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Results: 1-14 |
Results: 14
Genomic organization of the SLC1A1/EAAC1 gene and mutation screening in early-onset obsessive-compulsive disorder
Authors: Veenstra-VanderWeele, J Kim, SJ Gonen, D Hanna, GL Leventhal, BL Cook, EH
Citation: J. Veenstra-vanderweele et al., Genomic organization of the SLC1A1/EAAC1 gene and mutation screening in early-onset obsessive-compulsive disorder, MOL PSYCHI, 6(2), 2001, pp. 160-167
Double-blind, placebo-controlled study of amantadine hydrochloride in the treatment of children with autistic disorder
Authors: King, BH Wright, DM Handen, BL Sikich, I Zimmerman, AW McMahon, W Cantwell, E Davanzo, PA Dourish, CT Dykens, EM Hooper, SR Jaselskis, CA Leventhal, BL Levitt, J Lord, C Lubetsky, MJ Myers, SM Ozonoff, S Shah, BG Snape, M Shernoff, EW Williamson, K Cook, EH
Citation: Bh. King et al., Double-blind, placebo-controlled study of amantadine hydrochloride in the treatment of children with autistic disorder, J AM A CHIL, 40(6), 2001, pp. 658-665
Multisite, double-blind, placebo-controlled trial of porcine secretin in autism
Authors: Owley, T McMahon, W Cook, EH Laulhere, T South, M Mays, LZ Shernoff, ES Lainhart, J Modahl, CB Corsello, C Ozonoff, S Risi, S Lord, C Leventhal, BL Filipek, PA
Citation: T. Owley et al., Multisite, double-blind, placebo-controlled trial of porcine secretin in autism, J AM A CHIL, 40(11), 2001, pp. 1293-1299
Quantifying the phenotype in autism spectrum disorders
Authors: Lord, C Leventhal, BL Cook, EH
Citation: C. Lord et al., Quantifying the phenotype in autism spectrum disorders, AM J MED G, 105(1), 2001, pp. 36-38
Maternal age at first birth and boys' risk for conduct disorder
Authors: Wakschlag, LS Gordon, RA Lahey, BB Loeber, R Green, SM Leventhal, BL
Citation: Ls. Wakschlag et al., Maternal age at first birth and boys' risk for conduct disorder, J RES ADOLE, 10(4), 2000, pp. 417-441
Autism spectrum disorders
Authors: Lord, C Cook, EH Leventhal, BL Amaral, DG
Citation: C. Lord et al., Autism spectrum disorders, NEURON, 28(2), 2000, pp. 355-363
Deletion polymorphism in the coding region of the human NESP55 alternativetranscript of GNAS1
Authors: Kim, SJ Gonen, D Hanna, GL Leventhal, BL Cook, EH
Citation: Sj. Kim et al., Deletion polymorphism in the coding region of the human NESP55 alternativetranscript of GNAS1, MOL CELL PR, 14(3), 2000, pp. 191-194
Mutation screening of human 5-HT2B receptor gene in early-onset obsessive-compulsive disorder
Authors: Kim, SJ Veenstra-VanderWeele, J Hanna, GL Gonen, D Leventhal, BL Cook, EH
Citation: Sj. Kim et al., Mutation screening of human 5-HT2B receptor gene in early-onset obsessive-compulsive disorder, MOL CELL PR, 14(1), 2000, pp. 47-52
The association between maternal cigarette smoking and psychiatric diseases or criminal outcome in the offspring
Authors: Wakschlag, LS Pickett, KE Leventhal, BL
Citation: Ls. Wakschlag et al., The association between maternal cigarette smoking and psychiatric diseases or criminal outcome in the offspring, REPROD TOX, 14(6), 2000, pp. 579-579
The Autism Diagnostic Observation Schedule-Generic: A standard measure of social and communication deficits associated with the spectrum of autism
Authors: Lord, C Risi, S Lambrecht, L Cook, EH Leventhal, BL DiLavore, PC Pickles, A Rutter, M
Citation: C. Lord et al., The Autism Diagnostic Observation Schedule-Generic: A standard measure of social and communication deficits associated with the spectrum of autism, J AUTISM D, 30(3), 2000, pp. 205-223
High throughput fluorescent CE-SSCP SNP genotyping
Authors: Gonen, D Veenstra-VanderWeele, J Yang, Z Leventhal, BL Cook, EH
Citation: D. Gonen et al., High throughput fluorescent CE-SSCP SNP genotyping, MOL PSYCHI, 4(4), 1999, pp. 339-343
Mutation screening of the UBE3A/E6-AP gene in autistic disorder
Authors: Veenstra-VanderWeele, J Gonen, D Leventhal, BL Cook, EH
Citation: J. Veenstra-vanderweele et al., Mutation screening of the UBE3A/E6-AP gene in autistic disorder, MOL PSYCHI, 4(1), 1999, pp. 64-67
Bipolar disorder and ADHD
Authors: Stein, MA Roizen, NM Leventhal, BL
Citation: Ma. Stein et al., Bipolar disorder and ADHD, J AM A CHIL, 38(10), 1999, pp. 1208-1209
Physical mapping of the serotonin 5-HT7 receptor gene (HTR7) to chromosome10 and pseudogene (HTR7P) to chromosome 12, and testing of linkage disequilibrium between HTR7 and autistic disorder
Authors: Lassig, JP Vachirasomtoon, K Hartzell, K Leventhal, M Courchesne, E Courchesne, R Lord, C Leventhal, BL Cook, EH
Citation: Jp. Lassig et al., Physical mapping of the serotonin 5-HT7 receptor gene (HTR7) to chromosome10 and pseudogene (HTR7P) to chromosome 12, and testing of linkage disequilibrium between HTR7 and autistic disorder, AM J MED G, 88(5), 1999, pp. 472-475
Risultati: 1-14 |