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Nerwiakowłókniakowatość typu 1 (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Nerwiakowłókniakowatość typu 1" in Polish language version.

refsWebsite
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15nih.gov
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6doi.org
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doi.org

  • Wallace MR, Marchuk DA, Andersen LB, Letcher R, Odeh HM, Saulino AM, Fountain JW, Brereton A, Nicholson J, Mitchell AL, et al. Type 1 neurofibromatosis gene: identification of a larger transcript disrupted in three NF1 patients. „Science”. 249, s. 181–186, 1990. DOI: 10.1126/science.2134734. PMID: 2134734. 
  • Friedrich RE, Schmelzle R, Hartmann M, Fünsterer C, Mautner VF. Resection of small plexiform neurofibromas in neurofibromatosis type 1 children. „World Journal of Surgical Oncology”. 3. 6, 2005. DOI: 10.1186/1477-7819-3-6. PMID: 15683544. 
  • Fadare O, Hileeto D. Synchronously diagnosed pre-sacral neurofibroma and cutaneous spitzoid melanoma: a fortuitous association?. „World Journal of Surgical Oncology”. 2. 31, 2004. DOI: 10.1186/1477-7819-2-31. PMID: 15363097. 
  • Gkiokas A, Hadzimichalis S, Vasiliadis E, Katsalouli M, Kannas G. Painful rib hump: a new clinical sign for detecting intraspinal rib displacement in scoliosis due to neurofibromatosis. „Scoliosis”. 1. 10, 2006. DOI: 10.1186/1748-7161-1-10. PMID: 16774682. 
  • Ferner RE. Neurofibromatosis 1. „Eur J Hum Genet”. 15. 2, s. 131-8, 2007. DOI: 10.1038/sj.ejhg.5201676. PMID: 16957683. 
  • Rasmussen SA, Yang Q, Friedman JM. Mortality in neurofibromatosis. 1: An analysis using US death certificates. „Am J Hum Genet”. 68, s. 1110–1118, 2001. DOI: 10.1086/320121. PMID: 11283797. 

fda.gov

fda.gov

accessdata.fda.gov

nih.gov

ncbi.nlm.nih.gov

  • Wallace MR, Marchuk DA, Andersen LB, Letcher R, Odeh HM, Saulino AM, Fountain JW, Brereton A, Nicholson J, Mitchell AL, et al. Type 1 neurofibromatosis gene: identification of a larger transcript disrupted in three NF1 patients. „Science”. 249, s. 181–186, 1990. DOI: 10.1126/science.2134734. PMID: 2134734. 
  • Puisieux A. HNPCC syndrome, microsatellite instability and NF1 gene alteration]. „Bull Cancer”. 86. 10, s. 812-4, 1999. PMID: 10572231. 
  • Raevaara TE, Gerdes AM, Lönnqvist KE, Tybjaerg-Hansen A, Abdel-Rahman WM, Kariola R, Peltomäki P, Nyström-Lahti M. HNPCC mutation MLH1 P648S makes the functional protein unstable, and homozygosity predisposes to mild neurofibromatosis type 1. „Genes Chromosomes Cancer”. 40. 3, s. 261-5, 2004. PMID: 15139004. 
  • Huson SM, Compston DA, Clark P, Harper PS. A genetic study of von Recklinghausen neurofibromatosis in south east Wales. 1. Prevalence, fitness, mutation rate, and effect of parental transmission on severity. „J Med Genet”. 26. 11, s. 704–711, 1989. PMID: 2511318. 
  • Friedrich RE, Schmelzle R, Hartmann M, Fünsterer C, Mautner VF. Resection of small plexiform neurofibromas in neurofibromatosis type 1 children. „World Journal of Surgical Oncology”. 3. 6, 2005. DOI: 10.1186/1477-7819-3-6. PMID: 15683544. 
  • Fadare O, Hileeto D. Synchronously diagnosed pre-sacral neurofibroma and cutaneous spitzoid melanoma: a fortuitous association?. „World Journal of Surgical Oncology”. 2. 31, 2004. DOI: 10.1186/1477-7819-2-31. PMID: 15363097. 
  • Gkiokas A, Hadzimichalis S, Vasiliadis E, Katsalouli M, Kannas G. Painful rib hump: a new clinical sign for detecting intraspinal rib displacement in scoliosis due to neurofibromatosis. „Scoliosis”. 1. 10, 2006. DOI: 10.1186/1748-7161-1-10. PMID: 16774682. 
  • Singhal S, Birch JM, Kerr B, Lashford L, Evans DG. Neurofibromatosis type 1 and sporadic optic gliomas. „Arch Dis Child”. 87. 1, s. 65-70, 2002. PMID: 12089128. 
  • Evans DG, Baser ME, McGaughran J et al. Malignant peripheral nerve sheath tumours in neurofibromatosis 1. „J Med Genet”. 39. 5, s. 311–314, 2002. PMID: 12011145. 
  • Hyman SL, Shores A, North KN. The nature and frequency of cognitive deficits in children with neurofibromatosis type 1. „Neurology”. 65. 7, s. 1037-1044, 2005. PMID: 16217056. 
  • Hyman SL, Gill DS, Shores EA, Steinberg A, Joy P, Gibikote SV, North KN. Natural history of cognitive deficits and their relationship to MRI T2-hyperintensities in NF1. „Neurology”. 60. 7, s. 1139-1145, 2003. PMID: 12682321. 
  • Gutmann, DH, Aylsworth, A, Carey, JC, Korf, B, Marks, J, Pyeritz, RE, Rubenstein, A, Viskochil, D. The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. „JAMA”. 278. 1. s. 51-57. PMID: 9207339. 
  • Ferner RE. Neurofibromatosis 1. „Eur J Hum Genet”. 15. 2, s. 131-8, 2007. DOI: 10.1038/sj.ejhg.5201676. PMID: 16957683. 
  • Rasmussen SA, Yang Q, Friedman JM. Mortality in neurofibromatosis. 1: An analysis using US death certificates. „Am J Hum Genet”. 68, s. 1110–1118, 2001. DOI: 10.1086/320121. PMID: 11283797. 
  • Tibbles J, Cohen M. The Proteus syndrome: the Elephant Man diagnosed. „Br Med J (Clin Res Ed)”. 293. 6548, s. 683-685, 1986. PMID: 3092979.