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Maria Joana Lima Barbosa de Melo

AuthID: R-000-BT9

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Confirmed Publications: 18

1

TITLE: Cryptic 7q36.2q36.3 deletion causes multiple congenital eye anomalies and craniofacial dysmorphism Full Text
AUTHORS: Ana Beleza Meireles; Eunice Matoso; Lina Ramos; Joana B Melo ; Isabel M Carreira ; Eduardo D Silva ; Jorge M Saraiva;
PUBLISHED: 2013, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 161A, ISSUE: 3

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2

TITLE: Insertional Translocation Leading to a 4q13 Duplication Including the EPHA5 Gene in Two Siblings With Attention-Deficit Hyperactivity Disorder Full Text
AUTHORS: Eunice Matoso; Joana B Melo ; Susana I Ferreira; Ana Jardim; Teresa M Castelo; Anja Weise; Isabel M Carreira ;
PUBLISHED: 2013, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 161, ISSUE: 8

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3

TITLE: Potential Markers of Cisplatin Treatment Response Unveiled by NMR Metabolomics of Human Lung Cells Full Text
AUTHORS: Duarte, IF; Ladeirinha, AF; Lamego, I; Gil, AM; Carvalho, L; Carreira, IM ; Melo, JB ;
PUBLISHED: 2013, SOURCE: MOLECULAR PHARMACEUTICS, VOLUME: 10, ISSUE: 11

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4

TITLE: Critical region in 2q31.2q32.3 deletion syndrome: Report of two phenotypically distinct patients, one with an additional deletion in Alagille syndrome region Full Text
AUTHORS: Susana Isabel Ferreira; Eunice Matoso; Margarida Venancio; Jorge Saraiva; Joana B Melo ; Isabel Marques Carreira ;
PUBLISHED: 2012, SOURCE: MOLECULAR CYTOGENETICS, VOLUME: 5, ISSUE: 1

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5

TITLE: Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances
AUTHORS: Joana Barbosa Melo ; Liesbeth Backx; Joris R Vermeesch; Heloisa G Santos; Ana C Sousa; Nadezda Kosyakova; Anja Weise; Ferdinand von Eggeling; Thomas Liehr; Isabel Marques Carreira ;
PUBLISHED: 2011, SOURCE: JOURNAL OF APPLIED GENETICS, VOLUME: 52, ISSUE: 2

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6

TITLE: Metabolic Profiling of Human Lung Cancer Tissue by H-1 High Resolution Magic Angle Spinning (HRMAS) NMR Spectroscopy Full Text
AUTHORS: Rocha, CM; Barros, AS ; Gil, AM ; Goodfellow, BJ ; Humpfer, E; Spraul, M; Carreira, IM ; Melo, JB ; Bernardo, J; Gomes, A; Sousa, V; Carvalho, L ; Duarte, IF ;
PUBLISHED: 2010, SOURCE: JOURNAL OF PROTEOME RESEARCH, VOLUME: 9, ISSUE: 1

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7

TITLE: X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation Full Text
AUTHORS: Susana I Ferreira; Eunice Matoso; Marta Pinto; Joana Almeida; Thomas Liehr; Joana B Melo ; Isabel M Carreira ;
PUBLISHED: 2010, SOURCE: MOLECULAR CYTOGENETICS, VOLUME: 3, ISSUE: 1

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8

TITLE: Analytical Approaches toward Successful Human Cell Metabolome Studies by NMR Spectroscopy Full Text
AUTHORS: Iola F Duarte ; Joana Marques; Ana F Ladeirinha; Claudia Rocha; Ines Lamego; Rita Calheiros; Tania M Silva; Paula P M Marques ; Joana B Melo ; Isabel M Carreira ; Ana M Gil ;
PUBLISHED: 2009, SOURCE: ANALYTICAL CHEMISTRY, VOLUME: 81, ISSUE: 12

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9

TITLE: Galantamine protects against oxidative stress induced by amyloid-beta peptide in cortical neurons Full Text
AUTHORS: Joana B Melo ; Carla Sousa; Pedro Garcao; Catarina R Oliveira ; Paula Agostinho ;
PUBLISHED: 2009, SOURCE: EUROPEAN JOURNAL OF NEUROSCIENCE, VOLUME: 29, ISSUE: 3

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10

TITLE: Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 -> qter) detected in an autistic boy Full Text
AUTHORS: Isabel M Carreira ; Joana B Melo ; Carlos Rodrigues; Liesbeth Backx; Joris Vermeesch; Anja Weise; Nadezda Kosyakova; Guiomar Oliveira ; Eunice Matoso;
PUBLISHED: 2009, SOURCE: MOLECULAR CYTOGENETICS, VOLUME: 2, ISSUE: 1

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