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DR. KRISTIE H KOEHLER M.D.
M.D.
Pediatrics Physician
NPI: 1174856785Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
81939(AZ)4301096603(MI)
Research & Publications (20)
Serum testosterone and urinary excretion of steroid hormone metabolites after administration of a high-dose zinc supplement.
PMID 17882141·Eur J Clin Nutr·2009
3-trial
Population-based incidence of infection with selected bacterial enteric pathogens in children younger than five years of age, 1996-1998.
PMID 16462289·Pediatr Infect Dis J·2006
8-other
Association of folate intake and serum homocysteine in elderly persons according to vitamin supplementation and alcohol use.
PMID 11237942·Am J Clin Nutr·2001
8-other
Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome.
PMID 18551317·Eur J Pediatr·2009
5-case
Development of a sampler for total aerosol deposition in the human respiratory tract.
PMID 19638392·Ann Occup Hyg·2009
8-other
Genetic analysis of familial non-syndromic primary failure of eruption.
PMID 19419450·Orthod Craniofac Res·2009
8-other
Autosomal dominant neurohypophyseal diabetes insipidus in two families. Molecular analysis of the vasopressin-neurophysin II gene and functional studies of three missense mutations.
PMID 19129716·Horm Res·2009
7-preclinical
Identification of genetic markers for productive life in commercial sows.
PMID 19359509·J Anim Sci·2009
7-preclinical
Dietary supplement use among elite young German athletes.
PMID 19403956·Int J Sport Nutr Exerc Metab·2009
8-other
Effect of a controlled dietary change on carbon and nitrogen stable isotope ratios of human hair.
PMID 19603471·Rapid Commun Mass Spectrom·2009
7-preclinical
Three siblings with triple A syndrome with a novel frameshift mutation in the AAAS gene and a review of 17 independent patients with the frequent p.Ser263Pro mutation.
PMID 18172684·Eur J Pediatr·2008
5-case
Late-onset triple A syndrome: a risk of overlooked or delayed diagnosis and management.
PMID 18953174·Horm Res·2008
5-case
Familial glucocorticoid deficiency type 1 due to a novel compound heterozygous MC2R mutation.
PMID 18504396·Horm Res·2008
5-case
Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430Phe.
PMID 18628786·Eur J Hum Genet·2008
5-case
Water interaction with hydrophobic and hydrophilic soot particles.
PMID 18414725·Phys Chem Chem Phys·2008
8-other
Quantitative data analysis methods for bead-based DNA hybridization assays using generic flow cytometry platforms.
PMID 18338761·Cytometry A·2008
8-other
Nutritional supplements cross-contaminated and faked with doping substances.
PMID 18563865·J Mass Spectrom·2008
6-review
Acute metabolic responses of postpartal dairy cows to subcutaneous glucagon injections, oral glycerol, or both.
PMID 18765590·J Dairy Sci·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 1250 E. Michigan Avenue
Grayling, MI 49738 - Phone
- (989) 348-0550
Quick Facts
- NPI
- 1174856785
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 2
- Publications
- 20
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