BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 10424824)

  • 41. Ropinirole in a child with attention-deficit hyperactivity disorder and restless legs syndrome.
    Konofal E; Arnulf I; Lecendreux M; Mouren MC
    Pediatr Neurol; 2005 May; 32(5):350-1. PubMed ID: 15866437
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome.
    Neri G; Marini R; Cappa M; Borrelli P; Opitz JM
    Am J Med Genet; 1988; 30(1-2):287-99. PubMed ID: 3177455
    [TBL] [Abstract][Full Text] [Related]  

  • 43. The Aarskog-Scott syndrome in four brothers.
    Archibald RM; German J
    Birth Defects Orig Artic Ser; 1975; 11(2):25-9. PubMed ID: 1227529
    [No Abstract]   [Full Text] [Related]  

  • 44. Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.
    Lindsay S; Ireland M; O'Brien O; Clayton-Smith J; Hurst JA; Mann J; Cole T; Sampson J; Slaney S; Schlessinger D; Burn J; Pilia G
    J Med Genet; 1997 Jun; 34(6):480-3. PubMed ID: 9192268
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Growth and sexual maturation in children and adolescents with attention deficit hyperactivity disorder.
    Poulton A
    Curr Opin Pediatr; 2006 Aug; 18(4):427-34. PubMed ID: 16914999
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Extending the overlap of three congenital overgrowth syndromes.
    Coppin B; Moore I; Hatchwell E
    Clin Genet; 1997 Jun; 51(6):375-8. PubMed ID: 9237499
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome.
    Neri G; Gurrieri F; Zanni G; Lin A
    Am J Med Genet; 1998 Oct; 79(4):279-83. PubMed ID: 9781908
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Genital anomalies in three male siblings with Simpson-Golabi-Behmel syndrome.
    Griffith CB; Probert RC; Vance GH
    Am J Med Genet A; 2009 Nov; 149A(11):2484-8. PubMed ID: 19842194
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Hereditary factors in attention deficit hyperactivity disorder].
    Fliers EA; Franke B; Buitelaar JK
    Ned Tijdschr Geneeskd; 2005 Jul; 149(31):1726-9. PubMed ID: 16114287
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Electrocardiographic screening in children with attention-deficit hyperactivity disorder.
    Mahle WT; Hebson C; Strieper MJ
    Am J Cardiol; 2009 Nov; 104(9):1296-9. PubMed ID: 19840580
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Attention deficit hyperactivity syndrome].
    Sell-Salazar F
    Rev Neurol; 2003 Aug 16-31; 37(4):353-8. PubMed ID: 14533112
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Attention-deficit/hyperactivity-related symptoms among children with enterovirus 71 infection of the central nervous system.
    Gau SS; Chang LY; Huang LM; Fan TY; Wu YY; Lin TY
    Pediatrics; 2008 Aug; 122(2):e452-8. PubMed ID: 18606624
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Lymphoproliferative disorders in Sotos syndrome: observation of two cases.
    Corsello G; Giuffrè M; Carcione A; Cuzto ML; Piccione M; Ziino O
    Am J Med Genet; 1996 Sep; 64(4):588-93. PubMed ID: 8870927
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Analysis of visuospatial activity in preschool children with attention deficit disorder].
    Quintanar L; Solovieva Iu; Bonilla R
    Fiziol Cheloveka; 2006; 32(1):51-5. PubMed ID: 16526290
    [No Abstract]   [Full Text] [Related]  

  • 55. GPC3 mutations in seven patients with Simpson-Golabi-Behmel syndrome.
    Sakazume S; Okamoto N; Yamamoto T; Kurosawa K; Numabe H; Ohashi Y; Kako Y; Nagai T; Ohashi H
    Am J Med Genet A; 2007 Aug; 143A(15):1703-7. PubMed ID: 17603795
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Attention-deficit/hyperactivity disorder and callous-unemotional traits as moderators of conduct problems when examining impairment and aggression in elementary school children.
    Waschbusch DA; Willoughby MT
    Aggress Behav; 2008; 34(2):139-53. PubMed ID: 17696164
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Study of susceptibility loci located within Xp11 in attention deficit hyperactivity disorder].
    Jiang S; Xin R; Qian Y; Lin S; Li F; Wu X; Wang D; Tang G; Jiang K
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Jun; 18(3):169-72. PubMed ID: 11402442
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Psychosocial, cognitive, and motor functioning in patients with suspected Sotos syndrome: a comparison between patients with and without NSD1 gene alterations.
    de Boer L; Röder I; Wit JM
    Dev Med Child Neurol; 2006 Jul; 48(7):582-8. PubMed ID: 16780628
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma.
    Hienonen T; Sammalkorpi H; Isohanni P; Versteeg R; Karikoski R; Aaltonen LA
    J Med Genet; 2005 Jan; 42(1):e3. PubMed ID: 15635065
    [No Abstract]   [Full Text] [Related]  

  • 60. Germinal mosaicism in Simpson-Golabi-Behmel syndrome.
    Romanelli V; Arroyo I; Rodriguez JI; Magano L; Arias P; Incera I; Gracia-Bouthelier R; Lapunzina P
    Clin Genet; 2007 Oct; 72(4):384-6. PubMed ID: 17850639
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.