These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
245 related articles for article (PubMed ID: 15357690)
1. Two cases of generalized seizures and the Velocardiofacial syndrome -- a clinically significant association? El Tahir MO; Kerr M; Jones RG J Intellect Disabil Res; 2004 Oct; 48(Pt 7):695-8. PubMed ID: 15357690 [TBL] [Abstract][Full Text] [Related]
2. Velocardiofacial manifestations and microdeletions in schizophrenic inpatients. Gothelf D; Frisch A; Munitz H; Rockah R; Aviram A; Mozes T; Birger M; Weizman A; Frydman M Am J Med Genet; 1997 Nov; 72(4):455-61. PubMed ID: 9375731 [TBL] [Abstract][Full Text] [Related]
3. Childhood-onset schizophrenia associated with parkinsonism in a patient with a microdeletion of chromosome 22. Krahn LE; Maraganore DM; Michels VV Mayo Clin Proc; 1998 Oct; 73(10):956-9. PubMed ID: 9787744 [TBL] [Abstract][Full Text] [Related]
4. [Microdeletion 22q11: apropos of case of schizophrenia in an adolescent]. Pinquier C; Héron D; de Carvalho W; Lazar G; Mazet P; Cohen D Encephale; 2001; 27(1):45-50. PubMed ID: 11294038 [TBL] [Abstract][Full Text] [Related]
5. Velocardiofacial syndrome associated with atrophy of the shoulder girdle muscles and cervicomedullary narrowing. Bolland E; Manzur AY; Milward TM; Muntoni F Eur J Paediatr Neurol; 2000; 4(2):73-6. PubMed ID: 10817488 [TBL] [Abstract][Full Text] [Related]
7. Child with velocardiofacial syndrome and del (4)(q34.2): another critical region associated with a velocardiofacial syndrome-like phenotype. Tsai CH; Van Dyke DL; Feldman GL Am J Med Genet; 1999 Feb; 82(4):336-9. PubMed ID: 10051168 [TBL] [Abstract][Full Text] [Related]
8. Psychiatric inpatients and chromosome deletions within 22q11.2. Sugama S; Namihira T; Matsuoka R; Taira N; Eto Y; Maekawa K J Neurol Neurosurg Psychiatry; 1999 Dec; 67(6):803-6. PubMed ID: 10567504 [TBL] [Abstract][Full Text] [Related]
9. Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome. Lachman HM; Morrow B; Shprintzen R; Veit S; Parsia SS; Faedda G; Goldberg R; Kucherlapati R; Papolos DF Am J Med Genet; 1996 Sep; 67(5):468-72. PubMed ID: 8886163 [TBL] [Abstract][Full Text] [Related]
10. Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia. Murphy KC; Owen MJ Br J Psychiatry; 2001 Nov; 179():397-402. PubMed ID: 11689394 [TBL] [Abstract][Full Text] [Related]
11. Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2. Lund J; Chen F; Hua A; Roe B; Budarf M; Emanuel BS; Reeves RH Genomics; 2000 Feb; 63(3):374-83. PubMed ID: 10704284 [TBL] [Abstract][Full Text] [Related]
13. [Epilepsy in an adult with chromosome 22q11 micro-deletion]. Alla P; Philip N; Azulay JP; Attarian S; Pouget J Rev Neurol (Paris); 1999 Nov; 155(11):967-70. PubMed ID: 10603642 [TBL] [Abstract][Full Text] [Related]
14. Clozapine treatment of psychosis associated with velo-cardio-facial syndrome: benefits and risks. Gladston S; Clarke DJ J Intellect Disabil Res; 2005 Jul; 49(Pt 7):567-70. PubMed ID: 15966965 [TBL] [Abstract][Full Text] [Related]
15. [A bifid uvula in a patient with schizophrenia as a sign of 22q11 deletion syndrome]. Vorstman JA; de Ranitz AG; Udink ten Cate FE; Beemer FA; Kahn RS Ned Tijdschr Geneeskd; 2002 Oct; 146(43):2033-6. PubMed ID: 12428463 [TBL] [Abstract][Full Text] [Related]
17. Cytogenetic abnormalities in attention-deficit/hyperactivity disorder. Bastain TM; Lewczyk CM; Sharp WS; James RS; Long RT; Eagen PB; Ebens CL; Meck JM; Chan WY; Sidransky E; Rapoport JL; Castellanos FX J Am Acad Child Adolesc Psychiatry; 2002 Jul; 41(7):806-10. PubMed ID: 12108805 [TBL] [Abstract][Full Text] [Related]
18. Kousseff syndrome caused by deletion of chromosome 22q11-13. Forrester S; Kovach MJ; Smith RE; Rimer L; Wesson M; Kimonis VE Am J Med Genet; 2002 Nov; 112(4):338-42. PubMed ID: 12376934 [TBL] [Abstract][Full Text] [Related]
19. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases. Elia M; Striano P; Fichera M; Gaggero R; Castiglia L; Galesi O; Malacarne M; Pierluigi M; Amato C; Musumeci SA; Romano C; Majore S; Grammatico P; Zara F; Striano S; Faravelli F Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647 [TBL] [Abstract][Full Text] [Related]
20. 22q11 deletion syndrome and forensic research: can we go there? Harris V J Am Acad Psychiatry Law; 2005; 33(1):106-11. PubMed ID: 15809249 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]