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AMANDA PATCH, M.D.
M.D.
Family Medicine Physician
NPI: 1891060075IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
11015098A(IN)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
INDIANA UNIVERSITY SCHOOL OF MEDICINE
Class of 2012
Research & Publications (12)
Fingerprinting fission yeast: polymorphic markers for molecular genetic analysis of Schizosaccharomyces pombe strains.
PMID 17322209·Microbiology (Reading)·2007
8-other
Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period.
PMID 17919176·Diabetes Obes Metab·2007
8-other
Neonatal diabetes mellitus due to pancreas agenesis: a new case report and review of the literature.
PMID 19496968·Pediatr Diabetes·2009
5-case
Mutations in the ABCC8 (SUR1 subunit of the K(ATP) channel) gene are associated with a variable clinical phenotype.
PMID 19021632·Clin Endocrinol (Oxf)·2009
8-other
Effective treatment with oral sulfonylureas in patients with diabetes due to sulfonylurea receptor 1 (SUR1) mutations.
PMID 18025408·Diabetes Care·2008
8-other
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.
PMID 18162506·Diabetes·2008
8-other
Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetes.
PMID 18025464·Proc Natl Acad Sci U S A·2007
8-other
Insulin gene mutations as a cause of permanent neonatal diabetes.
PMID 17855560·Proc Natl Acad Sci U S A·2007
8-other
Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects.
PMID 17668386·Am J Hum Genet·2007
8-other
Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood.
PMID 17446535·Diabetes·2007
8-other
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity.
PMID 17434869·Science·2007
8-other
TRbase: a database relating tandem repeats to disease genes for the human genome.
PMID 15479712·Bioinformatics·2005
4-observational
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
- 5693 YMCA PARK DR W
FORT WAYNE, IN 46835 - Phone
- (260) 469-6603
Quick Facts
- NPI
- 1891060075
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 2
- Years in Practice
- 14
- Publications
- 12
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