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MARLENE MANCUSO, M.D.
M.D.
Surgery Physician
NPI: 1952561540IndividualAccepts Medicare
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
244998(NY)
CMS Specialties
PrimarySURGICAL ONCOLOGY
Education
ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
Class of 2001
Research & Publications (20)
Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation.
PMID 15607216·J Neurol Sci·2005
8-other
New DGK gene mutations in the hepatocerebral form of mitochondrial DNA depletion syndrome.
PMID 15883261·Arch Neurol·2005
8-other
POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness.
PMID 14745080·Neurology·2004
5-case
A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism.
PMID 15534189·Arch Neurol·2004
5-case
Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene.
PMID 12686403·J Neurol Sci·2003
5-case
Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.
PMID 12873860·Arch Neurol·2003
5-case
Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genes.
PMID 14568816·Arch Neurol·2003
5-case
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA.
PMID 12391347·Neurology·2002
5-case
No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort.
PMID 19632744·Neurobiol Aging·2011
8-other
Lack of association between the APEX1 Asp148Glu polymorphism and sporadic amyotrophic lateral sclerosis.
PMID 18482781·Neurobiol Aging·2010
8-other
Does sphenopalatine endoscopic ganglion block have an effect in paroxysmal hemicrania? A case report.
PMID 19438918·Cephalalgia·2010
5-case
G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype.
PMID 19488901·Amyotroph Lateral Scler·2010
8-other
Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature.
PMID 19597763·Neurol Sci·2009
5-case
Neuroprotective effects of tetracyclines: molecular targets, animal models and human disease.
PMID 19601819·CNS Neurol Disord Drug Targets·2009
6-review
A new syndrome with Stargardt macular degeneration, abnormalities of the corpus callosum, mental retardation, and dysmorphic features: a case report of two siblings.
PMID 19451813·Clin Dysmorphol·2009
5-case
Cellular source and amount of vascular endothelial growth factor and platelet-derived growth factor in tumors determine response to angiogenesis inhibitors.
PMID 19401451·Cancer Res·2009
7-preclinical
Activity of tyrosine kinase inhibitor Dasatinib in neuroblastoma cells in vitro and in orthotopic mouse model.
PMID 19623650·Int J Cancer·2009
7-preclinical
Effectiveness of an HbA1c tracking tool on primary care management of diabetes mellitus: glycaemic control, clinical practice and usability.
PMID 19490772·Inform Prim Care·2009
8-other
Development of a multiplex PCR assay for Photobacterium damselae subsp. piscicida identification in fish samples.
PMID 19500208·J Fish Dis·2009
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
- 1155 NORTHERN BLVD
MANHASSET, NY 11030 - Phone
- (516) 222-2022
Quick Facts
- NPI
- 1952561540
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 25
- Publications
- 20
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