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SAMANTHA SENECA, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1871237891Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Clinical and biochemical spectrum of mitochondrial complex III deficiency caused by mutations in the BCS1L gene.
PMID 19508421·Clin Genet·2009
5-case
Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects.
PMID 19181635·J Clin Pathol·2009
8-other
Preimplantation genetic diagnosis for myotonic dystrophy type 1: upon request to child.
PMID 19367318·Eur J Hum Genet·2009
8-other
Pathogenic mutations in the 5' untranslated region of BCS1L mRNA in mitochondrial complex III deficiency.
PMID 19389488·Mitochondrion·2009
5-case
Unusual findings in Leigh syndrome caused by T8993C mutation.
PMID 19046652·Eur J Paediatr Neurol·2009
8-other
Mitochondrial mosaics in the liver of 3 infants with mtDNA defects.
PMID 19500334·BMC Clin Pathol·2009
8-other
Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency.
PMID 18221507·BMC Genomics·2008
4-observational
Real and expected delivery rates of patients with myotonic dystrophy undergoing intracytoplasmic sperm injection and preimplantation genetic diagnosis.
PMID 18408243·Hum Reprod·2008
8-other
Further pitfalls in the diagnosis of mtDNA mutations: homoplasmic mt-tRNA mutations.
PMID 18178636·J Med Genet·2008
8-other
Experience and outcome of 3 years of a European EQA scheme for genetic testing of the spinocerebellar ataxias.
PMID 18301445·Eur J Hum Genet·2008
8-other
CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutation.
PMID 18577525·Mol Hum Reprod·2008
8-other
A single mutation in the GALC gene is responsible for the majority of late onset Krabbe disease patients in the Catania (Sicily, Italy) region.
PMID 17579360·Hum Mutat·2007
8-other
A new family with the mitochondrial tRNAGLU gene mutation m.14709T>C presenting with hydrops fetalis.
PMID 17161635·Eur J Paediatr Neurol·2007
5-case
Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy.
PMID 17846276·Arch Neurol·2007
5-case
The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disorders.
PMID 18072335·Acta Neurol Belg·2007
8-other
Linezolid-induced inhibition of mitochondrial protein synthesis.
PMID 16575728·Clin Infect Dis·2006
5-case
Mitochondrial dysfunction in Brooks-Wisniewski-Brown syndrome.
PMID 16477654·Am J Med Genet A·2006
5-case
A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failure.
PMID 16908752·Arch Neurol·2006
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 550 1ST AVE
NEW YORK, NY 10016 - Phone
- (212) 263-5506
Quick Facts
- NPI
- 1871237891
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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