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Profil bibliographique

Manuel Pérez

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

51Publications signalées
596Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Spinal Dysraphism and MalformationsCerebrospinal fluid and hydrocephalusFamily Support in IllnessAortic Disease and Treatment ApproachesMyasthenia Gravis and Thymoma

Les publications récentes

Accès ouvert 2024 article OpenAlex

Impact of chronic pain and depressive symptoms on the quality of life of adults with Chiari Malformation type I: A comparative study

Maitane García, Imanol Amayra, Manuel Pérez, Alicia Aurora Rodríguez et autres

Chiari Malformation type I (CM-I) is a neurological disorder characterized by cerebellar tonsillar herniation. Chronic pain, particularly headaches, is a prevalent symptom in CM-I patients, significantly impacting their quality of life. The objective of this study was to evaluate the perceived quality …

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2 citations Intractable & Rare Diseases Research
Accès ouvert 2023 article OpenAlex

Carga socioeconómica de la mielofibrosis en pacientes con y sin anemia en España

Garbiñe Lizeaga, Jaime Espín, Regina García, Valentín García‐Gutiérrez et autres

Objetivo: El objetivo del estudio fue estimar la carga socioeconómica, en relación con los costes sanitarios directos, indirectos e intangibles de los pacientes con mielofibrosis (MF) con y sin anemia en España. Material y métodos: Se realizó un estudio de la carga …

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0 citations Economía de la Salud
Accès ouvert 2023 review OpenAlex

Cognition in Chiari Malformation Type I: an Update of a Systematic Review

Maitane García, Imanol Amayra, Manuel Pérez, Mónika Salgueiro et autres

Chiari malformation has been classified as a group of posterior cranial fossa disorders characterized by hindbrain herniation. Chiari malformation type I (CM-I) is the most common subtype, ranging from asymptomatic patients to those with severe disorders. Research about clinical manifestations or medical …

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14 citations Neuropsychology Review
Accès ouvert 2023 article OpenAlex

Cognitive Functioning in Adults with Phenylketonuria in a Cohort of Spanish Patients

Paula María Luna, Juan Francisco López Paz, Maitane García, Imanol Amayra et autres

The early introduction of a low phenylalanine (Phe) diet has been demonstrated to be the most successful treatment in subjects with phenylketonuria (PKU), especially for preventing severe cognitive and neurological damages. However, it still concerns that even if treated in the first …

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11 citations Behavioural Neurology
Accès ouvert 2022 article OpenAlex

Neuropsychological Profile of Hereditary Ataxias: Study of 38 Patients

Maitane García, Idoia Rouco-Axpe, Imanol Amayra, Alfredo Rodríguez-Antigüedad et autres

Hereditary ataxias are a heterogeneous group of disorders characterized by degeneration of the cerebellum and its connections. It is known that patients with ataxia can manifest a broad spectrum of motor symptoms; however, current research has emphasized the relevance of cognitive disturbances. …

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5 citations Archives of Clinical Neuropsychology
Accès ouvert 2022 article OpenAlex

Comparison of Prophylactic Intravenous Antibiotic Regimens After Endoprosthetic Reconstruction for Lower Extremity Bone Tumors

Michelle Ghert, Patricia Schneider, Victoria Giglio, Andrew Duong et autres

IMPORTANCE: The use of perioperative, prophylactic, intravenous antibiotics is standard practice to reduce the risk of surgical site infection after oncologic resection and complex endoprosthetic reconstruction for lower extremity bone tumors. However, evidence guiding the duration of prophylactic treatment remains limited. OBJECTIVE: …

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95 citations JAMA Oncology
Accès ouvert 2021 article OpenAlex

Music therapy and Sanfilippo syndrome: an analysis of psychological and physiological variables of three case studies

Paula Pérez-Núñez, Esther Lázaro, Imanol Amayra, Juan Francisco López Paz et autres

INTRODUCTION: Mucopolysaccharidosis type III (MPS III) or Sanfilippo syndrome is a neurodegenerative disease caused by the accumulation of mucopolysaccharides in the body. As the symptoms are wide ranging, it is a challenge to provide a diagnosis and psychological treatment for affected children. …

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5 citations Orphanet Journal of Rare Diseases
Accès ouvert 2021 article OpenAlex

Diseases Costs and Impact of the Caring Role on Informal Carers of Children with Neuromuscular Disease

Alicia Aurora Rodríguez, Óscar Martínez, Imanol Amayra, Juan Francisco López Paz et autres

This study aims to evaluate the costs of informal care for children with neuromuscular disease and evaluate how physical and psychological health is associated with socio-demographic variables. A cross sectional design was used with a convenience sample of 110 carers that participated …

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28 citations International Journal of Environmental Research and Public Health
Accès ouvert 2021 article OpenAlex

Effects of Teleassistance on the Quality of Life of People With Rare Neuromuscular Diseases According to Their Degree of Disability

Óscar Martínez, Imanol Amayra, Juan Francisco López Paz, Esther Lázaro et autres

Rare neuromuscular diseases (RNMDs) are a group of pathologies characterized by a progressive loss of muscular strength, atrophy, fatigue, and other muscle-related symptoms, which affect quality of life (QoL) levels. The low prevalence, high geographical dispersion and disability of these individuals involve …

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15 citations Frontiers in Psychology

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