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Literature DB >> 19208384

The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome.

Christina Zaleski¹, Anne S Bassett, Karen Tam, Andrea L Shugar, Eva W C Chow, Elizabeth McPherson.

Abstract

Entities: Disease

Mesh：

Year: 2009 PMID： 19208384 PMCID： PMC3295831 DOI： 10.1002/ajmg.a.32650

Source DB: PubMed Journal: Am J Med Genet A ISSN： 1552-4825 Impact factor: 2.802

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20 in total

1. The effect of monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) polymorphisms on levodopa therapy in patients with sporadic Parkinson's disease.

Authors: M Białecka; M Droździk; G Kłodowska-Duda; K Honczarenko; B Gawrońska-Szklarz; G Opala; J Stankiewicz
Journal: Acta Neurol Scand Date: 2004-10 Impact factor: 3.209

2. Effect of 6-hydroxydopamine lesions of the medial prefrontal cortex on neurotransmitter systems in subcortical sites in the rat.

Authors: C J Pycock; C J Carter; R W Kerwin
Journal: J Neurochem Date: 1980-01 Impact factor: 5.372

3. Frontal, midbrain and striatal dopaminergic function in early and advanced Parkinson's disease A 3D [(18)F]dopa-PET study.

Authors: J S Rakshi; T Uema; K Ito; D L Bailey; P K Morrish; J Ashburner; A Dagher; I H Jenkins; K J Friston; D J Brooks
Journal: Brain Date: 1999-09 Impact factor: 13.501

4. A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.

Authors: Lorenzo D Botto; Kristin May; Paul M Fernhoff; Adolfo Correa; Karlene Coleman; Sonja A Rasmussen; Robert K Merritt; Leslie A O'Leary; Lee-Yang Wong; E Marsha Elixson; William T Mahle; Robert M Campbell
Journal: Pediatrics Date: 2003-07 Impact factor: 7.124

Review 5. Neuropsychological and perceptual defects in Parkinson's disease.

Authors: Ivan Bodis-Wollner
Journal: Parkinsonism Relat Disord Date: 2003-08 Impact factor: 4.891

6. Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden.

Authors: S Oskarsdóttir; M Vujic; A Fasth
Journal: Arch Dis Child Date: 2004-02 Impact factor: 3.791

7. Incidence of Parkinson's disease: variation by age, gender, and race/ethnicity.

Authors: Stephen K Van Den Eeden; Caroline M Tanner; Allan L Bernstein; Robin D Fross; Amethyst Leimpeter; Daniel A Bloch; Lorene M Nelson
Journal: Am J Epidemiol Date: 2003-06-01 Impact factor: 4.897

8. Childhood-onset schizophrenia associated with parkinsonism in a patient with a microdeletion of chromosome 22.

Authors: L E Krahn; D M Maraganore; V V Michels
Journal: Mayo Clin Proc Date: 1998-10 Impact factor: 7.616

9. Cerebellar atrophy in a patient with velocardiofacial syndrome.

Authors: D R Lynch; D M McDonald-McGinn; E H Zackai; B S Emanuel; D A Driscoll; L A Whitaker; K H Fischbeck
Journal: J Med Genet Date: 1995-07 Impact factor: 6.318

10. Planning ability in Parkinson's disease is influenced by the COMT val158met polymorphism.

Authors: Thomas Foltynie; Terry E Goldberg; Simon G J Lewis; Andrew D Blackwell; Bhaskar S Kolachana; Daniel R Weinberger; Trevor W Robbins; Roger A Barker
Journal: Mov Disord Date: 2004-08 Impact factor: 10.338

21 in total

Review 1. The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.

Authors: Rachel K Jonas; Caroline A Montojo; Carrie E Bearden
Journal: Biol Psychiatry Date: 2013-08-28 Impact factor: 13.382

2. The curious case of a violently ill woman.

Authors: John H Enterman; Dyllis van Dijk
Journal: Schizophr Bull Date: 2011-09-12 Impact factor: 9.306

Review 3. Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series.

Authors: Nancy J Butcher; Erik Boot; Anthony E Lang; Danielle Andrade; Jacob Vorstman; Donna McDonald-McGinn; Anne S Bassett
Journal: Am J Med Genet A Date: 2018-05-19 Impact factor: 2.802

4. Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and Behavior.

Authors: Avanti Gokhale; Cortnie Hartwig; Amanda A H Freeman; Julia L Bassell; Stephanie A Zlatic; Christie Sapp Savas; Trishna Vadlamudi; Farida Abudulai; Tyler T Pham; Amanda Crocker; Erica Werner; Zhexing Wen; Gabriela M Repetto; Joseph A Gogos; Steven M Claypool; Jennifer K Forsyth; Carrie E Bearden; Jill Glausier; David A Lewis; Nicholas T Seyfried; Jennifer Q Kwong; Victor Faundez
Journal: J Neurosci Date: 2019-03-04 Impact factor: 6.167

5. Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications.

Authors: Nancy J Butcher; Tim-Rasmus Kiehl; Lili-Naz Hazrati; Eva W C Chow; Ekaterina Rogaeva; Anthony E Lang; Anne S Bassett
Journal: JAMA Neurol Date: 2013-11 Impact factor: 18.302