Holger Blessing
Erlangen, BY, Germany
Last Updated: 09/26/2026
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Found 9 publications
Human ultrarare genetic disorders of sulfur metabolism demonstrate redundancies in H2S homeostasis.
Journal: Redox biology
Published: September 30, 2022
Clinical implementation of RNA sequencing for Mendelian disease diagnostics.
Journal: Genome medicine
Published: May 17, 2021
Newborn screening and disease variants predict neurological outcome in isovaleric aciduria.
Journal: Journal of inherited metabolic disease
Published: December 17, 2020
Diagnostic Challenges Using a 2-Tier Strategy for Methylmalonic Acidurias: Data from 1.2 Million Dried Blood Spots.
Journal: Annals of nutrition & metabolism
Published: March 18, 2020
Homozygous familial hypercholesterolemia with severe involvement of the aortic valve-A sibling-controlled case study on the efficacy of lipoprotein apheresis.
Journal: Journal of clinical apheresis
Published: January 31, 2020
Effect of dietary regime on metabolic control in phenylketonuria: Is exact calculation of phenylalanine intake really necessary?
Journal: Molecular genetics and metabolism reports
Published: August 21, 2015
Neonatal Cholestasis - Differential Diagnoses, Current Diagnostic Procedures, and Treatment.
Journal: Frontiers in pediatrics
Published: September 20, 2014
MAP4-dependent regulation of microtubule formation affects centrosome, cilia, and Golgi architecture as a central mechanism in growth regulation.
Journal: Human mutation
Published: July 03, 2014
Evaluation of plasma trace element and mineral status in children and adolescents with phenylketonuria using data from inductively-coupled-plasma atomic emission and mass spectrometric analysis.
Journal: Annals of nutrition & metabolism
Published: January 14, 2013
Showing 1-9 of 9
Last Updated: 09/26/2026