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CARMELA FRIDMAN, D.O
D.O
Psychiatry Physician
NPI: 1548541881IndividualAccepts Medicare
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
264464(NY)
CMS Specialties
PrimaryPSYCHIATRY
Education
NEW YORK COLLEGE OF OSTEO MEDICINE OF NEW YORK INSTITUTE OF TECHNOLOGY
Class of 2008
Research & Publications (15)
WITHDRAWN: Association between polymorphisms in genes of inflammatory response and axonal repair with spinal cord injury.
PMID 17893696·Spinal Cord·2007
8-other
Inv dup (15): is the electroclinical phenotype helpful for this challenging clinical diagnosis?
PMID 16495142·Clin Neurophysiol·2006
5-case
Epilepsy in patients with angelman syndrome caused by deletion of the chromosome 15q11-13.
PMID 16401744·Arch Neurol·2006
3-trial
Angelman syndrome: uniparental paternal disomy 15 determines mild epilepsy, but has no influence on EEG patterns.
PMID 16226874·Epilepsy Res·2005
8-other
Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene.
PMID 12749060·Am J Med Genet A·2003
5-case
Angelman syndrome: difficulties in EEG pattern recognition and possible misinterpretations.
PMID 12887436·Epilepsia·2003
8-other
Association of a new polymorphism in ALOX12 gene with bipolar disorder.
PMID 12664313·Eur Arch Psychiatry Clin Neurosci·2003
4-observational
Identification and characterisation of a group of cervical carcinoma patients with profound downregulation of intratumoral Type 1 (IFNgamma) and Type 2 (IL-4) cytokine mRNA expression.
PMID 12628838·Eur J Cancer·2003
8-other
Molecular and cytogenetic analyses on Brazilian youths with pervasive developmental disorders.
PMID 11916331·J Autism Dev Disord·2002
8-other
Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome.
PMID 10995513·Am J Med Genet·2000
8-other
Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patients.
PMID 10861661·Am J Med Genet·2000
8-other
A further Angelman syndrome patient with UPD15 due to paternal meiosis II nondisjunction.
PMID 10733242·Clin Genet·2000
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
- 2020 CONEY ISLAND AVE
BROOKLYN, NY 11223 - Phone
- (718) 676-4210
Quick Facts
- NPI
- 1548541881
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 18
- Publications
- 15
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