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 *

116 related articles for article (PubMed ID: 25602252)

  • 41. Role of ESSENCE for preschool children with neurodevelopmental disorders.
    Neville B
    Brain Dev; 2013 Feb; 35(2):128-32. PubMed ID: 22874529
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Bed-wetters, finicky eaters, stutterers. Great progress has been made in research into causes and treatment].
    Nissen G
    MMW Fortschr Med; 2003 Jul; 145(27-28):25. PubMed ID: 14587183
    [No Abstract]   [Full Text] [Related]  

  • 43. The state of the science.
    Connolly K
    Dev Med Child Neurol; 1991 Oct; 33(10):847-8. PubMed ID: 1720748
    [No Abstract]   [Full Text] [Related]  

  • 44. The pathophysiology, medical management and dental implications of fragile X, Rett, and Prader-Willi syndromes.
    Friedlander AH; Yagiela JA; Paterno VI; Mahler ME
    J Calif Dent Assoc; 2003 Sep; 31(9):693-702. PubMed ID: 14560873
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Prader-Willi syndrome.
    Wattendorf DJ; Muenke M
    Am Fam Physician; 2005 Sep; 72(5):827-30. PubMed ID: 16156341
    [TBL] [Abstract][Full Text] [Related]  

  • 46. The Prader-Willi phenotype of fragile X syndrome.
    Nowicki ST; Tassone F; Ono MY; Ferranti J; Croquette MF; Goodlin-Jones B; Hagerman RJ
    J Dev Behav Pediatr; 2007 Apr; 28(2):133-8. PubMed ID: 17435464
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Care of the patient with Prader-Willi syndrome.
    Yearwood EL; McCulloch MR; Tucker ML; Riley JB
    Medsurg Nurs; 2011; 20(3):113-22. PubMed ID: 21786486
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Approach to the genetic evaluation of the child with autism.
    Toriello HV
    Pediatr Clin North Am; 2012 Feb; 59(1):113-28, xi. PubMed ID: 22284797
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Behaviour phenotypes].
    Artigas-Pallarés J
    Rev Neurol; 2002 Feb; 34 Suppl 1():S38-48. PubMed ID: 12447788
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Activity levels of persons with Prader-Willi syndrome.
    Nardella MT; Sulzbacher SI; Worthington-Roberts BS
    Am J Ment Defic; 1983 Mar; 87(5):498-505. PubMed ID: 6837640
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Prader-Willi syndrome: an update and review for the primary pediatrician.
    Chen C; Visootsak J; Dills S; Graham JM
    Clin Pediatr (Phila); 2007 Sep; 46(7):580-91. PubMed ID: 17522286
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Social phenotypes in neurogenetic syndromes.
    Feinstein C; Singh S
    Child Adolesc Psychiatr Clin N Am; 2007 Jul; 16(3):631-47. PubMed ID: 17562583
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Clinical consult: developmental delay/fragile X syndrome.
    Wiesner GL; Cassidy SB; Grimes SJ; Matthews AL; Acheson LS
    Prim Care; 2004 Sep; 31(3):621-5, x. PubMed ID: 15331251
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Therapeutic implications of the mGluR theory of fragile X mental retardation.
    Bear MF
    Genes Brain Behav; 2005 Aug; 4(6):393-8. PubMed ID: 16098137
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Stress, locus of control, and family cohesion and adaptability in parents of children with Down, Williams, Fragile X, and Prader-Willi syndromes.
    Lanfranchi S; Vianello R
    Am J Intellect Dev Disabil; 2012 May; 117(3):207-24. PubMed ID: 22716263
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Epilepsy and autism spectrum disorders: are there common developmental mechanisms?
    Brooks-Kayal A
    Brain Dev; 2010 Oct; 32(9):731-8. PubMed ID: 20570072
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Pediatric neurology in China: challenges and solutions.
    Jiang Y
    Dev Med Child Neurol; 2018 Jul; 60(7):635. PubMed ID: 29882963
    [No Abstract]   [Full Text] [Related]  

  • 58. Psychiatric disorders in pre-schoolers.
    Kong DS
    Singapore Med J; 1995 Jun; 36(3):318-21. PubMed ID: 8553102
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Molecular advances in "non-mendelian" genetics. Implications for pediatrics].
    Pérez Jurado LA
    An Esp Pediatr; 1993 Jun; 38(6):479-87. PubMed ID: 8368674
    [No Abstract]   [Full Text] [Related]  

  • 60. Rett syndrome: natural history and management.
    Moeschler JB; Charman CE; Berg SZ; Graham JM
    Pediatrics; 1988 Jul; 82(1):1-10. PubMed ID: 2454443
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.