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VAROTE SHOTELERSUK, M.D.
M.D.
Student in an Organized Health Care Education/Training Program
NPI: 1730979709Individual
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)
Bilateral pheochromocytoma during the postpartum period.
PMID 19340440·Arch Gynecol Obstet·2009
5-case
Prenatal diagnosis of a novel mutation, c.529C>T (p.Q177X), in the BCKDHA gene in a family with maple syrup urine disease.
PMID 19240989·J Inherit Metab Dis·2009
5-case
Bilateral submandibular gland aplasia with clinico-radiological mass due to prolapsing sublingual salivary tissue through mylohyoid boutonniere: a case report and review.
PMID 19176656·Dentomaxillofac Radiol·2009
5-case
Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene.
PMID 18681856·Clin Endocrinol (Oxf)·2009
5-case
A novel SPINK1 gene mutation, c.206C>T, in a Thai patient with chronic alcoholic pancreatitis.
PMID 18182741·JOP·2008
5-case
Carbamazepine and phenytoin induced Stevens-Johnson syndrome is associated with HLA-B*1502 allele in Thai population.
PMID 18637831·Epilepsia·2008
8-other
Risk factors associated with the occurrence of frontoethmoidal encephalomeningocele.
PMID 17869141·Eur J Paediatr Neurol·2008
8-other
Study of the poliovirus receptor related-1 gene in Thai patients with non-syndromic cleft lip with or without cleft palate.
PMID 18356023·Int J Oral Maxillofac Surg·2008
4-observational
Three novel mutations in the PORCN gene underlying focal dermal hypoplasia.
PMID 18325042·Clin Genet·2008
5-case
Identification of mutations in the SRD5A2 gene in Thai patients with male pseudohermaphroditism.
PMID 18314109·Fertil Steril·2008
5-case
Identification of two novel aquaporin-2 mutations in a Thai girl with congenital nephrogenic diabetes insipidus.
PMID 18473191·Endocrine·2008
5-case
A novel germline mutation, IVS4+1G>A, of the POU1F1 gene underlying combined pituitary hormone deficiency.
PMID 18059085·Horm Res·2008
5-case
TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population.
PMID 17868388·Clin Genet·2007
8-other
Nonsense mutations of the CYBB gene in two Thai families with X-linked chronic granulomatous disease.
PMID 18402298·Asian Pac J Allergy Immunol·2007
8-other
An exceptionally low percentage of Thai expectant mothers and medical personnel with folic acid knowledge and peri-conceptional consumption urges an urgent education program and/or food fortification.
PMID 17566891·Int J Food Sci Nutr·2007
8-other
Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects.
PMID 17377962·Hum Mutat·2007
5-case
Two common and three novel PDS mutations in Thai patients with Pendred syndrome.
PMID 18250610·J Endocrinol Invest·2007
8-other
Prenatal exclusion of subtelomeric deletion 1p by fluorescent in situ hybridization.
PMID 16983561·Arch Gynecol Obstet·2007
5-case
PTEN c.511C>T nonsense mutation in a BRRS family disrupts a potential exonic splicing enhancer and causes exon skipping.
PMID 17043057·Jpn J Clin Oncol·2006
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3601 4TH STREET, STOP #9410
LUBBOCK, TX 79430 - Phone
- (806) 743-3641
Quick Facts
- NPI
- 1730979709
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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