Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Center Core Grants (P30)
Project #
5P30HD028202-02
Application #
2025310
Study Section
Mental Retardation Research Committee (HDMR)
Project Start
1995-08-31
Project End
2000-07-31
Budget Start
1996-08-01
Budget End
1997-07-31
Support Year
2
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of California Irvine
Department
Pediatrics
Type
Schools of Medicine
DUNS #
161202122
City
Irvine
State
CA
Country
United States
Zip Code
92697
Filipek, Pauline A; Juranek, Jenifer; Nguyen, Minh T et al. (2004) Relative carnitine deficiency in autism. J Autism Dev Disord 34:615-23
Wadhwa, P D; Sandman, C A; Garite, T J (2001) The neurobiology of stress in human pregnancy: implications for prematurity and development of the fetal central nervous system. Prog Brain Res 133:131-42
Sandman, C A; Hetrick, W; Talyor, D et al. (2000) Uncoupling of proopiomelanocortin (POMC) fragments is related to self-injury. Peptides 21:785-91
Swanson, J M; Flodman, P; Kennedy, J et al. (2000) Dopamine genes and ADHD. Neurosci Biobehav Rev 24:21-5
Sandman, C A; Hetrick, W; Taylor, D V et al. (2000) Long-term effects of naltrexone on self-injurious behavior. Am J Ment Retard 105:103-17
Filipek, P A; Accardo, P J; Ashwal, S et al. (2000) Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society. Neurology 55:468-79
Sandman, C A; Wadhwa, P D; Chicz-DeMet, A et al. (1999) Maternal corticotropin-releasing hormone and habituation in the human fetus. Dev Psychobiol 34:163-73
Filipek, P A; Accardo, P J; Baranek, G T et al. (1999) The screening and diagnosis of autistic spectrum disorders. J Autism Dev Disord 29:439-84
Filipek, P A (1999) Neuroimaging in the developmental disorders: the state of the science. J Child Psychol Psychiatry 40:113-28
Smith, M; Sperling, D (1999) Novel 23-base-pair duplication mutation in TSC1 exon 15 in an infant presenting with cardiac rhabdomyomas. Am J Med Genet 84:346-9

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