-
1
-
-
79955912970
-
-
American Psychiatric Association. Diagnostic and statistical manual of mental disorders. 4th, text revision ed. Washington: American Psychiatric Association
-
American Psychiatric Association. Diagnostic and statistical manual of mental disorders. 4th, text revision ed. Washington: American Psychiatric Association; 2000.
-
(2000)
-
-
-
2
-
-
70349656767
-
The heterogeneity of causes and courses of attention-deficit/hyperactivity disorder
-
Steinhausen H.C. The heterogeneity of causes and courses of attention-deficit/hyperactivity disorder. Acta Psychiatr Scand 2009, 120:392-399.
-
(2009)
Acta Psychiatr Scand
, vol.120
, pp. 392-399
-
-
Steinhausen, H.C.1
-
3
-
-
70350223638
-
Genetics of attention-deficit-hyperactivity disorder (ADHD)
-
Sharp S.I., McQuillin A., Gurling H.M. Genetics of attention-deficit-hyperactivity disorder (ADHD). Neuropharmacology 2009, 57:590-600.
-
(2009)
Neuropharmacology
, vol.57
, pp. 590-600
-
-
Sharp, S.I.1
McQuillin, A.2
Gurling, H.M.3
-
4
-
-
67651121684
-
Candidate gene studies of ADHD: a meta-analytic review
-
Gizer I.R., Ficks C., Waldman I.D. Candidate gene studies of ADHD: a meta-analytic review. Hum Genet 2009, 126:51-90.
-
(2009)
Hum Genet
, vol.126
, pp. 51-90
-
-
Gizer, I.R.1
Ficks, C.2
Waldman, I.D.3
-
5
-
-
67349098397
-
The neurobiology of attention deficit/hyperactivity disorder
-
Curatolo P., Paloscia C., D'Agati E., Moavero R., Pasini A. The neurobiology of attention deficit/hyperactivity disorder. Eur J Paediatr Neurol 2009, 13:299-304.
-
(2009)
Eur J Paediatr Neurol
, vol.13
, pp. 299-304
-
-
Curatolo, P.1
Paloscia, C.2
D'Agati, E.3
Moavero, R.4
Pasini, A.5
-
6
-
-
67651036217
-
Prenatal smoking and attention-deficit/hyperactivity disorder: DRD4-7R as a plasticity gene
-
Pluess M., Belsky J., Neuman R.J. Prenatal smoking and attention-deficit/hyperactivity disorder: DRD4-7R as a plasticity gene. Biol Psychiatry 2009, 66:e5-e6.
-
(2009)
Biol Psychiatry
, vol.66
-
-
Pluess, M.1
Belsky, J.2
Neuman, R.J.3
-
7
-
-
57349087262
-
A comparison of molecular alterations in environmental and genetic rat models of ADHD: a pilot study
-
B
-
DasBanerjee T., Middleton F.A., Berger D.F., Lambardo J.P., Sagvolden T., Faraone S.V. A comparison of molecular alterations in environmental and genetic rat models of ADHD: a pilot study. Am J Med Genet B Neuropsychiatr Genet 2008, 147B:1554-1563.
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147
, pp. 1554-1563
-
-
DasBanerjee, T.1
Middleton, F.A.2
Berger, D.F.3
Lambardo, J.P.4
Sagvolden, T.5
Faraone, S.V.6
-
8
-
-
0041624358
-
ADHD: topic update
-
Denckla M.B. ADHD: topic update. Brain Dev 2003, 25:383-389.
-
(2003)
Brain Dev
, vol.25
, pp. 383-389
-
-
Denckla, M.B.1
-
10
-
-
34447621203
-
The GABAA receptor: a novel target for treatment of fragile X?
-
D'Hulst C., Kooy R.F. The GABAA receptor: a novel target for treatment of fragile X?. Trends Neurosci 2007, 30:425-431.
-
(2007)
Trends Neurosci
, vol.30
, pp. 425-431
-
-
D'Hulst, C.1
Kooy, R.F.2
-
11
-
-
70349974168
-
The state of synapses in fragile X syndrome
-
Pfeiffer B.E., Huber K.M. The state of synapses in fragile X syndrome. Neuroscientist 2009, 15:549-567.
-
(2009)
Neuroscientist
, vol.15
, pp. 549-567
-
-
Pfeiffer, B.E.1
Huber, K.M.2
-
13
-
-
67649427508
-
Downregulation of tonic GABAergic inhibition in a mouse model of fragile X syndrome
-
Curia G., Papouin T., Seguela P., Avoli M. Downregulation of tonic GABAergic inhibition in a mouse model of fragile X syndrome. Cereb Cortex 2009, 19:1515-1520.
-
(2009)
Cereb Cortex
, vol.19
, pp. 1515-1520
-
-
Curia, G.1
Papouin, T.2
Seguela, P.3
Avoli, M.4
-
14
-
-
61349164873
-
Metabotropic glutamate receptor-mediated use-dependent down-regulation of synaptic excitability involves the fragile X mental retardation protein
-
Repicky S., Broadie K. Metabotropic glutamate receptor-mediated use-dependent down-regulation of synaptic excitability involves the fragile X mental retardation protein. J Neurophysiol 2009, 101:672-687.
-
(2009)
J Neurophysiol
, vol.101
, pp. 672-687
-
-
Repicky, S.1
Broadie, K.2
-
15
-
-
68649093278
-
Protein translation in synaptic plasticity: mGluR-LTD, fragile X
-
Waung M.W., Huber K.M. Protein translation in synaptic plasticity: mGluR-LTD, fragile X. Curr Opin Neurobiol 2009, 19:319-326.
-
(2009)
Curr Opin Neurobiol
, vol.19
, pp. 319-326
-
-
Waung, M.W.1
Huber, K.M.2
-
16
-
-
26444599545
-
The nature and frequency of cognitive deficits in children with neurofibromatosis type 1
-
Hyman S.L., Shores A., North K.N. The nature and frequency of cognitive deficits in children with neurofibromatosis type 1. Neurology 2005, 65:1037-1044.
-
(2005)
Neurology
, vol.65
, pp. 1037-1044
-
-
Hyman, S.L.1
Shores, A.2
North, K.N.3
-
18
-
-
0031007708
-
Requirement of Drosophila NF1 for activation of adenylyl cyclase by PACAP38-like neuropeptides
-
Guo H.F., The I., Hannan F., Bernards A., Zhong Y. Requirement of Drosophila NF1 for activation of adenylyl cyclase by PACAP38-like neuropeptides. Science 1997, 276:795-798.
-
(1997)
Science
, vol.276
, pp. 795-798
-
-
Guo, H.F.1
The, I.2
Hannan, F.3
Bernards, A.4
Zhong, Y.5
-
19
-
-
0031018226
-
A mouse model for the learning and memory deficits associated with neurofibromatosis type I
-
Silva A.J., Frankland P.W., Marowitz Z., Friedman E., Laszlo G.S., Cioffi D., et al. A mouse model for the learning and memory deficits associated with neurofibromatosis type I. Nat Genet 1997, 15:281-284.
-
(1997)
Nat Genet
, vol.15
, pp. 281-284
-
-
Silva, A.J.1
Frankland, P.W.2
Marowitz, Z.3
Friedman, E.4
Laszlo, G.S.5
Cioffi, D.6
-
20
-
-
0037203821
-
Mechanism for the learning deficits in a mouse model of neurofibromatosis type 1
-
Costa R.M., Federov N.B., Kogan J.H., Murphy G.G., Stern J., Ohno M., et al. Mechanism for the learning deficits in a mouse model of neurofibromatosis type 1. Nature 2002, 415:526-530.
-
(2002)
Nature
, vol.415
, pp. 526-530
-
-
Costa, R.M.1
Federov, N.B.2
Kogan, J.H.3
Murphy, G.G.4
Stern, J.5
Ohno, M.6
-
21
-
-
0038182584
-
Neurocognitive dysfunction in children with neurofibromatosis type 1
-
Rosser T.L., Packer R.J. Neurocognitive dysfunction in children with neurofibromatosis type 1. Curr Neurol Neurosci Rep 2003, 3:129-136.
-
(2003)
Curr Neurol Neurosci Rep
, vol.3
, pp. 129-136
-
-
Rosser, T.L.1
Packer, R.J.2
-
22
-
-
39049168113
-
Unidentified bright objects on brain MRI in children as a diagnostic criterion for neurofibromatosis type 1
-
Lopes Ferraz Filho J.R., Munis M.P., Soares Souza A., Goloni-Bertollo E.M., Pavarino-Bertelli E.C. Unidentified bright objects on brain MRI in children as a diagnostic criterion for neurofibromatosis type 1. Pediatr Radiol 2008, 38:305-310.
-
(2008)
Pediatr Radiol
, vol.38
, pp. 305-310
-
-
Lopes Ferraz Filho, J.R.1
Munis, M.P.2
Soares Souza, A.3
Goloni-Bertollo, E.M.4
Pavarino-Bertelli, E.C.5
-
23
-
-
0034075143
-
Thalamic involvement in neurofibromatosis type 1: evaluation with proton magnetic resonance spectroscopic imaging
-
Wang P.Y., Kaufmann W.E., Koth C.W., Denckla M.B., Barker P.B. Thalamic involvement in neurofibromatosis type 1: evaluation with proton magnetic resonance spectroscopic imaging. Ann Neurol 2000, 47:477-484.
-
(2000)
Ann Neurol
, vol.47
, pp. 477-484
-
-
Wang, P.Y.1
Kaufmann, W.E.2
Koth, C.W.3
Denckla, M.B.4
Barker, P.B.5
-
24
-
-
28444433354
-
Attention deficits in children with 22q.11 deletion syndrome
-
Niklasson L., Rasmussen P., Oskarsdottir S., Gillberg C. Attention deficits in children with 22q.11 deletion syndrome. Dev Med Child Neurol 2005, 47:803-807.
-
(2005)
Dev Med Child Neurol
, vol.47
, pp. 803-807
-
-
Niklasson, L.1
Rasmussen, P.2
Oskarsdottir, S.3
Gillberg, C.4
-
25
-
-
70350719204
-
The neuropsychology of 22q11 deletion syndrome. A neuropsychiatric study of 100 individuals
-
Niklasson L., Gillberg C. The neuropsychology of 22q11 deletion syndrome. A neuropsychiatric study of 100 individuals. Res Dev Disabil 2010, 31:185-194.
-
(2010)
Res Dev Disabil
, vol.31
, pp. 185-194
-
-
Niklasson, L.1
Gillberg, C.2
-
26
-
-
18044377629
-
Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome)
-
Antshel K.M., Conchelos J., Lanzetta G., Fremont W., Kates W.R. Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome). Psychiatry Res 2005, 138:235-245.
-
(2005)
Psychiatry Res
, vol.138
, pp. 235-245
-
-
Antshel, K.M.1
Conchelos, J.2
Lanzetta, G.3
Fremont, W.4
Kates, W.R.5
-
27
-
-
63449100481
-
Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults
-
B
-
Halleland H., Lundervold A.J., Halmoy A., Haavik J., Johansson S. Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults. Am J Med Genet B Neuropsychiatr Genet 2009, 150B:403-410.
-
(2009)
Am J Med Genet B Neuropsychiatr Genet
, vol.150
, pp. 403-410
-
-
Halleland, H.1
Lundervold, A.J.2
Halmoy, A.3
Haavik, J.4
Johansson, S.5
-
28
-
-
34247529566
-
The psychopathologies of children and adolescents with tuberous sclerosis complex (TSC): a postal survey of UK families
-
de Vries P.J., Hunt A., Bolton P.F. The psychopathologies of children and adolescents with tuberous sclerosis complex (TSC): a postal survey of UK families. Eur Child Adolesc Psychiatry 2007, 16:16-24.
-
(2007)
Eur Child Adolesc Psychiatry
, vol.16
, pp. 16-24
-
-
de Vries, P.J.1
Hunt, A.2
Bolton, P.F.3
-
29
-
-
36549010421
-
Psychiatric comorbid conditions in a clinic population of 241 patients with tuberous sclerosis complex
-
Muzykewicz D.A., Newberry P., Danforth N., Halpern E.F., Thiele E.A. Psychiatric comorbid conditions in a clinic population of 241 patients with tuberous sclerosis complex. Epilepsy Behav 2007, 11:506-513.
-
(2007)
Epilepsy Behav
, vol.11
, pp. 506-513
-
-
Muzykewicz, D.A.1
Newberry, P.2
Danforth, N.3
Halpern, E.F.4
Thiele, E.A.5
-
30
-
-
0027536381
-
Development, behaviour and seizures in 300 cases of tuberous sclerosis
-
Hunt A. Development, behaviour and seizures in 300 cases of tuberous sclerosis. J Intellect Disabil Res 1993, 37:41-51.
-
(1993)
J Intellect Disabil Res
, vol.37
, pp. 41-51
-
-
Hunt, A.1
-
32
-
-
2642525301
-
The relation of infantile spasms, tubers, and intelligence in tuberous sclerosis complex
-
O'Callaghan F.J., Harris T., Joinson C., Bolton P., Noakes M., Presdee D., et al. The relation of infantile spasms, tubers, and intelligence in tuberous sclerosis complex. Arch Dis Child 2004, 89:530-533.
-
(2004)
Arch Dis Child
, vol.89
, pp. 530-533
-
-
O'Callaghan, F.J.1
Harris, T.2
Joinson, C.3
Bolton, P.4
Noakes, M.5
Presdee, D.6
-
33
-
-
74949121901
-
Attention-deficit-hyperactivity disorder (ADHD) and tuberous sclerosis complex
-
D'Agati E., Moavero R., Cerminara C., Curatolo P. Attention-deficit-hyperactivity disorder (ADHD) and tuberous sclerosis complex. J Child Neurol 2009, 24:1282-1287.
-
(2009)
J Child Neurol
, vol.24
, pp. 1282-1287
-
-
D'Agati, E.1
Moavero, R.2
Cerminara, C.3
Curatolo, P.4
-
34
-
-
19044394761
-
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism
-
Smalley S.L., Kustanovich V., Minassian S.L., Stone J.L., Ogdie M.N., McGough J.J., et al. Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. Am J Hum Genet 2002, 71:959-963.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 959-963
-
-
Smalley, S.L.1
Kustanovich, V.2
Minassian, S.L.3
Stone, J.L.4
Ogdie, M.N.5
McGough, J.J.6
-
35
-
-
0028838709
-
The tuberous sclerosis 2 gene is expressed at high levels in the cerebellum and developing spinal cord
-
Geist R.T., Gutmann D.H. The tuberous sclerosis 2 gene is expressed at high levels in the cerebellum and developing spinal cord. Cell Growth Differ 1995, 6:1477-1483.
-
(1995)
Cell Growth Differ
, vol.6
, pp. 1477-1483
-
-
Geist, R.T.1
Gutmann, D.H.2
-
36
-
-
33748765792
-
Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effects
-
Russel H.F., Wallis D., Mazzocco M.M., Moshang T., Zackai E., Zim A.R., et al. Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effects. J Pediatr Psychol 2006, 31:945-955.
-
(2006)
J Pediatr Psychol
, vol.31
, pp. 945-955
-
-
Russel, H.F.1
Wallis, D.2
Mazzocco, M.M.3
Moshang, T.4
Zackai, E.5
Zim, A.R.6
-
37
-
-
0034810137
-
Functional neuroanatomy of visuo-spatial working memory in Turner syndrome
-
Haberecht M.F., Menon V., Warsofsky J.S., White C.D., Dyer-Friedman J., Glover G.H., et al. Functional neuroanatomy of visuo-spatial working memory in Turner syndrome. Hum Brain Mapp 2001, 14:96-107.
-
(2001)
Hum Brain Mapp
, vol.14
, pp. 96-107
-
-
Haberecht, M.F.1
Menon, V.2
Warsofsky, J.S.3
White, C.D.4
Dyer-Friedman, J.5
Glover, G.H.6
-
38
-
-
66049159361
-
Psychiatric characteristics in a self-selected sample of boys with Klinefelter syndrome
-
Bruining H., Swaab H., Kas M., van Engeland H. Psychiatric characteristics in a self-selected sample of boys with Klinefelter syndrome. Pediatrics 2009, 123:e865-e870.
-
(2009)
Pediatrics
, vol.123
-
-
Bruining, H.1
Swaab, H.2
Kas, M.3
van Engeland, H.4
-
39
-
-
44849133641
-
A new look at XXYY syndrome: medical and psychological features
-
Tartaglia N., Davis S., Hench A., Nimishakavi S., Beauregard R., Reynolds A., et al. A new look at XXYY syndrome: medical and psychological features. Am J Med Genet A 2008, 146:1509-1522.
-
(2008)
Am J Med Genet A
, vol.146
, pp. 1509-1522
-
-
Tartaglia, N.1
Davis, S.2
Hench, A.3
Nimishakavi, S.4
Beauregard, R.5
Reynolds, A.6
-
40
-
-
0035701427
-
Analysis of neurosteroid levels in attention deficit-hyperactivity disorder
-
Strous R.D., Spivak B., Yoran-Hegesh R., Maayan R., Averbuch E., Kotler M., et al. Analysis of neurosteroid levels in attention deficit-hyperactivity disorder. Int J Neuropsychopharmacol 2001, 4:259-264.
-
(2001)
Int J Neuropsychopharmacol
, vol.4
, pp. 259-264
-
-
Strous, R.D.1
Spivak, B.2
Yoran-Hegesh, R.3
Maayan, R.4
Averbuch, E.5
Kotler, M.6
-
41
-
-
33748946219
-
Prevalence of psychiatric disorders in 4 to 16-year-olds with Williams syndrome
-
Leyfer O.T., Woodruff-Borden J., Klein-Tasman B.P., Fricke J.S., Mervis C.B. Prevalence of psychiatric disorders in 4 to 16-year-olds with Williams syndrome. Am J Med Genet B Neuropsychiatr Genet 2006, 141:615-622.
-
(2006)
Am J Med Genet B Neuropsychiatr Genet
, vol.141
, pp. 615-622
-
-
Leyfer, O.T.1
Woodruff-Borden, J.2
Klein-Tasman, B.P.3
Fricke, J.S.4
Mervis, C.B.5
-
42
-
-
63449107365
-
The genomic basis of the Williams-Beuren syndrome
-
Schubert C. The genomic basis of the Williams-Beuren syndrome. Cell Mol Life Sci 2009, 66:1178-1197.
-
(2009)
Cell Mol Life Sci
, vol.66
, pp. 1178-1197
-
-
Schubert, C.1
-
43
-
-
31144479591
-
A brain-specific microRNA regulates dendritic spine development
-
Schratt G.M., Tuebing F., Nigh E.A., Kane C.G., Sabatini M.E., Kiebler M., et al. A brain-specific microRNA regulates dendritic spine development. Nature 2006, 439:283-289.
-
(2006)
Nature
, vol.439
, pp. 283-289
-
-
Schratt, G.M.1
Tuebing, F.2
Nigh, E.A.3
Kane, C.G.4
Sabatini, M.E.5
Kiebler, M.6
-
44
-
-
18444372636
-
Abnormal spine morphology and enhanced LTP in LIMK-1 knockout mice
-
Meng Y., Zhang Y., Tregoubov V., Janus C., Cruz L., Jackson M., et al. Abnormal spine morphology and enhanced LTP in LIMK-1 knockout mice. Neuron 2002, 35:121-133.
-
(2002)
Neuron
, vol.35
, pp. 121-133
-
-
Meng, Y.1
Zhang, Y.2
Tregoubov, V.3
Janus, C.4
Cruz, L.5
Jackson, M.6
-
45
-
-
61749083876
-
Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays
-
Dai L., Bellugi U., Chen X.N., Pulst-Korenberg A.M., Jarvinen-Pasley A., Tirosh-Wagner T., et al. Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays. Am J Med Genet A 2009, 149:302-314.
-
(2009)
Am J Med Genet A
, vol.149
, pp. 302-314
-
-
Dai, L.1
Bellugi, U.2
Chen, X.N.3
Pulst-Korenberg, A.M.4
Jarvinen-Pasley, A.5
Tirosh-Wagner, T.6
-
46
-
-
14144256013
-
The neuropsychiatry and multisystem features of the Smith-Magenis syndrome: a review
-
Shelley B.P., Robertson M.M. The neuropsychiatry and multisystem features of the Smith-Magenis syndrome: a review. J Neuropsychiatry Clin Neurosci 2005, 17:91-97.
-
(2005)
J Neuropsychiatry Clin Neurosci
, vol.17
, pp. 91-97
-
-
Shelley, B.P.1
Robertson, M.M.2
-
47
-
-
34147169956
-
Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype
-
Potocki L., Bi W., Treadwell-Deering D., Carvalho C.M., Eifert A., Friedman E.M., et al. Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype. Am J Hum Genet 2007, 80:633-649.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 633-649
-
-
Potocki, L.1
Bi, W.2
Treadwell-Deering, D.3
Carvalho, C.M.4
Eifert, A.5
Friedman, E.M.6
-
48
-
-
68749119659
-
Mouse models of genomic syndromes as tools for understanding the basis of complex traits: an example with the Smith-Magenis and the Potocki-Lupski syndromes
-
Carmona-Mora P., Molina J., Encina C.A., Walz K. Mouse models of genomic syndromes as tools for understanding the basis of complex traits: an example with the Smith-Magenis and the Potocki-Lupski syndromes. Curr Genomics 2009, 10:259-268.
-
(2009)
Curr Genomics
, vol.10
, pp. 259-268
-
-
Carmona-Mora, P.1
Molina, J.2
Encina, C.A.3
Walz, K.4
-
49
-
-
0037965627
-
Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice. phenotypic consequences of gene dosage imbalance
-
Walz K., Caratini-Rivera S., Bi W., Fonseca P., Mansouri D.L., Lynch J., et al. Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice. phenotypic consequences of gene dosage imbalance. Mol Cell Biol 2003, 23:3646-3655.
-
(2003)
Mol Cell Biol
, vol.23
, pp. 3646-3655
-
-
Walz, K.1
Caratini-Rivera, S.2
Bi, W.3
Fonseca, P.4
Mansouri, D.L.5
Lynch, J.6
-
50
-
-
34447504783
-
Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD
-
Lonardo F., Parenti G., Luquetti D.V., Annunziata I., Della Monica M., Perone L., et al. Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD. Eur J Med Genet 2007, 50:301-308.
-
(2007)
Eur J Med Genet
, vol.50
, pp. 301-308
-
-
Lonardo, F.1
Parenti, G.2
Luquetti, D.V.3
Annunziata, I.4
Della Monica, M.5
Perone, L.6
-
51
-
-
50049104212
-
X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit-hyperactivity disorder, autism and social communication deficits
-
Kent L., Emerton J., Bhadravathi V., Weisblatt E., Pasco G., Willat L.R., et al. X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit-hyperactivity disorder, autism and social communication deficits. J Med Genet 2008, 45:519-524.
-
(2008)
J Med Genet
, vol.45
, pp. 519-524
-
-
Kent, L.1
Emerton, J.2
Bhadravathi, V.3
Weisblatt, E.4
Pasco, G.5
Willat, L.R.6
-
52
-
-
67651154172
-
Converging pharmacological and genetic evidence indicates a role for steroid sulfatase in attention
-
Davies W., Humby T., Kong W., Otter T., Burgoyne P.S., Wilkinson L.S. Converging pharmacological and genetic evidence indicates a role for steroid sulfatase in attention. Biol Psychiatry 2009, 66:360-367.
-
(2009)
Biol Psychiatry
, vol.66
, pp. 360-367
-
-
Davies, W.1
Humby, T.2
Kong, W.3
Otter, T.4
Burgoyne, P.S.5
Wilkinson, L.S.6
-
53
-
-
0033614716
-
Sulfated and unsulfated steroids modulate gamma-aminobutyric acid A receptor function through distinct sites
-
Park-Chung M., Malayev A., Purdy R.H., Gibbs T.T., Farb D.H. Sulfated and unsulfated steroids modulate gamma-aminobutyric acid A receptor function through distinct sites. Brain Res 1999, 830:72-87.
-
(1999)
Brain Res
, vol.830
, pp. 72-87
-
-
Park-Chung, M.1
Malayev, A.2
Purdy, R.H.3
Gibbs, T.T.4
Farb, D.H.5
-
54
-
-
24944432300
-
Symptoms of ADHD and their correlates in children with intellectual disabilities
-
Hastings R.P., Beck A., Daley D., Hill C. Symptoms of ADHD and their correlates in children with intellectual disabilities. Res Dev Disabil 2005, 26:456-468.
-
(2005)
Res Dev Disabil
, vol.26
, pp. 456-468
-
-
Hastings, R.P.1
Beck, A.2
Daley, D.3
Hill, C.4
-
55
-
-
0033902791
-
Patterns of behavioral adjustment and maladjustment in mental retardation: comparison of children with and without ADHD
-
Pearson D.A., Lacher D., Loveland K.A., Santos C.W., Faria L.P., Azzam P.N., et al. Patterns of behavioral adjustment and maladjustment in mental retardation: comparison of children with and without ADHD. Am J Ment Retard 2000, 105:236-251.
-
(2000)
Am J Ment Retard
, vol.105
, pp. 236-251
-
-
Pearson, D.A.1
Lacher, D.2
Loveland, K.A.3
Santos, C.W.4
Faria, L.P.5
Azzam, P.N.6
-
56
-
-
21244504231
-
Consensus clinical guidelines for the assessment of cognitive and behavioural problems in Tuberous Sclerosis
-
de Vries P., Humphrey A., McCartney D., Prather P., Bolton P., Hunt A. Consensus clinical guidelines for the assessment of cognitive and behavioural problems in Tuberous Sclerosis. Eur Child Adolesc Psychiatry 2005, 14:183-190.
-
(2005)
Eur Child Adolesc Psychiatry
, vol.14
, pp. 183-190
-
-
de Vries, P.1
Humphrey, A.2
McCartney, D.3
Prather, P.4
Bolton, P.5
Hunt, A.6
-
57
-
-
33845716621
-
Optimizing therapy of seizures in children and adolescents with developmental disorders
-
Smith M.C. Optimizing therapy of seizures in children and adolescents with developmental disorders. Neurology 2006, 67:S52-S55.
-
(2006)
Neurology
, vol.67
-
-
Smith, M.C.1
-
58
-
-
34548618323
-
Clinical assessment and treatment of ADHD in children
-
Smoot L.C., Boothby L.A., Gillett R.C. Clinical assessment and treatment of ADHD in children. Int J Clin Pract 2007, 61:1730-1738.
-
(2007)
Int J Clin Pract
, vol.61
, pp. 1730-1738
-
-
Smoot, L.C.1
Boothby, L.A.2
Gillett, R.C.3
-
59
-
-
37749012096
-
Attention deficit/hyperactivity disorder in pediatric patients with epilepsy: review of pharmacological treatment
-
Torres A.R., Whitney J., Gonzalez-Heydrich J. Attention deficit/hyperactivity disorder in pediatric patients with epilepsy: review of pharmacological treatment. Epilepsy Behav 2008, 12:217-233.
-
(2008)
Epilepsy Behav
, vol.12
, pp. 217-233
-
-
Torres, A.R.1
Whitney, J.2
Gonzalez-Heydrich, J.3
-
60
-
-
0345700831
-
Use of methylphenidate for attention-deficit-hyperactivity disorder in patients with epilepsy or electroencephalographic abnormalities
-
Gucuyener K., Erdemoglu A.K., Senol S., Serdaroglu A., Soysal S., Kockar A.I. Use of methylphenidate for attention-deficit-hyperactivity disorder in patients with epilepsy or electroencephalographic abnormalities. J Child Neurol 2003, 18:109-112.
-
(2003)
J Child Neurol
, vol.18
, pp. 109-112
-
-
Gucuyener, K.1
Erdemoglu, A.K.2
Senol, S.3
Serdaroglu, A.4
Soysal, S.5
Kockar, A.I.6
-
61
-
-
34347401245
-
Seizure risk in patients with attention-deficit-hyperactivity disorder treated with atomoxetine
-
Wernicke J.F., Holdridge K.C., Jin L., Edison T., Zhang S., Bang M.E., et al. Seizure risk in patients with attention-deficit-hyperactivity disorder treated with atomoxetine. Dev Med Child Neurol 2007, 49:498-502.
-
(2007)
Dev Med Child Neurol
, vol.49
, pp. 498-502
-
-
Wernicke, J.F.1
Holdridge, K.C.2
Jin, L.3
Edison, T.4
Zhang, S.5
Bang, M.E.6
-
62
-
-
76249084241
-
Mammalian target of rapamycin (mTOR) inhibition as a potential antiepileptogenic therapy: from tuberous sclerosis to common acquired epilepsies
-
Wong M. Mammalian target of rapamycin (mTOR) inhibition as a potential antiepileptogenic therapy: from tuberous sclerosis to common acquired epilepsies. Epilepsia 2010, 51:27-36.
-
(2010)
Epilepsia
, vol.51
, pp. 27-36
-
-
Wong, M.1
-
63
-
-
69849090240
-
Fragile X syndrome: from molecular genetics to therapy
-
D'Hulst C., Kooy R.F. Fragile X syndrome: from molecular genetics to therapy. J Med Genet 2009, 46:577-584.
-
(2009)
J Med Genet
, vol.46
, pp. 577-584
-
-
D'Hulst, C.1
Kooy, R.F.2
|