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RICHARD BORGATTI, MD
MD
Orthopaedic Surgery Physician
NPI: 1871589952Individual
Specialties, Licenses & Credentials
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
MAO52680(NJ)
Research & Publications (20)
Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
PMID 18413471·Arch Neurol·2008
8-other
Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotype.
PMID 18648397·Eur J Hum Genet·2008
5-case
Academic performance in children with rolandic epilepsy.
PMID 18294216·Dev Med Child Neurol·2008
4-observational
Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis.
PMID 18178631·J Med Genet·2008
5-case
Disorders of cognitive and affective development in cerebellar malformations.
PMID 17872929·Brain·2007
8-other
Language and social communication in children with cerebellar dysgenesis.
PMID 17627129·Folia Phoniatr Logop·2007
6-review
Indicators of theory of mind in narrative production: a comparison between individuals with genetic syndromes and typically developing children.
PMID 17364616·Clin Linguist Phon·2007
8-other
Agenesis of the corpus callosum: clinical and genetic study in 63 young patients.
PMID 16504787·Pediatr Neurol·2006
8-other
Changes in the optic disc excavation of children affected by cerebral visual impairment: a tomographic analysis.
PMID 16431940·Invest Ophthalmol Vis Sci·2006
8-other
Is everybody always my friend? Perception of approachability in Williams syndrome.
PMID 16005478·Neuropsychologia·2006
2-rct
A 2.3 Mb duplication of chromosome 8q24.3 associated with severe mental retardation and epilepsy detected by standard karyotype.
PMID 15657611·Eur J Hum Genet·2005
5-case
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC).
PMID 16235065·Neurogenetics·2005
7-preclinical
Long-term neuropsychological deficits after cerebellar infarctions in two young adult twins.
PMID 14728925·Neuropsychologia·2004
5-case
Study of attentional processes in children with idiopathic epilepsy by Conners' Continuous Performance Test.
PMID 15526955·J Child Neurol·2004
8-other
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation.
PMID 15249611·Neurology·2004
5-case
Retrospective diagnosis of congenital cytomegalovirus infection and cortical maldevelopment.
PMID 12963772·Neurology·2003
8-other
Distal trisomy 6p and 20q owing to the concurrent transposition of distal 6p and 20q to the 22q telomere: a genomic polymorphism?
PMID 12920086·J Med Genet·2003
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
- 1430 HOOPER AVE, SUITE 202
TOMS RIVER, NJ 08753 - Phone
- (732) 244-4544
Quick Facts
- NPI
- 1871589952
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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