Back to Search
EDDY CADET, M.D.
M.D.
Internal Medicine Physician
NPI: 1447302898IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
185893(NY)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
OTHER
Class of 1985
Research & Publications (18)
The management of acromioclavicular joint osteoarthrosis: débride, resect, or leave it alone.
PMID 16958441·Instr Course Lect·2006
6-review
First identification of a point mutation at position -83 (G>A) of the beta-globin gene promoter.
PMID 19657844·Hemoglobin·2009
5-case
An unusual case of hemochromatosis due to a new compound heterozygosity in HFE (p.[Gly43Asp;His63Asp]+[Cys282Tyr]): structural implications with respect to binding with transferrin receptor 1.
PMID 18157833·Hum Mutat·2008
5-case
A novel beta-Thalassemic allele due to a two nucleotide deletion: beta76 (-GC).
PMID 17365003·Hemoglobin·2007
5-case
Juvenile hemochromatosis caused by a novel combination of hemojuvelin G320V/R176C mutations in a 5-year old girl.
PMID 17339196·Haematologica·2007
5-case
A survey of sports medicine specialists investigating the preferred management of contaminated anterior cruciate ligament grafts.
PMID 16325086·Arthroscopy·2005
8-other
Tendon-to-bone pressure distributions at a repaired rotator cuff footprint using transosseous suture and suture anchor fixation techniques.
PMID 16000662·Am J Sports Med·2005
4-observational
Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?
PMID 15863667·J Med Genet·2005
8-other
Recent advances in understanding haemochromatosis: a transition state.
PMID 15466004·J Med Genet·2004
6-review
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.
PMID 14729817·J Med Genet·2004
4-observational
Mechanisms responsible for longitudinal growth of the cortex: coalescence of trabecular bone into cortical bone.
PMID 12954833·J Bone Joint Surg Am·2003
7-preclinical
Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
PMID 12915468·Hum Mol Genet·2003
8-other
Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload.
PMID 12873829·J Hepatol·2003
5-case
A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis.
PMID 12542563·J Intern Med·2003
8-other
Hyperhomocysteinaemia, folate and vitamin B12 in unsupplemented haemodialysis patients: effect of oral therapy with folic acid and vitamin B12.
PMID 11865092·Nephrol Dial Transplant·2002
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
- 175 NAGLE AVE
NEW YORK, NY 10034 - Phone
- (212) 544-2001
Quick Facts
- NPI
- 1447302898
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 41
- Publications
- 18
Are you this provider?
Claim Your Profile