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RAUN MELMED, MD
MD
Developmental - Behavioral Pediatrics Physician
NPI: 1407876808Individual
Specialties, Licenses & Credentials
Developmental - Behavioral Pediatrics PhysicianPrimary
Pediatrics — Developmental - Behavioral Pediatrics
Code: 2080P0006X
13127(AZ)
Research & Publications (20)
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.
PMID 18607376·Mol Psychiatry·2010
8-other
Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression.
PMID 18317465·Mol Psychiatry·2009
8-other
Influence of adapted environment on the anxiety of medically treated children with developmental disability.
PMID 19232638·J Pediatr·2009
2-rct
A double-blind, placebo-controlled trial of oral human immunoglobulin for gastrointestinal dysfunction in children with autistic disorder.
PMID 19148734·J Autism Dev Disord·2009
2-rct
Long-term, open-label extension study of guanfacine extended release in children and adolescents with ADHD.
PMID 19179940·CNS Spectr·2008
3-trial
A randomized, double-blind, placebo-controlled, parallel-group study of methylphenidate transdermal system in pediatric patients with attention-deficit/hyperactivity disorder.
PMID 18312050·J Clin Psychiatry·2008
4-observational
A randomized, double-blind, placebo-controlled study of guanfacine extended release in children and adolescents with attention-deficit/hyperactivity disorder.
PMID 18166547·Pediatrics·2008
4-observational
Behavioural and physiological effect of dental environment sensory adaptation on children's dental anxiety.
PMID 18028056·Eur J Oral Sci·2007
2-rct
Clinical, morphological, and biochemical correlates of head circumference in autism.
PMID 17644070·Biol Psychiatry·2007
8-other
Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1.
PMID 17346350·BMC Med Genet·2007
8-other
HOXA1 gene variants influence head growth rates in humans.
PMID 17171652·Am J Med Genet B Neuropsychiatr Genet·2007
4-observational
Oral human immunoglobulin for children with autism and gastrointestinal dysfunction: a prospective, open-label study.
PMID 16845577·J Autism Dev Disord·2006
3-trial
A genetic variant that disrupts MET transcription is associated with autism.
PMID 17053076·Proc Natl Acad Sci U S A·2006
8-other
Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.
PMID 16027737·Mol Psychiatry·2005
8-other
Enhanced APOE2 transmission rates in families with autistic probands.
PMID 15167692·Psychiatr Genet·2004
8-other
Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism.
PMID 14960295·Biol Psychiatry·2004
4-observational
Volitional control of autonomic arousal: a functional magnetic resonance study.
PMID 12202079·Neuroimage·2002
8-other
Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children.
PMID 12192626·Mol Psychiatry·2002
8-other
No association between the 4g/5G polymorphism of the plasminogen activator inhibitor-1 gene promoter and autistic disorder.
PMID 11525425·Psychiatr Genet·2001
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 4848 E CACTUS RD STE 940
SCOTTSDALE, AZ 85254 - Phone
- (480) 443-0050
Quick Facts
- NPI
- 1407876808
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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