Chun-yiu Law

Lipid mediators of inflammation as novel plasma biomarkers to identify patients with bacteremia.

Samson S. Y. Wong, P. Woo, K. To, 2015, The Journal of infection.

A case of early-onset obesity, hypocortisolism, and skin pigmentation problem due to a novel homozygous mutation in the proopiomelanocortin (POMC) gene in an Indian boy

W. Poon, A. Chan, C. Law, 2012, Journal of pediatric endocrinology & metabolism : JPEM.

Analysis of inborn errors of metabolism: disease spectrum for expanded newborn screening in Hong Kong.

T. Siu, S. Tam, C. Lam, 2011, Chinese medical journal.

Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants

T. Siu, S. Tam, C. Lam, 2011, Journal of Human Genetics.

Whole-exome sequencing of a quartet family identifies DTYMK mutations in siblings with mitochondrial DNA depletion syndrome.

C. Lam, C. Law, Ka-chung Wong, 2019, Clinica chimica acta; international journal of clinical chemistry.

Mitochondrial diseases in Hong Kong: prevalence, clinical characteristics and genetic landscape

R. Rodenburg, J. Smeitink, C. Lam, 2023, Orphanet Journal of Rare Diseases.

Case Report: Prenatal Recurrent Microcephaly and Corpus Callosum Abnormalities in a Chinese Family with Novel Biallelic SASS6 Mutations

K. Choy, L. Poon, C. Law, 2023, Fetal Diagnosis and Therapy.

Thyroid Dysfunction in Relation to Immune Profile, Disease Status and Outcome in 191 Patients with COVID-19

K. To, A. Tam, I. Hung, 2020, The Journal of clinical endocrinology and metabolism.

Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy.

C. Lam, N. Fong, S. T. Chang, 2015, Clinica chimica acta; international journal of clinical chemistry.