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Orphanet Journal of Rare Diseases
|
May 12, 2019
Evaluation of the frequency of non-motor symptoms of Parkinson's disease in adult patients with Gaucher disease type 1
Matheus V M B Wilke, Alícia D Dornelles, Artur S Schuh, et al.
American Journal of Medical Genetics. Part A
|
May 25, 2021
Elevated holo-transcobalamin in Gaucher disease type II: A case report
Suelen Porto Basgalupp, Karina Carvalho Donis, Marina Siebert, et al.
Frontiers in Neurology
|
June 25, 2019
Are Cognitive Changes in Hereditary Spastic Paraplegias Restricted to Complicated Forms?
Laís Alves Jacinto-Scudeiro, Gustavo Dariva Machado, Annelise Ayres, et al.
Arquivos De Neuro-Psiquiatria
|
January 16, 2020
Prevalence of oropharyngeal dysphagia in hereditary spastic paraplegias
Laís Alves Jacinto-Scudeiro, Gustavo Dariva Machado, Annelise Ayres, et al.
Cardiology
|
September 8, 2025
MicroRNA Expression Pre-Trastuzumab Treatment in HER-2+ Early Breast Cancer Patients as a Predictor of Cancer Therapy-Related Cardiac Dysfunction: A Pilot Cohort Study
Fernando Pivatto Júnior, Ângela Barreto Santiago Santos, Eduarda Foresti Englert, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
February 17, 2022
Diagnostic yield of multi-gene panel for muscular dystrophies and other hereditary myopathies
Pablo Brea Winckler, Bruna Cristine Chwal, Marco Antonnio Rocha Dos Santos, et al.
Molecular Genetics and Metabolism Reports
|
February 27, 2020
Liver involvement in patients with Gaucher disease types I and III
Rodrigo Tzovenos Starosta, Filippo Pinto E Vairo, Alícia Dorneles Dornelles, et al.
Epilepsy Research
|
September 2, 2017
NTRK2 (TrkB gene) variants and temporal lobe epilepsy: A genetic association study
Carolina Machado Torres, Marina Siebert, Hugo Bock, et al.
Brain Communications
|
March 15, 2024
Serum myostatin as a candidate disease severity and progression biomarker of spinal muscular atrophy
Ana Letícia Amorim de Albuquerque, Júlia Kersting Chadanowicz, Giovanna Câmara Giudicelli, et al.
Oral Diseases
|
March 28, 2021
Risk factors associated with the development of oral mucositis in pediatric oncology patients: Systematic review and meta-analysis
Amanda de Farias Gabriel, Felipe Martins Silveira, Marina Curra, et al.
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Search research articles
Search
Showing results (31-40 of 46) with videos related to
Sort By:
Page
of 5
Orphanet Journal of Rare Diseases
|
May 12, 2019
Evaluation of the frequency of non-motor symptoms of Parkinson's disease in adult patients with Gaucher disease type 1
Matheus V M B Wilke, Alícia D Dornelles, Artur S Schuh, et al.
American Journal of Medical Genetics. Part A
|
May 25, 2021
Elevated holo-transcobalamin in Gaucher disease type II: A case report
Suelen Porto Basgalupp, Karina Carvalho Donis, Marina Siebert, et al.
Frontiers in Neurology
|
June 25, 2019
Are Cognitive Changes in Hereditary Spastic Paraplegias Restricted to Complicated Forms?
Laís Alves Jacinto-Scudeiro, Gustavo Dariva Machado, Annelise Ayres, et al.
Arquivos De Neuro-Psiquiatria
|
January 16, 2020
Prevalence of oropharyngeal dysphagia in hereditary spastic paraplegias
Laís Alves Jacinto-Scudeiro, Gustavo Dariva Machado, Annelise Ayres, et al.
Cardiology
|
September 8, 2025
MicroRNA Expression Pre-Trastuzumab Treatment in HER-2+ Early Breast Cancer Patients as a Predictor of Cancer Therapy-Related Cardiac Dysfunction: A Pilot Cohort Study
Fernando Pivatto Júnior, Ângela Barreto Santiago Santos, Eduarda Foresti Englert, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
February 17, 2022
Diagnostic yield of multi-gene panel for muscular dystrophies and other hereditary myopathies
Pablo Brea Winckler, Bruna Cristine Chwal, Marco Antonnio Rocha Dos Santos, et al.
Molecular Genetics and Metabolism Reports
|
February 27, 2020
Liver involvement in patients with Gaucher disease types I and III
Rodrigo Tzovenos Starosta, Filippo Pinto E Vairo, Alícia Dorneles Dornelles, et al.
Epilepsy Research
|
September 2, 2017
NTRK2 (TrkB gene) variants and temporal lobe epilepsy: A genetic association study
Carolina Machado Torres, Marina Siebert, Hugo Bock, et al.
Brain Communications
|
March 15, 2024
Serum myostatin as a candidate disease severity and progression biomarker of spinal muscular atrophy
Ana Letícia Amorim de Albuquerque, Júlia Kersting Chadanowicz, Giovanna Câmara Giudicelli, et al.
Oral Diseases
|
March 28, 2021
Risk factors associated with the development of oral mucositis in pediatric oncology patients: Systematic review and meta-analysis
Amanda de Farias Gabriel, Felipe Martins Silveira, Marina Curra, et al.
Page
of 5