Guenter Schwarz
Zuelpicher Str. 47
Koeln, NW 50674, Germany
Koeln, NW 50674, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 82 publications
Clinical and biochemical footprints of inherited cofactor disorders.
Journal: Molecular genetics and metabolism
Published: March 14, 2026
Lysophosphatidylcholine as a mechanistic and therapeutic nexus in atherosclerotic cardiovascular disease.
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: November 10, 2025
The Interplay between Gut Microbiota and Diet-Induced Kidney Protection.
Journal: Kidney360
Published: November 02, 2025
An electrochemical perspective on human sulfite oxidase as a potential nitrite reductase.
Journal: Journal of inorganic biochemistry
Published: October 14, 2025
A prevalent MOCS2 variant in the Roma population is associated with a novel mild form of molybdenum cofactor deficiency.
Journal: European journal of pediatrics
Published: June 17, 2025
Gephyrin filaments represent the molecular basis of inhibitory postsynaptic densities.
Journal: Nature communications
Published: February 04, 2025
Phosphoinositide- and Collybistin-Dependent Synaptic Clustering of Gephyrin.
Journal: Journal of neurochemistry
Published: November 29, 2024
cPMP rescue of a neonate with severe molybdenum cofactor deficiency after serendipitous early diagnosis, and characterisation of a novel MOCS1 variant.
Journal: Molecular genetics and metabolism
Published: August 20, 2024
Increased Survival in Patients With Molybdenum Cofactor Deficiency Type A Treated With Cyclic Pyranopterin Monophosphate.
Journal: Journal of inherited metabolic disease
Published: July 31, 2024
Sulfite oxidase deficiency causes persulfidation loss and hydrogen sulfide release.
Journal: The Journal of clinical investigation
Published: April 09, 2024
Last Updated: 09/26/2026