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COLLEEN CURRY, CD (DONA)
CD (DONA)
Doula
NPI: 1649508086Individual
Specialties, Licenses & Credentials
DoulaPrimary
Doula
Code: 374J00000X
6069(IL)
Research & Publications (20)
Notch inhibition in Kaposi's sarcoma tumor cells leads to mitotic catastrophe through nuclear factor-kappaB signaling.
PMID 17604336·Mol Cancer Ther·2007
8-other
Notch-independent regulation of Hes-1 expression by c-Jun N-terminal kinase signaling in human endothelial cells.
PMID 16732296·Lab Invest·2006
8-other
Gamma secretase inhibitor blocks Notch activation and induces apoptosis in Kaposi's sarcoma tumor cells.
PMID 15940249·Oncogene·2005
8-other
Rational evaluation of the adolescent with mental retardation.
PMID 11986040·Adolesc Med·2002
6-review
Elements of morphology: standard terminology for the lips, mouth, and oral region.
PMID 19125428·Am J Med Genet A·2009
8-other
Prognostic impact of C-REL expression in diffuse large B-cell lymphoma.
PMID 19669219·J Hematop·2009
8-other
Home care safety perspectives from clients, family members, caregivers and paid providers.
PMID 19667785·Healthc Q·2009
8-other
Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.
PMID 18536050·Am J Med Genet A·2008
8-other
Prospectively gated transverse coronary CT angiography versus retrospectively gated helical technique: improved image quality and reduced radiation dose.
PMID 18195386·Radiology·2008
4-observational
A perspective on developing emergency medicine as a specialty.
PMID 19384509·Int J Emerg Med·2008
8-other
Chondrodysplasia punctata associated with maternal autoimmune diseases: expanding the spectrum from systemic lupus erythematosus (SLE) to mixed connective tissue disease (MCTD) and scleroderma report of eight cases.
PMID 19006208·Am J Med Genet A·2008
5-case
Homozygous deletions of a copy number change detected by array CGH: a new cause for mental retardation?
PMID 18627067·Am J Med Genet A·2008
5-case
Clear cell sarcoma of soft tissue: diagnostic utility of fluorescence in situ hybridization and reverse transcriptase polymerase chain reaction.
PMID 18333903·J Cutan Pathol·2008
5-case
Mutations in the pericentrin (PCNT) gene cause primordial dwarfism.
PMID 18174396·Science·2008
8-other
Comparison of a low carbohydrate and low fat diet for weight maintenance in overweight or obese adults enrolled in a clinical weight management program.
PMID 17976244·Nutr J·2007
8-other
Diaphanospondylodysostosis: six new cases and exclusion of the candidate genes, PAX1 and MEOX1.
PMID 17764081·Am J Med Genet A·2007
5-case
Risk factors for perinatal arterial stroke: a study of 60 mother-child pairs.
PMID 17675024·Pediatr Neurol·2007
8-other
Effects of ACE inhibitors or beta-blockers in patients treated with the fixed-dose combination of isosorbide dinitrate/hydralazine in the African-American Heart Failure Trial.
PMID 18041162·Am J Cardiovasc Drugs·2007
3-trial
Role of host tissues for sustained humoral effects after endothelial progenitor cell transplantation into the ischemic heart.
PMID 18070934·J Exp Med·2007
7-preclinical
Homozygous myotonic dystrophy: clinical findings in two patients and review of the literature.
PMID 17663477·Am J Med Genet A·2007
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1613 CIMARRON DR
NEW LENOX, IL 60451 - Phone
- (708) 351-0935
Quick Facts
- NPI
- 1649508086
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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