170 related articles for article (PubMed ID: 11811651)
1. Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.
Niklasson L; Rasmussen P; Oskarsdóttir S; Gillberg C
Dev Med Child Neurol; 2002 Jan; 44(1):44-50. PubMed ID: 11811651
[TBL] [Abstract][Full Text] [Related]
2. CATCH 22 Syndrome.
Yonehara Y; Nakatsuka T; Ichioka S; Sasaki N; Kobayashi T
J Craniofac Surg; 2002 Sep; 13(5):623-6. PubMed ID: 12218787
[TBL] [Abstract][Full Text] [Related]
3. "CATCH 22" sans cardiac anomaly, thymic hypoplasia, cleft palate, and hypocalcaemia: cAtch 22. A common result of 22q11 deficiency?
Lipson A; Emanuel B; Colley P; Fagan K; Driscoll DA
J Med Genet; 1994 Sep; 31(9):741. PubMed ID: 7815448
[No Abstract] [Full Text] [Related]
4. [Chromosome 22q11 deletion syndrome and its relevance for child and adolescent psychiatry. An overview of etiology, physical symptoms, aspects of child development and psychiatric disorders].
Briegel W; Cohen M
Z Kinder Jugendpsychiatr Psychother; 2004 May; 32(2):107-15. PubMed ID: 15181786
[TBL] [Abstract][Full Text] [Related]
5. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
Sergi C; Serpi M; Müller-Navia J; Schnabel PA; Hagl S; Otto HF; Ulmer HE
Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461
[TBL] [Abstract][Full Text] [Related]
6. The neuropsychology of 22q11 deletion syndrome. A neuropsychiatric study of 100 individuals.
Niklasson L; Gillberg C
Res Dev Disabil; 2010; 31(1):185-94. PubMed ID: 19815377
[TBL] [Abstract][Full Text] [Related]
7. DiGeorge syndrome: part of CATCH 22.
Wilson DI; Burn J; Scambler P; Goodship J
J Med Genet; 1993 Oct; 30(10):852-6. PubMed ID: 8230162
[TBL] [Abstract][Full Text] [Related]
8. [CATCH 22].
Matsuo N; Yamagishi H
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):150-3. PubMed ID: 11057175
[No Abstract] [Full Text] [Related]
9. A review of neurocognitive and behavioral profiles associated with 22q11 deletion syndrome: implications for clinical evaluation and treatment.
Ousley O; Rockers K; Dell ML; Coleman K; Cubells JF
Curr Psychiatry Rep; 2007 Apr; 9(2):148-58. PubMed ID: 17389127
[TBL] [Abstract][Full Text] [Related]
10. Catch 22--microdeletion 22q11 screening in patients with congenital heart defects.
Von Beust G; Bartmus D; Bartels I
Genet Couns; 1998; 9(3):223-7. PubMed ID: 9777346
[No Abstract] [Full Text] [Related]
11. Neuropsychiatric disorders in the 22q11 deletion syndrome.
Niklasson L; Rasmussen P; Oskarsdóttir S; Gillberg C
Genet Med; 2001; 3(1):79-84. PubMed ID: 11339385
[TBL] [Abstract][Full Text] [Related]
12. Attention deficits in children with 22q.11 deletion syndrome.
Niklasson L; Rasmussen P; Oskarsdóttir S; Gillberg C
Dev Med Child Neurol; 2005 Dec; 47(12):803-7. PubMed ID: 16288669
[TBL] [Abstract][Full Text] [Related]
13. Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.
Swillen A; Devriendt K; Legius E; Eyskens B; Dumoulin M; Gewillig M; Fryns JP
J Med Genet; 1997 Jun; 34(6):453-8. PubMed ID: 9192263
[TBL] [Abstract][Full Text] [Related]
14. Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
Papolos DF; Faedda GL; Veit S; Goldberg R; Morrow B; Kucherlapati R; Shprintzen RJ
Am J Psychiatry; 1996 Dec; 153(12):1541-7. PubMed ID: 8942449
[TBL] [Abstract][Full Text] [Related]
15. Morphometry of the head of the caudate nucleus in patients with velocardiofacial syndrome (del 22q11.2).
Sugama S; Bingham PM; Wang PP; Moss EM; Kobayashi H; Eto Y
Acta Paediatr; 2000 May; 89(5):546-9. PubMed ID: 10852189
[TBL] [Abstract][Full Text] [Related]
16. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.
Alikaşifoğlu M; Malkoç N; Ceviz N; Ozme S; Uludoğan S; Tunçbilek E
Turk J Pediatr; 2000; 42(3):215-8. PubMed ID: 11105620
[TBL] [Abstract][Full Text] [Related]
17. Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.
Niklasson L; Rasmussen P; Oskarsdóttir S; Gillberg C
Res Dev Disabil; 2009; 30(4):763-73. PubMed ID: 19070990
[TBL] [Abstract][Full Text] [Related]
18. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.
Matsuoka R; Takao A; Kimura M; Imamura S; Kondo C; Joh-o K; Ikeda K; Nishibatake M; Ando M; Momma K
Am J Med Genet; 1994 Nov; 53(3):285-9. PubMed ID: 7856665
[TBL] [Abstract][Full Text] [Related]
19. DNA fluorescent probes for diagnosis of velocardiofacial and related syndromes.
Crifasi PA; Michels VV; Driscoll DJ; Jalal SM; Dewald GW
Mayo Clin Proc; 1995 Dec; 70(12):1148-53. PubMed ID: 7490915
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]