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A mostrar 1 - 20 resultados de 46 para a pesquisa '(( j nasr computers a non ) OR ((( 3 daily compared law now ) OR ( j can companies can ngoc ))))', tempo de pesquisa: 1.27seg Refinar resultados
1
AB129. Osteogenesis imperfecta: clinical features and bisphosphonate treatment outcome
“...BACKGROUND AND OBJECTIVE: Osteogenesis imperfecta (OI) comprises a group of disorders principally...”
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AB070. Mutations of SRD5A2 in Vietnamese patients: phenotype and genotype
“...A rare form of the 46,XY disorders of sex development (DSD), 5α-reductase deficiency was first...”
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AB132. Neonatal diabetes in Wolcott-Rallison syndrome: a case report
“... not find any sign of cholestasis. Sequencing analysis of patient’s EIF2AK3 gene has identified a homozygous...”
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AB124. Mucolipidosis type II: clinical features and laboratories
“... to the lysosomes I. As a consequence the enzymes are secreted into the extracellular space, and high activities can...”
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AB127. Enzyme replacement therapy in patient with mucopolysaccharidosis type II: a case report
“... analysis and management in a 4 years 6-month-old girl was study. Based on analysis of a patient’s clinical...”
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AB102. Vietnamese patient with Tyrosinemia type 1: a case report
“... symptoms at 1 and 1.5 months of age, respectively. Three days before admission, she presented with poor...”
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AB100. Phenotypes of primary hyperlipidemia in a Vietnamese referral center
“... management of pediatric hyperlipidemia can have a significant impact upon the disease course and can prevent...”
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AB125. Neonatal diabetes mellitus due to insulin gene mutation
“... with the feature of diabetic ketoacidosis with pH of 7.04±0.22; plasma glucose levels were 34.3±12.7 mmoL/L, HbA1C...”
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