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2 612 (0,095s) •

Project

Inproduction of the molecular genetic diagnosis in the most frequent genetic syndromes with deafness. (IZ2891)

FG - Pediatrie

  • 1995 - 1997
    • •
  • 1 044 tis. Kč
    • •
  • 1 044 tis. Kč
    • •
  • MZ
Project

Massive parallel sequencing (MPS) for elucidation of causes of early hereditary hearing loss in Czech patients without GJB2 mutations (NV16-31173A)

Early severe deafness has prevalence of 1:1000 and is the most frequent sensory deficit. More than 60% of the cases have genetic, monogenic origin, most frequently autosomal recessive and are non-syndromic. Hereditary deafness

FF - ORL, oftalmologie, stomatologie

  • 2016 - 2019
    • •
  • 6 907 tis. Kč
    • •
  • 6 907 tis. Kč
    • •
  • MZ
Project

The level of quality of the deaf education - a national research (RS99004)

After the research and description of present conditions for deaf education to work out some proposals to improve the deaf education as well as further education of spec. ed. teachers.......

AM - Pedagogika a školství

  • 1999 - 1999
    • •
  • 200 tis. Kč
    • •
  • 200 tis. Kč
    • •
  • MŠMT
Project

Theatre of the Deaf and New Ways (ICE8983201)

The paper exploresnew ways brought by using of sign language in theatre. Collecting of a historical material shows that theatre of the Deaf is an internally coherent theatre stream. Realization of projects "From a picture to a movement schoo...

AL - Umění, architektura, kulturní dědictví

  • 2002 - 2002
    • •
  • 230 tis. Kč
    • •
  • 222 tis. Kč
    • •
  • AV ČR
Project

Molecular genetic charakteristic of CFTR gne mutations with atypical course of cystic fibrosis. (IZ2899)

Detection of CFTR mutations leading to infertility,congenit. disordes of the uropoetic system,malabsorption,deafness,nasal polyp.,chronic respiratory infect.,asthma and chronic pancereatit. to improve their prevent.and therapy,in childhood a...

FG - Pediatrie

  • 1995 - 1999
    • •
  • 3 530 tis. Kč
    • •
  • 3 160 tis. Kč
    • •
  • MZ
Project

Unknown cause of DFNB1 deafness in patients with only one pathogenic GJB2 gene mutation – complex elucidation by new molecular genetic approaches. (NV16-31921A)

that mutations in the GJB2 gene cause up to 40 % of early nonsyndromic deafness in Czech for the hearing impairment in these patients. DNA samples of deaf heterozygotes with only one recurrent rearrangement would clarify the cause...

FF - ORL, oftalmologie, stomatologie

  • 2016 - 2020
    • •
  • 5 531 tis. Kč
    • •
  • 5 456 tis. Kč
    • •
  • MZ
Project

BAHA processor in patients with single-sided deafness (NT11543)

in patients with a single sided deafness, disregarding the aetiology. The uniqueness of the BAHA system in patients with a single sided deafness consists in a transformation with a single sided deafness is aiming to a hypo...

FF - ORL, oftalmologie, stomatologie

  • 2010 - 2015
    • •
  • 8 652 tis. Kč
    • •
  • 8 652 tis. Kč
    • •
  • MZ
Project

Research and application of time-frequency analysis in logopaedia, foreign language learning and learning speech of deaf pearson. (FT-TA2/072)

and improve the training of deaf peoples speaking....

JD - Využití počítačů, robotika a její aplikace

  • 2005 - 2009
    • •
  • 12 291 tis. Kč
    • •
  • 9 203 tis. Kč
    • •
  • MPO
Project

Mutation analysis of connexin 26 gene as the most frequent cause of prelingual nonsyndromic hearing loss. (NM7417)

Mutation analysis of the connexin 26 gene as the major gene for prelingual hearing loss in Czech patients and families with prelingual nonsydromic deafness and cochlear implant recipients.......

FF - ORL, oftalmologie, stomatologie

  • 2003 - 2005
    • •
  • 2 241 tis. Kč
    • •
  • 2 154 tis. Kč
    • •
  • MZ
Project

Electric stimulation in deaf-patients. (IZ1547)

9F - 9

  • 1993 - 1994
    • •
  • 0 tis. Kč
    • •
  • 0 tis. Kč
    • •
  • MZ
  • 1 - 10 out of 2 612