BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

776 related articles for article (PubMed ID: 11294038)

  • 1. [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]  

  • 2. [Cerebral polymicrogyria and 22q11 deletion syndrome].
    Arriola-Pereda G; Verdú-Pérez A; de Castro-De Castro P
    Rev Neurol; 2009 Feb 16-28; 48(4):188-90. PubMed ID: 19226486
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. [22q11.2 microdeletion].
    Schneider M; Eliez S
    Arch Pediatr; 2010 Apr; 17(4):431-4. PubMed ID: 19942416
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome].
    Muñoz S; Garay F; Flores I; Heusser F; Talesnik E; Aracena M; Mellado C; Méndez C; Arnaiz P; Repetto G
    Rev Med Chil; 2001 May; 129(5):515-21. PubMed ID: 11464533
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [22q11 deletion syndrome: an expanding phenotype].
    Moreno Izco F; Zuazo Zamalloa E; González Alvaredo S; Bereciartu Irastorza P
    Neurologia; 2009; 24(1):69-71. PubMed ID: 19214819
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.
    Gerdes M; Solot C; Wang PP; Moss E; LaRossa D; Randall P; Goldmuntz E; Clark BJ; Driscoll DA; Jawad A; Emanuel BS; McDonald-McGinn DM; Batshaw ML; Zackai EH
    Am J Med Genet; 1999 Jul; 85(2):127-33. PubMed ID: 10406665
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Velocardiofacial syndrome in childhood-onset schizophrenia.
    Usiskin SI; Nicolson R; Krasnewich DM; Yan W; Lenane M; Wudarsky M; Hamburger SD; Rapoport JL
    J Am Acad Child Adolesc Psychiatry; 1999 Dec; 38(12):1536-43. PubMed ID: 10596254
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Phenotypic variability of deletion 22q11.2. An analysis of 16 observations with special emphasis on the neurological manifestations].
    Eirís-Puñal J; Iglesias-Meleiro JM; Blanco-Barca MO; Fuster-Siebert M; Barros-Angueira F; Ansede A; Castro-Gago M
    Rev Neurol; 2003 Oct 1-15; 37(7):601-7. PubMed ID: 14582013
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
    Kitsiou-Tzeli S; Kolialexi A; Fryssira H; Galla-Voumvouraki A; Salavoura K; Kanariou M; Tsangaris GT; Kanavakis E; Mavrou A
    In Vivo; 2004; 18(5):603-8. PubMed ID: 15523900
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. 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]  

  • 16. Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome.
    Shashi V; Muddasani S; Santos CC; Berry MN; Kwapil TR; Lewandowski E; Keshavan MS
    Neuroimage; 2004 Apr; 21(4):1399-406. PubMed ID: 15050565
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hypocalcemia and chromosome 22q11 microdeletion.
    Garabédian M
    Genet Couns; 1999; 10(4):389-94. PubMed ID: 10631928
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2: report of five families with a review of the literature.
    Leana-Cox J; Pangkanon S; Eanet KR; Curtin MS; Wulfsberg EA
    Am J Med Genet; 1996 Nov; 65(4):309-16. PubMed ID: 8923941
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Altered functioning of the cingulate gyrus in two cases of chromosome 22q11 deletion syndrome.
    Reif A; Fallgatter AJ; Ehlis AC; Lesch KP
    Psychiatry Res; 2004 Dec; 132(3):273-8. PubMed ID: 15664798
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 39.