Recommendations for Assessment and Management of Health-Related Quality of Life in Patients with Mucopolysaccharidoses in Latin America (2019)
- Authors:
- Autor USP: KIM, CHONG AE - FM
- Unidade: FM
- DOI: 10.1590/2326-4594-jiems-2019-0004
- Subjects: GLICOSAMINOGLICANAS; ERROS INATOS DO METABOLISMO; QUALIDADE DE VIDA; TERAPÊUTICA; QUESTIONÁRIOS
- Language: Inglês
- Imprenta:
- Publisher place: Porto Alegre
- Date published: 2019
- Source:
- Título do periódico: Journal of inborn errors of metabolism and screening
- ISSN: 2326-4594
- Volume/Número/Paginação/Ano: v. 7, p. e20190004, 2019
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
GIUGLIANI, Roberto et al. Recommendations for Assessment and Management of Health-Related Quality of Life in Patients with Mucopolysaccharidoses in Latin America. Journal of inborn errors of metabolism and screening, v. 7, p. e20190004, 2019Tradução . . Disponível em: https://doi.org/10.1590/2326-4594-jiems-2019-0004. Acesso em: 24 abr. 2024. -
APA
Giugliani, R., Fainboim, A., Kim, C. A., Horovitz, D. D. G., Sakata, E. T., Damiano, A. P., et al. (2019). Recommendations for Assessment and Management of Health-Related Quality of Life in Patients with Mucopolysaccharidoses in Latin America. Journal of inborn errors of metabolism and screening, 7, e20190004. doi:10.1590/2326-4594-jiems-2019-0004 -
NLM
Giugliani R, Fainboim A, Kim CA, Horovitz DDG, Sakata ET, Damiano AP, Magalhães TSPC, Villareal MS. Recommendations for Assessment and Management of Health-Related Quality of Life in Patients with Mucopolysaccharidoses in Latin America [Internet]. Journal of inborn errors of metabolism and screening. 2019 ; 7 e20190004.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1590/2326-4594-jiems-2019-0004 -
Vancouver
Giugliani R, Fainboim A, Kim CA, Horovitz DDG, Sakata ET, Damiano AP, Magalhães TSPC, Villareal MS. Recommendations for Assessment and Management of Health-Related Quality of Life in Patients with Mucopolysaccharidoses in Latin America [Internet]. Journal of inborn errors of metabolism and screening. 2019 ; 7 e20190004.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1590/2326-4594-jiems-2019-0004 - Caracterização clínico-laboratorial das Síndromes de Williams-Beuren e de Noonan
- Advantages of early replacement therapy for mucopolysaccharidosis type VI: Echocardiographic follow-up of siblings
- Mowat-Wilson syndrome: Neurological and molecular study in seven patients
- Complex structural rearrangement features suggesting chromoanagenesis mechanism in a case of 1p36 deletion syndrome
- Investigação da variação no número de cópias gênicas em crianças com defeito cardíaco conotruncal
- CD4+CD25highFoxp3+ Treg deficiency in a Brazilian patient with Gaucher disease and lupus nephritis
- Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with "corner fractures"
- Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndrome
- The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry
- Cri-du-Chat Syndrome: revealing a familial atypical seletion in 5p
Informações sobre o DOI: 10.1590/2326-4594-jiems-2019-0004 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
