Les références

  1. Haymond, M. Early recognition of growth abnormalities permitting early intervention. Acta Paediatrica 2013.
  2. Rogol AD, Hayden GF. J Pediatr 2014 (v1.0) – rule of fives (p.2)
  3. KidsHealth. Growth Disorders. (v1.0)
  4. Growth disorders. Nature. (v1.0) 
  5. Ciresi A, Giordano C. 2018. (v1.0) – If growth disorders are left untreated, it can lead to further health problems later in life (p.2)
  6. Moller N et al 2009 Effects of Growth Hormone on glucose, lipid and protein metabolism… (v1.0)
  7. Finken MJJ, et al. Endocr Rev 2018. (v1.0)
  8. Kelberman D, et al. Endocr Rev 2009. (v1.0)
  9. Consensus Guidelines for the Diagnosis and Treatment of Growth Hormone (GH) Deficiency in Childhood (v1.0)
  10. National Organization for Rare Disorders (NORD). Growth hormone deficiency. 2016 (v1.0)
  11. de Marqui ABT. Rev Paul Pediatr. 2015 (v1.0) 
  12. Tanaka T, et al. Growth Horm IGF Res 2002 (v1.0)
  13. Recommendations for the diagnosis and management of Prader-Willi syndrome (v1.0)
  14. Siklar, Berberoglu_Syndromic Disorders with Short Stature_J Clin Res Pediatr Endocrinol 2014;6(1)1-8 (v1.0) 
  15. Silverstein DM. Front Pediatr 2018 (v1.0)
  16. American academy of pediatrics. Chronic Kidney disease in children (v1.0)
  17. Rogol AD, Hayden GF. J Pediatr 2014.
  18. Stochholm K et al 2006 Incidence of GH deficiency – a nationwide study (v1.0)
  19. Prevalence and demographic features of childhood growthhormone deficiency in Belgium during the peri (v1.0)
  20. National Organization for Rare Disorders (NORD). Growth hormone deficiency. 2016 (v1.0)
  21. Schoenmakers N, et al. Journal of Endocrinology 2015 (v1.0)
  22. The Challenge of Defining and Investigating the Causes of Idiopathic Short Stature and Finding… (v1.0)
  23. Novel genetic cause of idiopathic short stature (v1.0)
  24. Cooke, et al. In: Williams Textbook of Endocrinology. 12th ed. Philadelphia, PA: Elsevier Inc.; 2011.
  25. Noonan syndrome (v1.0) – Noonan Syndrome/p1/para1 (p.1)
  26. Mendez HMM, Opitz JM. Am J Med Genet. 1985 (v1.0)
  27. Butler MG, et al. Curr Pediatr Rev. 2016 (v1.0)
  28. Bar C, et al. Orphanet J Rare Dis. 2017 (v1.0) 
  29. Stipančić G, et al. Acta Clin Croat. 2018 (v1.0) 
  30. Prader-Willi syndrome – Diagnosis – NHS (v1.0)
  31. Finken MJJ, et al. Endocr Rev 2018. (v1.0) 
  32. Boonstra VH, et al. 2006 (v1.0) – MTH_SGA_appetite (p.1)
  33. Krakow D. Clin Perinatol. 2015 (v1.0) 
  34. Geister KA and Camper SA. Annu Rev Genomics Hum Genet. 2017 (v1.0)
  35. Ireland PJ, et al. The Application of Clinical Genetics 2014:7;117–125 (v1.0)
  36. Gordon N. Brain Dev 2000. (v1.0)
  37. Pediatrics. 2005 ; 116 : 771- 83. (v1.0)
  38. Saal HM, et al. GeneReviews®. 2002 (v1.0)
  39. Ishida M. Epigenomics 2016 (v1.0) 
  40. Gravholt CH. 2017. Clinical practice guidelines for the care of girls (v1.0)
  41. Bondy CA, et al. Care of Girls and Women with Turner Syndrome: A Guideline of the Turner Syndrome Study Group. J Clin Endocrinol Metab. 2007.
  42. Turner – know your body (v1.0)
  43. Pelentsov LJ et al. BMC Family Practice 2016; 17: 88. (v1.0)
  44. Living with a rare condition. Contact a Family (v1.0)
  45. Coming to terms with your child’s diagnosis. SCOPE (v1.0) 
  46. Pelentsov LJ et al. BMC Family Practice 2016; 17: 88. (v1.0)
  47. Lipman Arch Dis Child 2004 (v1.0) 
  48. How to help your child thrive and succeed at school (v1.0)
  49. Adult-onset growth hormone deficiency. You and your Hormones (v1.0) 
  50. Brod M, et al. Qual Life Res 2017; 26: 1673–1686. (v1.0)
  51. Growth Hormone Deficiency in Adults. Serono Symposia Australasia (v1.0) 
  52. Impact of adult growth hormone deficiency on daily functioning and well-being (v1.0)