BackgroundClassical galactosemia (CG), an inborn error of galactose metabolism, results in long-term complications including cognitive impairment and movement disorders, despite early diagnosis and dietary treatment. Two decades ago, lower motor-, cognitive- and social health related quality of life (HRQoL) was demonstrated in pediatric and adult patients. Since then, the diet has been relaxed, newborn screening was implemented and new international guidelines resulted in major changes in follow-up. The aim of this study was to assess HRQoL of CG by means of online self- and/or proxy-HRQoL-questionnaires focusing on the main areas of concern of CG (i.e. anxiety, depression, cognition, fatigue, social- and upper extremity function) within th...
Patients with classic galactosemia suffer from several long term effects of their disease. Research ...
Classic galactosemia is a rare inborn error of carbohydrate metabolism, caused by a severe deficienc...
Classical galactosemia is an autosomal recessive inborn error of metabolism leading to toxic accumul...
BackgroundClassical galactosemia (CG), an inborn error of galactose metabolism, results in long-term...
BACKGROUND: Classic galactosemia is an autosomal recessive disorder due to galactose-1-phosphate uri...
Abstract Background Classical galactosemia (CG) is due to a severe deficiency of the galactose-1-pho...
BACKGROUND Classical galactosemia (CG) is due to a severe deficiency of the galactose-1-phosphate...
For classical galactosemia, (CG), an autosomal recessive inborn error of galactose metabolism, a gal...
Background: Despite early diagnosis and treatment, Classical Galactosemia (CG) patients frequently d...
Although movement disorders (MDs) are known complications, the exact frequency and severity remains ...
Purpose: Classical galactosaemia is an inborn error of galactose metabolism which may lead to impair...
A number of previous studies have identified reduced language outcomes across the lifespan in indivi...
Background: Patients with the metabolic disorder classical galactosemia suffer from long-term compli...
BACKGROUND: Despite early diagnosis and treatment, Classical Galactosemia (CG) patients frequently d...
Patients with classic galactosemia suffer from several long term effects of their disease. Research ...
Classic galactosemia is a rare inborn error of carbohydrate metabolism, caused by a severe deficienc...
Classical galactosemia is an autosomal recessive inborn error of metabolism leading to toxic accumul...
BackgroundClassical galactosemia (CG), an inborn error of galactose metabolism, results in long-term...
BACKGROUND: Classic galactosemia is an autosomal recessive disorder due to galactose-1-phosphate uri...
Abstract Background Classical galactosemia (CG) is due to a severe deficiency of the galactose-1-pho...
BACKGROUND Classical galactosemia (CG) is due to a severe deficiency of the galactose-1-phosphate...
For classical galactosemia, (CG), an autosomal recessive inborn error of galactose metabolism, a gal...
Background: Despite early diagnosis and treatment, Classical Galactosemia (CG) patients frequently d...
Although movement disorders (MDs) are known complications, the exact frequency and severity remains ...
Purpose: Classical galactosaemia is an inborn error of galactose metabolism which may lead to impair...
A number of previous studies have identified reduced language outcomes across the lifespan in indivi...
Background: Patients with the metabolic disorder classical galactosemia suffer from long-term compli...
BACKGROUND: Despite early diagnosis and treatment, Classical Galactosemia (CG) patients frequently d...
Patients with classic galactosemia suffer from several long term effects of their disease. Research ...
Classic galactosemia is a rare inborn error of carbohydrate metabolism, caused by a severe deficienc...
Classical galactosemia is an autosomal recessive inborn error of metabolism leading to toxic accumul...