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TITLE: Novel MTO1 mutations associated with an intrafamilial phenotypic variability  Full Text
AUTHORS: Almeida, Catarina Maria; Rodrigues, Esmeralda; Campos, Teresa Almeida; Vilarinho, Laura; Teles, Elisa Leao;
PUBLISHED: 2023, SOURCE: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, VOLUME: 24, ISSUE: 1
INDEXED IN: Scopus WOS
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TITLE: Diagnosis across a cohort of atypical atypical and complex parkinsonism  Full Text
AUTHORS: Malaquias, Maria Joao; Igreja, Liliana; Nogueira, Celia; Pereira, Cristina; Vilarinho, Laura; Quelhas, Dulce; Freixo, Joao Parente; Oliveira, Jorge; Magalha, Marina;
PUBLISHED: 2023, SOURCE: PARKINSONISM & RELATED DISORDERS, VOLUME: 111
INDEXED IN: Scopus WOS
3
TITLE: Leigh Syndrome Spectrum: A Portuguese Population Cohort in an Evolutionary Genetic Era  Full Text
AUTHORS: Baldo, Manuela Schubert; Nogueira, Celia; Pereira, Cristina; Janeiro, Patricia; Ferreira, Sara; Lourenco, Charles M.; Bandeira, Anabela; Martins, Esmeralda ; Magalhaes, Marina; Rodrigues, Esmeralda; Santos, Helena; Ferreira, Ana Cristina; Vilarinho, Laura;
PUBLISHED: 2023, SOURCE: GENES, VOLUME: 14, ISSUE: 8
INDEXED IN: Scopus WOS
5
TITLE: Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement
AUTHORS: Kaiyrzhanov, Rauan; Mohammed, Sami E. M.; Maroofian, Reza; Husain, Ralf A.; Catania, Alessia; Torraco, Alessandra; Alahmad, Ahmad; Dutra Clarke, Marina; Gronborg, Sabine; Sudarsanam, Annapurna; Vogt, Julie; Arrigoni, Filippo; Baptista, Julia; Haider, Shahzad; Feichtinger, Rene G.; Bernardi, Paolo; Zulian, Alessandra; Gusic, Mirjana; Efthymiou, Stephanie; Bai, Renkui; Bibi, Farah; Horga, Alejandro; Martinez Agosto, Julian A.; Lam, Amanda; Manole, Andreea; Rodriguez, Diego Perez; Durigon, Romina; Pyle, Angela; Albash, Buthaina; Dionisi Vici, Carlo; Murphy, David; Martinelli, Diego; Bugiardini, Enrico; Allis, Katrina; Lamperti, Costanza; Reipert, Siegfried; Risom, Lotte; Laugwitz, Lucia; Di Nottia, Michela; McFarland, Robert; Vilarinho, Laura; Hanna, Michael; Prokisch, Holger; Mayr, Johannes A.; Bertini, Enrico Silvio; Ghezzi, Daniele; Ostergaard, Elsebet; Wortmann, Saskia B.; Carrozzo, Rosalba; Haack, Tobias B.; Taylor, Robert W.; Spinazzola, Antonella; Nowikovsky, Karin; Houlden, Henry; ...More
PUBLISHED: 2022, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 109, ISSUE: 9
INDEXED IN: Scopus WOS
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TITLE: Acquired Vitamin B12 Deficiency in Newborns: Positive Impact on Newborn Health through Early Detection  Full Text
AUTHORS: Pinto, Patricia Lipari; Florindo, Cristina; Janeiro, Patricia; Santos, Rita Loureiro; Mexia, Sandra; Rocha, Hugo; de Almeida, Isabel Tavares; Vilarinho, Laura; Gaspar, Ana;
PUBLISHED: 2022, SOURCE: NUTRIENTS, VOLUME: 14, ISSUE: 20
INDEXED IN: Scopus WOS
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TITLE: Neonatal Screening in Europe Revisited: An ISNS Perspective on the Current State and Developments Since 2010
AUTHORS: Loeber, JG; Platis, D; Zetterstrom, RH; Almashanu, S; Boemer, F; Bonham, JR; Borde, P; Brincat, I; Cheillan, D; Dekkers, E; Dimitrov, D; Fingerhut, R; Franzson, L; Groselj, U; Hougaard, D; Knapkova, M; Kocova, M; Kotori, V; Kozich, V; Kremezna, A; Kurkijarvi, R; La Marca, G; Mikelsaar, R; Milenkovic, T; Mitkin, V; Moldovanu, F; Ceglarek, U; O'Grady, L; Oltarzewski, M; Pettersen, RD; Ramadza, D; Salimbayeva, D; Samardzic, M; Shamsiddinova, M; Songailiene, J; Szatmari, I; Tabatadze, N; Tezel, B; Toromanovic, A; Tovmasyan, I; Usurelu, N; Vevere, P; Vilarinho, L; Vogazianos, M; Yahyaoui, R; Zeyda, M; Schielen, PCJI; ...More
PUBLISHED: 2021, SOURCE: INTERNATIONAL JOURNAL OF NEONATAL SCREENING, VOLUME: 7, ISSUE: 1
INDEXED IN: WOS
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TITLE: Role of RNA in Molecular Diagnosis of MADD Patients
AUTHORS: Nogueira, C; Silva, L; Marcao, A; Sousa, C; Fonseca, H; Rocha, H; Campos, T; Teles, EL; Rodrigues, E; Janeiro, P; Gaspar, A; Vilarinho, L;
PUBLISHED: 2021, SOURCE: BIOMEDICINES, VOLUME: 9, ISSUE: 5
INDEXED IN: Scopus WOS
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TITLE: Molecular basis of Leigh syndrome: a current look  Full Text
AUTHORS: Manuela Baldo Schubert; Laura Vilarinho;
PUBLISHED: 2020, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 15, ISSUE: 1
INDEXED IN: Scopus WOS
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