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Genes
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May 1, 2020
Application of CRISPR Tools for Variant Interpretation and Disease Modeling in Inherited Retinal Dystrophies
Carla Fuster-García, Belén García-Bohórquez, Ana Rodríguez-Muñoz, et al.
Clinical Chemistry and Laboratory Medicine
|
July 26, 2017
The importance of biochemical and genetic findings in the diagnosis of atypical Norrie disease
Ana Rodríguez-Muñoz, Gema García-García, Francisco Menor, et al.
Frontiers in Cell and Developmental Biology
|
July 30, 2021
Updating the Genetic Landscape of Inherited Retinal Dystrophies
Belén García Bohórquez, Elena Aller, Ana Rodríguez Muñoz, et al.
Endocrine
|
June 24, 2015
Levels of regulatory T cells CD69(+)NKG2D(+)IL-10(+) are increased in patients with autoimmune thyroid disorders
Ana Rodríguez-Muñoz, Marlen Vitales-Noyola, Ana Ramos-Levi, et al.
Journal of Clinical Laboratory Analysis
|
December 30, 2014
When an Analytical Interference Is a Useful Diagnostic Tool: Finding Monoclonal Gammopathies in Routine Analysis
Carmen Quiñones-Torrelo, María Pilar Villanueva-Gil, Ana Rodríguez-Muñoz, et al.
International Journal of Molecular Sciences
|
July 2, 2021
Usher Syndrome: Genetics of a Human Ciliopathy
Carla Fuster-García, Belén García-Bohórquez, Ana Rodríguez-Muñoz, et al.
Retina (Philadelphia, Pa.)
|
January 7, 2021
CONCOMITANT MUTATIONS IN INHERITED RETINAL DYSTROPHIES: Why the Reproductive and Therapeutic Counseling Should Be Addressed Cautiously
Ana Rodríguez-Muñoz, Belén García-Bohórquez, Patricia Udaondo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 20, 2015
Circulating Microvesicles Regulate Treg and Th17 Differentiation in Human Autoimmune Thyroid Disorders
Ana Rodríguez-Muñoz, Rebeca Martínez-Hernández, Ana M Ramos-Leví, et al.
Plos One
|
April 17, 2015
Graves' disease is associated with a defective expression of the immune regulatory molecule galectin-9 in antigen-presenting dendritic cells
Susanna Leskela, Ana Serrano, Hortensia de la Fuente, et al.
The Journal of Molecular Diagnostics : JMD
|
February 10, 2020
Expanding the Clinical and Molecular Heterogeneity of Nonsyndromic Inherited Retinal Dystrophies
Ana Rodríguez-Muñoz, Elena Aller, Teresa Jaijo, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Genes
|
May 1, 2020
Application of CRISPR Tools for Variant Interpretation and Disease Modeling in Inherited Retinal Dystrophies
Carla Fuster-García, Belén García-Bohórquez, Ana Rodríguez-Muñoz, et al.
Clinical Chemistry and Laboratory Medicine
|
July 26, 2017
The importance of biochemical and genetic findings in the diagnosis of atypical Norrie disease
Ana Rodríguez-Muñoz, Gema García-García, Francisco Menor, et al.
Frontiers in Cell and Developmental Biology
|
July 30, 2021
Updating the Genetic Landscape of Inherited Retinal Dystrophies
Belén García Bohórquez, Elena Aller, Ana Rodríguez Muñoz, et al.
Endocrine
|
June 24, 2015
Levels of regulatory T cells CD69(+)NKG2D(+)IL-10(+) are increased in patients with autoimmune thyroid disorders
Ana Rodríguez-Muñoz, Marlen Vitales-Noyola, Ana Ramos-Levi, et al.
Journal of Clinical Laboratory Analysis
|
December 30, 2014
When an Analytical Interference Is a Useful Diagnostic Tool: Finding Monoclonal Gammopathies in Routine Analysis
Carmen Quiñones-Torrelo, María Pilar Villanueva-Gil, Ana Rodríguez-Muñoz, et al.
International Journal of Molecular Sciences
|
July 2, 2021
Usher Syndrome: Genetics of a Human Ciliopathy
Carla Fuster-García, Belén García-Bohórquez, Ana Rodríguez-Muñoz, et al.
Retina (Philadelphia, Pa.)
|
January 7, 2021
CONCOMITANT MUTATIONS IN INHERITED RETINAL DYSTROPHIES: Why the Reproductive and Therapeutic Counseling Should Be Addressed Cautiously
Ana Rodríguez-Muñoz, Belén García-Bohórquez, Patricia Udaondo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 20, 2015
Circulating Microvesicles Regulate Treg and Th17 Differentiation in Human Autoimmune Thyroid Disorders
Ana Rodríguez-Muñoz, Rebeca Martínez-Hernández, Ana M Ramos-Leví, et al.
Plos One
|
April 17, 2015
Graves' disease is associated with a defective expression of the immune regulatory molecule galectin-9 in antigen-presenting dendritic cells
Susanna Leskela, Ana Serrano, Hortensia de la Fuente, et al.
The Journal of Molecular Diagnostics : JMD
|
February 10, 2020
Expanding the Clinical and Molecular Heterogeneity of Nonsyndromic Inherited Retinal Dystrophies
Ana Rodríguez-Muñoz, Elena Aller, Teresa Jaijo, et al.
Page
of 2