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Inflammatory Bowel Diseases|July 13, 2015
Pediatric IBD-unclassified Is Less Common than Previously Reported; Results of an 8-Year Audit of the EUROKIDS RegistryDwight A Winter, Katarzyna Karolewska-Bochenek, Izabella Lazowska-Przeorek, et al.
American Journal of Human Genetics|December 3, 2016
Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent EpilepsyNiklas Darin, Emma Reid, Laurence Prunetti, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|March 3, 2018
Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experienceC M Mak, S Pl Chen, N S Mok, et al.
Journal of Clinical Microbiology|September 21, 2007
MP1 homologue-based multilocus sequence system for typing the pathogenic fungus Penicillium marneffei: a novel approach using lineage-specific genesPatrick C Y Woo, Candy C Y Lau, Ken T K Chong, et al.
AIDS Research and Human Retroviruses|February 10, 1996
A multicenter proton magnetic resonance spectroscopy study of neurological complications of AIDSM Paley, P J Cozzone, J Alonso, et al.
Journal of the American College of Radiology : JACR|October 2, 2020
Mapping the Ultrasound Landscape to Define Point-of-Care Ultrasound and Diagnostic Ultrasound: A Proposal From the Society of Radiologists in Ultrasound and ACR Commission on UltrasoundMaitray D Patel, Mindy M Horrow, Aya Kamaya, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 16, 2026
WSB.APP/PS1 mice develop age-dependent cerebral amyloid angiopathy, cerebrovascular dysfunction, and white matter deficitsOlivia J Marola, Asli Uyar, Kelly J Keezer, et al.
Human Molecular Genetics|September 10, 2013
Epigenome-wide DNA methylation landscape of melanoma progression to brain metastasis reveals aberrations on homeobox D cluster associated with prognosisDiego M Marzese, Richard A Scolyer, Jamie L Huynh, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
WSB.APP/PS1 mice develop age-dependent cerebral amyloid angiopathy, cerebrovascular deficits, and white matter damage, which are modified by humanized APOE allelesKristen D Onos, Olivia J Marola, Asli Uyar, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|January 24, 2019
Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical evaluation of their first-degree relativesC M Mak, N S Mok, H C Shum, et al.
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