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MARIA SUPER, D.O.
D.O.
Internal Medicine Physician
NPI: 1619310422IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
5635(OK)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
OTHER
Class of 2013
Research & Publications (15)
A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome.
PMID 15549396·Hum Genet·2005
8-other
Blood pressure and the cystic fibrosis gene: evidence for lower pressure rises with age in female carriers.
PMID 15477385·Hypertension·2004
8-other
Case 4: assessment. An adolescent aged 14 has cystic fibrosis.
PMID 14692404·Paediatr Respir Rev·2003
5-case
Cystic fibrosis newborn screening and detection of carriers.
PMID 14602687·Arch Dis Child Fetal Neonatal Ed·2003
8-other
End-organ dysfunction in cystic fibrosis: association with angiotensin I converting enzyme and cytokine gene polymorphisms.
PMID 12554626·Am J Respir Crit Care Med·2003
8-other
Antidisialoganglioside/granulocyte macrophage-colony-stimulating factor fusion protein facilitates neutrophil antibody-dependent cellular cytotoxicity and depends on FcgammaRII (CD32) and Mac-1 (CD11b/CD18) for enhanced effector cell adhesion and azurophil granule exocytosis.
PMID 12010822·Blood·2002
8-other
Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein.
PMID 11283202·J Med Genet·2001
8-other
Clinical studies on submicroscopic subtelomeric rearrangements: a checklist.
PMID 11238680·J Med Genet·2001
8-other
Failure to refer for testing for cystic fibrosis. Doctors must ensure that those with a family history are advised appropriately.
PMID 11159639·BMJ·2001
8-other
Sibs with developmental delay, hirsutism and nail hypoplasia: a new syndrome.
PMID 11045578·Clin Dysmorphol·2000
5-case
Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations.
PMID 10937553·Invest Ophthalmol Vis Sci·2000
8-other
TGF-beta(1) genotype and accelerated decline in lung function of patients with cystic fibrosis.
PMID 10817792·Thorax·2000
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
- 2000 S WHEELING AVE STE 701
TULSA, OK 74104 - Phone
- (918) 403-7801
Quick Facts
- NPI
- 1619310422
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 13
- Publications
- 15
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