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ANNIKA CROSBY, MD
MD
Internal Medicine Physician
NPI: 1831158294Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
37100(MN)
Research & Publications (20)
Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair.
PMID 18957847·Cardiology·2009
5-case
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
Regulation of growth differentiation factor 15 expression by intracellular iron.
PMID 19047680·Blood·2009
3-trial
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
Lethal cystic kidney disease in Amish neonates associated with homozygous nonsense mutation of NPHP3.
PMID 19303681·Am J Kidney Dis·2009
4-observational
Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia.
PMID 18855023·Neurogenetics·2009
8-other
CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.
PMID 19439420·Brain·2009
4-observational
A mutation in NFkappaB interacting protein 1 causes cardiomyopathy and woolly haircoat syndrome of Poll Hereford cattle.
PMID 19016676·Anim Genet·2009
7-preclinical
Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia.
PMID 19250384·Clin Genet·2009
5-case
Refinement of the locus for distal hereditary motor neuronopathy VII (dHMN-VII) and exclusion of candidate genes.
PMID 18956029·Genome·2008
5-case
Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration.
PMID 18252231·Am J Hum Genet·2008
4-observational
Patterns of abuse among unintentional pharmaceutical overdose fatalities.
PMID 19066381·JAMA·2008
8-other
Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish.
PMID 18467358·Heart·2008
8-other
A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.
PMID 18463364·Neurology·2008
8-other
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
Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms.
PMID 19007737·Lancet Neurol·2008
6-review
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
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 800 E 28TH ST, MAIL ROUTE 11326
MINNEAPOLIS, MN 55407 - Phone
- (612) 863-5576
Quick Facts
- NPI
- 1831158294
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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