010
Optimizing strategies for CFTR molecular testingJavier Gimenez, Maria D Ramos, Teresa Casals
American Journal of Human Genetics|November 20, 2001
Can a place of origin of the main cystic fibrosis mutations be identified?Eva Mateu, Francesc Calafell, Maria Dolors Ramos, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 25, 2012
GUSB and ATP2B4 are suitable reference genes for CFTR gene expression data normalization in nasal epithelium cellsLaia Masvidal, Antoni Alvarez, Laura Ruano, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|January 18, 2006
Patients' perceptions of health related quality of life in rheumatoid arthritis and chronic low back painMontserrat Núñez, Alex Sanchez, Esther Nuñez, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 30, 2005
Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutationsSatu Kinnunen, Sandra Bonache, Teresa Casals, et al.
Genetic Testing and Molecular Biomarkers|October 9, 2009
The p.Arg258Gly mutation in intracellular loop 2 of CFTR is associated with CFTR-related disordersLaia Masvidal, Javier Giménez, María D Ramos, et al.
Pharmaceutical Research|July 24, 2002
Quantitative assessment of chimeraplast stability in biological fluids by polyacrylamide gel electrophoresis and laser-assisted fluorescence analysisDavid de Semir, Anna Avinyó, Sara Larriba, et al.
Human Molecular Genetics|April 30, 2003
New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12Franco Pagani, Cristiana Stuani, Maria Tzetis, et al.
Clinical Chemistry|October 27, 2004
Multimutational analysis of eleven cystic fibrosis mutations common in the Mediterranean areasM Esther Farez-Vidal, Carolina Gómez-Llorente, Sonia Blanco, et al.
Pageof 4