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Journal Abstract Search

551 related items for PubMed ID: 28448680

  • 21.
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  • 23. 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; 7():27. PubMed ID: 27158440
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  • 24. [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
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  • 25. Epileptology of the first tonic-clonic seizure in adults and prediction of seizure recurrence.
    Koutroumanidis M, Bruno E.
    Epileptic Disord; 2018 Dec 01; 20(6):490-501. PubMed ID: 30530414
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  • 26. [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 01; 41(3):266-73. PubMed ID: 25523123
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  • 29. [Genetic and clinical characteristics of 22q11.2 deletion syndrome].
    Kozlova IuO, Zabnenkova VV, Shilova NV, Min'zhenkova ME, Antonenko VG, Kotlukova NP, Simonova LV, Kazanceva IA, Levchenko EG, Bombardirova TD, Zolotukhina TV, Poliakov AV.
    Genetika; 2014 May 01; 50(5):602-10. PubMed ID: 25715476
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  • 34. The impact of hypocalcemia on full scale IQ in patients with 22q11.2 deletion syndrome.
    Grand K, Levitt Katz LE, Crowley TB, Moss E, Lessig M, Bamba V, Lord K, Zackai EH, Emanuel BS, Valverde K, McDonald-McGinn DM.
    Am J Med Genet A; 2018 Oct 01; 176(10):2167-2171. PubMed ID: 30380188
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  • 35. Association of airway abnormalities with 22q11.2 deletion syndrome.
    Sacca R, Zur KB, Crowley TB, Zackai EH, Valverde KD, McDonald-McGinn DM.
    Int J Pediatr Otorhinolaryngol; 2017 May 01; 96():11-14. PubMed ID: 28390597
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  • 36. 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 01; 182(3):461-468. PubMed ID: 31837200
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  • 37. Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.
    Prasad SE, Howley S, Murphy KC.
    Dev Disabil Res Rev; 2008 Mar 01; 14(1):26-34. PubMed ID: 18636634
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  • 38. All-cause mortality and survival in adults with 22q11.2 deletion syndrome.
    Van L, Heung T, Graffi J, Ng E, Malecki S, Van Mil S, Boot E, Corral M, Chow EWC, Hodgkinson KA, Silversides C, Bassett AS.
    Genet Med; 2019 Oct 01; 21(10):2328-2335. PubMed ID: 30948858
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  • 39. A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.
    Vaz SO, Pires R, Pires LM, Carreira IM, Anjos R, Maciel P, Mota-Vieira L.
    BMC Pediatr; 2015 Aug 22; 15():95. PubMed ID: 26297018
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