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ADAM WILL, MD
MD
Family Medicine Physician
NPI: 1821529025Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
35.134595(OH)
Research & Publications (20)
The mutation spectrum associated with type 3 von Willebrand disease in a cohort of patients from the north west of England.
PMID 19601990·Haemophilia·2009
8-other
Results of an intervention in an academic Internal Medicine Clinic to continue, step-down, or discontinue proton pump inhibitor therapy related to a tennessee medicaid formulary change.
PMID 19422274·J Manag Care Pharm·2009
8-other
A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3.
PMID 19372260·Blood·2009
8-other
Successful treatment of human metapneumovirus pneumonia using combination therapy with intravenous ribavirin and immune globulin.
PMID 19344395·Br J Haematol·2009
5-case
Complicated sternal dehiscence: reconstruction with plates, cables, and cannulated screws.
PMID 19324187·Ann Thorac Surg·2009
5-case
First successful aortic valve implantation with the CoreValve ReValving System via right subclavian artery access: a case report.
PMID 18948247·Heart Surg Forum·2008
5-case
Sternal reconstruction with titanium plates in complicated sternal dehiscence.
PMID 18455410·Eur J Cardiothorac Surg·2008
8-other
Platelet count has no influence on traumatic and bloody lumbar puncture in children undergoing intrathecal chemotherapy.
PMID 17156399·Br J Haematol·2007
8-other
First successful transapical aortic valve implantation with the Corevalve Revalving system: a case report.
PMID 18187382·Heart Surg Forum·2007
5-case
Partial median "I" sternotomy: minimally invasive alternate approach for aortic valve replacement.
PMID 17720441·Ann Thorac Surg·2007
8-other
Improved noninvasive assessment of coronary artery bypass grafts with 64-slice computed tomographic angiography in an unselected patient population.
PMID 17336717·J Am Coll Cardiol·2007
4-observational
Use of anterior tibial translation in the management of patellofemoral pain syndrome in older patients: a case series.
PMID 19066670·J Man Manip Ther·2007
8-other
Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption.
PMID 17243162·Genes Chromosomes Cancer·2007
8-other
Stent-grafting of the descending aorta: value of early postinterventional computed tomographic control.
PMID 17140933·J Thorac Cardiovasc Surg·2006
5-case
Acquired chemosensitivity after insect bite in a boy with leukaemia.
PMID 16846487·Br J Haematol·2006
5-case
No evidence of significant silencing of Fanconi genes FANCF and FANCB or Nijmegen breakage syndrome gene NBS1 by DNA hyper-methylation in sporadic childhood leukaemia.
PMID 16803569·Br J Haematol·2006
8-other
Spectrum and significance of variants and mutations in the Fanconi anaemia group G gene in children with sporadic acute myeloid leukaemia.
PMID 16643430·Br J Haematol·2006
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
- 100 BREWSTER BLVD
CAMP LEJEUNE, NC 28547 - Phone
- (910) 450-4357
Quick Facts
- NPI
- 1821529025
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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