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KERRICK STOUT, MD
MD
Family Medicine Physician
NPI: 1710961172IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
4902(AK)34237(KY)
Emergency Medicine Physician
Emergency Medicine
Code: 207P00000X
34237(KY)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
UNIVERSITY OF LOUISVILLE SCHOOL OF MEDICINE
Class of 1997
Research & Publications (20)
Distorted cardiac anatomy: the congenital (R)evolution.
PMID 19187854·J Am Soc Echocardiogr·2009
8-other
A novel method for the evaluation and treatment of obstructive sleep apnea in four adults with complex congenital heart disease and Fontan repairs.
PMID 19449048·Sleep Breath·2009
8-other
Percutaneous right ventricular assist device as support for cardiogenic shock due to right ventricular infarction.
PMID 18599906·J Invasive Cardiol·2008
5-case
The bicuspid aortic valve: an integrated phenotypic classification of leaflet morphology and aortic root shape.
PMID 18308868·Heart·2008
4-observational
How many leaflets does that valve have? Diagnosis and significance in congenital aortic valve disease.
PMID 18256561·Am Heart Hosp J·2008
5-case
Development of a screening tool predicting the transition from acute to chronic low back pain for patients in a GP setting: protocol of a multinational prospective cohort study.
PMID 19099569·BMC Musculoskelet Disord·2008
3-trial
Repaired tetralogy of Fallot in the adult: monitoring and management.
PMID 19011142·Heart·2008
6-review
Changes in hospitalization patterns among patients with congenital heart disease during the transition from adolescence to adulthood.
PMID 17320746·J Am Coll Cardiol·2007
8-other
Distorted cardiac anatomy: role of echocardiography in diagnosis of complex congenital heart disease.
PMID 17982295·Am Heart Hosp J·2007
5-case
Management of obstructive sleep apnea in patients with congenital heart disease and Fontan procedures.
PMID 17512247·Sleep Med·2007
5-case
Usefulness of bicuspid aortic valve phenotype to predict elastic properties of the ascending aorta.
PMID 17317372·Am J Cardiol·2007
8-other
Disruption of TCBA1 associated with a de novo t(1;6)(q32.2;q22.3) presenting in a child with developmental delay and recurrent infections.
PMID 15908570·J Med Genet·2006
5-case
Pregnancy in women with congenital heart disease: the importance of evaluation and counselling.
PMID 15894757·Heart·2005
8-other
A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation.
PMID 12070244·J Med Genet·2002
5-case
Chicken microchromosomes are hypermethylated and can be identified by specific painting probes.
PMID 11528124·Cytogenet Cell Genet·2001
7-preclinical
Two supernumerary marker chromosomes, originating from chromosomes 6 and 11, in a child with developmental delay and craniofacial dysmorphism.
PMID 11528110·Cytogenet Cell Genet·2001
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
- 6000 KANAKANAK RD
DILLINGHAM, AK 99576 - Phone
- (907) 842-5201
Quick Facts
- NPI
- 1710961172
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 29
- Publications
- 20
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