Luisa Maria Abreu Freire Diogo Matos
AuthID: R-001-YQS
1
TITLE: THE IMPACT OF A TAILORED END USER ENGAGEMENT FRAMEWORK ON A PEER-TO-PEER ENERGY SHARING INITIATIVE: AN EMPIRICAL STUDY
AUTHORS: Lurian Klein; Luisa Matos; Giovanni Allegretti;
PUBLISHED: 2019, SOURCE: 4th International Conference on Energy and Environment - Bringing together Engineering and Economics (ICEE) in PROCEEDINGS OF THE 4TH INTERNATIONAL CONFERENCE ON ENERGY & ENVIRONMENT (ICEE 2019): BRINGING TOGETHER ENGINEERING AND ECONOMICS
AUTHORS: Lurian Klein; Luisa Matos; Giovanni Allegretti;
PUBLISHED: 2019, SOURCE: 4th International Conference on Energy and Environment - Bringing together Engineering and Economics (ICEE) in PROCEEDINGS OF THE 4TH INTERNATIONAL CONFERENCE ON ENERGY & ENVIRONMENT (ICEE 2019): BRINGING TOGETHER ENGINEERING AND ECONOMICS
INDEXED IN: 
WOS
WOS2
TITLE: Acute liver failure related to inherited metabolic diseases in young children
AUTHORS: Filipa Dias Costa; Rita Moinho; Sandra Ferreira; Paula Garcia; Luisa Diogo; Isabel Goncalves; Carla Pinto;
PUBLISHED: 2018, SOURCE: ANALES DE PEDIATRIA, VOLUME: 88, ISSUE: 2
AUTHORS: Filipa Dias Costa; Rita Moinho; Sandra Ferreira; Paula Garcia; Luisa Diogo; Isabel Goncalves; Carla Pinto;
PUBLISHED: 2018, SOURCE: ANALES DE PEDIATRIA, VOLUME: 88, ISSUE: 2
INDEXED IN: WOS
WOS3
TITLE: Phenotyping GABA transaminase deficiency: a case description and literature review Full Text
AUTHORS: Pedro Louro ; Lina Ramos; Conceicao Robalo; Candida Cancelinha; Alexandra Dinis; Ricardo Veiga; Raquel Pina; Olinda Rebelo; Ana Pop; Luisa Diogo; Gajja S Salomons; Paula Garcia;
PUBLISHED: 2016, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 39, ISSUE: 5
AUTHORS: Pedro Louro ; Lina Ramos; Conceicao Robalo; Candida Cancelinha; Alexandra Dinis; Ricardo Veiga; Raquel Pina; Olinda Rebelo; Ana Pop; Luisa Diogo; Gajja S Salomons; Paula Garcia;
PUBLISHED: 2016, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 39, ISSUE: 5
4
TITLE: A Novel SUCLA2 Mutation in a Portuguese Child Associated With "Mild" Methylmalonic Aciduria
AUTHORS: Celia Nogueira; Maria Chiara Meschini; Claudia Nesti; Paula Garcia; Luisa Diogo; Carla Valongo; Ricardo Costa; Arnaldo Videira; Laura Vilarinho; Filippo M Santorelli;
PUBLISHED: 2015, SOURCE: JOURNAL OF CHILD NEUROLOGY, VOLUME: 30, ISSUE: 2
AUTHORS: Celia Nogueira; Maria Chiara Meschini; Claudia Nesti; Paula Garcia; Luisa Diogo; Carla Valongo; Ricardo Costa; Arnaldo Videira; Laura Vilarinho; Filippo M Santorelli;
PUBLISHED: 2015, SOURCE: JOURNAL OF CHILD NEUROLOGY, VOLUME: 30, ISSUE: 2
5
TITLE: Nonketotic Hyperglycinemia: A Cause of Encephalopathy in Children
AUTHORS: Carla Verissimo; Paula Garcia; Marta Simoes; Conceicao Robalo; Raquel Henriques; Luisa Diogo; Manuela Grazina ;
PUBLISHED: 2013, SOURCE: JOURNAL OF CHILD NEUROLOGY, VOLUME: 28, ISSUE: 2
AUTHORS: Carla Verissimo; Paula Garcia; Marta Simoes; Conceicao Robalo; Raquel Henriques; Luisa Diogo; Manuela Grazina ;
PUBLISHED: 2013, SOURCE: JOURNAL OF CHILD NEUROLOGY, VOLUME: 28, ISSUE: 2
6
TITLE: Coenzyme Q(10) deficiency in mitochondrial DNA depletion syndromes Full Text
AUTHORS: Raquel Montero; Manuela Grazina ; Ester Lopez Gallardo; Julio Montoya; Paz Briones; Aleix Navarro Sastre; John M Land; Iain P Hargreaves; Rafael Artuch; Maria D del Mar O'Callaghan; Cristina Jou; Cecilia Jimenez; Nuria Bujan; Merce Pineda; Angels Garcia Cazorla; Andres Nascimento; Belen Perez Duenas; Eduardo Ruiz Pesini; Carl Fratter; Leonardo Salviati; ...More
PUBLISHED: 2013, SOURCE: MITOCHONDRION, VOLUME: 13, ISSUE: 4
AUTHORS: Raquel Montero; Manuela Grazina ; Ester Lopez Gallardo; Julio Montoya; Paz Briones; Aleix Navarro Sastre; John M Land; Iain P Hargreaves; Rafael Artuch; Maria D del Mar O'Callaghan; Cristina Jou; Cecilia Jimenez; Nuria Bujan; Merce Pineda; Angels Garcia Cazorla; Andres Nascimento; Belen Perez Duenas; Eduardo Ruiz Pesini; Carl Fratter; Leonardo Salviati; ...More
PUBLISHED: 2013, SOURCE: MITOCHONDRION, VOLUME: 13, ISSUE: 4
7
TITLE: A novel SUCLA2 mutation in a Portuguese patient Full Text
AUTHORS: Celia Nogueira; Paula Garcia; Luisa Diogo; Carla Valongo; Filippo M Santorelli; Laura Vilarinho;
PUBLISHED: 2013, SOURCE: MITOCHONDRION, VOLUME: 13, ISSUE: 6
AUTHORS: Celia Nogueira; Paula Garcia; Luisa Diogo; Carla Valongo; Filippo M Santorelli; Laura Vilarinho;
PUBLISHED: 2013, SOURCE: MITOCHONDRION, VOLUME: 13, ISSUE: 6
INDEXED IN: WOS 
CrossRef
WOS CrossRef8
TITLE: Off licence use of medications: Off-label-off law?
AUTHORS: Matos, MF;
PUBLISHED: 2013, SOURCE: Legal and Forensic Medicine
AUTHORS: Matos, MF;
PUBLISHED: 2013, SOURCE: Legal and Forensic Medicine
INDEXED IN: 
Scopus
Scopus9
TITLE: Mitochondrial DNA 8993T > G Mutation in a Child With Ornithine Transcarbamylase Deficiency and Leigh Syndrome: An Unexpected Association
AUTHORS: Margarida Henriques; Luisa Diogo; Paula Garcia; Joao Pratas; Marta Simoes; Manuela Grazina ;
PUBLISHED: 2012, SOURCE: JOURNAL OF CHILD NEUROLOGY, VOLUME: 27, ISSUE: 8
AUTHORS: Margarida Henriques; Luisa Diogo; Paula Garcia; Joao Pratas; Marta Simoes; Manuela Grazina ;
PUBLISHED: 2012, SOURCE: JOURNAL OF CHILD NEUROLOGY, VOLUME: 27, ISSUE: 8
10
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
AUTHORS: Paula Garcia; Fidjy Rodrigues; Carla Valongo; Gajja S Salomons; Luisa Diogo;
PUBLISHED: 2012, SOURCE: PEDIATRIC NEUROLOGY, VOLUME: 46, ISSUE: 1
