1
TITLE: Understanding Hypertriglyceridemia: Integrating Genetic Insights  Full Text
AUTHORS: Alves, Mara; Laranjeira, Francisco ; Correia da Silva, Georgina ;
PUBLISHED: 2024, SOURCE: GENES, VOLUME: 15, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 1
2
TITLE: Impact of Structural GLA Protein Changes on Peripheral GLA Activity and Substrate Accumulation in Fabry Disease Patients
AUTHORS: Jorge Diogo Da Silva; Isaura Ribeiro; Carla Caseiro; Eugénia Pinto; Sónia Rocha; Helena Ribeiro; Célia Ferreira; Elisabete Silva; Francisco Laranjeira ; Nataliya Tkachenko; Lúcia Lacerda; Dulce Quelhas;
PUBLISHED: 2023, SOURCE: Endocrine, Metabolic & Immune Disorders - Drug Targets, VOLUME: 23
INDEXED IN: CrossRef: 1
3
TITLE: Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition  Full Text
AUTHORS: Palmer, Elizabeth E.; Pusch, Michael; Picollo, Alessandra; Forwood, Caitlin; Nguyen, Matthew H.; Suckow, Vanessa; Gibbons, Jessica; Hoff, Alva; Sigfrid, Lisa; Megarbane, Andre; Nizon, Mathilde; Cogne, Benjamin; Beneteau, Claire; Alkuraya, Fowzan S.; Chedrawi, Aziza; Hashem, Mais O.; Stamberger, Hannah; Weckhuysen, Sarah; Vanlander, Arnaud; Ceulemans, Berten; Rajagopalan, Sulekha; Nunn, Kenneth; Arpin, Stephanie; Raynaud, Martine; Motter, Constance S.; Ward Melver, Catherine; Janssens, Katrien; Meuwissen, Marije; Beysen, Diane; Dikow, Nicola; Grimmel, Mona; Haack, Tobias B.; Clement, Emma; McTague, Amy; Hunt, David; Townshend, Sharron; Ward, Michelle; Richards, Linda J.; Simons, Cas; Costain, Gregory; Dupuis, Lucie; Mendoza Londono, Roberto; Dudding Byth, Tracy; Boyle, Jackie; Saunders, Carol; Fleming, Emily; El Chehadeh, Salima; Spitz, Marie Aude; Piton, Amelie; Gerard, Benedicte; Warde, Marie Therese Abi; Rea, Gillian; McKenna, Caoimhe; Douzgou, Sofia; Banka, Siddharth; Akman, Cigdem; Bain, Jennifer M.; Sands, Tristan T.; Wilson, Golder N.; Silvertooth, Erin J.; Miller, Lauren; Lederer, Damien; Sachdev, Rani; Macintosh, Rebecca; Monestier, Olivier; Karadurmus, Deniz; Collins, Felicity; Carter, Melissa; Rohena, Luis; Willemsen, Marjolein H.; Ockeloen, Charlotte W.; Pfundt, Rolph; Kroft, Sanne D.; Field, Michael; Laranjeira, Francisco E. R. ; Fortuna, Ana M.; Soares, Ana R.; Michaud, Vincent; Naudion, Sophie; Golla, Sailaja; Weaver, David D.; Bird, Lynne M.; Friedman, Jennifer; Clowes, Virginia; Joss, Shelagh; Polsler, Laura; Campeau, Philippe M.; Blazo, Maria; Bijlsma, Emilia K.; Rosenfeld, Jill A.; Beetz, Christian; Powis, Zoe; McWalter, Kirsty; Brandt, Tracy; Torti, Erin; Mathot, Mikael; Mohammad, Shekeeb S.; Armstrong, Ruth; Kalscheuer, Vera M.; ...More
PUBLISHED: 2022, SOURCE: MOLECULAR PSYCHIATRY, VOLUME: 28, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 18
4
TITLE: Maturity-onset diabetes of the young in a large Portuguese cohort  Full Text
AUTHORS: Monteiro, Silvia Santos; Santos, Tiago da Silva; Fonseca, Liliana; Assuncao, Guilherme; Lopes, Ana M.; Duarte, Diana B.; Soares, Ana Rita; Laranjeira, Francisco ; Ribeiro, Isaura ; Pinto, Eugenia; Rocha, Sonia; Gouveia, Sofia Barbosa; Vazquez Mosquera, Maria Eugenia; Oliveira, Maria Joao; Borges, Teresa; Cardoso, Maria Helena;
PUBLISHED: 2022, SOURCE: ACTA DIABETOLOGICA, VOLUME: 60, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 1
5
TITLE: Case Report: Diffuse Polymicrogyria Associated With a Novel <i>ADGRG1</i> Variant
AUTHORS: Carneiro, Fabio; Duarte, Julia; Laranjeira, Francisco ; Barbosa Gouveia, Sofia; Couce, Maria Luz; Fonseca, Maria Jose;
PUBLISHED: 2021, SOURCE: FRONTIERS IN PEDIATRICS, VOLUME: 9
INDEXED IN: Scopus WOS CrossRef
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TITLE: Congenital Disorders of Glycosylation in Portugal-Two Decades of Experience  Full Text
AUTHORS: Quelhas, D ; Martins, E ; Azevedo, L ; Bandeira, A; Diogo, L; Garcia, P; Sequeira, S; Ferreira, AC; Teles, EL; Rodrigues, E; Fortuna, AM; Mendonca, C; Fernandes, HC; Medeira, A; Gaspar, A; Janeiro, P; Oliveira, A; Laranjeira, F ; Ribeiro, I ; Souche, E; Race, V; Keldermans, L; Matthijs, G; Jaeken, J; ...More
PUBLISHED: 2021, SOURCE: JOURNAL OF PEDIATRICS, VOLUME: 231
INDEXED IN: Scopus WOS CrossRef: 1
7
TITLE: Dorfman-Chanarin Syndrome: A Rare Cause of Metabolic Associated Fatty Liver Disease Related to Homozygosity of the Nonsense Mutation c.934C&amp;#x3e;T (p.R312*)
AUTHORS: Rita Quelhas da Costa; Francisco Laranjeira ; Isaura Duarte Ribeiro; António Filipe Santos; Filipe Nery;
PUBLISHED: 2021, SOURCE: GE - Portuguese Journal of Gastroenterology, VOLUME: 29, ISSUE: 4
INDEXED IN: CrossRef
8
TITLE: Utility of Gene Panels for the Diagnosis of Inborn Errors of Metabolism in a Metabolic Reference Center  Full Text
AUTHORS: Sofia Barbosa-Gouveia; María E Vázquez-Mosquera; Emiliano González-Vioque; José V Álvarez; Roi Chans; Francisco Laranjeira ; Esmeralda Martins; Ana Cristina Ferreira; Alejandro Avila-Alvarez; María L Couce;
PUBLISHED: 2021, SOURCE: Genes, VOLUME: 12, ISSUE: 8
INDEXED IN: CrossRef: 4
9
TITLE: Genotype-phenotype correlations and BH4 estimated responsiveness in patients with phenylketonuria from Rio de Janeiro, Southeast Brazil
AUTHORS: Neto, EV; Laranjeira, F ; Quelhas, D ; Ribeiro, I; Seabra, A; Mineiro, N; Carvalho, LM; Lacerda, L; Ribeiro, MG;
PUBLISHED: 2019, SOURCE: MOLECULAR GENETICS & GENOMIC MEDICINE, VOLUME: 7, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 7
10
TITLE: Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients  Full Text
AUTHORS: Ana Fernández-Marmiesse; Iria Roca; Felícitas Díaz-Flores; Verónica Cantarín; Mª Socorro Pérez-Poyato; Ana Fontalba; Francisco Laranjeira ; Sofia Quintans; Oana Moldovan; Blanca Felgueroso; Montserrat Rodríguez-Pedreira; Rogelio Simón; Ana Camacho; Pilar Quijada; Salvador Ibanez-Mico; Mª Rosario Domingno; Carmen Benito; Rocío Calvo; Antonia Pérez-Cejas; Mª Llanos Carrasco; Feliciano Ramos; Mª Luz Couce; Mª Luz Ruiz-Falcó; Luis Gutierrez-Solana; Margarita Martínez-Atienza; ...More
PUBLISHED: 2019, SOURCE: Frontiers in Neuroscience, VOLUME: 13
INDEXED IN: CrossRef: 32
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