Sort   by:  
 Page size 
UnknownIntrafamilial oocyte donation in classic galactosemia: ethical and societal aspects.
Not available
S-EPMC6133175 | biostudies-literature
UnknownPathophysiology and targets for treatment in hereditary galactosemia: A systematic review of animal and cellular models.
Not available
S-EPMC7317974 | biostudies-literature
UnknownClassical galactosemia: neuropsychological and psychosocial functioning beyond intellectual abilities.
Not available
S-EPMC7007688 | biostudies-literature
UnknownInternational clinical guideline for the management of classical galactosemia: diagnosis, treatment, and follow-up.
Not available
S-EPMC5306419 | biostudies-literature
UnknownDynamic tracing of sugar metabolism reveals the mechanisms of action of synthetic sugar analogs.
Not available
S-EPMC8966471 | biostudies-literature
UnknownGalactose epimerase deficiency: lessons from the GalNet registry.
Not available
S-EPMC9438182 | biostudies-literature
UnknownEvaluation of Newborn Screening for Diseases Using C5-OH as a Marker: Systematic Review of the Literature and Evaluation of 17 Years of C5-OH Screening in the Netherlands.
Not available
S-EPMC12426815 | biostudies-literature
UnknownBrain function in classic galactosemia, a galactosemia network (GalNet) members review.
Not available
S-EPMC10902464 | biostudies-literature
UnknownCLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder.
Not available
S-EPMC4320260 | biostudies-literature
UnknownThe natural history of classic galactosemia: lessons from the GalNet registry.
Not available
S-EPMC6486996 | biostudies-literature
Sort   by:  
 Page size