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DR. MONAZZA AZAM MD
MD
Internal Medicine Physician
NPI: 1497384366Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
2023-01554(NC)
Research & Publications (20)
Activation of tyrosine kinases by mutation of the gatekeeper threonine.
PMID 18794843·Nat Struct Mol Biol·2008
8-other
Use of ACTH and prednisolone in infantile spasms: experience from a developing country.
PMID 16183305·Seizure·2005
3-trial
Cloning and characterization of the 5'-flanking region of the oxalate decarboxylase gene from Flammulina velutipes.
PMID 12020349·Biochem J·2002
8-other
Disruption of the mouse mu-calpain gene reveals an essential role in platelet function.
PMID 11238954·Mol Cell Biol·2001
7-preclinical
A secretion signal is present in the Collybia velutipes oxalate decarboxylase gene.
PMID 11735117·Biochem Biophys Res Commun·2001
8-other
Lin28 promotes transformation and is associated with advanced human malignancies.
PMID 19483683·Nat Genet·2009
7-preclinical
Synthesis and spectroscopic studies on complexes of N,N'-bis-(2-pyridinecarboxaldimine)-1,8-diaminonaphthalene (L); DNA binding studies on Cu(II) complex.
PMID 18722156·Spectrochim Acta A Mol Biomol Spectrosc·2009
8-other
Arginase promotes neointima formation in rat injured carotid arteries.
PMID 19164802·Arterioscler Thromb Vasc Biol·2009
7-preclinical
9-(Arenethenyl)purines as dual Src/Abl kinase inhibitors targeting the inactive conformation: design, synthesis, and biological evaluation.
PMID 19572547·J Med Chem·2009
7-preclinical
Template synthesis and physico-chemical characterization of 14-membered tetraimine macrocyclic complexes, [MLX(2)] [M=Co(II), Ni(II), Cu(II) and Zn(II)]. DNA binding study on [CoLCl(2)] complex.
PMID 19119063·Spectrochim Acta A Mol Biomol Spectrosc·2009
7-preclinical
Intracranial cavernous hemangioma and seizures in a newborn infant.
PMID 19619757·J Pediatr·2009
5-case
ICSBP-mediated immune protection against BCR-ABL-induced leukemia requires the CCL6 and CCL9 chemokines.
PMID 19171873·Blood·2009
7-preclinical
CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa.
PMID 18387594·Am J Hum Genet·2008
7-preclinical
Non-invasive diagnosis of H pylori infection: evaluation of serological tests with and without current infection marker CIM.
PMID 18300349·World J Gastroenterol·2008
8-other
Addendum. CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa.
PMID 19068953·Am J Hum Genet·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 303 PARKWAY DR NE # 430
ATLANTA, GA 30312 - Phone
- (770) 265-4919
Quick Facts
- NPI
- 1497384366
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 2
- Publications
- 20
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