Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Clement K M Ho"'
Publikováno v:
Endocrine Abstracts.
Autor:
Mei Yoke Chan, Clement K M Ho, Prasad Iyer, Ragavendra Kalyanasundaram, Rajat Bhattacharyya, Wen Qi Cher
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 5, Iss 3, Pp 96-99 (2020)
Profound hyperferritinaemia of >10,000 μg/L has been suggested to be highly specific for the diagnosis of paediatric haemophagocytic lymphohistiocytosis (HLH) in western literature but similar studies are lacking in Asian children. We did a single-c
Autor:
Choong-Weng Lam, Grace Lay Lay Lee, Mee-Yin Lee, Tze Ping Loh, Moh Sim Wong, Chin Pin Yeo, Tong Kooi Lee, Pallavi Chincholkar, Clement K M Ho, Hafash Khalid, Bih-Yann Ng, Tang Lin Teo, Hong Liu, Sharine Lim, Sharon Yong, Qinde Liu, Sunil Sethi, Robert C. Hawkins, Lingkai Wong, Sok Fong Maria Lim, Shelia Marie Delos Santos Cosio, Johnson W.S. Setoh
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 57:648-658
Background The measurement of hemoglobin A1c (HbA1c) is important for diagnosing diabetes mellitus as well as assessing glycemic control in diabetic patients. Commutable whole blood certified reference materials (CRMs) are needed in the measurement o
Publikováno v:
Journal of Clinical Pathology. 71:932-935
BackgroundIt is often impractical for each laboratory to establish its own paediatric reference intervals. This is particularly true for specimen types collected using invasive procedures, for example, cerebrospinal fluid (CSF).MethodsPublished CSF r
Publikováno v:
Journal of clinical pathology. 72(8)
Clinical indications for the measurement of serum or plasma concentrations of inorganic phosphate (hereafter referred to as phosphate) in paediatric patients include metabolic bone disorders, parathyroid abnormalities, malnutrition, renal failure and
Publikováno v:
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 52:680-684
Familial hypercholesterolaemia, one of the most common inherited diseases in the general population, is associated with mutations in at least three different genes including the low density lipoprotein receptor ( LDLR), apolipoprotein B ( APOB) and p
Autor:
Mor Jack Ng, Kok Hian Tan, George S. H. Yeo, Nancy W S Tee, Bernard Chern, Edward T H Tan, Clement K M Ho, Kenneth Kwek
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 55
Background:Thyroid disorders are common during pregnancy. To date, a limited number of studies have reported differences in serum thyroid hormone concentrations between different ethnic groups. We sought to establish gestational age-specific referenc
Autor:
Clement K M Ho, Robert Finnie, Sara Jenks, Christine Bell, Peter Bloomfield, Nicola Shand, Simon W Walker
Publikováno v:
The British Journal of Diabetes & Vascular Disease. 12:243-247
As in other areas of Western Europe, familial hypercholesterolaemia (FH) is one of the most frequent genetic disorders in the UK. Genetic testing for this condition is available in Scotland. This observational study describes the genetic variants fou
Publikováno v:
Prostate Cancer and Prostatic Diseases. 15:365-368
Both genetics and the environment are implicated as risk factors for prostate cancer (PCa). This population-based case-control study evaluated four single-nucleotide polymorphisms (SNPs) previously identified by genome-wide association studies to be
Publikováno v:
Pediatric Dermatology. 34:e104-e105
This is a case report of a 4-month-old full-term, fully breastfed boy who presented with a persistent periorificial and groin rash associated with poor weight gain and irritability. His serum zinc level was low. The mother's breast milk zinc level wa