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VICKI MICHELS, PHD
PHD
Psychologist
NPI: 1912088311Individual
Specialties, Licenses & Credentials
PsychologistPrimary
Psychologist
Code: 103T00000X
301(ND)
Research & Publications (20)
Frequency of development of idiopathic dilated cardiomyopathy among relatives of patients with idiopathic dilated cardiomyopathy.
PMID 12767445·Am J Cardiol·2003
8-other
Progression of familial and non-familial dilated cardiomyopathy: long term follow up.
PMID 12807850·Heart·2003
4-observational
Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology.
PMID 18651846·Clin Genet·2008
8-other
A multicentre, prospective study to evaluate costs of septic patients in Brazilian intensive care units.
PMID 18429658·Pharmacoeconomics·2008
4-observational
[Clinical case of the month. Hepatitis B reactivation in an Ag HBs negative patient].
PMID 17511378·Rev Med Liege·2007
5-case
Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature review.
PMID 16835934·Am J Med Genet A·2006
5-case
Phase II trial of pirfenidone in adults with neurofibromatosis type 1.
PMID 17035676·Neurology·2006
3-trial
Genetic testing: practical, ethical, and counseling considerations.
PMID 15667031·Mayo Clin Proc·2005
5-case
Usual interstitial pneumonia complicating dyskeratosis congenita.
PMID 15945534·Mayo Clin Proc·2005
5-case
Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.
PMID 15708709·J Am Coll Cardiol·2005
8-other
Sodium channel mutations and susceptibility to heart failure and atrial fibrillation.
PMID 15671429·JAMA·2005
8-other
[Clinical case of the month. Adult onset Still's disease: a rare cause of acute febrile hepatitis].
PMID 14978846·Rev Med Liege·2003
5-case
Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.
PMID 14526392·Am J Hum Genet·2003
8-other
Left ventricular function in the Marfan syndrome without significant valvular regurgitation.
PMID 12667591·Am J Cardiol·2003
4-observational
Familial frontotemporal dementia associated with a novel presenilin-1 mutation.
PMID 12053127·Dement Geriatr Cogn Disord·2002
8-other
Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: a role for laparoscopic and cortical-sparing surgery.
PMID 12049539·Arch Surg·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
- 1900-8TH AVE. S.E.
MINOT, ND 58701 - Phone
- (701) 857-5998
Quick Facts
- NPI
- 1912088311
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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