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TITLE: Phenotypic Variability in a Portuguese Family With X-Linked Creatine Transport Deficiency  Full Text
AUTHORS: Paula Garcia; Fidjy Rodrigues; Carla Valongo; Gajja S Salomons; Luisa Diogo;
PUBLISHED: 2012, SOURCE: PEDIATRIC NEUROLOGY, VOLUME: 46, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 5
12
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
15
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
16
TITLE: NMR derivatives for quantification of H-2 and C-13-enrichment of human glucuronide from metabolic tracers  Full Text
AUTHORS: John G Jones ; Cristina Barosa ; Filipe Gomes; Ana Carina Mendes; Teresa C Delgado; Luisa Diogo; Paula Garcia; Margarida Bastos; Luisa Barros; Ana Fagulha; Carla Baptista; Manuela Carvalheiro; Madalena M Caldeira;
PUBLISHED: 2006, SOURCE: 6th International Meeting of the Portuguese-Carbohydrate-Group/3rd Iberian Carbohydrate Meeting (Glupor VI) in JOURNAL OF CARBOHYDRATE CHEMISTRY, VOLUME: 25, ISSUE: 2-3
INDEXED IN: Scopus WOS CrossRef: 24
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