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Material Type: Artigo
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Intervenção fisioterapêutica em criança com leucinose: estudo de caso; Physiotherapeutic intervention in child with leucinosis: case reportMarcucci, Fernando César IwamotoFisioterapia e Pesquisa; Vol. 11 No. 1 (2004); 32-38Universidade de São Paulo. Faculdade de Medicina 2004-06-30Acesso online |
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Material Type: Artigo
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Living related versus deceased donor liver transplantation for maple syrup urine diseaseFlavia Feier Ida Vanessa D Schwartz; Abigail R Benkert; Joao Seda Neto; Irene Miura; Paulo Chapchap; Eduardo Antunes da Fonseca; Sandra Vieira; Maria Lúcia Zanotelli; Filippo Pinto e Vairo; José Simon Camelo Júnior; Ana Vitoria Barban Margutti; George V Mazariegos; Erik G Puffenberger; Kevin A StraussMolecular Genetics and Metabolism Waltham v. 117, n. 3, p. 336-343, 2016Waltham 2016Localização: FMRP - Fac. Medicina de Ribeirão Preto (pcd 2785755 Estantes Deslizantes )(Acessar) |
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Material Type: Artigo
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Maple syrup urine disease in Brazilian patients variants and clinical phenotype heterogeneityAna Vitoria Barban Margutti Wilson Araújo da Silva Junior; Daniel Fantozzi Garcia; Greice Andreotti de Molfetta; Adriana Aparecida Marques; Tatiana Amorim; Vânia Mesquita Gadelha Prazeres; Raquel Tavares Boy da Silva; Irene Kazue Miura; Joao Seda Neto; Emerson de Santana Santos; Mara Lúcia Schmitz Ferreira Santos; Charles Marques Lourenço; Tássia Tonon; Fernanda Sperb-ludwig; Carolina Fischinger Moura de Souza; Ida Vanessa Döederlein Schwartz; José Simon Camelo JúniorOrphanet Journal of Rare Diseases London v. 15, art. 309, 2020London 2020Localização: FMRP - Fac. Medicina de Ribeirão Preto (pcd 3021069 Acervo Digital )(Acessar) |
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Material Type: Artigo
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Nutrition management guideline for maple syrup urine disease: An evidence- and consensus-based approachFrazier, Dianne M. ; Allgeier, Courtney ; Homer, Caroline ; Marriage, Barbara J. ; Ogata, Beth ; Rohr, Frances ; Splett, Patricia L. ; Stembridge, Adrya ; Singh, Rani H.Molecular genetics and metabolism, 2014-07, Vol.112 (3), p.210-217 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Brain Branched-Chain Amino Acids in Maple Syrup Urine Disease: Implications for Neurological DisordersXu, Jing ; Jakher, Youseff ; Ahrens-Nicklas, Rebecca CInternational journal of molecular sciences, 2020-10, Vol.21 (20), p.7490 [Periódico revisado por pares]Switzerland: MDPI AGTexto completo disponível |
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Material Type: Artigo
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Neonatal gene therapy achieves sustained disease rescue of maple syrup urine disease in micePontoizeau, Clément ; Simon-Sola, Marcelo ; Gaborit, Clovis ; Nguyen, Vincent ; Rotaru, Irina ; Tual, Nolan ; Colella, Pasqualina ; Girard, Muriel ; Biferi, Maria-Grazia ; Arnoux, Jean-Baptiste ; Rötig, Agnès ; Ottolenghi, Chris ; de Lonlay, Pascale ; Mingozzi, Federico ; Cavazzana, Marina ; Schiff, ManuelNature communications, 2022-06, Vol.13 (1), p.3278-3278, Article 3278 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Metabolic Control and “Ideal” Outcomes in Liver Transplantation for Maple Syrup Urine DiseaseEwing, Caroline B. ; Soltys, Kyle A. ; Strauss, Kevin A. ; Sindhi, Rakesh ; Vockley, Jerry ; McKiernan, Patrick ; Squires, Robert H. ; Bond, Geoffrey ; Ganoza, Armando ; Khanna, Ajai ; Mazariegos, George V. ; Squires, James E.The Journal of pediatrics, 2021-10, Vol.237, p.59-64.e1 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Neonatal maple syrup urine disease case report and literature reviewLiu, Qiao ; Li, Fang ; Zhou, Jingjing ; Liu, Xiaoyu ; Peng, Jidong ; Gong, LianggengMedicine (Baltimore), 2022-12, Vol.101 (50), p.e32174-e32174 [Periódico revisado por pares]United States: Lippincott Williams & WilkinsTexto completo disponível |
9 |
Material Type: Artigo
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Neonatal maple syrup urine disease in China: two novel mutations in the BCKDHB gene and literature reviewJiang, Hong‐Hua ; Guo, Yan ; Shen, Xian ; Wang, Ying ; Dai, Ting-Ting ; Rong, Hui ; Cheng, Rui ; Zhao, FeiJournal of Pediatric Endocrinology & Metabolism, 2021-09, Vol.34 (9), p.1147-1156 [Periódico revisado por pares]Germany: De GruyterTexto completo disponível |
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Material Type: Artigo
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Successful treatment of severe MSUD in Bckdhb−/− mice with neonatal AAV gene therapyPontoizeau, Clément ; Gaborit, Clovis ; Tual, Nolan ; Simon‐Sola, Marcelo ; Rotaru, Irina ; Benoist, Marion ; Colella, Pasqualina ; Lamazière, Antonin ; Brassier, Anaïs ; Arnoux, Jean‐Baptiste ; Rötig, Agnès ; Ottolenghi, Chris ; Lonlay, Pascale ; Mingozzi, Federico ; Cavazzana, Marina ; Schiff, ManuelJournal of inherited metabolic disease, 2024-01, Vol.47 (1), p.41-49 [Periódico revisado por pares]Hoboken, USA: John Wiley & Sons, IncTexto completo disponível |