Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Gago MF"'
Publikováno v:
Clinical Interventions in Aging, Vol Volume 12, Pp 1843-1857 (2017)
Nafiseh Mollaei,1 Estela Bicho,1 Nuno Sousa,2,3 Miguel Fernandes Gago2–4 1Centro Algoritmi, Campus Azurem, University of Minho, Guimarães, 2Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, 3ICVS-
Externí odkaz:
https://doaj.org/article/8ce7ad1cf79d413592c9b427fb5109ef
Akademický článek
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Autor:
Brigas HC; Department of Research and Development, BIAL, 4745-457, Trofa, Portugal. Electronic address: helena.brigas@bial.com., Rodrigues AM; Department of Neurology, ULS Braga, Hospital de Braga, 4710-243, Braga, Portugal; CNS - Campus Neurológico, 4710-452, Braga, Portugal., Morgadinho A; Department of Neurology, Hospital da Luz Coimbra, 3020-479, Coimbra, Portugal., Gago MF; CNS - Campus Neurológico, 4710-452, Braga, Portugal; Department of Neurology, ULS Alto Ave, Hospital da Senhora da Oliveira, 4835-044, Guimarães, Portugal; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057, Braga, Portugal., Simões RM; CNS - Campus Neurológico, 4710-452, Braga, Portugal; Department of Neurology, ULS Loures-Odivelas, Hospital de Loures, 2674-514 Loures, Portugal.
Publikováno v:
Parkinsonism & related disorders [Parkinsonism Relat Disord] 2024 Nov; Vol. 128, pp. 107124. Date of Electronic Publication: 2024 Sep 02.
Autor:
Gago MF; Neurology Department, Hospital da Senhora da Oliveira, Guimarães, Portugal; School of Medicine, Life and Health Sciences Research Institute (ICVS), University of Minho, Braga, Portugal. Electronic address: miguelfgago@yahoo.com., Ferreira F; Algoritmi Centre, School of Engineering, University of Minho, Portugal; Centre of Mathematics, School of Sciences, University of Minho, Portugal., Bicho E; Algoritmi Centre, School of Engineering, University of Minho, Portugal.
Publikováno v:
Clinical neurology and neurosurgery [Clin Neurol Neurosurg] 2022 Oct; Vol. 221, pp. 107405. Date of Electronic Publication: 2022 Aug 02.
Autor:
Fernandes C; Algoritmi Center, University of Minho, Portugal. Electronic address: carlos.rafael.fernandes@hotmail.com., Ferreira F; Center of Mathematics, University of Minho, Portugal., Lopes RL; INESC TEC, Porto, Portugal., Bicho E; Algoritmi Center, University of Minho, Portugal. Electronic address: estela.bicho@dei.uminho.pt., Erlhagen W; Center of Mathematics, University of Minho, Portugal. Electronic address: wolfram.erlhagen@math.uminho.pt., Sousa N; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Portugal; ICVS-3Bs PT Government Associate Laboratory, Portugal. Electronic address: njcsousa@ecsaude.uminho.pt., Gago MF; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Portugal; ICVS-3Bs PT Government Associate Laboratory, Portugal; Neurology Department, Hospital da Senhora da Oliveira, Guimarães, EPE, Portugal.
Publikováno v:
Journal of biomechanics [J Biomech] 2021 Aug 26; Vol. 125, pp. 110214. Date of Electronic Publication: 2021 May 11.
Autor:
Azevedo O; Cardiology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, 4835-044 Guimarães, Portugal.; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, 4805-017 Braga/Guimarães, Portugal., Cordeiro F; Cardiology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, 4835-044 Guimarães, Portugal., Gago MF; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, 4805-017 Braga/Guimarães, Portugal.; Neurology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, 4835-044 Guimarães, Portugal., Miltenberger-Miltenyi G; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, 4805-017 Braga/Guimarães, Portugal.; Genetics Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, 4835-044 Guimarães, Portugal., Ferreira C; Cardiology Department, Centro Hospitalar Trás-os-Montes e Alto Douro, 5000-508 Vila Real, Portugal.; Faculdade de Ciências da Saúde, Centro de Investigação em Ciências da Saúde, Universidade da Beira Interior, 6200-506 Covilhã, Portugal., Sousa N; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, 4805-017 Braga/Guimarães, Portugal., Cunha D; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, 4805-017 Braga/Guimarães, Portugal.
Publikováno v:
International journal of molecular sciences [Int J Mol Sci] 2021 Apr 23; Vol. 22 (9). Date of Electronic Publication: 2021 Apr 23.
Autor:
Azevedo O; Cardiology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, 4835-044 Guimarães, Portugal.; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, 4805-017 Braga/Guimarães, Portugal., Gago MF; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, 4805-017 Braga/Guimarães, Portugal.; Neurology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, 4835-044 Guimarães, Portugal., Miltenberger-Miltenyi G; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, 4805-017 Braga/Guimarães, Portugal.; Genetics Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, 4835-044 Guimarães, Portugal., Sousa N; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, 4805-017 Braga/Guimarães, Portugal., Cunha D; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, 4710-057 Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, 4805-017 Braga/Guimarães, Portugal.
Publikováno v:
International journal of molecular sciences [Int J Mol Sci] 2020 Dec 28; Vol. 22 (1). Date of Electronic Publication: 2020 Dec 28.
Autor:
Azevedo O; Cardiology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal, member of the European Reference Network on Hereditary Metabolic Disorders (MetabERN).; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal., Gago MF; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal.; Neurology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal, member of the European Reference Network on Hereditary Metabolic Disorders (MetabERN)., Miltenberger-Miltenyi G; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal.; Genetics Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal, member of the European Reference Network on Hereditary Metabolic Disorders (MetabERN)., Robles AR; Otorhinolaryngology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal, member of the European Reference Network on Hereditary Metabolic Disorders (MetabERN)., Costa MA; Ophthalmology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal, member of the European Reference Network on Hereditary Metabolic Disorders (MetabERN)., Pereira O; Dermatology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal, member of the European Reference Network on Hereditary Metabolic Disorders (MetabERN)., Vide AT; Neurorradiology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal, member of the European Reference Network on Hereditary Metabolic Disorders (MetabERN)., Castelo Branco G; Internal Medicine Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal, member of the European Reference Network on Hereditary Metabolic Disorders (MetabERN)., Simões S; Psychiatry Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal, member of the European Reference Network on Hereditary Metabolic Disorders (MetabERN)., Guimarães MJ; Pneumology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal, member of the European Reference Network on Hereditary Metabolic Disorders (MetabERN)., Salgado A; Radiology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal, member of the European Reference Network on Hereditary Metabolic Disorders (MetabERN)., Sousa N; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal., Cunha D; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal.; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal.
Publikováno v:
Molecular genetics and metabolism reports [Mol Genet Metab Rep] 2020 Feb 15; Vol. 22, pp. 100565. Date of Electronic Publication: 2020 Feb 15 (Print Publication: 2020).
Founder effect of Fabry disease due to p.F113L mutation: Clinical profile of a late-onset phenotype.
Autor:
Azevedo O; Cardiology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal. Electronic address: olgaazevedo@hospitaldeguimaraes.min-saude.pt., Gal A; Labor Dr. Heidrich & Kollegen MVZ GmbH, Hamburg, Germany., Faria R; Communication and Society Research Centre, University of Minho, Braga, Portugal., Gaspar P; Organelle Biogenesis & Function (OBF) Group, Institute of Molecular and Cell Biology (IBMC), Instituto de Investigação e Inovação em Saúde (I3S), Porto, Portugal., Miltenberger-Miltenyi G; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal; Genetics Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal., Gago MF; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal; Neurology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal., Dias F; Transdisciplinary Culture, Space and Memory Research Centre - History of Populations Group, University of Minho, Braga, Portugal., Martins A; Transdisciplinary Culture, Space and Memory Research Centre - History of Populations Group, University of Minho, Braga, Portugal., Rodrigues J; Otorhinolaryngology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal., Reimão P; Ophthalmology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal., Pereira O; Dermatology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal., Simões S; Psychiatry Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal., Lopes E; Internal Medicine Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal., Guimarães MJ; Pneumology Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal., Sousa N; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal., Cunha D; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal.
Publikováno v:
Molecular genetics and metabolism [Mol Genet Metab] 2020 Feb; Vol. 129 (2), pp. 150-160. Date of Electronic Publication: 2019 Jul 24.
Autor:
Gago MF; Neurology Department, Reference Center on Lysosomal Storage Disorders, Hospital da Senhora da Oliveira, EPE, Guimarães, Portugal.; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal.; European Reference Network for Hereditary Metabolic Disorders (MetabERN)., Azevedo O; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal.; Cardiology Department, Reference Center on Lysosomal Storage Disorders, Hospital da Senhora da Oliveira, EPE, Guimarães, Portugal.; European Reference Network for Hereditary Metabolic Disorders (MetabERN)., Guimarães A; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal., Teresa Vide A; Neuroradiology Department, Reference Center on Lysosomal Storage Disorders, Hospital da Senhora da Oliveira, EPE, Guimarães, Portugal.; European Reference Network for Hereditary Metabolic Disorders (MetabERN)., Lamas NJ; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal.; Anatomic Pathology Service, Pathology Department, Hospital and University Center of Porto, Porto, Portugal., Oliveira TG; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal., Gaspar P; Newborn Screening, Metabolism and Genetic Unit, Genetics Department, National Institute for Health Doutor Ricardo Jorge (INSA)., Bicho E; Centro Algoritmi, Campus Azurem, University of Minho, Guimarães, Braga, Portugal., Miltenberger-Miltenyi G; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal.; Genetics Department, Reference Center on Lysosomal Storage Disorders, Hospital Senhora da Oliveira, Guimarães, Portugal.; European Reference Network for Hereditary Metabolic Disorders (MetabERN)., Ferreira J; Laboratory of Clinical Pharmacology and Therapeutics, Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal; Instituto de Medicina Molecular, Lisbon, Portugal; CNS - Campus Neurológico Sénior, Torres Vedras, Portugal., Sousa N; Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal; ICVS/3Bs PT Government Associate Laboratory, Braga/Guimarães, Portugal.
Publikováno v:
Journal of Parkinson's disease [J Parkinsons Dis] 2020; Vol. 10 (1), pp. 141-152.