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Journal Abstract Search

279 related items for PubMed ID: 28190295

  • 1. High prevalence of fatigue in adults with a 22q11.2 deletion syndrome.
    Vergaelen E, Claes S, Kempke S, Swillen A.
    Am J Med Genet A; 2017 Apr; 173(4):858-867. PubMed ID: 28190295
    [Abstract] [Full Text] [Related]

  • 2. [Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].
    Demily C, Rossi M, Schneider M, Edery P, Leleu A, d'Amato T, Franck N, Eliez S.
    Encephale; 2015 Jun; 41(3):266-73. PubMed ID: 25523123
    [Abstract] [Full Text] [Related]

  • 3. Exploring the potential association among sleep disturbances, cognitive impairments, and immune activation in 22q11.2 deletion syndrome.
    Yirmiya ET, Mekori-Domachevsky E, Weinberger R, Taler M, Carmel M, Gothelf D.
    Am J Med Genet A; 2020 Mar; 182(3):461-468. PubMed ID: 31837200
    [Abstract] [Full Text] [Related]

  • 4. Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.
    Unolt M, DiCairano L, Schlechtweg K, Barry J, Howell L, Kasperski S, Nance M, Adzick NS, Zackai EH, McDonald-McGinn DM.
    Am J Med Genet A; 2017 Jan; 173(1):135-142. PubMed ID: 27682988
    [Abstract] [Full Text] [Related]

  • 5. An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndrome.
    Angkustsiri K, Leckliter I, Tartaglia N, Beaton EA, Enriquez J, Simon TJ.
    J Dev Behav Pediatr; 2012 Jan; 33(9):713-20. PubMed ID: 23117596
    [Abstract] [Full Text] [Related]

  • 6. Developmental trajectories in 22q11.2 deletion.
    Swillen A, McDonald-McGinn D.
    Am J Med Genet C Semin Med Genet; 2015 Jun; 169(2):172-81. PubMed ID: 25989227
    [Abstract] [Full Text] [Related]

  • 7. [22q11.2DS Syndrome as a Genetic Subtype of Schizophrenia].
    Huertas-Rodríguez CK, Payán-Gómez C, Forero-Castro RM.
    Rev Colomb Psiquiatr; 2015 Jun; 44(1):50-60. PubMed ID: 26578219
    [Abstract] [Full Text] [Related]

  • 8. The role of 22q11.2 deletion syndrome in the relationship between congenital heart disease and scoliosis.
    Homans JF, de Reuver S, Heung T, Silversides CK, Oechslin EN, Houben ML, McDonald-McGinn DM, Kruyt MC, Castelein RM, Bassett AS.
    Spine J; 2020 Jun; 20(6):956-963. PubMed ID: 31958577
    [Abstract] [Full Text] [Related]

  • 9. Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.
    Monks S, Niarchou M, Davies AR, Walters JT, Williams N, Owen MJ, van den Bree MB, Murphy KC.
    Schizophr Res; 2014 Mar; 153(1-3):231-6. PubMed ID: 24534796
    [Abstract] [Full Text] [Related]

  • 10. Scoliosis in association with the 22q11.2 deletion syndrome: an observational study.
    Homans JF, Baldew VGM, Brink RC, Kruyt MC, Schlösser TPC, Houben ML, Deeney VFX, Crowley TB, Castelein RM, McDonald-McGinn DM.
    Arch Dis Child; 2019 Jan; 104(1):19-24. PubMed ID: 29627765
    [Abstract] [Full Text] [Related]

  • 11. [22q11.2 microdeletion syndrome: Analysis of the care pathway before the genetic diagnosis].
    Ingrao T, Lambert L, Valduga M, Bosser G, Albuisson E, Leheup B.
    Arch Pediatr; 2017 Nov; 24(11):1067-1075. PubMed ID: 28967605
    [Abstract] [Full Text] [Related]

  • 12. 22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy.
    Wither RG, Borlot F, MacDonald A, Butcher NJ, Chow EWC, Bassett AS, Andrade DM.
    Epilepsia; 2017 Jun; 58(6):1095-1101. PubMed ID: 28448680
    [Abstract] [Full Text] [Related]

  • 13. Differences in speech and language abilities between children with 22q11.2 deletion syndrome and children with phenotypic features of 22q11.2 deletion syndrome but without microdeletion.
    Rakonjac M, Cuturilo G, Stevanovic M, Jelicic L, Subotic M, Jovanovic I, Drakulic D.
    Res Dev Disabil; 2016 Aug; 55():322-9. PubMed ID: 27235769
    [Abstract] [Full Text] [Related]

  • 14. Untargeted metabolomic, and proteomic analysis identifies metabolic biomarkers and pathway alterations in individuals with 22q11.2 deletion syndrome.
    Zafarullah M, Angkustsiri K, Quach A, Yeo S, Durbin-Johnson BP, Bowling H, Tassone F.
    Metabolomics; 2024 Feb 28; 20(2):31. PubMed ID: 38418685
    [Abstract] [Full Text] [Related]

  • 15. Identifying patterns of anxiety and depression in children with chromosome 22q11.2 deletion syndrome: comorbidity predicts behavioral difficulties and impaired functional communications.
    Stephenson DD, Beaton EA, Weems CF, Angkustsiri K, Simon TJ.
    Behav Brain Res; 2015 Jan 01; 276():190-8. PubMed ID: 24906195
    [Abstract] [Full Text] [Related]

  • 16. The dimensional structure of psychopathology in 22q11.2 Deletion Syndrome.
    Niarchou M, Moore TM, Tang SX, Calkins ME, McDonald-McGuinn DM, Zackai EH, Emanuel BS, Gur RC, Gur RE.
    J Psychiatr Res; 2017 Sep 01; 92():124-131. PubMed ID: 28433949
    [Abstract] [Full Text] [Related]

  • 17. 22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening.
    Wenger TL, Miller JS, DePolo LM, de Marchena AB, Clements CC, Emanuel BS, Zackai EH, McDonald-McGinn DM, Schultz RT.
    Mol Autism; 2016 Sep 01; 7():27. PubMed ID: 27158440
    [Abstract] [Full Text] [Related]

  • 18. Craniofacial dysmorphology in 22q11.2 deletion syndrome by 3D laser surface imaging and geometric morphometrics: illuminating the developmental relationship to risk for psychosis.
    Prasad S, Katina S, Hennessy RJ, Murphy KC, Bowman AW, Waddington JL.
    Am J Med Genet A; 2015 Mar 01; 167A(3):529-36. PubMed ID: 25691406
    [Abstract] [Full Text] [Related]

  • 19. Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson's disease.
    Butcher NJ, Marras C, Pondal M, Rusjan P, Boot E, Christopher L, Repetto GM, Fritsch R, Chow EWC, Masellis M, Strafella AP, Lang AE, Bassett AS.
    Brain; 2017 May 01; 140(5):1371-1383. PubMed ID: 28369257
    [Abstract] [Full Text] [Related]

  • 20. Risk factors and the evolution of psychosis in 22q11.2 deletion syndrome: a longitudinal 2-site study.
    Gothelf D, Schneider M, Green T, Debbané M, Frisch A, Glaser B, Zilkha H, Schaer M, Weizman A, Eliez S.
    J Am Acad Child Adolesc Psychiatry; 2013 Nov 01; 52(11):1192-1203.e3. PubMed ID: 24157393
    [Abstract] [Full Text] [Related]

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