C. Law

发表

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.

The first territory-wide expanded newborn screening for inborn errors of metabolism in Hong Kong: a pilot study

C. Lam, C. Mak, A. Chan, 2017 .

NMR-based metabolomic urinalysis: a rapid screening test for urinary tract infection.

K. To, K. Yuen, Kim-Chung Lee, 2014, Clinica chimica acta; international journal of clinical chemistry.

The Independent Association of TSH and Free Triiodothyronine Levels With Lymphocyte Counts Among COVID-19 Patients

K. To, A. Tam, I. Hung, 2022, Frontiers in Endocrinology.

Centrosome-associated CDC25B is a novel disease-causing gene for a syndrome with cataracts, dilated cardiomyopathy, and multiple endocrinopathies.

Xinqi Cheng, C. Lam, N. Fong, 2020, Clinica chimica acta; international journal of clinical chemistry.

Pleural effusion lipoproteins measured by NMR spectroscopy for diagnosis of exudative pleural effusions: a novel tool for pore-size estimation.

C. Lam, C. Law, 2014, Journal of proteome research.

NMR-based urinalysis for beta-ketothiolase deficiency.

C. Lam, Chi-kong Lai, Kin-Cheong Eric Yau, 2015, Clinica chimica acta; international journal of clinical chemistry.

Electronic chemical pathology consultation service and dried blood spot metabolic screening in hospital patients

C. Lam, W. Poon, Hencher Han-Chih Lee, 2012, Journal of Clinical Pathology.

Quantitative metabolomics of urine for rapid etiological diagnosis of urinary tract infection: evaluation of a microbial-mammalian co-metabolite as a diagnostic biomarker.

K. To, K. Sze, C. Lam, 2015, Clinica chimica acta; international journal of clinical chemistry.

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.

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.

Nuclear magnetic resonance spectroscopy-based urinalysis for a young girl with extreme hypoglycaemia.

C. Lam, C. Law, Ka-chung Wong, 2021, Pathology.

Role of non‐thyroidal illness syndrome in predicting adverse outcomes in COVID‐19 patients predominantly of mild‐to‐moderate severity

K. To, A. Tam, I. Hung, 2021, Clinical endocrinology.

Global developmental delay and intellectual disability associated with a de novo TOP2B mutation.

C. Lam, C. Law, W. Yeung, 2017, Clinica chimica acta; international journal of clinical chemistry.

Insights from a Prospective Follow-up of Thyroid Function and Autoimmunity among COVID-19 Survivors

K. To, A. Tam, I. Hung, 2021, Endocrinology and metabolism.

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.

Higher SARS-CoV-2 viral loads correlated with smaller thyroid volumes on ultrasound among male COVID-19 survivors

K. To, A. Tam, I. Hung, 2021, Endocrine.

Paediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2: a case report.

M. Levin, N. Fong, J. Yam, 2022, Hong Kong medical journal = Xianggang yi xue za zhi.

A prospective follow-up on thyroid function, thyroid autoimmunity and long COVID among 250 COVID-19 survivors

K. To, A. Tam, I. Hung, 2023, Endocrine.

Serum ceruloplasmin monitoring in a case of silver intoxication due to intravenous silver infusion

Ching-lung Lai, C. Lam, C. Law, 2021, Clinical toxicology.

Gelsemium poisoning mediated by the non‐toxic plant Cassytha filiformis parasitizing Gelsemium elegans

Y. Lam, T. Mak, Hencher Han-Chih Lee, 2018, Toxicon.

Non-invasive screening of HLA-DPA1 and HLA-DPB1 alleles for persistent hepatitis B virus infection: susceptibility for vertical transmission and toward a personalized approach for vaccination and treatment.

C. Lam, P. Chan, W. Poon, 2011, Clinica chimica acta; international journal of clinical chemistry.

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.

Untargeted mass spectrometry-based metabolomic profiling of pleural effusions: fatty acids as novel cancer biomarkers for malignant pleural effusions.

C. Lam, C. Law, 2014, Journal of proteome research.

The Impact of Interferon Beta-1b Therapy on Thyroid Function and Autoimmunity Among COVID-19 Survivors

K. To, A. Tam, I. Hung, 2021, Frontiers in Endocrinology.

Novel POLG mutation in a patient with sensory ataxia, neuropathy, ophthalmoparesis and stroke.

C. Lam, C. Fung, Hencher Han-Chih Lee, 2015, Clinica chimica acta; international journal of clinical chemistry.

Limb girdle myasthenia with digenic RAPSN and a novel disease gene AK9 mutations

H. Leung, C. Lam, C. Law, 2017, European Journal of Human Genetics.

Lipid metabolites as potential diagnostic and prognostic biomarkers for acute community acquired pneumonia

Samson S. Y. Wong, Kong-Hung Sze, K. To, 2016, Diagnostic Microbiology and Infectious Disease.

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

C. Lam, N. Fong, C. Law, 2015, 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.

A common COQ4 mutation in undiagnosed mitochondrial disease: a local case series

W. Chu, G. Brea-Calvo, C. Lam, 2019, Pathology (Sydney).

Clinical whole-exome sequencing reveals a common pathogenic variant in patients with COQ10 deficiency: An underdiagnosed cause of mitochondriopathy.

W. Chu, G. Brea-Calvo, C. Lam, 2019, Clinica chimica acta; international journal of clinical chemistry.

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.

Novel large deletion in AVPR2 gene causing copy number variation in a patient with X-linked nephrogenic diabetes insipidus.

C. Lam, C. Law, K. Ng, 2016, Clinica chimica acta; international journal of clinical chemistry.

Long COVID in Patients With Mild to Moderate Disease: Do Thyroid Function and Autoimmunity Play a Role?

K. To, A. Tam, I. Hung, 2021, Endocrine Practice.

C-terminal truncated SPOP causing a mixed type 1 and type 2 Nabais Sa-de Vries syndrome.

C. Law, Ching-wan Lam, 2022, Clinica chimica acta; international journal of clinical chemistry.

Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumors

G. Wong, C. Lam, C. Mak, 2011, Familial Cancer.

NMR-based urinalysis for rapid diagnosis of β-ureidopropionase deficiency in a patient with Dravet syndrome.

C. Lam, Kwok-Yin Chan, C. Mak, 2015, Clinica chimica acta; international journal of clinical chemistry.

Limb girdle myasthenia with digenic RAPSN and a novel disease gene AK9 mutations

C. Lam, C. Law, Ka-Sing Wong, 2016, European Journal of Human Genetics.

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.

A prospective follow-up on thyroid function, thyroid autoimmunity and long COVID among 250 COVID-19 survivors

K. To, A. Tam, I. Hung, 2023, Endocrine.

2,4-Dinitrophenol: a threat to Chinese body-conscious groups.

Y. Lam, A. Chan, T. Mak, 2014, Journal of the Chinese Medical Association : JCMA.

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.

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

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

A prospective follow-up of thyroid volume and thyroiditis features on ultrasonography among survivors of predominantly mild to moderate COVID-19

K. To, A. Tam, I. Hung, 2023, PeerJ.

Insights From Prospective Follow-up of Thyroid Function and Autoimmunity Among Covid-19 Survivors

K. To, A. Tam, I. Hung, 2021, Journal of the Endocrine Society.

Parental attitudes on expanded newborn screening in Hong Kong.

C. Lam, C. Mak, W. Siu, 2012, Public health.

Novel POLG mutation in a patient with sensory ataxia, neuropathy, ophthalmoparesis and stroke.

C. Lam, C. Fung, Hencher Han-Chih Lee, 2015, Clinica chimica acta; international journal of clinical chemistry.

NMR-based urinalysis for beta-ketothiolase deficiency.

C. Lam, C. Mak, C. Ching, 2015, Clinica chimica acta; international journal of clinical chemistry.