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446 (0,164s)

Result

Histopathological features in subsequent muscle biopsies in a warmblood mare with myotonic dystrophy

FH - Neurologie, neurochirurgie, neurovědy

  • 2012
  • Jx
  • Link
Result

Sequestration of MBNL1 protein by mutant ZNF9 RNA in lymphocytes of patients with myotonic dystrophy type 2

FH - Neurologie, neurochirurgie, neurovědy

  • 2011
  • O
Result

Sequestration of MBNL1 in tissues of patients with myotonic dystrophy type 2

FH - Neurologie, neurochirurgie, neurovědy

  • 2012
  • Jx
  • Link
Result

Myotonická dystrofie – Jednota v různosti

Myotonická dystrofie je nejčastější svalová dystrofie dospělého věku. Jde o autozomálně dominantní onemocnění charakterizované klíčovou triádou příznaků: svalová slabost, myotonie a katarakta. Podstatou je expanze trinukleotidových sekvencí CTG v gen...

Clinical neurology

  • 2017
  • Jimp
  • Link
Result

Molecular genetic diagnostics of myotonic dystrophy and facioscapulohumeral muscular dystrophy in Czech patients

EB - Genetika a molekulární biologie

  • 2006
  • O
Result

Sequestration of MBNL1 Protein by Mutant ZNF9 mRNA in Lymphocytes of Patients with Myotonic Dystrophy Type 2

BO - Biofyzika

  • 2012
  • Jx
Result

Strategies for Neuromuscular Blockade in Patients with Myotonic Dystrophy

FH - Neurologie, neurochirurgie, neurovědy

  • 2015
  • C
Result

Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease

Neurosciences (including psychophysiology)

  • 2018
  • Jimp
  • Link
Result

Sugammadex in a parturient with myotonic dystrophy

FK - Gynekologie a porodnictví

  • 2013
  • Jx
  • Link
  • 1 - 10 out of 446