Zobrazeno 1 - 10 of 33 pro vyhledávání: '"Sandra Obikawa Kyosen"'
1
Akademický článek
Oxidative stress assessment by glutathione peroxidase activity and glutathione levels in response to selenium supplementation in patients with Mucopolysaccharidosis I, II and VI
Autor: José Araújo de Oliveira-Silva, Joyce Umbelino Pinto Yamamoto, Renata Bernardes de Oliveira, Vaneisse Cristina Lima Monteiro, Beatriz Jurkiewcz Frangipani, Sandra Obikawa Kyosen, Ana Maria Martins, Vânia D’Almeida
Publikováno v: Genetics and Molecular Biology, Vol 42, Iss 1, Pp 1-8 (2019)
Abstract We assessed levels of plasma selenium (Se), selenoproteins and their change after Se supplementation in patients with mucopolysaccharidosis (MPS) types I, II and VI. This was done in a retrospective study of the medical records of 30 patient
Externí odkaz: https://doaj.org/article/0d74852cf84948caae4a19ffa099ee40
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2
Akademický článek
A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report
Autor: Caio Perez Gomes, Maryana Mara Marins, Fabiana Louise Motta, Sandra Obikawa Kyosen, Marco Antonio Curiati, Vânia D’Almeida, Ana Maria Martins, João Bosco Pesquero
Publikováno v: Frontiers in Genetics, Vol 10 (2020)
RationaleMucopolysaccharidosis type II (Hunter syndrome) is an X-linked multisystem disorder, caused by deficiency of the lysosomal enzyme iduronate-2-sulfatase (I2S). The clinical manifestations of this disease are severe skeletal deformities, airwa
Externí odkaz: https://doaj.org/article/a4f5bd92168646bfb00757766f44ce4c
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3
Akademický článek
Short stature as a presenting symptom of attenuated Mucopolysaccharidosis type I: case report and clinical insights
Autor: Ana Maria Martins, Kristin Lindstrom, Sandra Obikawa Kyosen, Maria Veronica Munoz-Rojas, Nathan Thibault, Lynda E. Polgreen
Publikováno v: BMC Endocrine Disorders, Vol 18, Iss 1, Pp 1-7 (2018)
Abstract Background Mucopolysaccharidosis type I (MPS I) results in significant disease burden and early treatment is important for optimal outcomes. Recognition of short stature and growth failure as symptoms of MPS I among pediatric endocrinologist
Externí odkaz: https://doaj.org/article/5e5e3a81bd744956854a3849775f2a7e
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4
Akademický článek
CASE SERIES OF PATIENTS UNDER BIWEEKLY TREATMENT WITH LARONIDASE: A REPORT OF A SINGLE CENTER EXPERIENCE
Autor: Sandra Obikawa Kyosen, Leny Toma, Helena Bonciani Nader, Marion Coting Braga, Vanessa Gonçalves Pereira, Sueli Canossa, João Bosco Pesquero, Vânia D’Almeida, Ana Maria Martins
Publikováno v: Revista Paulista de Pediatria, Iss 0 (2019)
ABSTRACT Objective: To report the stabilization of urinary glycosaminoglicans (GAG) excretion and clinical improvements in patients with mucopolysaccharidosis type I (MPS I) under an alternative dose regimen of laronidase of 1.2 mg/kg every other wee
Externí odkaz: https://doaj.org/article/38637534098d49dc82dca4878f97d736
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5
Akademický článek
Lysosomal Acid Lipase Deficiency: Report of Five Cases across the Age Spectrum
Autor: Marco Antonio Curiati, Sandra Obikawa Kyosen, Vanessa Gonçalves Pereira, Francy Reis da Silva Patrício, Ana Maria Martins
Publikováno v: Case Reports in Pediatrics, Vol 2018 (2018)
Lysosomal acid lipase (LAL) deficiency is an autosomal recessive lysosomal storage disorder caused by mutations in the LIPA gene that leads to premature organ damage and mortality. We present retrospective data from medical records of 5 Brazilian pat
Externí odkaz: https://doaj.org/article/4ee8a02c0c7d4fefa85144f3f4afcf03
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7
ÓXIDO NÍTRICO COMO TRATAMENTO DA HIPERTENSÃO PULMONAR EM NEONATOS
Autor: Rita de Cássia Lompa Juelg, Paula Myllena, Patricia Ikeda, Verônica Campos Resende, Sandra Obikawa Kyosen
Publikováno v: Anais do Congresso Médico Acadêmico da Universidade Nove de Julho.
Introdução: A hipertensão pulmonar em recém-nascido é um problema comum com característica e mortalidade significativas e limita a quantidade de sangue que vai para os pulmões. O uso de óxido nítrico (NO) é um vasodilatador que relaxa o mú
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e4700ddfa08006001c039ad4765fd7f2
https://doi.org/10.5585/comamedvg.2022.22
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8
CASE SERIES OF PATIENTS UNDER BIWEEKLY TREATMENT WITH LARONIDASE: A REPORT OF A SINGLE CENTER EXPERIENCE
Autor: Helena B. Nader, Marion Coting Braga, Vânia D'Almeida, Sandra Obikawa Kyosen, João Bosco Pesquero, Ana Maria Martins, Leny Toma, Vanessa Gonçalves Pereira, Sueli Canossa
Publikováno v: Revista Paulista de Pediatria, Iss 0 (2019)
Revista Paulista de Pediatria v.37 n.3 2019
Revista Paulista de Pediatria (Ed. Português. Online)
Sociedade de Pediatria de São Paulo (SPSP)
instacron:SPSP
Revista Paulista de Pediatria
Objective: To report the stabilization of urinary glycosaminoglicans (GAG) excretion and clinical improvements in patients with mucopolysaccharidosis type I (MPS I) under an alternative dose regimen of laronidase of 1.2 mg/kg every other week. Method
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b8e7206b86e2bcd34e70a3c8c8e06b4
https://doi.org/10.1590/1984-0462/
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9
A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report
Autor: Ana Maria Martins, Caio Perez Gomes, Sandra Obikawa Kyosen, Vânia D'Almeida, Maryana Mara Marins, João Bosco Pesquero, Marco A. Curiati, Fabiana Louise Motta
Publikováno v: Frontiers in Genetics
Frontiers in Genetics, Vol 10 (2020)
Rationale Mucopolysaccharidosis type II (Hunter syndrome) is an X-linked multisystem disorder, caused by deficiency of the lysosomal enzyme iduronate-2-sulfatase (I2S). The clinical manifestations of this disease are severe skeletal deformities, airw
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea8878d81a369354e3cc3d7f30f7b57a
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10
Oxidative stress assessment by glutathione peroxidase activity and glutathione levels in response to selenium supplementation in patients with Mucopolysaccharidosis I, II and VI
Autor: Vânia D'Almeida, Renata B. Oliveira, Beatriz Jurkiewcz Frangipani, Sandra Obikawa Kyosen, Vaneisse Cristina Lima Monteiro, Joyce Umbelino Pinto Yamamoto, José Araújo de Oliveira-Silva, Ana Maria Martins
Publikováno v: Genetics and Molecular Biology v.42 n.1 2019
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Issue: ahead, Published: 14 FEB 2019
Genetics and Molecular Biology, Volume: 42, Issue: 1, Pages: 1-8, Published: 14 FEB 2019
Genetics and Molecular Biology, Vol 42, Iss 1, Pp 1-8 (2019)
We assessed levels of plasma selenium (Se), selenoproteins and their change after Se supplementation in patients with mucopolysaccharidosis (MPS) types I, II and VI. This was done in a retrospective study of the medical records of 30 patients with MP
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb691e7160a2033d0ba2f1d7be8fa6d6
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572019000100001
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