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DR. STEVEN K BRENNAN MD
MD
Pediatric Pulmonology Physician
NPI: 1356754451IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
2017022832(MO)
Pediatric Emergency Medicine (Pediatrics) Physician
Pediatrics — Pediatric Emergency Medicine
Code: 2080P0204X
2017022832(MO)
Pediatric Pulmonology PhysicianPrimary
Pediatrics — Pediatric Pulmonology
Code: 2080P0214X
2017022832(MO)
Education
OTHER
Class of 2013
Research & Publications (20)
A second case of Hb Fontainebleau [alpha21(B2)Ala-->Pro] in an individual with microcytosis.
PMID 19657841·Hemoglobin·2009
5-case
The mRNA-destabilizing protein tristetraprolin is suppressed in many cancers, altering tumorigenic phenotypes and patient prognosis.
PMID 19491267·Cancer Res·2009
8-other
Regulation of cellular signal transduction pathways by the extracellular calcium-sensing receptor.
PMID 19355937·Curr Pharm Biotechnol·2009
6-review
Deletion of five residues from the coiled coil of fibrinogen (Bbeta Asn167_Glu171del) associated with bleeding and hypodysfibrinogenemia.
PMID 19229055·Haematologica·2009
5-case
BMD in population-based adult women is associated with socioeconomic status.
PMID 19113909·J Bone Miner Res·2009
8-other
The association between socioeconomic status and osteoporotic fracture in population-based adults: a systematic review.
PMID 19107382·Osteoporos Int·2009
1-meta
Imaging of late complications from mantle field radiation in lymphoma patients.
PMID 18619388·Radiol Clin North Am·2008
6-review
Novel hemoglobin alpha chain elongation resulting from a 15-residue insertion and tandem duplication of the F helix.
PMID 18571503·Clin Biochem·2008
8-other
Congenital hypodysfibrinogenaemia (Fibrinogen Des Moines) due to a gamma320Asp deletion at the Ca2+ binding site.
PMID 17721633·Thromb Haemost·2007
5-case
Hypofibrinogenaemia resulting from novel single nucleotide deletion at codon Bbeta58 (3404del A) associated with thrombotic stroke in infancy.
PMID 16601848·Thromb Haemost·2006
5-case
Hypofibrinogenaemia associated with common gamma82Ala-->Gly mutation is not mediated by altered mRNA splicing.
PMID 17003934·Thromb Haemost·2006
5-case
Novel gamma230 Asn-->Asp substitution in fibrinogen Middlemore associated hypofibrinogenaemia.
PMID 15968409·Thromb Haemost·2005
5-case
Hb riccarton [alpha51(CE9)Gly-->Ser]: a variant arising from a novel mutation in the alpha1 gene.
PMID 15768556·Hemoglobin·2005
8-other
Hb taradale [beta82(EF6)Lys-->Arg]: a novel mutation at a 2,3-diphosphoglycerate binding site.
PMID 16370489·Hemoglobin·2005
5-case
Hb Lusaka [alpha131(H14)Ser-->phe (alpha1)]: a new variant found in a woman heterozygous for Hb S [beta6(A3)G1u-->Val].
PMID 12908802·Hemoglobin·2003
5-case
Hb Manawatu [alpha 37(C2)Pro-->Leu]: a new mildly unstable mutation at an invariant proline residue.
PMID 12484634·Hemoglobin·2002
8-other
Novel fibrinogen gamma375 Arg-->Trp mutation (fibrinogen aguadilla) causes hepatic endoplasmic reticulum storage and hypofibrinogenemia.
PMID 12198657·Hepatology·2002
8-other
Hb Canterbury [beta112(G14)Cys-->Phe]: a new, mildly unstable variant.
PMID 11939514·Hemoglobin·2002
8-other
Gamma371 Thr-->Ile substitution in the fibrinogen gammaD domain causes hypofibrinogenaemia.
PMID 11755207·Biochim Biophys Acta·2001
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
- 1 CHILDRENS PL, DIV PED ALLERGY/IMMUNO/PULMO
SAINT LOUIS, MO 63110 - Phone
- (314) 454-2694
Quick Facts
- NPI
- 1356754451
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 13
- Publications
- 20
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