Get started
Author

Marina Magalhães

Observed names: M Magalhães, M. Magalhães, Marina J. Magalhães, Marina Magalhaes
Observed institutions: University of Lisbon, Universidade do Porto, Hospital de São João, Hospital Padre Américo, Instituto Português de Oncologia Francisco Gentil, Hospital de Egas Moniz, Hospital de Santa Cruz, Centro Hospitalar do Tâmega e Sousa, Centro Hospitalar de Lisboa Ocidental, Hospital de Santo António, Rede de Química e Tecnologia, Centro Hospitalar do Porto, i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Instituto de Biologia Molecular e Celular, LAQV Requimte, Unidade Local de Saúde de Santo António EPE, UCL Queen Square Institute of Neurology
ORCID: 0009-0003-5480-2084
Observed ORCID: 0009-0003-5480-2084
OpenAlex ID: A5103184315
Clinical features and natural history of multiple system atrophy: An analysis of 100 cases
1994 · G. K. Wenning, Y. Ben Shlomo, et al. · Brain · 796
DJ-1 linked parkinsonism (PARK7) is associated with Lewy body pathology
2016 · Ricardo Taipa, Conceição Pereira, et al. · Brain · 137
Autonomic dysfunction in pathologically confirmed multiple system atrophy and idiopathic Parkinson's disease - a retrospective comparison
2009 · M. Magalhães, G. K. Wenning, et al. · Acta Neurologica Scandinavica · 131
Clinical rating scale for pantothenate kinase‐associated neurodegeneration: A pilot study
2017 · Alejandra Darling, Cristina Tello, et al. · Movement Disorders · 31
Multisystemic RFC1 -Related Disorder: Expanding the Phenotype Beyond Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome
2023 · Maria João Malaquias, Luis Braz, et al. · Neurology Clinical Practice · 29
PDF
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype
2006 · Maria do Carmo Costa, Andreia Teixeira-Castro, et al. · Journal of Human Genetics · 29
PDF
Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice
2003 · Maria do Carmo Costa, Paula Magalhães, et al. · European Journal of Human Genetics · 26
PDF
Task-specific contribution of the human striatum to perceptual–motor skill learning
2010 · Sara Cavaco, Steven W. Anderson, et al. · Journal of Clinical and Experimental Neuropsychology · 23
Acquired hepatocerebral degeneration and hepatic encephalopathy: one or two entities?
2020 · M. J. Malaquias, C. M. Pinto, et al. · European Journal of Neurology · 22
Diagnosis of Aicardi‐Goutières Syndrome in Adults: A Case Series
2020 · Gonçalo Videira, Maria João Malaquias, et al. · Movement Disorders Clinical Practice · 20
PDF
Targeted next generation sequencing identifies novel pathogenic variants and provides molecular diagnoses in a cohort of pediatric and adult patients with unexplained mitochondrial dysfunction
2019 · Célia Nogueira, Lisbeth Silva, et al. · Mitochondrion · 20
The genetic landscape of mitochondrial diseases in the next-generation sequencing era: a Portuguese cohort study
2024 · C. Nogueira, C. Pereira, et al. · Frontiers in Cell and Developmental Biology · 18
GNAO1 mutation presenting as dyskinetic cerebral palsy
2019 · Maria João Malaquias, Isabel Fineza, et al. · Neurological Sciences · 17
Gordon Holmes syndrome due to compound heterozygosity of two new PNPLA6 variants – A diagnostic challenge
2018 · Paula Salgado, Rui Carvalho, et al. · eNeurologicalSci · 16
PDF
A Coincidental Case of Young-Onset Parkinson Disease and Multiple Sclerosis
2011 · Joana Damásio, Cristina Ramos, et al. · The Neurologist · 12
Tremor and white matter lesions in Klinefelter syndrome
2010 · Ester Coutinho, José Pedro Pereira, et al. · Movement Disorders · 12
Tremor as the first neurological manifestation of Sneddon's syndrome
2004 · A. Martins Da Silva, N. Rocha, et al. · Movement Disorders · 12
Wilson’s Disease and Ulcerative Colitis in the Same Patient: Just A Coincidence? A Case Report and Literature Review
2011 · Filipe Nery, Irene Marques, et al. · Gastroenterology Research · 11
PDF
Clinical spectrum of C9orf72 expansion in a cohort of Huntington’s disease phenocopies
2018 · Joana Martins, Joana Damásio, et al. · Neurological Sciences · 10
Trace Element Imbalances in Acquired Hepatocerebral Degeneration and Changes after Liver Transplant
2023 · Henrique Nascimento, Maria João Malaquias, et al. · Biology · 9
PDF
Perry syndrome with progressive supranuclear palsy-like phenotype in a Portuguese family – Long-term clinical follow-up
2021 · Rui Duarte Barreto, Rita Rodrigues, et al. · Parkinsonism & Related Disorders · 9
Correlation between neuroimaging, neurological phenotype, and functional outcomes in Wilson’s disease
2024 · João Moura, Catarina Pinto, et al. · Neurological Sciences · 8
Leigh Syndrome Spectrum: A Portuguese Population Cohort in an Evolutionary Genetic Era
2023 · Manuela Schubert Baldo, Célia Nogueira, et al. · Genes · 8
PDF
Brain MRI in the Decision for Liver Transplantation in Pediatric Neurological Wilson's Disease
2022 · Catarina Pinto, Maria João Malaquias, et al. · Movement Disorders Clinical Practice · 8
PDF
A Case of YY1 ‐Related Isolated Dystonia with Severe Oromandibular Involvement
2021 · Maria João Malaquias, Joana Damásio, et al. · Movement Disorders · 8
Works count: 57
Citation count: 1,506
H-index: 14
I10-index: 19
Year
Topic
Type