Author

Latife Salomão Tyszler

Observed name: Tyszler Latife Salomao

Observed institution: Instituto Estadual de Diabetes e Endocrinologia Luiz Capriglione

OpenAlex ID: A5079699996

A newborn screening pilot study using methylation-sensitive high resolution melting on dried blood spots to detect Prader-Willi and Angelman syndromes

2020 · Igor Ribeiro Ferreira, Régis Afonso Costa, et al. · Scientific Reports · 27

Avaliação do valor de corte de TSH em amostras de filtro na triagem neonatal para diagnóstico de hipotireoidismo congênito no Programa "Primeiros Passos" - IEDE/RJ

2013 · Bianca Barone, Clarisse Lourandes da Silva Lopes, et al. · Arquivos Brasileiros de Endocrinologia & Metabologia · 13

Investigating the correlation between genotype and phenotype in Prader-Willi syndrome: a study of 45 cases from Brazil

2024 · Hiago Azevedo Cintra, Danielle Nascimento Rocha, et al. · Orphanet Journal of Rare Diseases · 7

Posicionamento Brasileiro sobre Avaliação e Tratamento da Obesidade Pediátrica

2026 · Louise Cominato, Cresio de Aragão Dantas Alves, et al. · Conectando Pessoas eBooks

SAT-206 Development of a Minimum Dataset (MDS) for the Monitoring of Growth Hormone Therapy in Children with Prader Willi Syndrome (PWS) - A GloBE-Reg Initiative

2025 · Ashley Leong, Suet Ching Chen, et al. · Journal of the Endocrine Society

Development of a minimum dataset (MDS) for the monitoring of growth hormone therapy in children with prader willi syndrome (PWS) - a globe-reg initiative

2025 · Ashley Leong, Chen Suet Ching, et al. · Endocrine Abstracts

Works count: 6

Citation count: 47

H-index: 3

I10-index: 2