Search results
- 1.0496875 - FLÚ 2019 RIV FR fre M - Monography Chapter
Fulka, Josef
La surdité et la langue des signes dans l’histoire de la philosophie.
[Deafness and sign language in the history of philosophy.]
Tous à l’école! Bonheurs, malentendus et paradoxes de l’éducation inclusive. Pessac: Presses universitaires de Bordeaux, 2018 - (Kohout-Diaz, M.), s. 81-90. Études sur l’éducation (Talence). ISBN 979-10-300-0224-9
Institutional support: RVO:67985955
Keywords : deafness * sign language * history
OECD category: Philosophy, History and Philosophy of science and technology
Permanent Link: http://hdl.handle.net/11104/0290255 - 2.0469548 - FGÚ 2017 RIV GB eng J - Journal Article
Ng, Y. S. - Alston, Ch. L. - Diodato, D. - Morris, A. A. - Ulrick, N. - Kmoch, S. - Houštěk, Josef - Martinelli, D. - Haghighi, A. - Atiq, M. - Gamero, M. A. - Garcia-Martinez, E. - Kratochvílová, H. - Santra, S. - Brown, R. M. - Brown, G. K. - Ragge, N. - Monavari, A. - Pysden, K. - Ravn, K. - Casey, J. P. - Khan, A. - Chakrapani, A. - Vassallo, G. - Simons, C. - McKeever, K. - O´Sullivan, S. - Childs, A.-M. - Ostergaard, E. - Vanderver, A. - Goldstein, A. - Vogt, J. - Taylor, R. W. - McFarland, R.
The clinical, biochemical and genetic features associated with RMND1-related mitochondrial disease.
Journal of Medical Genetics. Roč. 53, č. 11 (2016), s. 768-775. ISSN 0022-2593. E-ISSN 1468-6244
R&D Projects: GA ČR(CZ) GB14-36804G
Institutional support: RVO:67985823
Keywords : congenital sensorineural deafness * lactic acidosis * mitochondrial respiratory chain deficiencies * prognosis * renal disease
Subject RIV: EB - Genetics ; Molecular Biology
Impact factor: 5.451, year: 2016
Permanent Link: http://hdl.handle.net/11104/0267352 - 3.0425276 - ÚMG 2014 RIV DK eng J - Journal Article
Lisková, P. - Ulmanová, O. - Těšina, Petr - Melsová, H. - Diblik, P. - Hansíková, H. - Tesařová, M. - Votruba, M.
Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder.
Acta Ophthalmologica. Roč. 91, č. 3 (2013), e225-e231. ISSN 1755-375X. E-ISSN 1755-3768
Institutional research plan: CEZ:AV0Z50520514
Keywords : ataxia * autosomal dominant * deafness * encephalomyopathy
Subject RIV: EB - Genetics ; Molecular Biology
Impact factor: 2.512, year: 2013
Permanent Link: http://hdl.handle.net/11104/0231199 - 4.0392766 - ÚOCHB 2014 RIV DK eng J - Journal Article
Lisková, P. - Ulmanová, O. - Těšina, Petr - Melsová, H. - Diblik, P. - Hansíková, H. - Tesařová, M. - Votruba, M.
Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder.
Acta Ophthalmologica. Roč. 91, č. 3 (2013), E225-E231. ISSN 1755-375X. E-ISSN 1755-3768
Grant - others:GA MZd(CZ) NT11190
Institutional research plan: CEZ:AV0Z40550506
Keywords : ataxia * autosomal dominant * deafness * encephalomyopathy
Subject RIV: FF - HEENT, Dentistry
Impact factor: 2.512, year: 2013
Permanent Link: http://hdl.handle.net/11104/0221562 - 5.0137820 - UEF-S 20039022 RIV DE cze R - Book Review
Šálek, Cyril
[Recenze].
[Emmanuel Vlček et al.: Bedřich Smetana. Physical personality and deafness, Vesmír, Prague 2001. Review.]
[VLČEK, E. (ed.).: Bedřich Smetana. Fyzická osobnost a hluchota. - Praha, 2001.]. Hudební věda. Ústav dějin umění AV ČR, v. v. i. Roč. 39, č. 1 (2002), s. 76-78. ISSN 0018-7003
Institutional research plan: CEZ:AV0Z8059909
Keywords : Smetana * deafness * anthropology
Subject RIV: AL - Art, Architecture, Cultural Heritage
Permanent Link: http://hdl.handle.net/11104/0000832