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NEENA PHILIP, MD

MD

Internal Medicine Physician

NPI: 1346244365IndividualAccepts Medicare

Specialties, Licenses & Credentials

Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

20673(OK)

CMS Specialties

PrimaryINTERNAL MEDICINE

Education

OTHER

Class of 1986

Research & Publications (20)

Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum hypoplasia.
PMID 19635726·J Med Genet·2010
7-preclinical
Varenicline augmentation in depressed smokers: an 8-week, open-label study.
PMID 19323966·J Clin Psychiatry·2009
4-observational
LIS1-related isolated lissencephaly: spectrum of mutations and relationships with malformation severity.
PMID 19667223·Arch Neurol·2009
8-other
The clinical variability of the MECP2 duplication syndrome: description of two families with duplications excluding L1CAM and FLNA.
PMID 19018795·Clin Genet·2009
8-other
TCF4 deletions in Pitt-Hopkins Syndrome.
PMID 18781613·Hum Mutat·2008
8-other
The Case: Hypocalcemia, chronic renal failure and dysmorphism.
PMID 19008915·Kidney Int·2008
5-case
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations.
PMID 18728072·J Med Genet·2008
8-other
[Hypocalcemia and microdeletion 22q11.2].
PMID 18582701·Arch Pediatr·2008
8-other
Subjective and objective quality assessment in wireless teleultrasonography imaging.
PMID 19163925·Annu Int Conf IEEE Eng Med Biol Soc·2008
8-other
Augmentation of antidepressants with atypical antipsychotics: a review of the current literature.
PMID 18212601·J Psychiatr Pract·2008
6-review
Characterization of a UBC13 kinase in Plasmodium falciparum.
PMID 17452636·Proc Natl Acad Sci U S A·2007
7-preclinical
A cluster of translocation breakpoints in 2q37 is associated with overexpression of NPPC in patients with a similar overgrowth phenotype.
PMID 17676597·Hum Mutat·2007
5-case
ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophrenia.
PMID 17728672·Psychiatr Genet·2007
8-other
Molecular and in silico analyses of the full-length isoform of usherin identify new pathogenic alleles in Usher type II patients.
PMID 17405132·Hum Mutat·2007
8-other
A cross-layer approach for wireless medical video streaming in robotic teleultrasonography.
PMID 18002645·Annu Int Conf IEEE Eng Med Biol Soc·2007
8-other
Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
PMID 17135275·Hum Mol Genet·2007
8-other
Truncation of NHEJ1 in a patient with polymicrogyria.
PMID 17191205·Hum Mutat·2007
5-case
Feasibility of fetal cardiac magnetic resonance imaging: preliminary experience.
PMID 17201007·Ultrasound Obstet Gynecol·2007
8-other
Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndrome.
PMID 16813605·Clin Genet·2006
8-other
Altered blood pressure responses and normal cardiac phenotype in ACE2-null mice.
PMID 16878172·J Clin Invest·2006
7-preclinical

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
3433 NW 56TH ST, STE 800
OKLAHOMA CITY, OK 73112

Location

Practice Location

3433 NW 56TH ST, OKLAHOMA CITY, OK
(405) 946-9831

Quick Facts

NPI
1346244365
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
40
Publications
20

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