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PETER B CRINO MD
MD
Neurology Physician
NPI: 1982638656IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
MD047970L(PA)
Education
YALE UNIVERSITY SCHOOL OF MEDICINE
Class of 1990
Research & Publications (20)
Focal brain malformations: a spectrum of disorders along the mTOR cascade.
PMID 18494264·Novartis Found Symp·2007
6-review
Gene expression, genetics, and genomics in epilepsy: some answers, more questions.
PMID 17571352·Epilepsia·2007
6-review
Gene profiling in temporal lobe epilepsy tissue and dysplastic lesions.
PMID 17054681·Epilepsia·2006
6-review
Molecular pathogenesis of focal cortical dysplasia and hemimegalencephaly.
PMID 15921235·J Child Neurol·2005
8-other
Malformations of cortical development: molecular pathogenesis and experimental strategies.
PMID 15250594·Adv Exp Med Biol·2004
6-review
Molecular pathogenesis of tuber formation in tuberous sclerosis complex.
PMID 15563019·J Child Neurol·2004
6-review
Increased expression of the neuronal glutamate transporter (EAAT3/EAAC1) in hippocampal and neocortical epilepsy.
PMID 11906504·Epilepsia·2002
7-preclinical
Gene expression analysis as a strategy to understand the molecular pathogenesis of infantile spasms.
PMID 12040902·Int Rev Neurobiol·2002
6-review
Neurodevelopmental disorders as a cause of seizures: neuropathologic, genetic, and mechanistic considerations.
PMID 11958376·Brain Pathol·2002
6-review
Differential expression of glutamate and GABA-A receptor subunit mRNA in cortical dysplasia.
PMID 11294928·Neurology·2001
8-other
Inflammatory processes in cortical tubers and subependymal giant cell tumors of tuberous sclerosis complex.
PMID 18023148·Epilepsy Res·2008
8-other
Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex.
PMID 18410267·Neuropathology·2008
5-case
Rapamycin and tuberous sclerosis complex: from Easter Island to epilepsy.
PMID 18360828·Ann Neurol·2008
7-preclinical
A neuropathological study of two autopsy cases of syndromic hemimegalencephaly.
PMID 17617874·Neuropathol Appl Neurobiol·2007
5-case
Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5.
PMID 17522105·Brain·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
- 3400 SPRUCE STREET, 2 RAVDIN
PHILADELPHIA, PA 19104 - Phone
- (215) 662-3606
Quick Facts
- NPI
- 1982638656
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 36
- Publications
- 20
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