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KELVIN LOKE, DO
DO
Student in an Organized Health Care Education/Training Program
NPI: 1730934563Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
A case of X-linked adrenal hypoplasia congenita, central precocious puberty and absence of the DAX-1 gene: implications for pubertal regulation.
PMID 19339795·Horm Res·2009
8-other
Diagnostic accuracy of anthropometric indices for obesity screening among Asian adolescents.
PMID 19221664·Ann Acad Med Singap·2009
8-other
Role of Tc-99m DMSA (V) scanning and serum calcitonin monitoring in the management of medullary thyroid carcinoma.
PMID 18204763·Singapore Med J·2008
8-other
Gonadal mosaicism 45,X/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal dysgenesis.
PMID 18418530·Singapore Med J·2008
5-case
Association of raised liver transaminases with physical inactivity, increased waist-hip ratio, and other metabolic morbidities in severely obese children.
PMID 18664869·J Pediatr Gastroenterol Nutr·2008
8-other
Novel melanocortin 4 receptor gene mutations in severely obese children.
PMID 17941900·Clin Endocrinol (Oxf)·2008
4-observational
3rd College of paediatrics and child health lecture--the past, the present and the shape of things to come...
PMID 18536833·Ann Acad Med Singap·2008
8-other
Isolated haploinsufficiency of exon 1 of the SHOX gene in a patient with idiopathic short stature.
PMID 16803952·J Clin Pathol·2006
5-case
Making $ense of growth hormone therapy for normal short children.
PMID 16453036·Ann Acad Med Singap·2005
8-other
Quantitative real-time polymerase chain reaction (RQ-PCR) for the rapid detection of SHOX haploinsufficiency in Leri-Weill Syndrome.
PMID 16319696·Diagn Mol Pathol·2005
8-other
Mitochondrial respiratory abnormalities in patients with end-stage congenital heart disease.
PMID 14734130·J Heart Lung Transplant·2004
8-other
A distinctive type of metaphyseal chondrodysplasia with characteristic thickening of the distal ulna and radius: possible metaphyseal chondrodysplasia-Rosenberg.
PMID 12707959·Am J Med Genet A·2003
5-case
Detection through screening of maternal thyrotoxicosis induced central hypothyroidism in newborns.
PMID 15906722·Southeast Asian J Trop Med Public Health·2003
5-case
Epidemiology of 21-hydroxylase deficiency in Singapore.
PMID 12008686·J Pediatr Endocrinol Metab·2002
8-other
Maternal thyrotoxicosis causing central hypothyroidism in infants.
PMID 12031010·J Paediatr Child Health·2002
5-case
Tyrosine phosphatase-like protein (IA-2) and glutamic acid decarboxylase (GAD65) autoantibodies: a study of Chinese patients with diabetes mellitus.
PMID 12073931·Autoimmunity·2002
8-other
Evidence of autoantibodies to glutamic acid decarboxylase in oral fluid of type 1 diabetic patients.
PMID 12126766·Diabetes Res Clin Pract·2002
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 15855 19 MILE RD
CLINTON TOWNSHIP, MI 48038 - Phone
- (952) 393-9735
Quick Facts
- NPI
- 1730934563
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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