Ulrike Och
Muenster, NW 48149, Germany
Last Updated: 09/26/2026
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Found 22 publications
Use of a cholesterol emulsion in Smith-Lemli-Opitz syndrome (SLOS): A single-center observational study, retrospective analysis and structured caregiver interview.
Journal: Lipids in health and disease
Published: August 12, 2025
Effects of dietary management for medium-chain acyl-CoA dehydrogenase deficiency (MCADD) on eating behaviour in childhood, adolescence and young adulthood.
Journal: BMC nutrition
Published: May 30, 2025
Neurocognitive functioning remained unchanged in adults with phenylketonuria: Report of a 15-year follow-up.
Journal: Acta paediatrica (Oslo, Norway : 1992)
Published: May 10, 2024
DGAT-1 deficiency: Congenital diarrhea and dietary treatment.
Journal: JPGN reports
Published: April 27, 2024
Children and Adolescents with Early Treated Phenylketonuria: Cognitive Development and Fluctuations of Blood Phenylalanine Levels.
Journal: International journal of environmental research and public health
Published: February 27, 2024
Treatment of AICA ribosiduria by suppression of de novo purine synthesis.
Journal: Molecular genetics and metabolism
Published: August 24, 2023
Impact of pregnancy planning and preconceptual dietary training on metabolic control and offspring's outcome in phenylketonuria.
Journal: Journal of inherited metabolic disease
Published: March 14, 2022
Preventing maternal phenylketonuria (PKU) syndrome: important factors to achieve good metabolic control throughout pregnancy.
Journal: Orphanet journal of rare diseases
Published: September 02, 2021
Metabolic control during the neonatal period in phenylketonuria: associations with childhood IQ.
Journal: Pediatric research
Published: February 26, 2021
A mutation in the neonatal isoform of SCN2A causes neonatal-onset epilepsy.
Journal: American journal of medical genetics. Part A
Published: February 13, 2021
Hepatorenal Tyrosinaemia: Impact of a Simplified Diet on Metabolic Control and Clinical Outcome.
Journal: Nutrients
Published: November 15, 2020
3-Hydroxyisobutyrate dehydrogenase (HIBADH) deficiency-A novel disorder of valine metabolism.
Journal: Journal of inherited metabolic disease
Published: October 30, 2020
Last Updated: 09/26/2026