Sign In

Login

Password

Forgot Password ? Sign Up

Dystonia torsyjna typu 1 (Polish Wikipedia)

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

refsWebsite
Global rank Polish rank
26nih.gov
4th place
7th place
11doi.org
2nd place
6th place
2whonamedit.com
2,888th place
496th place

doi.org

  • Nutt JG, Muenter MD, Aronson A, Kurland LT, Melton LJ. Epidemiology of focal and generalized dystonia in Rochester, Minnesota. „Mov Disord”. 3. 3, s. 188-94, 1989. DOI: 10.1002/mds.870030302. PMID: 3264051. 
  • Risch N, de Leon D, Ozelius L, Kramer P, Almasy L, Singer B, Fahn S, Breakefield X, Bressman S. Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population. „Nat Genet”. 9. 2, s. 152-9, 1995. DOI: 10.1038/ng0295-152. PMID: 7719342. 
  • Bressman SB, de Leon D, Brin MF, Risch N, Burke RE, Greene PE, Shale H, Fahn S. Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance. „Ann Neurol”. 26. 5, s. 612-20, 1989. DOI: 10.1002/ana.410260505. PMID: 2817837. 
  • Asanuma K, Ma Y, Okulski J, Dhawan V, Chaly T, Carbon M, Bressman SB, Eidelberg D. Decreased striatal D2 receptor binding in non-manifesting carriers of the DYT1 dystonia mutation. „Neurology”. 64. 2, s. 347-9, 2005. DOI: 10.1212/01.WNL.0000149764.34953.BF. PMID: 15668438. 
  • Greene P, Kang UJ, Fahn S. Spread of symptoms in idiopathic torsion dystonia. „Mov Disord”. 10. 2, s. 143-52, 1995. DOI: 10.1002/mds.870100204. PMID: 7753056. 
  • Burke RE, Brin MF, Fahn S, Bressman SB, Moskowitz C. Analysis of the clinical course of non-Jewish, autosomal dominant torsion dystonia. „Movement Disorders”. 1 (3), s. 163-78, 1989. DOI: 10.1002/mds.870010302. PMID: 3504242. 
  • Kamm C. Early onset torsion dystonia (Oppenheim's dystonia). „Orphanet J Rare Dis”. 1, s. 48, 2006. DOI: 10.1186/1750-1172-1-48. PMID: 17129379. 
  • Ahmad F, Davis MB, Waddy HM, Oley CA, Marsden CD., Harding AE. Evidence for locus heterogeneity in autosomal dominant torsion dystonia. „Genomics”. 1 (15), s. 9-12, styczeń 1993. DOI: 10.1006/geno.1993.1003. PMID: 8432555. 
  • Parker N. Hereditary whispering dysphonia.. „J Neurol Neurosurg Psychiatry”. 3 (48), s. 218-24, marzec 1985. PMID: 3156966.  Almasy L, Bressman SB, Raymond D, Kramer PL, Greene PE, Heiman GA, Ford B, Yount J, de Leon D, Chouinard S, Saunders-Pullman R, Brin MF, Kapoor RP, Jones AC, Shen H, Fahn S., Risch NJ, Nygaard TG. Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families. „Ann Neurol”. 42. 4, s. 670-3, 1997. DOI: 10.1002/ana.410420421. PMID: 9382482. 
  • Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. „Nature”. 392. 6676, s. 605-8, 1998. DOI: 10.1038/33416. PMID: 9560156. 
  • Vidailhet M, Vercueil L, Houeto JL, Krystkowiak P, Benabid AL, Cornu P, Lagrange C, Tézenas du Montcel S, Dormont D, Grand S, Blond S, Detante O, Pillon B, Ardouin C, Agid Y, Destée A, Pollak P. Bilateral deep-brain stimulation of the globus pallidus in primary generalized dystonia. „N Engl J Med”. 352. 5, s. 459-67, 2005. DOI: 10.1056/NEJMoa042187. PMID: 15689584. 

nih.gov

ncbi.nlm.nih.gov

  • Barraquer-Bordas L, Giménez-Roldán S. Idiopathic torsion dystonia as described by Barraquer-Roviralta. „Adv Neurol”. 50, s. 665-6, 1988. PMID: 3041765. 
  • Pearce JM. Lluis Barraquer i Roviralta and the origins of torsion dystonia. „J Neurol Neurosurg Psychiatry”. 75. 4, s. 582, 2004. PMID: 15026501. 
  • Nutt JG, Muenter MD, Aronson A, Kurland LT, Melton LJ. Epidemiology of focal and generalized dystonia in Rochester, Minnesota. „Mov Disord”. 3. 3, s. 188-94, 1989. DOI: 10.1002/mds.870030302. PMID: 3264051. 
  • Zeman W, Dyken P. Dystonia musculorum deformans. Clinical, genetic and pathoanatomical studies. „Psychiatr Neurol Neurochir”. 70. 2, s. 77-121, 1967. PMID: 6050693. 
  • Risch N, de Leon D, Ozelius L, Kramer P, Almasy L, Singer B, Fahn S, Breakefield X, Bressman S. Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population. „Nat Genet”. 9. 2, s. 152-9, 1995. DOI: 10.1038/ng0295-152. PMID: 7719342. 
  • Ozelius LJ, Hewett J, Kramer P, Bressman SB, Shalish C, de Leon D, Rutter M, Risch N, Brin MF, Markova ED, Limborska SA, Ivanova-Smolenskaya IA, McCormick MK, Fahn S, Buckler AJ, Gusella JF, Breakefield XO. Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium. „Genome Res”. 5 (7), s. 483-94, maj 1997. PMID: 9149944. 
  • Bressman SB, de Leon D, Brin MF, Risch N, Burke RE, Greene PE, Shale H, Fahn S. Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance. „Ann Neurol”. 26. 5, s. 612-20, 1989. DOI: 10.1002/ana.410260505. PMID: 2817837. 
  • Konakova M, Huynh DP, Yong W, Pulst SM. Cellular distribution of torsin A and torsin B in normal human brain. „Arch Neurol”. 58. 6, s. 921-7, 2001. PMID: 11405807. 
  • Asanuma K, Ma Y, Okulski J, Dhawan V, Chaly T, Carbon M, Bressman SB, Eidelberg D. Decreased striatal D2 receptor binding in non-manifesting carriers of the DYT1 dystonia mutation. „Neurology”. 64. 2, s. 347-9, 2005. DOI: 10.1212/01.WNL.0000149764.34953.BF. PMID: 15668438. 
  • Bressman SB, Sabatti C, Raymond D, de Leon D, Klein C, Kramer PL, Brin MF, Fahn S, Breakefield X, Ozelius LJ, Risch NJ. The DYT1 phenotype and guidelines for diagnostic testing. „Neurology”. 54. 9, s. 1746-52, 2000. PMID: 10802779. 
  • Greene P, Kang UJ, Fahn S. Spread of symptoms in idiopathic torsion dystonia. „Mov Disord”. 10. 2, s. 143-52, 1995. DOI: 10.1002/mds.870100204. PMID: 7753056. 
  • Marsden CD. Investigation of dystonia.. „Adv Neurol”. 50, s. 35-44, 1988. PMID: 3041758. 
  • Burke RE, Brin MF, Fahn S, Bressman SB, Moskowitz C. Analysis of the clinical course of non-Jewish, autosomal dominant torsion dystonia. „Movement Disorders”. 1 (3), s. 163-78, 1989. DOI: 10.1002/mds.870010302. PMID: 3504242. 
  • Heiman GA, Ottman R, Saunders-Pullman RJ, Ozelius LJ, Risch NJ, Bressman SB. Increased risk for recurrent major depression in DYT1 dystonia mutation carriers. „Neurology”. 63. 4, s. 631-7, 2004. PMID: 15326234. 
  • Kamm C. Early onset torsion dystonia (Oppenheim's dystonia). „Orphanet J Rare Dis”. 1, s. 48, 2006. DOI: 10.1186/1750-1172-1-48. PMID: 17129379. 
  • Fletcher NA. The genetics of idiopathic torsion dystonia. „J Med Genet”. 27. 7, s. 409-12, 1990. PMID: 2203908. 
  • Ahmad F, Davis MB, Waddy HM, Oley CA, Marsden CD., Harding AE. Evidence for locus heterogeneity in autosomal dominant torsion dystonia. „Genomics”. 1 (15), s. 9-12, styczeń 1993. DOI: 10.1006/geno.1993.1003. PMID: 8432555. 
  • Parker N. Hereditary whispering dysphonia. „J Neurol Neurosurg Psychiatry”. 48. 3, s. 218-24, 1985. PMID: 3156966. 
  • Parker N. Hereditary whispering dysphonia.. „J Neurol Neurosurg Psychiatry”. 3 (48), s. 218-24, marzec 1985. PMID: 3156966.  Almasy L, Bressman SB, Raymond D, Kramer PL, Greene PE, Heiman GA, Ford B, Yount J, de Leon D, Chouinard S, Saunders-Pullman R, Brin MF, Kapoor RP, Jones AC, Shen H, Fahn S., Risch NJ, Nygaard TG. Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families. „Ann Neurol”. 42. 4, s. 670-3, 1997. DOI: 10.1002/ana.410420421. PMID: 9382482. 
  • Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. „Nature”. 392. 6676, s. 605-8, 1998. DOI: 10.1038/33416. PMID: 9560156. 
  • Lücking CB, Dürr A, Bonifati V, Vaughan J, De Michele G, Gasser T, Harhangi BS, Meco G, Denèfle P, Wood NW, Agid Y, Brice A. Association between early-onset Parkinson's disease and mutations in the parkin gene. „N Engl J Med”. 342. 21, s. 1560-7, 2000. PMID: 10824074. 
  • Burke RE, Fahn S, Marsden CD. Torsion dystonia: a double-blind, prospective trial of high-dosage trihexyphenidyl. „Neurology”. 36. 2, s. 160-4, 1986. PMID: 3511401. 
  • Walker RH, Danisi FO, Swope DM, Goodman RR, Germano IM, Brin MF. Intrathecal baclofen for dystonia: benefits and complications during six years of experience. „Mov Disord”. 15. 6, s. 1242-7, 2001. PMID: 11104213. 
  • Jankovic J. Dystonia: medical therapy and botulinum toxin. „Adv Neurol”. 94, s. 275-86, 2003. PMID: 14509685. 
  • Vercueil L, Krack P, Pollak P. Results of deep brain stimulation for dystonia: a critical reappraisal. „Mov Disord”. 17 Suppl 3, s. S89-93, 2002. PMID: 11948761. 
  • Vidailhet M, Vercueil L, Houeto JL, Krystkowiak P, Benabid AL, Cornu P, Lagrange C, Tézenas du Montcel S, Dormont D, Grand S, Blond S, Detante O, Pillon B, Ardouin C, Agid Y, Destée A, Pollak P. Bilateral deep-brain stimulation of the globus pallidus in primary generalized dystonia. „N Engl J Med”. 352. 5, s. 459-67, 2005. DOI: 10.1056/NEJMoa042187. PMID: 15689584. 

whonamedit.com