Robin M. Satanovskij
Munich, BY, Germany
Last Updated: 09/26/2026
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Found 11 publications
The Hypomorphic Variant p.(Gly624Asp) in COL4A5 as a Possible Cause for an Unexpected Severe Phenotype in a Family With X-Linked Alport Syndrome.
Journal: Frontiers in pediatrics
Published: September 03, 2019
Cognitive Impairment is Associated with Mortality in Hemodialysis Patients.
Journal: Journal of Alzheimer's disease : JAD
Published: November 10, 2018
Heterozygous COL4A3 Variants in Histologically Diagnosed Focal Segmental Glomerulosclerosis.
Journal: Frontiers in pediatrics
Published: March 25, 2018
Cognitive impairment in hemodialysis patients: Implementation of cut-off values for the Montreal Cognitive Assessment (MoCA)-test for feasible screening.
Journal: PloS one
Published: April 03, 2017
Pulse wave velocity is associated with cognitive impairment in hemodialysis patients.
Journal: Clinical science (London, England : 1979)
Published: January 29, 2017
A new missense mutation in UMOD gene leads to severely reduced serum uromodulin concentrations - A tool for the diagnosis of uromodulin-associated kidney disease.
Journal: Clinical biochemistry
Published: June 30, 2016
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 05, 2015
Plasma total C-terminal agrin fragment (tCAF) as a marker for kidney function in patients with chronic kidney disease.
Journal: Clinical chemistry and laboratory medicine
Published: October 21, 2015
Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy.
Journal: American journal of human genetics
Published: October 05, 2015
Showing 1-11 of 11
Last Updated: 09/26/2026