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DANIEL CAMPAGNA, MD
MD
Emergency Medicine Physician
NPI: 1437262557IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
036100598(IL)
CMS Specialties
PrimaryEMERGENCY MEDICINE
Education
UNIVERSITY OF ILLINOIS COLLEGE OF MED (CHI/PEOR/ROCK/CHM-URB)
Class of 1997
Research & Publications (20)
Poststreptococcal glomerulonephritis presenting as impending airway obstruction.
PMID 11574804·Ann Emerg Med·2001
5-case
Negative relationships between erythrocyte Ca-pump activity and lead levels in mothers and newborns.
PMID 11191638·Life Sci·2000
8-other
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia.
PMID 19412178·Nat Genet·2009
7-preclinical
Identification of a Steap3 endosomal targeting motif essential for normal iron metabolism.
PMID 18955558·Blood·2009
7-preclinical
Gene expression profiles associated with advanced pancreatic cancer.
PMID 18784821·Int J Clin Exp Pathol·2008
8-other
hem6: an ENU-induced recessive hypochromic microcytic anemia mutation in the mouse.
PMID 18780836·Blood·2008
7-preclinical
Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA).
PMID 18408718·Nat Genet·2008
8-other
PABS: an online platform to assist BAC-by-BAC sequencing projects.
PMID 18254380·Biotechniques·2008
8-other
Primary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1.
PMID 18039845·Mol Cell Biol·2008
7-preclinical
Mutations in the serum/glucocorticoid regulated kinase 3 (Sgk3) are responsible for the mouse fuzzy (fz) hair phenotype.
PMID 17914447·J Invest Dermatol·2008
7-preclinical
Evaluation of GATA-4 and GATA-5 methylation profiles in human pancreatic cancers indicate promoter methylation patterns distinct from other human tumor types.
PMID 17912029·Cancer Biol Ther·2007
4-observational
Genetic variation in Mon1a affects protein trafficking and modifies macrophage iron loading in mice.
PMID 17632513·Nat Genet·2007
7-preclinical
Abcb7, the gene responsible for X-linked sideroblastic anemia with ataxia, is essential for hematopoiesis.
PMID 17192398·Blood·2007
7-preclinical
Loss of the acyl-CoA binding protein (Acbp) results in fatty acid metabolism abnormalities in mouse hair and skin.
PMID 16902415·J Invest Dermatol·2007
7-preclinical
The mitochondrial ATP-binding cassette transporter Abcb7 is essential in mice and participates in cytosolic iron-sulfur cluster biogenesis.
PMID 16467350·Hum Mol Genet·2006
7-preclinical
Identification of a ferrireductase required for efficient transferrin-dependent iron uptake in erythroid cells.
PMID 16227996·Nat Genet·2005
7-preclinical
nm1054: a spontaneous, recessive, hypochromic, microcytic anemia mutation in the mouse.
PMID 15994289·Blood·2005
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 4201 W MEDICAL CENTER DR
MCHENRY, IL 60050 - Phone
- (815) 759-3100
Quick Facts
- NPI
- 1437262557
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 29
- Publications
- 20
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