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Volumn 33, Issue 6, 2011, Pages 456-461

ADHD and genetic syndromes

Author keywords

Attention Deficit Hyperactivity Disorder; Fragile X Syndrome; Genetic syndromes; Mental retardation; Neurofibromatosis type 1; Sexual aneuploidies; Tuberous Sclerosis Complex; Williams Syndrome

Indexed keywords

METHYLPHENIDATE;

EID: 79955887086     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.braindev.2010.05.011     Document Type: Review
Times cited : (45)

References (63)
  • 1
    • 79955912970 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 6
    • 67651036217 scopus 로고    scopus 로고
    • 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
  • 8
    • 0041624358 scopus 로고    scopus 로고
    • 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
  • 9
    • 33750592235 scopus 로고    scopus 로고
    • ADHD symptoms in children with FXS
    • Sullivan K., Hatton D., Hammer J., et al. ADHD symptoms in children with FXS. Am J Med Genet A 2006, 140:2275-2288.
    • (2006) Am J Med Genet A , vol.140 , pp. 2275-2288
    • Sullivan, K.1    Hatton, D.2    Hammer, J.3
  • 10
    • 34447621203 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 17
    • 0034046743 scopus 로고    scopus 로고
    • Behavioral phenotype of neurofibromatosis, type 1
    • Kayl A.E., Moore B.D. Behavioral phenotype of neurofibromatosis, type 1. Ment Retard Dev Disabil Res Rev 2000, 6:117-124.
    • (2000) Ment Retard Dev Disabil Res Rev , vol.6 , pp. 117-124
    • Kayl, A.E.1    Moore, B.D.2
  • 18
    • 0031007708 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 23
    • 0034075143 scopus 로고    scopus 로고
    • 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
  • 25
    • 70350719204 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 38
    • 66049159361 scopus 로고    scopus 로고
    • 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
  • 42
    • 63449107365 scopus 로고    scopus 로고
    • 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
  • 44
    • 18444372636 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.