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DORA COMAN, PHD
PHD
Clinical Psychologist
NPI: 1437633294Individual
Specialties, Licenses & Credentials
Clinical PsychologistPrimary
Psychologist — Clinical
Code: 103TC0700X
35SI00597000(NJ)
Research & Publications (20)
Brain temperature and pH measured by (1)H chemical shift imaging of a thulium agent.
PMID 19130468·NMR Biomed·2009
7-preclinical
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice.
PMID 19015223·J Med Genet·2009
8-other
Temperament as a predictor of symptomotology and adaptive functioning in adolescents with high-functioning autism.
PMID 19165586·J Autism Dev Disord·2009
8-other
Self-referenced memory, social cognition, and symptom presentation in autism.
PMID 19298471·J Child Psychol Psychiatry·2009
8-other
Prenatal cardiac ultrasound finding in congenital disorder of glycosylation type 1a.
PMID 19176971·Fetal Diagn Ther·2009
5-case
Enzyme replacement therapy for mucopolysaccharidoses: opinions of patients and families.
PMID 18410781·J Pediatr·2008
8-other
Primary skeletal dysplasia as a major manifesting feature in an infant with congenital disorder of glycosylation type Ia.
PMID 18203160·Am J Med Genet A·2008
5-case
Spondylocostal dysostosis in a pregnancy complicated by confined placental mosaicism for tetrasomy 9p.
PMID 18627039·Am J Med Genet A·2008
5-case
Diagnostic dilemma's: the congenital disorders of glycosylation are clinical chameleons.
PMID 18075505·Eur J Hum Genet·2008
8-other
Unrelated cord blood transplantation in a girl with Hoyeraal-Hreidarsson syndrome.
PMID 18560411·Bone Marrow Transplant·2008
5-case
The skeletal manifestations of the congenital disorders of glycosylation.
PMID 18462449·Clin Genet·2008
6-review
Two siblings with 46,XY DSD, congenital adrenal hypoplasia, aniridia, craniofacial, and skeletal abnormalities and intrauterine growth retardation: a new syndrome?
PMID 17702017·Am J Med Genet A·2007
5-case
Energetics of neuronal signaling and fMRI activity.
PMID 18079290·Proc Natl Acad Sci U S A·2007
7-preclinical
A novel splice site mutation in EYA4 causes DFNA10 hearing loss.
PMID 17568404·Am J Med Genet A·2007
8-other
Congenital disorder of glycosylation type 1a: three siblings with a mild neurological phenotype.
PMID 17451957·J Clin Neurosci·2007
8-other
Renal transplantation in a 14-year-old girl with vitamin B12-responsive cblA-type methylmalonic acidaemia.
PMID 16247646·Pediatr Nephrol·2006
5-case
Long-term follow-up of patients with idiopathic infantile hypercalcaemia.
PMID 16932902·Pediatr Nephrol·2006
8-other
Seizures, ataxia, developmental delay and the general paediatrician: glucose transporter 1 deficiency syndrome.
PMID 16712556·J Paediatr Child Health·2006
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
- 741 MOUNT LUCAS RD
PRINCETON, NJ 08540 - Phone
- (609) 613-4854
Quick Facts
- NPI
- 1437633294
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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