Buscar
Mostrando ítems 1-10 de 89
Morbid obesity in an adolescent with Prader-Willi syndrome
(Sociedad Médica de Santiago, 2009)
Diagnóstico molecular de los síndromes de Prader-Willi y de Angelman: análisis de metilación, citogenética y FISH
(Sociedad Médica de Santiago, 2001)
Playing to Create New Ways of Playing: A Child with Prader-Willi Syndrome
(SPRINGER/PLENUM PUBLISHERS, 2009)
This investigation evaluates the possibility of constructing new ways of playing for a child with Prader-Willi syndrome, by means of occupational therapy. It is a qualitative study which makes use of the case study ...
Lack of evidence for monosomy 1p36 in patients with Prader-Willi-like phenotype
(Associação Brasileira de Divulgação Científica, 2008)
Monosomy 1p36 is the most common subtelomeric microdeletion syndrome with an incidence rate estimated to be 1 in 5000 births. A hypothesis of a similarity between patients with 1p36 deletion and those with Prader-Willi ...
Cognitive and behavioral heterogeneity in genetic syndromes
(Soc Brasil PediatriaRio De Janeiro, RjBrasil, 2014)
Use of Growth Hormone in Prader Willi SyndromeUso de hormona del crecimiento en el síndrome de Prader-Willi
(Intituto Tecnológico de Santo Domingo (INTEC), 2017)
Síndrome de Prader-Willi. Tratamiento con hormona de crecimiento en dos casos: Report of two cases
(Sociedad Médica de Santiago, 2001)
A clinical follow-up of 35 Brazilian patients with Prader-Willi Syndrome
(Faculdade de Medicina / USP, 2012)
OBJECTIVE: Prader-Willi Syndrome is a common etiology of syndromic obesity that is typically caused by either a paternal microdeletion of a region in chromosome 15 (microdeletions) or a maternal uniparental disomy of this ...