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SALVATORE CALANDRA, MD
MD
Internal Medicine Physician
NPI: 1659307528IndividualAccepts Medicare
Specialties, Licenses & Credentials
Cardiovascular Disease Physician
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
164085(NY)
Geriatric Medicine (Internal Medicine) Physician
Internal Medicine — Geriatric Medicine
Code: 207RG0300X
164085(NY)
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
164085-1(NY)
Education
STATE UNIVERSITY OF NEW YORK AT BUFFALO SCHOOL OF MEDICINE
Class of 1985
Research & Publications (20)
A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region.
PMID 19393826·Clin Chim Acta·2009
8-other
The type of LDLR gene mutation predicts cardiovascular risk in children with familial hypercholesterolemia.
PMID 19446849·J Pediatr·2009
8-other
Severe HDL deficiency due to novel defects in the ABCA1 transporter.
PMID 19019193·J Intern Med·2009
8-other
Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia.
PMID 19084451·Mol Genet Metab·2009
7-preclinical
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a Caucasian kindred.
PMID 19200546·Atherosclerosis·2009
5-case
An apparent inconsistency in parent to offspring transmission of point mutations of LDLR gene in familial hypercholesterolemia.
PMID 19467224·Clin Chim Acta·2009
5-case
Cholesteryl Ester Storage Disease (CESD) due to novel mutations in the LIPA gene.
PMID 19307143·Mol Genet Metab·2009
8-other
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian patients: identification and structural modeling of novel mutations.
PMID 19252935·Neurogenetics·2009
8-other
Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations.
PMID 18492086·Clin Genet·2008
8-other
A novel mutation of the apolipoprotein A-I gene in a family with familial combined hyperlipidemia.
PMID 17950741·Atherosclerosis·2008
8-other
Hypertriglyceridaemia and low plasma HDL in a patient with apolipoprotein A-V deficiency due to a novel mutation in the APOA5 gene.
PMID 18324930·J Intern Med·2008
5-case
Genetics and molecular biology: proprotein convertase subtilisin/kexin type 9 and LDL receptor--an intriguing story.
PMID 18388699·Curr Opin Lipidol·2008
7-preclinical
Therapeutic management of a new case of LCAT deficiency with a multifactorial long-term approach based on high doses of angiotensin II receptor blockers (ARBs).
PMID 18397721·Clin Nephrol·2008
5-case
Molecular diagnosis of hypobetalipoproteinemia: an ENID review.
PMID 17570373·Atherosclerosis·2007
6-review
Rational approach to the treatment for heterozygous familial hypercholesterolemia in childhood and adolescence: a review.
PMID 17923804·J Endocrinol Invest·2007
6-review
Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients.
PMID 17140581·Atherosclerosis·2007
3-trial
Abnormal apolipoprotein B pre-mRNA splicing in patients with familial hypobetalipoproteinaemia.
PMID 17158591·J Med Genet·2007
7-preclinical
Molecular characterization of two patients with severe LCAT deficiency.
PMID 17526537·Nephrol Dial Transplant·2007
5-case
APOA5 and triglyceride metabolism, lesson from human APOA5 deficiency.
PMID 16531747·Curr Opin Lipidol·2006
6-review
A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemia.
PMID 16687148·Atherosclerosis·2006
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
- 50 LAKEFRONT BLVD STE 208
BUFFALO, NY 14202 - Phone
- (716) 893-1010
Quick Facts
- NPI
- 1659307528
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 41
- Publications
- 20
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