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MARK MANCUSO, MD
MD
Anesthesiology Physician
NPI: 1467441899IndividualAccepts Medicare
Education
STATE UNIVERSITY OF NEW YORK AT BUFFALO SCHOOL OF MEDICINE
Class of 1991
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1555 LONG POND RD
ROCHESTER, NY 14626 - Phone
- (585) 255-8966
Quick Facts
- NPI
- 1467441899
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 35
- Publications
- 20
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