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ANTHONY ORRICO, DMD
DMD
General Practice Dentistry
NPI: 1649348855Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
22DI015678010(NJ)
Research & Publications (20)
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies.
PMID 19522081·Clin Genet·2009
8-other
Novel PTEN mutations in neurodevelopmental disorders and macrocephaly.
PMID 18759867·Clin Genet·2009
8-other
Late-onset Lennox-Gastaut syndrome in a patient with 15q11.2-q13.1 duplication.
PMID 19396834·Am J Med Genet A·2009
5-case
Muscle biopsy and in vitro contracture test in subjects with idiopathic HyperCKemia.
PMID 18813041·Anesthesiology·2008
8-other
A truncation in the RYR1 gene associated with central core lesions in skeletal muscle fibres.
PMID 17293538·J Med Genet·2007
5-case
Inheritance of a novel RYR1 mutation in a family with myotonic dystrophy type 1.
PMID 17204054·Clin Genet·2007
5-case
Unusually severe expression of craniofacial features in Aarskog-Scott syndrome due to a novel truncating mutation of the FGD1 gene.
PMID 17152066·Am J Med Genet A·2007
5-case
Unilateral focal polymicrogyria in a patient with classical Aarskog-Scott syndrome due to a novel missense mutation in an evolutionary conserved RhoGEF domain of the faciogenital dysplasia gene FGD1.
PMID 17847065·Am J Med Genet A·2007
5-case
Haploinsufficiency of TCF4 causes syndromal mental retardation with intermittent hyperventilation (Pitt-Hopkins syndrome).
PMID 17436255·Am J Hum Genet·2007
5-case
SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy.
PMID 16505326·Neurology·2006
5-case
Frequency and localization of mutations in the 106 exons of the RYR1 gene in 50 individuals with malignant hyperthermia.
PMID 16835904·Hum Mutat·2006
8-other
Cortical damage in brains of patients with adult-form of myotonic dystrophy type 1 and no or minimal MRI abnormalities.
PMID 16786209·J Neurol·2006
8-other
Resequencing the G6PT1 gene reveals a novel splicing mutation in a patient with glycogen storage disease type 1b.
PMID 16716283·Clin Chim Acta·2006
8-other
Classification and risk stratification of invasive breast carcinomas using a real-time quantitative RT-PCR assay.
PMID 16626501·Breast Cancer Res·2006
4-observational
Spastic paraparesis, cerebellar ataxia, and intention tremor: a severe variant of FXTAS?
PMID 15689437·J Med Genet·2005
5-case
Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q).
PMID 15809997·Am J Med Genet A·2005
5-case
Autonomic dysfunction in mental retardation and spastic paraparesis with MECP2 mutation.
PMID 15704871·J Child Neurol·2004
8-other
Phenotypic and molecular characterisation of the Aarskog-Scott syndrome: a survey of the clinical variability in light of FGD1 mutation analysis in 46 patients.
PMID 14560308·Eur J Hum Genet·2004
5-case
Retinochoroidal atrophy in two adult patients with Angelman syndrome.
PMID 12955768·Am J Med Genet A·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
- 532 SUMMIT AVENUE
JERSEY CITY, NJ 07306 - Phone
- (201) 653-2288
Quick Facts
- NPI
- 1649348855
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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