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IRINI SALAMA, PHARMD
PHARMD
Pharmacist
NPI: 1538539044Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
PH236279(MA)
Research & Publications (15)
Structure-selectivity investigations of D2-like receptor ligands by CoMFA and CoMSIA guiding the discovery of D3 selective PET radioligands.
PMID 17266201·J Med Chem·2007
7-preclinical
CoMFA and CoMSIA investigations of dopamine D3 receptor ligands leading to the prediction, synthesis, and evaluation of rigidized FAUC 365 analogues.
PMID 16750374·Bioorg Med Chem·2006
8-other
Utility of a voice-activated system in minimally invasive surgery.
PMID 16185114·J Laparoendosc Adv Surg Tech A·2005
8-other
Laparoscopic devascularization of the lower esophagus and upper stomach: experimental study in the pig.
PMID 12676025·J Laparoendosc Adv Surg Tech A·2003
7-preclinical
Genetic heterogeneity in two consanguineous families segregating early onset retinal degeneration: the pitfalls of homozygosity mapping.
PMID 19140180·Am J Med Genet A·2009
5-case
High prevalence of occult hepatitis B in hepatitis C-infected Egyptian children with haematological disorders and malignancies.
PMID 19192168·Liver Int·2009
8-other
Patients seeking liver transplant turn to China: outcomes of 15 Egyptian patients who went to China for a deceased-donor liver transplant.
PMID 18954296·Exp Clin Transplant·2008
8-other
18F-Labeled FAUC 346 and BP 897 derivatives as subtype-selective potential PET radioligands for the dopamine D3 receptor.
PMID 18306190·ChemMedChem·2008
8-other
Retrospective analysis of the causes of rejection of potential donors for living related liver transplantation.
PMID 19669338·Hepatol Int·2007
8-other
No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation.
PMID 15670773·Biochem Biophys Res Commun·2005
4-observational
Liver disease is a major cause of mortality following allogeneic bone-marrow transplantation.
PMID 15618844·Eur J Gastroenterol Hepatol·2004
8-other
The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy.
PMID 15147877·FEBS Lett·2004
7-preclinical
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy.
PMID 12847185·Neurology·2003
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
- 470 MEMORIAL DR, APT 302
CHICOPEE, MA 01020 - Phone
- (347) 368-9478
Quick Facts
- NPI
- 1538539044
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 15
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