Marina Magalhães - Concepedia

Author

Marina Magalhães

Also Known As

F Jácome, Joo Freixo, M J C MAGALHAES, M Magalhães, M. Magalhães, MARCO ANTÔNIO PERÍGOLO MAGALHÃES, MAYLA STEFANNE SANTOS MAGALHAES, Magalhães, M., Magalhães, Marina, Marcelo Magalhães

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

Centro Hospitalar do Porto Universidade do Porto Hospital de Santo António University of Minho Instituto de Biologia Molecular e Celular

About

Marina Magalhães is an author at Centro Hospitalar do Porto specializing in medicine, genetic epidemiology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	843
2	Neurology	2	2	803
3	Genetic Medicine	1	1	25
4	Molecular Biology	1	1	29
5	Molecular Genetics	1	1	29

Marina Magalhães

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
Clinical features and natural history of multiple system atrophy Gregor K. Wenning, Y. Ben Shlomo, Marina Magalhães, Brain Motor DysfunctionNeurological DisorderCorticobasal DegenerationMultiple System AtrophyDiagnosis	1994	778
DJ-1 linked parkinsonism (PARK7) is associated with Lewy body pathology Ricardo Taipa, Conceição Pereira, Inês Reis, Brain	2016	127
Autonomic dysfunction in pathologically confirmed multiple system atrophy and idiopathic Parkinson's disease - a retrospective comparison Marina Magalhães, Gregor K. Wenning, S. E. Daniel, Acta Neurologica Scandinavica	2009	126
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 Maria do Carmo Costa, Andreia Teixeira‐Castro, Marco Constante, Journal of Human Genetics Huntington-like PhenotypeMendelian DisorderGenetic DisorderMedicineGenetics	2006	29
Clinical rating scale for pantothenate kinase‐associated neurodegeneration: A pilot study Alejandra Darling, Cristina Tello, M. J. Martí, Movement Disorders	2017	28
Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice Maria do Carmo Costa, Paula Magalhães, Fátima Ferreirinha, European Journal of Human Genetics Molecular DiagnosisGenetic TestingMendelian DisorderGenetic DisorderGenetics	2003	25
Task-specific contribution of the human striatum to perceptual–motor skill learning Sara Cavaco, Steven W. Anderson, Manuel Correia, Journal of Clinical and Experimental Neuropsychology	2010	22
Acquired hepatocerebral degeneration and hepatic encephalopathy: one or two entities? Maria João Malaquias, Catarina Pinto, Cristina Ramos, European Journal of Neurology	2020	19
Diagnosis of Aicardi‐Goutières Syndrome in Adults: A Case Series Gonçalo Videira, Maria João Malaquias, Inês Laranjinha, Movement Disorders Clinical Practice	2020	18
Multisystemic <i>RFC1</i> -Related Disorder Maria João Malaquias, Luís Braz, Cláudia Santos Silva, Neurology Clinical Practice	2023	18

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