Back to Search
MARIA CARISSA PINEDA, M.D.
M.D.
Neurology Physician
NPI: 1346260130Individual
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
MD417593(PA)
Vascular Neurology Physician
Psychiatry & Neurology — Vascular Neurology
Code: 2084V0102X
MD417593(PA)
Research & Publications (20)
Miglustat in patients with Niemann-Pick disease Type C (NP-C): a multicenter observational retrospective cohort study.
PMID 19656703·Mol Genet Metab·2009
4-observational
External noise-induced phenomena in CO oxidation on single crystal surfaces.
PMID 19334869·J Chem Phys·2009
8-other
Vanishing white matter disease associated with progressive macrocephaly.
PMID 18504679·Neuropediatrics·2008
5-case
Non-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in the MSH2 gene.
PMID 18181177·Genes Chromosomes Cancer·2008
5-case
Idebenone treatment in paediatric and adult patients with Friedreich ataxia: long-term follow-up.
PMID 18234531·Eur J Paediatr Neurol·2008
8-other
Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion.
PMID 16365882·Ann Neurol·2006
5-case
The amino acid transporter asc-1 is not involved in cystinuria.
PMID 15458438·Kidney Int·2004
7-preclinical
Cystinuria-specific rBAT(R365W) mutation reveals two translocation pathways in the amino acid transporter rBAT-b0,+AT.
PMID 14561219·Biochem J·2004
7-preclinical
Peripheral neuropathy with ataxia in childhood as a result of the G8363A mutation in mitochondrial DNA.
PMID 15128915·Pediatr Res·2004
8-other
3-phosphoglycerate dehydrogenase deficiency in a patient with West syndrome.
PMID 11034457·Dev Med Child Neurol·2000
5-case
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.
PMID 19578037·J Med Genet·2010
8-other
Molecular analysis of the GNPTAB and GNPTG genes in 13 patients with mucolipidosis type II or type III - identification of eight novel mutations.
PMID 19659762·Clin Genet·2009
8-other
Nonsense-mediated mRNA decay process in nine alleles of Niemann-Pick type C patients from Spain.
PMID 19223215·Mol Genet Metab·2009
8-other
Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in Kazakhstan.
PMID 19138047·Radiat Res·2009
8-other
Brain injury in glutaric aciduria type I: the value of functional techniques in magnetic resonance imaging.
PMID 19167251·Eur J Paediatr Neurol·2009
8-other
Human papillomavirus type 16 variants in cervical intraepithelial neoplasia and invasive carcinoma in San Luis Potosí City, Mexico.
PMID 19216802·Infect Agent Cancer·2009
8-other
Adipose triglyceride lipase is implicated in fuel- and non-fuel-stimulated insulin secretion.
PMID 19389712·J Biol Chem·2009
7-preclinical
Mutations in the urocanase gene UROC1 are associated with urocanic aciduria.
PMID 19304569·J Med Genet·2009
5-case
Seizures versus dystonia in encephalopathic crisis of glutaric aciduria type I.
PMID 19433275·Pediatr Neurol·2009
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
- 909 WALNUT ST, 2ND FLOOR
PHILADELPHIA, PA 19107 - Phone
- (215) 955-1234
Quick Facts
- NPI
- 1346260130
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile