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KRISTEN HUCK, PHARMD

PHARMD

Pharmacist

NPI: 1861081390Individual

Specialties, Licenses & Credentials

PharmacistPrimary

Pharmacist

Code: 183500000X

03129314(OH)

Research & Publications (15)

Peripheral magnetic resonance angiography with continuous table movement in combination with high spatial and temporal resolution time-resolved MRA With a total single dose (0.1 mmol/kg) of gadobutrol at 3.0 T.
PMID 19652610·Invest Radiol·2009
8-other
Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation.
PMID 19425169·J Clin Invest·2009
5-case
Memory B cell function in HIV-infected children-decreased memory B cells despite ART.
PMID 19390488·Pediatr Res·2009
8-other
Memory B-cells in healthy and antibody-deficient children.
PMID 19162556·Clin Immunol·2009
8-other
Dual-energy CT angiography in peripheral arterial occlusive disease.
PMID 19130122·Cardiovasc Intervent Radiol·2009
4-observational
An immunodeficiency disease with RAG mutations and granulomas.
PMID 18463379·N Engl J Med·2008
5-case
Treatment of hemodynamic insufficiency in chronic CCA occlusion using a short saphenous vein interposition graft: diagnostic and technical considerations. An illustrative case report.
PMID 17912562·Neurosurg Rev·2008
5-case
Fanconi anaemia - response to Manoharan.
PMID 16925571·Br J Haematol·2006
8-other
Immune reconstitution inflammatory syndrome (IRIS) due to Bacille Calmette Guerin (BCG) in an HIV-positive child.
PMID 16857624·Scand J Infect Dis·2006
5-case
Three cases of renal relapse after allogeneic hematopoietic stem cell transplantation for childhood acute lymphoblastic leukemia.
PMID 16709515·Haematologica·2006
5-case
Delayed diagnosis and complications of Fanconi anaemia at advanced age--a paradigm.
PMID 16611311·Br J Haematol·2006
5-case
Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p.
PMID 12819251·J Am Soc Nephrol·2003
8-other
Refinement of the gene locus for autosomal dominant medullary cystic kidney disease type 1 (MCKD1) and construction of a physical and partial transcriptional map of the region.
PMID 11401443·Genomics·2001
8-other
Impact of a guideline-based disease management team on outcomes of hospitalized patients with congestive heart failure.
PMID 11176730·Arch Intern Med·2001
8-other
Evidence of further genetic heterogeneity in autosomal dominant medullary cystic kidney disease.
PMID 10831633·Nephrol Dial Transplant·2000
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
44519 MARIETTA RD
CALDWELL, OH 43724

Location

Practice Location

44519 MARIETTA RD, CALDWELL, OH
(740) 732-7201

Quick Facts

NPI
1861081390
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
15

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