Back to Search
JONATHAN MAKIELSKI, MD
MD
Cardiovascular Disease Physician
NPI: 1255308193IndividualAccepts Medicare
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
36851(WI)
CMS Specialties
PrimaryCARDIOVASCULAR DISEASE (CARDIOLOGY)
Education
UNIVERSITY OF CHICAGO, PRITZKER SCHOOL OF MEDICINE
Class of 1979
Research & Publications (20)
SIDS: genetic and environmental influences may cause arrhythmia in this silent killer.
PMID 16453014·J Clin Invest·2006
6-review
Na(+) current in human ventricle: implications for sodium loading and homeostasis.
PMID 16686671·J Cardiovasc Electrophysiol·2006
6-review
Ranolazine and late cardiac sodium current--a therapeutic target for angina, arrhythmia and more?
PMID 16520741·Br J Pharmacol·2006
7-preclinical
A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels.
PMID 14500339·Circ Res·2003
8-other
Differential modulation of late sodium current by protein kinase A in R1623Q mutant of LQT3.
PMID 19167409·Life Sci·2009
8-other
GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A.
PMID 19666841·Am J Physiol Heart Circ Physiol·2009
8-other
Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A.
PMID 19632629·Heart Rhythm·2009
5-case
Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy.
PMID 19056759·Am J Physiol Gastrointest Liver Physiol·2009
8-other
Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex.
PMID 18591664·Proc Natl Acad Sci U S A·2008
7-preclinical
Cardiac sulfonylurea receptor short form-based channels confer a glibenclamide-insensitive KATP activity.
PMID 18001767·J Mol Cell Cardiol·2008
7-preclinical
Suppression of atrial fibrillation with mexiletine pharmacotherapy in a young woman with type 1 long QT syndrome.
PMID 18313609·Heart Rhythm·2008
5-case
A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia.
PMID 17897635·Cardiovasc Res·2007
5-case
Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome.
PMID 17967976·Circulation·2007
8-other
Mice lacking sulfonylurea receptor 2 (SUR2) ATP-sensitive potassium channels are resistant to acute cardiovascular stress.
PMID 17765261·J Mol Cell Cardiol·2007
7-preclinical
Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.
PMID 17275750·Heart Rhythm·2007
8-other
KCNJ2 mutations in arrhythmia patients referred for LQT testing: a mutation T305A with novel effect on rectification properties.
PMID 17341397·Heart Rhythm·2007
8-other
SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome.
PMID 17592081·Circulation·2007
5-case
Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function.
PMID 17998470·Circulation·2007
8-other
The single nucleotide polymorphisms of I(Ks) potassium channel genes and their association with atrial fibrillation in a Chinese population.
PMID 17016049·Cardiology·2007
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
- 2738 RICHARDSON ST
FITCHBURG, WI 53711 - Phone
- (608) 276-4070
Quick Facts
- NPI
- 1255308193
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 47
- Publications
- 20
Are you this provider?
Claim Your Profile