Boris Rolinski
Riesa, SN, Germany
Last Updated: 09/26/2026
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Found 12 publications
Development and validation of a simple HPLC-MS/MS method for the quantification of methylmalonic acid in human serum without a derivatization step.
Journal: Biomedical chromatography : BMC
Published: October 12, 2022
SARS-CoV-2 rapid antigen testing in the healthcare sector: A clinical prediction model for identifying false negative results.
Journal: International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
Published: July 19, 2021
A new HPLC-MS/MS analytical method for quantification of tazobactam, piperacillin, and meropenem in human plasma.
Journal: Journal of separation science
Published: February 01, 2021
A new HPLC-MS/MS method for simultaneous determination of Cyclosporine A, Tacrolimus, Sirolimus and Everolimus for routine therapeutic drug monitoring.
Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
Published: June 23, 2019
Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective?
Journal: Orphanet journal of rare diseases
Published: November 05, 2017
Affection of the Respiratory Muscles in Combined Complex I and IV Deficiency.
Journal: The open neurology journal
Published: August 29, 2016
Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency.
Journal: Frontiers in genetics
Published: January 16, 2015
Spectrum of combined respiratory chain defects.
Journal: Journal of inherited metabolic disease
Published: December 03, 2014
Presumed mitochondrial disease manifesting with recurrent syncopes.
Journal: Journal of cardiovascular medicine (Hagerstown, Md.)
Published: February 14, 2014
Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosis.
Journal: Neurogenetics
Published: December 12, 2012
Homozygous missense mutation in BOLA3 causes multiple mitochondrial dysfunctions syndrome in two siblings.
Journal: Journal of inherited metabolic disease
Published: February 07, 2012
Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9.
Journal: Journal of medical genetics
Published: December 28, 2011
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Last Updated: 09/26/2026