166 related articles for article (PubMed ID: 10935843)
1. Dystonia in a patient with deletion of 18p.
Tezzon F; Zanoni T; Passarin MG; Ferrari G
Ital J Neurol Sci; 1998 Apr; 19(2):90-3. PubMed ID: 10935843
[TBL] [Abstract][Full Text] [Related]
2. Progressive dystonia in a child with chromosome 18p deletion, treated with intrathecal baclofen.
Awaad Y; Munoz S; Nigro M
J Child Neurol; 1999 Feb; 14(2):75-7. PubMed ID: 10073426
[TBL] [Abstract][Full Text] [Related]
3. Characteristics of dystonia in the 18p deletion syndrome, including a new case.
Postma AG; Verschuuren-Bemelmans CC; Kok K; van Laar T
Clin Neurol Neurosurg; 2009 Dec; 111(10):880-2. PubMed ID: 19699028
[TBL] [Abstract][Full Text] [Related]
4. Genetic analysis of three patients with an 18p- syndrome and dystonia.
Klein C; Page CE; LeWitt P; Gordon MF; de Leon D; Awaad Y; Breakefield XO; Brin MF; Ozelius LJ
Neurology; 1999 Feb; 52(3):649-51. PubMed ID: 10025808
[TBL] [Abstract][Full Text] [Related]
5. Dystonia in a patient with deletion of 18q.
Gordon MF; Bressman S; Brin MF; de Leon D; Warburton D; Yeboa K; Fahn S
Mov Disord; 1995 Jul; 10(4):496-9. PubMed ID: 7565832
[TBL] [Abstract][Full Text] [Related]
6. [18p-syndrome with bilateral pyramidal tract signs, dystonia of the lower extremities and concentric visual field defect].
Kakinuma S; Sasabe F; Negoro K; Nogaki H; Morimatsu M
Rinsho Shinkeigaku; 1994 May; 34(5):474-8. PubMed ID: 7924061
[TBL] [Abstract][Full Text] [Related]
7. Familial deletion 18p syndrome: case report.
Maranda B; Lemieux N; Lemyre E
BMC Med Genet; 2006 Jul; 7():60. PubMed ID: 16842614
[TBL] [Abstract][Full Text] [Related]
8. Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation.
Babovic-Vuksanovic D; Jenkins SC; Ensenauer R; Newman DC; Jalal SM
Am J Med Genet A; 2004 Jan; 124A(3):318-22. PubMed ID: 14708108
[TBL] [Abstract][Full Text] [Related]
9. Unbalanced whole arm translocation resulting in loss of 18p in dystonia.
Nasir J; Frima N; Pickard B; Malloy MP; Zhan L; Grünewald R
Mov Disord; 2006 Jun; 21(6):859-63. PubMed ID: 16541453
[TBL] [Abstract][Full Text] [Related]
10. Spectrum of Movement Disorders in 18p Deletion Syndrome.
Crosiers D; Blaumeiser B; Van Goethem G
Mov Disord Clin Pract; 2019 Jan; 6(1):70-73. PubMed ID: 30746419
[TBL] [Abstract][Full Text] [Related]
11. Detection of a rare de novo 18p terminal deletion with inverted duplication in a Chinese pregnant woman.
Zhu J; Qi H; Cao S; Cai L; Wen X; Tang G; Wan Q; Chen C; Wang J; Zeng W; Luo Y
Mol Genet Genomic Med; 2019 Sep; 7(9):e868. PubMed ID: 31317671
[TBL] [Abstract][Full Text] [Related]
12. Pure and complete trisomy 18p due to a supernumerary marker chromosome associated with moderate mental retardation.
Mabboux P; Brisset S; Aboura A; Pineau D; Koubi V; Joannidis S; Labrune P; Tachdjian G
Am J Med Genet A; 2007 Apr; 143A(7):727-33. PubMed ID: 17330860
[TBL] [Abstract][Full Text] [Related]
13. GNAL deletion as a probable cause of dystonia in a patient with the 18p- syndrome.
Esposito F; Addor MC; Humm AM; Vingerhoets F; Wider C
Parkinsonism Relat Disord; 2014 Mar; 20(3):351-2. PubMed ID: 24405754
[No Abstract] [Full Text] [Related]
14. Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.
Brenk CH; Prott EC; Trost D; Hoischen A; Walldorf C; Radlwimmer B; Wieczorek D; Propping P; Gillessen-Kaesbach G; Weber RG; Engels H
Eur J Hum Genet; 2007 Jan; 15(1):35-44. PubMed ID: 17024214
[TBL] [Abstract][Full Text] [Related]
15. Paroxysmal oculogyric dystonia associated with a de novo 3q29 microdeletion.
Kaur H; Thom RP; Neumeyer AM; Bilancia CG; Wray SH; McDougle CJ
Psychiatr Genet; 2020 Aug; 30(4):119-123. PubMed ID: 32459710
[TBL] [Abstract][Full Text] [Related]
16. 18p deletion syndrome with a 45, XY, t (14; 18) (p11;q11.2), -18, karyotype.
Rao VB; Kerketta L; Korgaonkar S; Ghosh K; Mohanty D
Ann Genet; 2001; 44(4):187-90. PubMed ID: 11755103
[TBL] [Abstract][Full Text] [Related]
17. A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbows.
Chen CP; Lin SP; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2018 Aug; 57(4):583-587. PubMed ID: 30122583
[TBL] [Abstract][Full Text] [Related]
18. Optic disk and white matter abnormalities in a patient with a de novo 18p partial monosomy.
Abu-Amero KK; Hellani A; Salih MA; Alorainy IA; Zidan G; Kern KC; Sicotte NL; Bosley TM
Ophthalmic Genet; 2010 Sep; 31(3):147-54. PubMed ID: 20565246
[TBL] [Abstract][Full Text] [Related]
19. 18p Deletion Syndrome Originating from Rare Unbalanced Whole-Arm Translocation between Chromosomes 13 and 18: A Case Report and Literature Review.
Choi JY; Moon JU; Yoon DH; Yim J; Kim M; Jung MH
Children (Basel); 2022 Jul; 9(7):. PubMed ID: 35883971
[TBL] [Abstract][Full Text] [Related]
20. Monosomy 18p.
Turleau C
Orphanet J Rare Dis; 2008 Feb; 3():4. PubMed ID: 18284672
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
