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DANIEL MAREK, M.D.
M.D.
Orthopaedic Hand Surgery Physician
NPI: 1912190075IndividualAccepts Medicare
Specialties, Licenses & Credentials
Orthopaedic Surgery Physician
Orthopaedic Surgery
Code: 207X00000X
MD60158633(WA)49566(MN)
Orthopaedic Hand Surgery PhysicianPrimary
Orthopaedic Surgery — Hand Surgery
Code: 207XS0106X
49566(MN)
Education
UNIVERSITY OF MINNESOTA MEDICAL SCHOOL
Class of 2005
Research & Publications (20)
Case report: reconstruction of a recalcitrant scapular neck nonunion and literature review.
PMID 19082865·Clin Orthop Relat Res·2009
5-case
Micro MRI of the mouse brain using a novel 400 MHz cryogenic quadrature RF probe.
PMID 19536757·NMR Biomed·2009
7-preclinical
The effects of candesartan on left ventricular hypertrophy and function in nonobstructive hypertrophic cardiomyopathy: a pilot, randomized study.
PMID 19074594·J Mol Diagn·2009
2-rct
Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset.
PMID 18987351·Neurology·2009
4-observational
Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome.
PMID 18452888·Am J Hum Genet·2008
8-other
Mistakes in dealing with aortic dissection. Lessons from three warning cases.
PMID 19219221·Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub·2008
5-case
Performance of a 200-MHz cryogenic RF probe designed for MRI and MRS of the murine brain.
PMID 18421696·Magn Reson Med·2008
7-preclinical
Activity level in young patients with primary total hip arthroplasty: a 5-year minimum follow-up.
PMID 17197307·J Arthroplasty·2007
8-other
[Long term results of cardiac resynchronisation therapy for patients with severe heart failure].
PMID 18277624·Vnitr Lek·2007
8-other
[Chronic benign exsudative pericarditis--a case of familiar incidence].
PMID 18072439·Vnitr Lek·2007
5-case
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8.
PMID 17804834·Neurology·2007
8-other
Point mutation in the HCN4 cardiac ion channel pore affecting synthesis, trafficking, and functional expression is associated with familial asymptomatic sinus bradycardia.
PMID 17646576·Circulation·2007
7-preclinical
R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation.
PMID 17149721·Mov Disord·2007
8-other
Mutations in LRRK2 other than G2019S are rare in a north American-based sample of familial Parkinson's disease.
PMID 17078063·Mov Disord·2006
4-observational
Acute severe mitral regurgitation with cardiogenic shock caused by two-step complete anterior papillary muscle rupture during acute myocardial infarction.
PMID 17426796·Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub·2006
5-case
Mapping of a gene causing brittle cornea syndrome in Tunisian jews to 16q24.
PMID 17122114·Invest Ophthalmol Vis Sci·2006
8-other
Incidence of pericardial effusion in females stimulated in "in vitro fertilization" program.
PMID 16999690·Echocardiography·2006
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
- 560 S MAPLE ST, SUITE 200
WACONIA, MN 55387 - Phone
- (952) 442-2163
Quick Facts
- NPI
- 1912190075
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 21
- Publications
- 20
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