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SHADY FATTOUM, M.D
M.D
Internal Medicine Physician
NPI: 1538575915IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
270697(MA)
CMS Specialties
PrimaryHOSPITALIST
Education
OTHER
Class of 2007
Research & Publications (16)
An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET project.
PMID 19657830·Hemoglobin·2009
8-other
alpha-Thalassaemia in Tunisia: some epidemiological and molecular data.
PMID 19147907·J Genet·2008
8-other
[Clinical characteristics and outcome of cystic fibrosis: report of 16 cases].
PMID 19216450·Tunis Med·2008
8-other
Point: Sickle cell trait should be considered asymptomatic and as a benign condition during physical activity.
PMID 17395764·J Appl Physiol (1985)·2007
8-other
[Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].
PMID 17294892·Tunis Med·2006
4-observational
Detection of two rare beta-thalassemia alleles found in the Tunisian population: codon 47 (+A) and codons 106/107 (+G).
PMID 16987798·Hemoglobin·2006
8-other
Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia.
PMID 16798642·Hemoglobin·2006
8-other
A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia.
PMID 16352812·Blood·2006
3-trial
First description in Tunisia of a point mutation at codon 119 (CCT-->TCT) in the alpha1-globin gene: Hb Groene Hart in association with the -alpha3.7 deletion.
PMID 16370486·Hemoglobin·2005
5-case
[Prevalence and causal factors of anemia in children in Tunisia].
PMID 16383194·Tunis Med·2005
8-other
A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene (GAG-->TAG) in a Tunisian family.
PMID 15481894·Hemoglobin·2004
5-case
Molecular basis of beta-thalassemia in the population of Tunisia.
PMID 15481884·Hemoglobin·2004
8-other
HbHope/HbS and HbS/beta-thal double compound heterozygosity in a Mauritanian family: clinical and biochemical studies.
PMID 12764548·Ann Hematol·2003
5-case
Hemoglobin A2' (HbA2delta') in the Mauritanian population: first results of a preliminary survey.
PMID 12185509·Ann Hematol·2002
8-other
Epidemiological profile of hemoglobinopathies in the Mauritanian population.
PMID 12107561·Ann Hematol·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
Via practice · 2 locations total
- Address
- 1555 LONG POND RD
ROCHESTER, NY 14626 - Phone
- (585) 723-7769
Quick Facts
- NPI
- 1538575915
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 19
- Publications
- 16
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