Maria Manuela Monteiro Grazina


AuthID: R-000-CA1

Confirmed Publications: 26



11
TITLE: Neonatal liver failure due to deoxyguanosine kinase deficiency
AUTHORS: Nobre, S; Grazina, M ; Silva, F; Pinto, C; Goncalves, I; Diogo, L;
PUBLISHED: 2012, SOURCE: BMJ Case Reports
INDEXED IN: Scopus
IN MY: ORCID
12
TITLE: Pharmacogenetics in Latin American populations: Regulatory aspects, application to herbal medicine, cardiovascular and psychiatric disorders
AUTHORS: Rodeiro, I; Remirez Figueredo, D; Garcia Mesa, M; Dorado, P; Llerena, A; Moya, GE; Ferrero, V; Tarazona Santos, E; Fiedler, J; Herrera, L; Rojas Ponce, R; Sarmiento Sanchez, AP; Borbon Orejuela, A; Barrantes, R; Jimenez Arce, G; Cespedes, C; Alvarez, M; Perez, B; Calzadilla, L; Delgado, R; Remirez, D; Teran, E; Heras, N; Beltran, L; Hernandez, F; Doredo, P; Penas Lledo, EM; Cobaleda, J; Gonzalez Naranjo, ME; De Andres, F; Ortiz Lopez, R; Rojas Martinez, A; Garza Ocanas, L; Perez Paramo, YX; Lopez Lopez, M; Ortega Vazquez, A; Alonso Vilatela, E; Monroy Jaramillo, N; Vazquez, TC; Yescas Gomez, P; Ochoa Morales, A; Sosa Macias, MG; Galaviz Hernandez, C; Lares, I; Lazalde, B; Ramirez Roa, R; Grazina, M ; Estevez Carrizo, FE; Gonzalez Vacarezza, N; ...More
PUBLISHED: 2012, SOURCE: Drug Metabolism and Drug Interactions, VOLUME: 27, ISSUE: 1
INDEXED IN: Scopus CrossRef: 4
IN MY: ORCID
13
14
TITLE: Value of Brain Magnetic Resonance Imaging in Mitochondrial Respiratory Chain Disorders  Full Text
AUTHORS: Luisa Diogo; Miguel Cordeiro; Paula Garcia; Isabel Fineza; Cristina Moura; Catarina Resende Oliveira ; Margarida Veiga; Teresa Garcia; Manuela Grazina ;
PUBLISHED: 2010, SOURCE: PEDIATRIC NEUROLOGY, VOLUME: 42, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 9
IN MY: ORCID
15
16
TITLE: The brain-heart connection in mitochondrial respiratory chain diseases
AUTHORS: Cordeiro, M; Scaglia, F; Lopes Da Silva, S; Garcia, P; Grazina, M ; Moura, C; Diogol, L;
PUBLISHED: 2009, SOURCE: Neuroradiology Journal, VOLUME: 22, ISSUE: 5
INDEXED IN: Scopus
IN MY: ORCID
17
TITLE: Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G > A point mutation - A case report  Full Text
AUTHORS: Manuela M Grazina ; Luisa M Diogo; Paula C Garcia; Eduardo D Silva ; Teresa D Garcia; Conceicao B Robalo; Catarina R Oliveira ;
PUBLISHED: 2007, SOURCE: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, VOLUME: 11, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 17
IN MY: ORCID
18
TITLE: Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: No association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene  Full Text
AUTHORS: Catarina Correia; Ana M Coutinho; Luisa Diogo; Manuela Grazina ; Carla Marques; Teresa Miguel; Assuncao Ataide; Joana Almeida; Luis Borges; Catarina Oliveira ; Guiomar Oliveira ; Astrid M Vicente ;
PUBLISHED: 2006, SOURCE: JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, VOLUME: 36, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 52
IN MY: ORCID
19
TITLE: Genetic basis of Alzheimer's dementia: Role of mtDNA mutations  Full Text
AUTHORS: Grazina, M ; Pratas, J; Silva, F; Oliveira, S; Santana, I ; Oliveira, C ;
PUBLISHED: 2006, SOURCE: Genes, Brain and Behavior, VOLUME: 5, ISSUE: SUPPL. 2
INDEXED IN: Scopus CrossRef
IN MY: ORCID
20
TITLE: Genetic basis of Alzheimer's dementia: role of mtDNA mutations
AUTHORS: Grazina, M ; Pratas, J; Silva, F; Oliveira, S; Santana, I ; Oliveira, C ;
PUBLISHED: 2006, SOURCE: GENES BRAIN AND BEHAVIOR, VOLUME: 5
INDEXED IN: WOS
Page 2 of 3. Total results: 26.

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