Raquel Baviera Muñoz

Instituto de Investigación Sanitaria La Fe

Spain

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Articles (16)

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2025

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2025

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2025

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2024

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2024

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2023

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2020

Collaborators (7)

Olivia Belbin

Assistant Professor

Hospital de la Santa Creu i Sant Pau

SPAIN

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Irene Martinez-Torres

Head of the Movement Disorders Unit

Hospital Universitari i Politècnic La Fe

SPAIN

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Amparo Andres Borderia

Titulada Superior en actividades Técnicas y Profesionales

Instituto de Agroquímica y Tecnología de Alimentos

SPAIN

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Pablo Mir

SPAIN

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pilar sanchez

Head of neurodegenerative disease and movement disorders

Hospital Universitario Puerta del Hierro Majadahonda

SPAIN

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Juan Carlos Martinez Castrillo

Head. Neurodegenerative Diseases

HOSPITAL UNIVERSITARIO RAMÓN Y CAJAL

SPAIN

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Rafael Sivera

Universidad CEU Cardenal Herrera Facultad de Ciencias de la Salud

SPAIN

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Raquel Baviera Muñoz

Research Interests

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Articles (16)

Profile of People With Parkinson's Disease Treated With a Device‐Aided Therapy in Spain. A Comparative Multicenter Observational Study

A Spanish-Portuguese GWAS of progressive supranuclear palsy reveals a novel risk locus in NFASC

Safety and efficacy of bilateral staged focused ultrasound thalamotomy in refractory essential tremor

STUB1 Mutations as Possible Genetic Modifiers in Spinocerebellar Ataxia Type 8

Use of the MNCD Classification to Monitor Clinical Stage and Response to Levodopa-Entacapone-Carbidopa Intestinal Gel Infusion in Advanced Parkinson’s Disease

MRgFUS subthalamotomy in Parkinson’s disease: an approach aimed at minimizing Lesion Volume

Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain

Estimulación cerebral profunda combinada del núcleo subtalámico y el globo pálido interno en la enfermedad de Parkinson

Diagnostic Efficacy of Genetic Studies in a Series of Hereditary Cerebellar Ataxias in Eastern Spain

Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias

[Adverse effects and complications of continuous intestinal infusion of levodopa-carbidopa in a cohort of patients with Parkinson's disease in a tertiary hospital].

A 3.9-Mb Deletion on 2p11.2 Comprising the REEP1 Gene Causes Early-Onset Atypical Parkinsonism

Estatus epiléptico refractario por déficit de vitamina B6 en paciente con enfermedad de Parkinson e infusión intestinal de levodopa/carbidopa

Clinical and genetic characteristics of 21 Spanish patients with biallelic pathogenic SPG7 mutations

Hereditary Spastic Paraplegia 7 Presenting as Multifocal Dystonia with Prominent Cranio‐Cervical Involvement

El índice de pulsatilidad intracraneal elevado apoya el diagnóstico de parkinsonismo vascular frente a enfermedad de Parkinson idiopática

Collaborators (7)

Olivia Belbin

Irene Martinez-Torres

Amparo Andres Borderia

Pablo Mir

pilar sanchez

Juan Carlos Martinez Castrillo

Rafael Sivera

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