Sign In

Login

Password

Forgot Password ? Sign Up

Spinobulbäre Muskelatrophie Typ Kennedy (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Spinobulbäre Muskelatrophie Typ Kennedy" in German language version.

refsWebsite
Global rank German rank
11nih.gov
4th place
7th place
1doi.org
2nd place
3rd place
1orpha.net
3,537th place
429th place
1omim.org
4,380th place
781st place

doi.org

  • G. Kuhlenbäumer u. a.: Die X-chromosomal rezessive spinobulbäre Muskelatrophie (Typ Kennedy) Beschreibung einer Familie, Klinik, molekulare Genetik, Differentialdiagnose und Therapie. In: Der Nervenarzt 69, 1998, S. 660–665. doi:10.1007/s001150050325.

nih.gov

ncbi.nlm.nih.gov

  • A. E. Harding u. a.: X-linked recessive bulbospinal neuronopathy: a report of ten cases. In: J. Neurol. Neurosurg. Psychiat. 45, 1982, S. 1012–1019. PMID 6890989.
  • B. J. Schmidt u. a.: Expression of X-linked bulbospinal muscular atrophy (Kennedy disease) in two homozygous women. In: Neurology 59, 2002, S. 770–772. PMID 12221177.
  • B. Udd u. a.: High prevalence of Kennedy’s disease in western Finland: is the syndrome underdiagnosed? In: Acta Neurol. Scand., 98, 1998, S. 128–133. PMID 9724012.
  • A. Lund u. a.: Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia. In: Europ. J. Hum. Genet., 8, 2000, S. 631–636. PMID 10951525.
  • I. Georgiou u. a.: Preimplantation genetic diagnosis for spinal and bulbar muscular atrophy (SBMA). In: Hum. Genet. 108, 2001, S. 494–498. PMID 11499674.
  • M. Minamiyama u. a.: Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy. In: Hum. Molec. Genet. 13, 2004, S. 1183–1192. PMID 15102712.
  • M. Katsuno u. a.: Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy. In: Nature Med 9, 2003, S. 768–773. PMID 12754502.
  • Z. Yang u. a.: ASC-J9 ameliorates spinal and bulbar muscular atrophy phenotype via degradation of androgen receptor. In: Nature Med 13, 2007, S. 348–353. PMID 17334372.
  • W. R. Kennedy u. a.: Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait. In: Neurology 18, 1968, S, 671–680. PMID 4233749.
  • H. Tsukagoshi u. a.: Hereditary, proximal, neurogenic muscular atrophy in adult. In: Arch. Neurol., 12, 1965, S. 597–603. PMID 14295959.
  • A. R. La Spada u. a.: Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. In: Nature, 352, 1991, S. 77–79. PMID 2062380.

omim.org

orpha.net