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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 38790224)

  • 21. Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome.
    Korteling D; Boks MP; Fiksinski AM; van Hoek IN; Vorstman JAS; Verhoeven-Duif NM; Jans JJM; Zinkstok JR
    Transl Psychiatry; 2022 Mar; 12(1):97. PubMed ID: 35264571
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders.
    Eaton CB; Thomas RH; Hamandi K; Payne GC; Kerr MP; Linden DEJ; Owen MJ; Cunningham AC; Bartsch U; Struik SS; van den Bree MBM
    Epilepsia; 2019 May; 60(5):818-829. PubMed ID: 30977115
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The clinical presentation of attention deficit-hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome.
    Niarchou M; Martin J; Thapar A; Owen MJ; van den Bree MB
    Am J Med Genet B Neuropsychiatr Genet; 2015 Dec; 168(8):730-8. PubMed ID: 26400629
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 22q11.2DS deletion syndrome: developmental milestones in infants and toddlers.
    Roizen NJ; Antshel KM; Fremont W; AbdulSabur N; Higgins AM; Shprintzen RJ; Kates WR
    J Dev Behav Pediatr; 2007 Apr; 28(2):119-24. PubMed ID: 17435462
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome.
    Cunningham AC; Delport S; Cumines W; Busse M; Linden DEJ; Hall J; Owen MJ; van den Bree MBM
    Br J Psychiatry; 2018 Jan; 212(1):27-33. PubMed ID: 29433607
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome.
    Palmer LD; Butcher NJ; Boot E; Hodgkinson KA; Heung T; Chow EWC; Guna A; Crowley TB; Zackai E; McDonald-McGinn DM; Bassett AS
    Am J Med Genet A; 2018 Apr; 176(4):936-944. PubMed ID: 29575622
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Negative subthreshold psychotic symptoms distinguish 22q11.2 deletion syndrome from other neurodevelopmental disorders: A two-site study.
    Mekori-Domachevsky E; Guri Y; Yi J; Weisman O; Calkins ME; Tang SX; Gross R; McDonald-McGinn DM; Emanuel BS; Zackai EH; Zalsman G; Weizman A; Gur RC; Gur RE; Gothelf D
    Schizophr Res; 2017 Oct; 188():42-49. PubMed ID: 28041919
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Childhood Executive Functioning Predicts Young Adult Outcomes in 22q11.2 Deletion Syndrome.
    Albert AB; Abu-Ramadan T; Kates WR; Fremont W; Antshel KM
    J Int Neuropsychol Soc; 2018 Oct; 24(9):905-916. PubMed ID: 30375321
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Atypical language characteristics and trajectories in children with 22q11.2 deletion syndrome.
    Van Den Heuvel E; Manders E; Swillen A; Zink I
    J Commun Disord; 2018; 75():37-56. PubMed ID: 30005318
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndrome.
    Yuen T; Chow EW; Silversides CK; Bassett AS
    Schizophr Res; 2013 Dec; 151(1-3):221-5. PubMed ID: 24262682
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 3 generation pedigree with paternal transmission of the 22q11.2 deletion syndrome: Intrafamilial phenotypic variability.
    Vergaelen E; Swillen A; Van Esch H; Claes S; Van Goethem G; Devriendt K
    Eur J Med Genet; 2015 Apr; 58(4):244-8. PubMed ID: 25655469
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.
    Gothelf D; Law AJ; Frisch A; Chen J; Zarchi O; Michaelovsky E; Ren-Patterson R; Lipska BK; Carmel M; Kolachana B; Weizman A; Weinberger DR
    Biol Psychiatry; 2014 Mar; 75(5):406-13. PubMed ID: 23992923
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Time-based prospective memory in children and adolescents with 22q11.2 deletion syndrome.
    Souchay C; Dubourg L; Ballhausen N; Schneider M; Cerf C; Schnitzspahn K; Faivre L; Kliegel M; Eliez S
    Clin Neuropsychol; 2018 Jul; 32(5):981-992. PubMed ID: 29132265
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The motor profile of primary school-age children with a 22q11.2 deletion syndrome (22q11.2DS) and an age- and IQ-matched control group.
    Van Aken K; Caeyenberghs K; Smits-Engelsman B; Swillen A
    Child Neuropsychol; 2009 Nov; 15(6):532-42. PubMed ID: 19280375
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Deep psychophysiological phenotyping of adolescents and adults with 22q11.2 deletion syndrome: a multilevel approach to defining core disease processes.
    Parker DA; Cubells JF; Imes SL; Ruban GA; Henshey BT; Massa NM; Walker EF; Duncan EJ; Ousley OY
    BMC Psychiatry; 2023 Jun; 23(1):425. PubMed ID: 37312091
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome.
    Hooper SR; Curtiss K; Schoch K; Keshavan MS; Allen A; Shashi V
    Res Dev Disabil; 2013 May; 34(5):1758-69. PubMed ID: 23506790
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders.
    Jalal R; Nair A; Lin A; Eckfeld A; Kushan L; Zinberg J; Karlsgodt KH; Cannon TD; Bearden CE
    J Neurodev Disord; 2021 Apr; 13(1):15. PubMed ID: 33863277
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Intellectual, adaptive and behavioural characteristics in four patients with 18p deletion syndrome.
    Mello CB; Bueno OFA; Benedetto LM; Pimenta LSE; Takeno SS; Melaragno MI; Meloni VA
    J Intellect Disabil Res; 2019 Mar; 63(3):225-232. PubMed ID: 30536814
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.