-
1
-
-
49649124127
-
Schizophrenia and 22q11.2 deletion syndrome
-
Bassett AS, Chow EW. 2008. Schizophrenia and 22q11.2 deletion syndrome. Curr Psychiatry Rep 10:148-157.
-
(2008)
Curr Psychiatry Rep
, vol.10
, pp. 148-157
-
-
Bassett, A.S.1
Chow, E.W.2
-
2
-
-
27444447025
-
Clinical features of 78 adults with 22q11 deletion syndrome
-
Bassett AS, Chow EW, Husted J, Weksberg R, Caluseriu O, Webb GD, Gatzoulis MA. 2005. Clinical features of 78 adults with 22q11 deletion syndrome. Am J Med Genet Part A 138A:307-313.
-
(2005)
Am J Med Genet
, vol.138 A
, Issue.PART A
, pp. 307-313
-
-
Bassett, A.S.1
Chow, E.W.2
Husted, J.3
Weksberg, R.4
Caluseriu, O.5
Webb, G.D.6
Gatzoulis, M.A.7
-
3
-
-
34247636739
-
Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome
-
Bassett AS, Caluseriu O, Weksberg R, Young D, Chow EW. 2007. Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome. Biol Psychiatry 61:1135-1140.
-
(2007)
Biol Psychiatry
, vol.61
, pp. 1135-1140
-
-
Bassett, A.S.1
Caluseriu, O.2
Weksberg, R.3
Young, D.4
Chow, E.W.5
-
4
-
-
4644328053
-
The effect of monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) polymorphisms on levodopa therapy in patients with sporadic Parkinson's disease
-
Bialecka M, Drozdzik M, Klodowska-Duda G, Honczarenko K, Gawronska-Szklarz B, Opala G, Stankiewicz J. 2004. The effect of monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) polymorphisms on levodopa therapy in patients with sporadic Parkinson's disease. Acta Neurol Scand 110:260-266.
-
(2004)
Acta Neurol Scand
, vol.110
, pp. 260-266
-
-
Bialecka, M.1
Drozdzik, M.2
Klodowska-Duda, G.3
Honczarenko, K.4
Gawronska-Szklarz, B.5
Opala, G.6
Stankiewicz, J.7
-
5
-
-
20544449204
-
Catechol-O-methyltransferase and monoamine oxidase B genes and susceptibility to sporadic Parkinson's disease in a Polish population
-
Bialecka M, Drozdzik M, Honczarenko K, Gawronska-Szklarz B, Stankiewicz J, Dabrowska E, Kubisiak M, Klodowska-Duda G, Opala G. 2005. Catechol-O-methyltransferase and monoamine oxidase B genes and susceptibility to sporadic Parkinson's disease in a Polish population. Eur Neurol 53:68-73.
-
(2005)
Eur Neurol
, vol.53
, pp. 68-73
-
-
Bialecka, M.1
Drozdzik, M.2
Honczarenko, K.3
Gawronska-Szklarz, B.4
Stankiewicz, J.5
Dabrowska, E.6
Kubisiak, M.7
Klodowska-Duda, G.8
Opala, G.9
-
6
-
-
0042661268
-
Neuropsychological and perceptual defects in Parkinson's disease
-
Bodis-Wollner I. 2003. Neuropsychological and perceptual defects in Parkinson's disease. Parkinsonism Relat Disord 9:S83-S89.
-
(2003)
Parkinsonism Relat Disord
, vol.9
-
-
Bodis-Wollner, I.1
-
7
-
-
0038419517
-
A population-based study of the 22q11.2 deletion: Phenotype, incidence, and contribution to major birth defects in the population
-
Botto LD, May K, Fernhoff PM, Correa A, Coleman K, Rasmussen SA, Merritt RK, O'Leary LA, Wong LY, Elixson EM, Mahle WT, Campbell RM. 2003. A population-based study of the 22q11.2 deletion: Phenotype, incidence, and contribution to major birth defects in the population. Pediatrics 112:101-107.
-
(2003)
Pediatrics
, vol.112
, pp. 101-107
-
-
Botto, L.D.1
May, K.2
Fernhoff, P.M.3
Correa, A.4
Coleman, K.5
Rasmussen, S.A.6
Merritt, R.K.7
O'Leary, L.A.8
Wong, L.Y.9
Elixson, E.M.10
Mahle, W.T.11
Campbell, R.M.12
-
8
-
-
33748895740
-
Neurocognitive profile in 22q11 deletion syndrome and schizophrenia
-
Chow EW, Watson M, Young DA, Bassett AS. 2006. Neurocognitive profile in 22q11 deletion syndrome and schizophrenia. Schizophr Res 87:270-278.
-
(2006)
Schizophr Res
, vol.87
, pp. 270-278
-
-
Chow, E.W.1
Watson, M.2
Young, D.A.3
Bassett, A.S.4
-
9
-
-
0036137526
-
Risk tables for parkinsonism and Parkinson's disease
-
Elbaz A, Bower JH, Maraganore DM, McDonnell SK, Peterson BJ, Ahlskog JE, Schaid DJ, Rocca WA. 2002. Risk tables for parkinsonism and Parkinson's disease. J Clin Epidemiol 55:25-31.
-
(2002)
J Clin Epidemiol
, vol.55
, pp. 25-31
-
-
Elbaz, A.1
Bower, J.H.2
Maraganore, D.M.3
McDonnell, S.K.4
Peterson, B.J.5
Ahlskog, J.E.6
Schaid, D.J.7
Rocca, W.A.8
-
10
-
-
4444264056
-
Planning ability in Parkinson's disease is influenced by the COMT val158met polymorphism
-
Foltynie T, Goldberg TE, Lewis SG, Blackwell AD, Kolachana BS, Weinberger DR, Robbins TW, Barker RA. 2004. Planning ability in Parkinson's disease is influenced by the COMT val158met polymorphism. Mov Disord 19:885-891.
-
(2004)
Mov Disord
, vol.19
, pp. 885-891
-
-
Foltynie, T.1
Goldberg, T.E.2
Lewis, S.G.3
Blackwell, A.D.4
Kolachana, B.S.5
Weinberger, D.R.6
Robbins, T.W.7
Barker, R.A.8
-
11
-
-
33748340878
-
What is the evidence for a premorbid parkinsonian personality: A systematic review
-
Ishihara L, Brayne C. 2006. What is the evidence for a premorbid parkinsonian personality: A systematic review. Mov Disord 21:1006-1072.
-
(2006)
Mov Disord
, vol.21
, pp. 1006-1072
-
-
Ishihara, L.1
Brayne, C.2
-
12
-
-
0034981451
-
Increased frontal [(18)F]fluorodopa uptake in early Parkinson's disease: Sex differences in the prefrontal cortex
-
Kaasinen V, Nurmi E, Bruck A, Eskola O, Bergman J, Solin O, Rinne JO. 2001. Increased frontal [(18)F]fluorodopa uptake in early Parkinson's disease: Sex differences in the prefrontal cortex. Brain 124:1125-1130.
-
(2001)
Brain
, vol.124
, pp. 1125-1130
-
-
Kaasinen, V.1
Nurmi, E.2
Bruck, A.3
Eskola, O.4
Bergman, J.5
Solin, O.6
Rinne, J.O.7
-
13
-
-
0031671235
-
Childhood-onset schizophrenia associated with parkinsonism in a patient with a microdeletion of chromosome 22
-
Krahn LE, Maraganore DM, Michels VV. 1998. Childhood-onset schizophrenia associated with parkinsonism in a patient with a microdeletion of chromosome 22. Mayo Clin Proc 73:956-959.
-
(1998)
Mayo Clin Proc
, vol.73
, pp. 956-959
-
-
Krahn, L.E.1
Maraganore, D.M.2
Michels, V.V.3
-
14
-
-
0029166983
-
Cerebellar atrophy in a patient with velocardiofacial syndrome
-
Lynch DR, McDonald-McGinn DM, Zackei EH, Emanuel BS, Driscoll DA, Whitaker LA, Fishbeck KH. 1995. Cerebellar atrophy in a patient with velocardiofacial syndrome. J Med Genet 32:561-563.
-
(1995)
J Med Genet
, vol.32
, pp. 561-563
-
-
Lynch, D.R.1
McDonald-McGinn, D.M.2
Zackei, E.H.3
Emanuel, B.S.4
Driscoll, D.A.5
Whitaker, L.A.6
Fishbeck, K.H.7
-
15
-
-
0842327784
-
Incidence and prevalence of the 22q11 deletion syndrome: Apopulation-based study in Western Sweden
-
Oskarsdottir S, Vujic M, Fasth A. 2004. Incidence and prevalence of the 22q11 deletion syndrome: Apopulation-based study in Western Sweden. Arch Dis Child 89:148-151.
-
(2004)
Arch Dis Child
, vol.89
, pp. 148-151
-
-
Oskarsdottir, S.1
Vujic, M.2
Fasth, A.3
-
16
-
-
0018903573
-
Effect of 6-hydroxydopamine lesions of the medial prefrontal cortex on neurotransmitter systems in subcortical sites in the rat
-
Pycock CJ, Carter CJ, Kerwin RW. 1980. Effect of 6-hydroxydopamine lesions of the medial prefrontal cortex on neurotransmitter systems in subcortical sites in the rat. J Neurochem 34:91-99.
-
(1980)
J Neurochem
, vol.34
, pp. 91-99
-
-
Pycock, C.J.1
Carter, C.J.2
Kerwin, R.W.3
-
17
-
-
0032870202
-
Frontal, midbrain and striatal dopaminergic function in early and advanced Parkinson's disease A 3D [(18)F]dopa-PET study
-
Rakshi JS, Uema T, Ito K, Bailey DL, Morrish PK, Ashburner J, Dagher A, Jenkins IH, Friston KJ, Brooks DJ. 1999. Frontal, midbrain and striatal dopaminergic function in early and advanced Parkinson's disease A 3D [(18)F]dopa-PET study. Brain 122:1637-1650.
-
(1999)
Brain
, vol.122
, pp. 1637-1650
-
-
Rakshi, J.S.1
Uema, T.2
Ito, K.3
Bailey, D.L.4
Morrish, P.K.5
Ashburner, J.6
Dagher, A.7
Jenkins, I.H.8
Friston, K.J.9
Brooks, D.J.10
-
18
-
-
21744438839
-
Velo-cardio-facial syndrome
-
Cassidy SB, Allanson JE, editors, 2nd edition. New York: Wiley-Liss. pp
-
Shprintzen R. 2005. Velo-cardio-facial syndrome. In: Cassidy SB, Allanson JE, editors. Management of genetic syndromes, 2nd edition. New York: Wiley-Liss. pp 615-631.
-
(2005)
Management of genetic syndromes
, pp. 615-631
-
-
Shprintzen, R.1
-
19
-
-
0036837762
-
Prevalence of Parkinson's disease in Estonia
-
Taba P, Asser T. 2002. Prevalence of Parkinson's disease in Estonia. Acta Neurol Scand 106:276-281.
-
(2002)
Acta Neurol Scand
, vol.106
, pp. 276-281
-
-
Taba, P.1
Asser, T.2
-
20
-
-
61749087071
-
The co-occurrence of 22q11 deletion syndrome and Parkinson disease: A new neurological feature?
-
Toronto, Available at:, accessed August 7, 2008
-
Tam K, Bassett A, Chow E. 2004. The co-occurrence of 22q11 deletion syndrome and Parkinson disease: A new neurological feature? American Society of Human Genetics Meeting, Toronto, 2004. Available at: http://www.ashg.org/ genetics/abstracts/abs04/f769.htm (accessed August 7, 2008).
-
(2004)
American Society of Human Genetics Meeting
-
-
Tam, K.1
Bassett, A.2
Chow, E.3
-
21
-
-
0037675042
-
Incidence of Parkinson's disease: Variation by age, gender, and race/ethnicity
-
Van Den Eeden SK, Tanner CM, Bernstein AL, Fross RD, Leimpeter A, Bloch DA, Nelson LM. 2003. Incidence of Parkinson's disease: Variation by age, gender, and race/ethnicity. Am J Epidemiol 157:1015-1022.
-
(2003)
Am J Epidemiol
, vol.157
, pp. 1015-1022
-
-
Van Den Eeden, S.K.1
Tanner, C.M.2
Bernstein, A.L.3
Fross, R.D.4
Leimpeter, A.5
Bloch, D.A.6
Nelson, L.M.7
-
22
-
-
34247897260
-
Catechol O-methyltransferase val158Met genotype influences frontoparietal activity during planning in patients with Parkinson's disease
-
Williams-Gray CH, Hampshire A, Robbins TW, Owen AM, Barker RA. 2007. Catechol O-methyltransferase val158Met genotype influences frontoparietal activity during planning in patients with Parkinson's disease. J Neurosci 27:4832-4838.
-
(2007)
J Neurosci
, vol.27
, pp. 4832-4838
-
-
Williams-Gray, C.H.1
Hampshire, A.2
Robbins, T.W.3
Owen, A.M.4
Barker, R.A.5
-
23
-
-
0000491950
-
Minimum prevalence of chromosome 22q11 deletions
-
Wilson DI, Cross IE, Wren C, Scambler PJ, Burn J, Goodship J. 1994. Minimum prevalence of chromosome 22q11 deletions. Am J Hum Genet 55:A169.
-
(1994)
Am J Hum Genet
, vol.55
-
-
Wilson, D.I.1
Cross, I.E.2
Wren, C.3
Scambler, P.J.4
Burn, J.5
Goodship, J.6
|