Detection of mucopolysaccharidosis III-A (Sanfilippo Syndrome-A) in dried blood spots (DBS) by tandem mass spectrometry
2018 · Molecular Genetics and Metabolism · 18 citations
https://doi.org/10.1016/j.ymgme.2018.05.005
X
Xinying Hong
Claim or correct this author profile
Claim this profile or suggest corrections to the name, affiliation, bio, photo, or paper titles. Approved changes appear as verified CitedEvidence overlays.
75
Papers
738
Citations
15
h-index
20
i10-index
Xinying Hong is an academic researcher from Children's Hospital of Philadelphia. The author has contributed to research in topics: Lysosomal Storage Disorders Research & Cytomegalovirus and herpesvirus research & Metabolism and Genetic Disorders. The author has an h-index of 15, co-authored 64 publications.
ORCID: 0000-0002-7517-5193Papers by this author
worksMalate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature
2022 · Molecular Genetics and Metabolism Reports · 17 citations
https://doi.org/10.1016/j.ymgmr.2022.100931
Additional file 5 of Predicting disease severity in metachromatic leukodystrophy using protein activity and a patient phenotype matrix
2023 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.23730866
Additional file 8 of Predicting disease severity in metachromatic leukodystrophy using protein activity and a patient phenotype matrix
2023 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.23730878
Additional file 11 of Predicting disease severity in metachromatic leukodystrophy using protein activity and a patient phenotype matrix
2023 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.23730890
Additional file 6 of Predicting disease severity in metachromatic leukodystrophy using protein activity and a patient phenotype matrix
2023 · Figshare · 0 citations
https://doi.org/10.6084/m9.figshare.23730869
Research topics
topicsChat about Author
Papers
Chat
Click to start Chat