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ASHLEY CROSBY, MD
MD
Anatomic Pathology & Clinical Pathology Physician
NPI: 1932781671IndividualAccepts Medicare
Specialties, Licenses & Credentials
Anatomic Pathology & Clinical Pathology PhysicianPrimary
Pathology — Anatomic Pathology & Clinical Pathology
Code: 207ZP0102X
2023-03419(NC)
CMS Specialties
PrimaryPATHOLOGY
Education
UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL SCHOOL OF MEDICINE
Class of 2021
Research & Publications (20)
Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11.
PMID 15690106·J Hum Genet·2005
5-case
Lethal cystic kidney disease in Amish neonates associated with homozygous nonsense mutation of NPHP3.
PMID 19303681·Am J Kidney Dis·2009
4-observational
CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.
PMID 19439420·Brain·2009
4-observational
Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia.
PMID 19250384·Clin Genet·2009
5-case
Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair.
PMID 18957847·Cardiology·2009
5-case
Altered bone morphogenetic protein and transforming growth factor-beta signaling in rat models of pulmonary hypertension: potential for activin receptor-like kinase-5 inhibition in prevention and progression of disease.
PMID 19153267·Circulation·2009
7-preclinical
A mutation in NFkappaB interacting protein 1 causes cardiomyopathy and woolly haircoat syndrome of Poll Hereford cattle.
PMID 19016676·Anim Genet·2009
7-preclinical
Activin-like kinase 5 (ALK5) mediates abnormal proliferation of vascular smooth muscle cells from patients with familial pulmonary arterial hypertension and is involved in the progression of experimental pulmonary arterial hypertension induced by monocrotaline.
PMID 19116361·Am J Pathol·2009
7-preclinical
Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia.
PMID 18855023·Neurogenetics·2009
8-other
Regulation of growth differentiation factor 15 expression by intracellular iron.
PMID 19047680·Blood·2009
3-trial
The effectiveness of interventions to reduce psychological harm from traumatic events among children and adolescents: a systematic review.
PMID 18692745·Am J Prev Med·2008
1-meta
Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish.
PMID 18467358·Heart·2008
8-other
Patterns of abuse among unintentional pharmaceutical overdose fatalities.
PMID 19066381·JAMA·2008
8-other
Characteristics of perpetrators in homicide-followed-by-suicide incidents: National Violent Death Reporting System--17 US States, 2003-2005.
PMID 18794221·Am J Epidemiol·2008
8-other
Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms.
PMID 19007737·Lancet Neurol·2008
6-review
Refinement of the locus for distal hereditary motor neuronopathy VII (dHMN-VII) and exclusion of candidate genes.
PMID 18956029·Genome·2008
5-case
Photo-cross-linked PLA-PEO-PLA hydrogels from self-assembled physical networks: mechanical properties and influence of assumed constitutive relationships.
PMID 18817440·Biomacromolecules·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
- Address
- MEDICAL CENTER BOULEVARD
WINSTON SALEM, NC 27157 - Phone
- (336) 716-3770
Quick Facts
- NPI
- 1932781671
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 5
- Publications
- 20
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