INTRODUCTION Cognitive impairment is a well-known complication of classical galactosemia (CG). Differences in patient characteristics and test methods have hampered final conclusions regarding the extent of intellectual disabilities in CG. The primary aim of this systematic review was to assess intellectual performance in early-treated (≤4 weeks of life) individuals with confirmed CG (defined by absent or barely detectable GALT enzyme activity and/or the presence of two null or severe missense variations), assessed with comparable test instruments. The full-scale IQ (FSIQ) was the variable of interest. METHODS A clinical librarian developed search strategies, and two independent investigators performed the study selection, risk of ...
BACKGROUND: Classic galactosemia is an autosomal recessive disorder due to galactose-1-phosphate uri...
Duarte galactosemia is a variant form of galactosemia that on average results in a reduction of the ...
BackgroundClassical galactosemia (CG), an inborn error of galactose metabolism, results in long-term...
Background: Despite early diagnosis and treatment, Classical Galactosemia (CG) patients frequently d...
BACKGROUND: Despite early diagnosis and treatment, Classical Galactosemia (CG) patients frequently d...
Background: Patients with the metabolic disorder classical galactosemia suffer from long-term compli...
BACKGROUND Classical galactosemia (CG) is due to a severe deficiency of the galactose-1-phosphate...
Abstract Background Classical galactosemia (CG) is due to a severe deficiency of the galactose-1-pho...
Cross-sectional methodologies have revealed age-related deterioration in cognitive performance, refl...
Classical Galactosemia is an inborn error of metabolism, a disease in which galactose (milk sugar) i...
Early diagnosis and dietary treatment do not prevent long-term complications, which mostly affect th...
Early diagnosis and dietary treatment do not prevent long-term complications, which mostly affect th...
Background: The high variability in clinical outcome of patients with Classical Galactosemia (CG) is...
For classical galactosemia, (CG), an autosomal recessive inborn error of galactose metabolism, a gal...
PURPOSE: Classical galactosaemia is an inborn error of galactose metabolism which may lead to impair...
BACKGROUND: Classic galactosemia is an autosomal recessive disorder due to galactose-1-phosphate uri...
Duarte galactosemia is a variant form of galactosemia that on average results in a reduction of the ...
BackgroundClassical galactosemia (CG), an inborn error of galactose metabolism, results in long-term...
Background: Despite early diagnosis and treatment, Classical Galactosemia (CG) patients frequently d...
BACKGROUND: Despite early diagnosis and treatment, Classical Galactosemia (CG) patients frequently d...
Background: Patients with the metabolic disorder classical galactosemia suffer from long-term compli...
BACKGROUND Classical galactosemia (CG) is due to a severe deficiency of the galactose-1-phosphate...
Abstract Background Classical galactosemia (CG) is due to a severe deficiency of the galactose-1-pho...
Cross-sectional methodologies have revealed age-related deterioration in cognitive performance, refl...
Classical Galactosemia is an inborn error of metabolism, a disease in which galactose (milk sugar) i...
Early diagnosis and dietary treatment do not prevent long-term complications, which mostly affect th...
Early diagnosis and dietary treatment do not prevent long-term complications, which mostly affect th...
Background: The high variability in clinical outcome of patients with Classical Galactosemia (CG) is...
For classical galactosemia, (CG), an autosomal recessive inborn error of galactose metabolism, a gal...
PURPOSE: Classical galactosaemia is an inborn error of galactose metabolism which may lead to impair...
BACKGROUND: Classic galactosemia is an autosomal recessive disorder due to galactose-1-phosphate uri...
Duarte galactosemia is a variant form of galactosemia that on average results in a reduction of the ...
BackgroundClassical galactosemia (CG), an inborn error of galactose metabolism, results in long-term...