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You searched for: Author/Creator Huidekoper, Hidde H.

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1. Abnormal VLCADD newborn screening resembling MADD in four neonates with decreased riboflavin levels and VLCAD activity. Issue 1 (7th May 2021)

2. Autism spectrum disorder: an early and frequent feature in cerebrotendinous xanthomatosis. Issue 4 (11th September 2017)

3. High prevalence of complementary and alternative medicine use in patients with genetically proven mitochondrial disorders. Issue 3 (11th October 2014)

5. Managing CLN2 disease: a treatable neurodegenerative condition among other treatable early childhood epilepsies. (2nd November 2021)

6. Multi‐omics in classical galactosemia: Evidence for the involvement of multiple metabolic pathways. Issue 6 (25th August 2022)

8. Prediction of disease severity in multiple acyl‐CoA dehydrogenase deficiency: A retrospective and laboratory cohort study. Issue 5 (17th July 2019)

9. Quantification of naive and memory T-cell turnover during HIV-1 infection. (23rd October 2015)

10. The 1‐13C galactose breath test in GALT deficient patients distinguishes NBS detected variant patients but does not predict outcome in classical phenotypes. Issue 3 (22nd January 2020)