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Kristen Liedtke
Observed names:
Kris L. Liedtke,
Kris Liedtke,
Kristen L Liedtke,
Kristen L. Liedtke
Institution:
Mayo Clinic
Observed institution:
Mayo Clinic
OpenAlex ID:
A5074508641
Novel congenital disorder of O -linked glycosylation caused by GALNT2 loss of function
2020
·
Monica Zilmer
, Andrew C Edmondson
, et al.
·
Brain
·
82
PDF
Clinical, biochemical and genetic characteristics of MOGS-CDG: a rare congenital disorder of glycosylation
2022
·
Shino Shimada
, Bobby G Ng
, et al.
·
Journal of Medical Genetics
·
22
A new D‐galactose treatment monitoring index for PGM1‐CDG
2021
·
Ester Perales‐Clemente
, Kristen Liedtke
, et al.
·
Journal of Inherited Metabolic Disease
·
17
Immune dysfunction in MGAT2‐CDG : A clinical report and review of the literature
2020
·
Sheri A. Poskanzer
, Matthew J. Schultz
, et al.
·
American Journal of Medical Genetics Part A
·
14
Biochemical genetic testing for congenital disorders of glycosylation after sequencing produces equivocal results
2026
·
Matthew J. Schultz
, Kristen L. Liedtke
, et al.
·
Molecular Genetics and Metabolism
In support of transferrin testing for PMM2-CDG: The experience at a reference laboratory
2024
·
Dayebgadoh Gerald
, Dietrich Matern
, et al.
·
Molecular Genetics and Metabolism
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Works count:
6
Citation count:
135
H-index:
4
I10-index:
4
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