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Irene Valenzuela

Showing results (1-10 of 102) with videos related to

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Physical Review Letters|May 17, 2024
Universal Pattern in Quantum Gravity at Infinite DistanceAlberto Castellano, Ignacio Ruiz, Irene Valenzuela
Calcified Tissue International|February 17, 2025
Severe Osteoporosis in an Adult Subject with RNU4-2 Gene MutationJoshua Peñafiel-Sam, Irene Valenzuela, Pilar Peris
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2026
Response to Saleem et alIrene Valenzuela, Marta Codina-Solà, Eduardo F Tizzano
Revista Espanola De Cardiologia (English Ed.)|September 10, 2014
Nonsyndromic familial aortic disease: an underdiagnosed entityGisela Teixidó-Turà, Irene Valenzuela, Laura Gutiérrez, et al.
Journal of Clinical Research in Pediatric Endocrinology|October 25, 2021
Prolyl Endopeptidase-like Deficiency Associated with Growth Hormone DeficiencyLaura Sayol-Torres, Maria Irene Valenzuela, Rosangela Tomasini, et al.
Prenatal Diagnosis|September 21, 2024
Parental or Trio Magnetic Resonance Imaging to Improve Prenatal Counseling in Brain AnomaliesCarlota Rodó, Nerea Maiz, Élida Vázquez, et al.
Breast Cancer Research and Treatment|April 30, 2013
Germline mutations in NF1 and BRCA1 in a family with neurofibromatosis type 1 and early-onset breast cancerBerta Campos, Judith Balmaña, Josep Gardenyes, et al.
American Journal of Medical Genetics. Part A|September 8, 2020
Expanding the phenotype of cerebellar-facial-dental syndrome: Two siblings with a novel variant in BRF1Irene Valenzuela, Marta Codina, Paula Fernández-Álvarez, et al.
European Journal of Medical Genetics|March 28, 2017
Arthrogryposis as neonatal presentation of Loeys-Dietz syndrome due to a novel TGFBR2 mutationIrene Valenzuela, Paula Fernández-Alvarez, Francina Munell, et al.
European Journal of Medical Genetics|July 15, 2018
Further delineation of the phenotype caused by loss of function mutations in PRMT7Irene Valenzuela, Maria Segura-Puimedon, Benjamín Rodríguez-Santiago, et al.
Pageof 11

Showing results (1-10 of 102) with videos related to

Sort By:
Pageof 11
Physical Review Letters|May 17, 2024
Universal Pattern in Quantum Gravity at Infinite DistanceAlberto Castellano, Ignacio Ruiz, Irene Valenzuela
Calcified Tissue International|February 17, 2025
Severe Osteoporosis in an Adult Subject with RNU4-2 Gene MutationJoshua Peñafiel-Sam, Irene Valenzuela, Pilar Peris
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2026
Response to Saleem et alIrene Valenzuela, Marta Codina-Solà, Eduardo F Tizzano
Revista Espanola De Cardiologia (English Ed.)|September 10, 2014
Nonsyndromic familial aortic disease: an underdiagnosed entityGisela Teixidó-Turà, Irene Valenzuela, Laura Gutiérrez, et al.
Journal of Clinical Research in Pediatric Endocrinology|October 25, 2021
Prolyl Endopeptidase-like Deficiency Associated with Growth Hormone DeficiencyLaura Sayol-Torres, Maria Irene Valenzuela, Rosangela Tomasini, et al.
Prenatal Diagnosis|September 21, 2024
Parental or Trio Magnetic Resonance Imaging to Improve Prenatal Counseling in Brain AnomaliesCarlota Rodó, Nerea Maiz, Élida Vázquez, et al.
Breast Cancer Research and Treatment|April 30, 2013
Germline mutations in NF1 and BRCA1 in a family with neurofibromatosis type 1 and early-onset breast cancerBerta Campos, Judith Balmaña, Josep Gardenyes, et al.
American Journal of Medical Genetics. Part A|September 8, 2020
Expanding the phenotype of cerebellar-facial-dental syndrome: Two siblings with a novel variant in BRF1Irene Valenzuela, Marta Codina, Paula Fernández-Álvarez, et al.
European Journal of Medical Genetics|March 28, 2017
Arthrogryposis as neonatal presentation of Loeys-Dietz syndrome due to a novel TGFBR2 mutationIrene Valenzuela, Paula Fernández-Alvarez, Francina Munell, et al.
European Journal of Medical Genetics|July 15, 2018
Further delineation of the phenotype caused by loss of function mutations in PRMT7Irene Valenzuela, Maria Segura-Puimedon, Benjamín Rodríguez-Santiago, et al.
Pageof 11