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 *

109 related articles for article (PubMed ID: 12940658)

  • 1. Neurologic aspects of 49,XXXXY syndrome.
    Galasso C; Arpino C; Fabbri F; Curatolo P
    J Child Neurol; 2003 Jul; 18(7):501-4. PubMed ID: 12940658
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Further magnetic resonance imaging (MRI) brain delineation of 49,XXXXY syndrome.
    Tabarki B; Shafi SA; Adwani NA; Shahwan SA
    J Child Neurol; 2012 May; 27(5):650-3. PubMed ID: 22156792
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 49,XXXXY syndrome: behavioural and developmental profiles.
    Lomelino CA; Reiss AL
    J Med Genet; 1991 Sep; 28(9):609-12. PubMed ID: 1956059
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 49, XXXXY syndrome with severe vesico-ureteral reflux and hydronephrosis: report of one case.
    Chang JT; Chiu PC; Chen YY; Chao MC; Hsieh KS
    Acta Paediatr Taiwan; 2005; 46(1):35-8. PubMed ID: 16302576
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 49,XXXXY syndrome with diabetes mellitus.
    Kim HJ; Kim D; Shin JM; Chung HK; Lee G
    Horm Res; 2006; 65(1):14-7. PubMed ID: 16357485
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Frontal Aslant Tract Abnormality on Diffusion Tensor Imaging in an Aphasic Patient With 49, XXXXY Syndrome.
    Dhakar MB; Ilyas M; Jeong JW; Behen ME; Chugani HT
    Pediatr Neurol; 2016 Feb; 55():64-7. PubMed ID: 26706051
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Case report of 49,XXXXY syndrome with cleft palate, diabetes, hypothyroidism, and cataracts.
    Wei L; Liu Y; Sun S; Tang Y; Chen S; Song G
    Medicine (Baltimore); 2019 Sep; 98(39):e17342. PubMed ID: 31574874
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A male phenotype with Aicardi syndrome.
    Zubairi MS; Carter RF; Ronen GM
    J Child Neurol; 2009 Feb; 24(2):204-7. PubMed ID: 19182158
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal sonographic diagnosis of the 49,XXXXY syndrome.
    Schluth C; Doray B; Girard-Lemaire F; Kohler M; Langer B; Gasser B; Lindner V; Flori E
    Prenat Diagn; 2002 Dec; 22(13):1177-80. PubMed ID: 12478628
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical variability and novel neurodevelopmental findings in 49, XXXXY syndrome.
    Gropman AL; Rogol A; Fennoy I; Sadeghin T; Sinn S; Jameson R; Mitchell F; Clabaugh J; Lutz-Armstrong M; Samango-Sprouse CA
    Am J Med Genet A; 2010 Jun; 152A(6):1523-30. PubMed ID: 20503329
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Speech and language development in children with 49,XXXXY syndrome.
    Samango-Sprouse CA; Lasutschinkow PC; McLeod M; Porter GF; Powell S; St Laurent J; Sadeghin T; Gropman AL
    Am J Med Genet A; 2021 Dec; 185(12):3567-3575. PubMed ID: 32725750
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Commentary: Unravelling the effects of additional sex chromosomes on cognition and communication--reflections on Lee et al. (2012).
    Bishop DV
    J Child Psychol Psychiatry; 2012 Oct; 53(10):1082-3. PubMed ID: 22934737
    [No Abstract]   [Full Text] [Related]  

  • 13. Severe myelinopathy in 49,XXXXY syndrome.
    Buller MA; Pfeifer CM
    Neuroradiol J; 2018 Oct; 31(5):523-525. PubMed ID: 28627968
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Expanding the spectrum of acquired cerebral hemiatrophy.
    Kumar N; Drubach DA; Black DF
    J Neuroimaging; 2005 Apr; 15(2):200-2. PubMed ID: 15746235
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sex chromosome pentasomy 49,XXXXY connected with hypothyroidism. Case report.
    Wikiera B; Głab E; Slezak R; Wójcik E; Noczyńska A
    Pediatr Endocrinol Diabetes Metab; 2009; 15(2):125-7. PubMed ID: 19772821
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 49, XXXXY syndrome.
    Hou JW
    Chang Gung Med J; 2004 Jul; 27(7):551-4. PubMed ID: 15508879
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pentasomy 49,XXXXY diagnosed in utero: case report and systematic review of antenatal findings.
    Peitsidis P; Manolakos E; Peitsidou A; Petersen MB; Tsoplou P; Kadir R; Agapitos E
    Fetal Diagn Ther; 2009; 26(1):1-5. PubMed ID: 19816022
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes.
    Simşek PO; Utine GE; Alikaşifoğlu A; Alanay Y; Boduroğlu K; Kandemir N
    Turk J Pediatr; 2009; 51(3):294-7. PubMed ID: 19817277
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A rare case of ambiguous genitalia.
    Ng SF; Boo NY; Wu LL; Shuib S
    Singapore Med J; 2007 Sep; 48(9):858-61. PubMed ID: 17728969
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
    Elia M; Striano P; Fichera M; Gaggero R; Castiglia L; Galesi O; Malacarne M; Pierluigi M; Amato C; Musumeci SA; Romano C; Majore S; Grammatico P; Zara F; Striano S; Faravelli F
    Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.