Publications by authors named "Kimiyo M Raymond"

13Publications

Laboratory monitoring of patients with hereditary tyrosinemia type I.

Mol Genet Metab 2020 08 6;130(4):247-254. Epub 2020 Jun 6.

Biochemical Genetics Laboratory, Mayo Clinic College of Medicine, Rochester, MN, USA. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ymgme.2020.06.001DOI Listing
August 2020

Urine oligosaccharide screening by MALDI-TOF for the identification of NGLY1 deficiency.

Mol Genet Metab 2018 05 10;124(1):82-86. Epub 2018 Mar 10.

Biochemical Genetics Laboratory, Department of Laboratory Medicine and Pathology Mayo Clinic College of Medicine, Rochester, MN, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ymgme.2018.03.002DOI Listing
May 2018

Simultaneous Testing for 6 Lysosomal Storage Disorders and X-Adrenoleukodystrophy in Dried Blood Spots by Tandem Mass Spectrometry.

Clin Chem 2016 09 20;62(9):1248-54. Epub 2016 Jul 20.

Biochemical Genetics Laboratory, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1373/clinchem.2016.256255DOI Listing
September 2016

Discordant results between biochemical and molecular transthyretin assays: lessons learned from a unique testing algorithm at the Mayo Clinic.

J Genet 2013 Dec;92(3):599-604

Molecular Laboratories, Department of Laboratory Medicine and Pathology, Mayo Clinic School of Medicine, Rochester, MN, 55905, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s12041-013-0303-6DOI Listing
December 2013