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ANGELICA SAADA, M.D.
M.D.
Internal Medicine Physician
NPI: 1205369584Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
304922(NY)
Research & Publications (20)
Exocrine pancreatic insufficiency, dyserythropoeitic anemia, and calvarial hyperostosis are caused by a mutation in the COX4I2 gene.
PMID 19268275·Am J Hum Genet·2009
8-other
Nonylphenol ethoxylate plastic additives inhibit mitochondrial respiratory chain complex I.
PMID 19617286·Clin Chem·2009
8-other
Antibiotic effects on mitochondrial translation and in patients with mitochondrial translational defects.
PMID 19671450·Mitochondrion·2009
8-other
Mice deficient in ribosomal protein S6 phosphorylation suffer from muscle weakness that reflects a growth defect and energy deficit.
PMID 19479038·PLoS One·2009
7-preclinical
Mutated NDUFS6 is the cause of fatal neonatal lactic acidemia in Caucasus Jews.
PMID 19259137·Eur J Hum Genet·2009
5-case
Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease.
PMID 19463981·Am J Hum Genet·2009
5-case
NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvement.
PMID 19364667·Mol Genet Metab·2009
5-case
Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ.
PMID 18439546·Am J Hum Genet·2008
8-other
Cardiac-targeted transgenic mutant mitochondrial enzymes: mtDNA defects, antiretroviral toxicity and cardiomyopathy.
PMID 18446447·Cardiovasc Toxicol·2008
7-preclinical
The effect of mutated mitochondrial ribosomal proteins S16 and S22 on the assembly of the small and large ribosomal subunits in human mitochondria.
PMID 18539099·Mitochondrion·2008
8-other
Mitochondrial deoxyribonucleotide pools in deoxyguanosine kinase deficiency.
PMID 18723380·Mol Genet Metab·2008
8-other
FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency.
PMID 18771761·Am J Hum Genet·2008
7-preclinical
Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia.
PMID 19068277·Am J Hum Genet·2008
8-other
TAT-mediated delivery of LAD restores pyruvate dehydrogenase complex activity in the mitochondria of patients with LAD deficiency.
PMID 18362926·Mol Ther·2008
8-other
Mitochondrial complex I deficiency caused by a deleterious NDUFA11 mutation.
PMID 18306244·Ann Neurol·2008
5-case
The unique neuroradiology of complex I deficiency due to NDUFA12L defect.
PMID 18180188·Mol Genet Metab·2008
5-case
Mutations in LPIN1 cause recurrent acute myoglobinuria in childhood.
PMID 18817903·Am J Hum Genet·2008
5-case
Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia.
PMID 17847012·Am J Hum Genet·2007
5-case
Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation.
PMID 17873122·J Med Genet·2007
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
- 462 FIRST AVENUE, AMBULATORY CARE BUILDING - 2D
NEW YORK, NY 10016 - Phone
- (212) 562-5555
Quick Facts
- NPI
- 1205369584
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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