Listar por autor "Álvarez Martínez, María Victoria"

A series of cases with Huntington-like phenotype and intermediate repeats in HTT

Reguera Acuña, A.; Suárez San Martín, E.; García Fernández, C.; Fernández Menéndez, Santiago; Blázquez Estrada, Marta

; Amorín Díaz, M.; Menéndez González, Manuel

; Álvarez Martínez, María Victoria

(2021)

Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms

Fernández Cardo, Lucía

; Coto García, Eliecer

; Mena Álvarez, Lorena de

; Ribacoba Montero, Renée

; Mata, Ignacio F.; Menéndez González, Manuel

; Morís de la Tassa, Germán

; Álvarez Martínez, María Victoria

(Elsevier, 2014)

Amyloid Precursor Protein Gene (APP) Variation in Late-Onset Alzheimer's Disease

Miar Cuervo, Ana Belén

; Álvarez Martínez, María Victoria

; Corao Trueba, Ana Isabel

; Díaz González, Marta Elvira

; Alonso González, Belén

; Martínez Rodríguez, Carmen

; Calatayud Noguera, María Teresa

; Menéndez González, Manuel

; Morís de la Tassa, Germán

; Coto García, Eliecer

(2011)

Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain

Dols Icardo, O.; Nebot, I.; Gorostidi, A.; Álvarez Martínez, María Victoria

(2015)

Analysis of the Micro-RNA-133 and PITX3 Genes in Parkinson's Disease

Mena Álvarez, Lorena de

; Coto García, Eliecer

; Fernández Cardo, Lucía

; Díaz González, Marta Elvira

; Blázquez Estrada, Marta

; Ribacoba Montero, Renée

; Salvador Aguiar, Carlos

; Pastor Muñoz, Pau; Samaranch Gusí, Lluís; Morís de la Tassa, Germán

; Menéndez González, Manuel

; Corao Trueba, Ana Isabel

; Álvarez Martínez, María Victoria

(2010)

Association between a common KCNJ11 polymorphism (rs5219) and new-onset posttransplant diabetes in patients treated with Tacrolimus

Tavira Iglesias, Beatriz

; Coto García, Eliecer

; Torres, Armando; Díaz Corte, María del Carmen

; Díaz Molina, Beatriz

; Ortega Suárez, Francisco José

; Arias, Manuel; Díaz, Juan Manuel; Selgas, Rafael; López Larrea, Carlos

; Ruiz Ortega, Marta; Ortiz, Alberto; González, Elena; Campistol Plana, José María; Álvarez Martínez, María Victoria

(Elsevier, 2012)

Association between heroin dependence and 5-HT2A receptor gene polymorphisms

Saiz Martínez, Pilar Alejandra

; García-Portilla González, María Paz

; Arango López, Celso; Morales Cañabete, Blanca

; Martínez Barrondo, Sara

; Álvarez Díaz, César Esteban; San Narciso Izquierdo, Gemma Isabel

; Carreño Rendueles, José Eduardo; Álvarez Martínez, María Victoria

; Coto García, Eliecer

; Bobes, Julio

(2008)

Association between the A-1438G polymorphism of the serotonin 2A receptor gene and nonimpulsive suicide attempts

Saiz Martínez, Pilar Alejandra

; García-Portilla González, María Paz

; Paredes Ojanguren, María Begoña; Arango López, Celso; Morales Cañabete, Blanca

; Álvarez Martínez, María Victoria

; Coto García, Eliecer

; Bascarán Fernández, María Teresa

; Bousoño García, Manuel Víctor

; Bobes, Julio

(2008)

Association between the Stin2 VNTR polymorphism of the Serotonin transporter gene and treatment outcome in alcohol-dependent patients

Flórez Menéndez, Gerardo; Saiz Martínez, Pilar Alejandra

; García-Portilla González, María Paz

; Álvarez González, Sandra; Nogueiras Fernández, Luis; Morales Cañabete, Blanca

; Álvarez Martínez, María Victoria

; Coto García, Eliecer

; Bobes, Julio

(2008)

Association study between obsessive-compulsive disorder and serotonergic candidate genes

Saiz Martínez, Pilar Alejandra

; García-Portilla González, María Paz

; Arango López, Celso; Morales Cañabete, Blanca

; Bascarán Fernández, María Teresa

; Martínez Barrondo, Sara

; Álvarez Martínez, María Victoria

; Coto García, Eliecer

; Fernández Domínguez, Juan María

; Bousoño García, Manuel Víctor

; Bobes, Julio

(2008)

Association study of the interleukin-1 gene complex and tumor necrosis factor alpha gene with suicide attempts

Saiz Martínez, Pilar Alejandra

; García-Portilla González, María Paz

; Paredes Ojanguren, María Begoña; Arango López, Celso; Morales Cañabete, Blanca

; Álvarez Martínez, María Victoria

; Coto García, Eliecer

; Bascarán Fernández, María Teresa

; Bousoño García, Manuel Víctor

; Bobes, Julio

(2008)

Characterization of B27 haplotypes by oligotyping and genomic sequencing in the Mexican Mestizo population with ankylosing spondylitis: Juvenile and adult onset

López Larrea, Carlos

; González Roces, Severino; Peña Concepción, Mercedes; Domínguez, Orlando; Coto García, Eliecer

; Álvarez Martínez, María Victoria

; Moreno, Mónica; Hernández, Ofelia; Burgos Vargas, Rubén; Gorodezky, Clara (1995)

Characterization of interleukin-8 receptors in non-human primates

Álvarez Martínez, María Victoria

; Coto García, Eliecer

; Setién Baranda, Fernando; González Rodríguez, Segundo

; González Roces, Severino; López Larrea, Carlos

(1996)

Cold-Induced Sweating Syndrome Type 1, with a CRLF1 Level Mutation, Previously Associated with Crisponi Syndrome

González Fernández, Daniel; Lazaro Pérez, M.; Santiallán Garzón, S.; Álvarez Martínez, María Victoria

; Encinas Madrazo, A.; Fernández Toral, Joaquín

; Pérez Oliva, Narciso

(2013)

Differential role of serotonergic polymorphisms in alcohol and heroin dependence

Saiz Martínez, Pilar Alejandra

; García-Portilla González, María Paz

; Flórez Menéndez, Gerardo; Arango López, Celso; Corcoran, Denis Paul

; Morales Cañabete, Blanca

; Bascarán Fernández, María Teresa

; Álvarez Díaz, César Esteban; San Narciso Izquierdo, Gemma Isabel

; Carreño Rendueles, José Eduardo; Álvarez Martínez, María Victoria

; Coto García, Eliecer

; Bobes, Julio

(2009)

Enfermedad de Parkinson: caracterización de la región 3UTR de los genes SNCA y LRRK2 y del miRNOMA de tejido cerebral y plasma sanguíneo

Fernández Cardo, Lucía

(2014-09-12)

Enfermedad de Parkinson: papel de la variación genética en regiones reguladoras de la expresión de los genes de Parkina y microRNAs asociados

Mena Álvarez, Lorena de

(Universidad de Oviedo, 2013-03-22)

Espectro mutacional de los genes ATL1, SPAST y SPG7 e influencia de la variación genética mitocondrial en pacientes españoles con paraparesia espática hereditaria

Sánchez Ferrero, Elena

(Universidad de Oviedo, 2012-11-30)

Espectro mutacional de los genes snca, prkn, pink1 y lrrk2 en la enfermedad de Parkinson

Fernández Mata, Ignacio (2005)

A family with a milder form of adult dominant polycystic Kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes

Ariza-Prota, Miguel Ángel; Álvarez Martínez, María Victoria

; Marín Iranzo, Rafael José

; Aguado de la Paz, Sara

; López Larrea, Carlos

; Álvarez Piñera, Jorge

; Menéndez, M. J.; Coto García, Eliecer

(BMJ Publishing Group, 1997)

Listar por autor "Álvarez Martínez, María Victoria"

A series of cases with Huntington-like phenotype and intermediate repeats in HTT ﻿

Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms ﻿

Amyloid Precursor Protein Gene (APP) Variation in Late-Onset Alzheimer's Disease ﻿

Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain ﻿

Analysis of the Micro-RNA-133 and PITX3 Genes in Parkinson's Disease ﻿

Association between a common KCNJ11 polymorphism (rs5219) and new-onset posttransplant diabetes in patients treated with Tacrolimus ﻿

Association between heroin dependence and 5-HT2A receptor gene polymorphisms ﻿

Association between the A-1438G polymorphism of the serotonin 2A receptor gene and nonimpulsive suicide attempts ﻿

Association between the Stin2 VNTR polymorphism of the Serotonin transporter gene and treatment outcome in alcohol-dependent patients ﻿

Association study between obsessive-compulsive disorder and serotonergic candidate genes ﻿

Association study of the interleukin-1 gene complex and tumor necrosis factor alpha gene with suicide attempts ﻿

Characterization of B27 haplotypes by oligotyping and genomic sequencing in the Mexican Mestizo population with ankylosing spondylitis: Juvenile and adult onset ﻿

Characterization of interleukin-8 receptors in non-human primates ﻿

Cold-Induced Sweating Syndrome Type 1, with a CRLF1 Level Mutation, Previously Associated with Crisponi Syndrome ﻿

Differential role of serotonergic polymorphisms in alcohol and heroin dependence ﻿

Enfermedad de Parkinson: caracterización de la región 3UTR de los genes SNCA y LRRK2 y del miRNOMA de tejido cerebral y plasma sanguíneo ﻿

Enfermedad de Parkinson: papel de la variación genética en regiones reguladoras de la expresión de los genes de Parkina y microRNAs asociados ﻿

Espectro mutacional de los genes ATL1, SPAST y SPG7 e influencia de la variación genética mitocondrial en pacientes españoles con paraparesia espática hereditaria ﻿

Espectro mutacional de los genes snca, prkn, pink1 y lrrk2 en la enfermedad de Parkinson ﻿

A family with a milder form of adult dominant polycystic Kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes ﻿

A series of cases with Huntington-like phenotype and intermediate repeats in HTT

Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms

Amyloid Precursor Protein Gene (APP) Variation in Late-Onset Alzheimer's Disease

Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain

Analysis of the Micro-RNA-133 and PITX3 Genes in Parkinson's Disease

Association between a common KCNJ11 polymorphism (rs5219) and new-onset posttransplant diabetes in patients treated with Tacrolimus

Association between heroin dependence and 5-HT2A receptor gene polymorphisms

Association between the A-1438G polymorphism of the serotonin 2A receptor gene and nonimpulsive suicide attempts

Association between the Stin2 VNTR polymorphism of the Serotonin transporter gene and treatment outcome in alcohol-dependent patients

Association study between obsessive-compulsive disorder and serotonergic candidate genes

Association study of the interleukin-1 gene complex and tumor necrosis factor alpha gene with suicide attempts

Characterization of B27 haplotypes by oligotyping and genomic sequencing in the Mexican Mestizo population with ankylosing spondylitis: Juvenile and adult onset

Characterization of interleukin-8 receptors in non-human primates

Cold-Induced Sweating Syndrome Type 1, with a CRLF1 Level Mutation, Previously Associated with Crisponi Syndrome

Differential role of serotonergic polymorphisms in alcohol and heroin dependence

Enfermedad de Parkinson: caracterización de la región 3UTR de los genes SNCA y LRRK2 y del miRNOMA de tejido cerebral y plasma sanguíneo

Enfermedad de Parkinson: papel de la variación genética en regiones reguladoras de la expresión de los genes de Parkina y microRNAs asociados

Espectro mutacional de los genes ATL1, SPAST y SPG7 e influencia de la variación genética mitocondrial en pacientes españoles con paraparesia espática hereditaria

Espectro mutacional de los genes snca, prkn, pink1 y lrrk2 en la enfermedad de Parkinson

A family with a milder form of adult dominant polycystic Kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes