222 results on '"MAZANEC, R."'
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2. Signatures of natural selection in a foundation tree along Mediterranean climatic gradients
3. Quambalaria shoot blight resistance in marri (Corymbia calophylla): Genetic parameters and correlations between growth rate and blight resistance
4. Resistance to quambalaria shoot blight and myrtle rust in Corymbia calophylla seedlings
5. Muscular dystrophies and myopathies: the spectrum of mutated genes in the Czech Republic
6. Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom
7. Pletencové svalové dystrofie.
8. Mosaicism for GJB1 mutation causes milder Charcot-Marie-Tooth X1 phenotype in a heterozygous man than in a manifesting heterozygous woman
9. Lower urinary tract functions in a series of Charcot–Marie–Tooth neuropathy patients
10. Genetic parameters and potential gains from breeding for biomass and cineole production in three-year-old Eucalyptus polybractea progeny trials
11. Effect of thinning and fertilizer on growth and allometry of Eucalyptus marginata
12. High frequency of SH3TC2 mutations in Czech HMSN I patients
13. Demyelinating Charcot–Marie–Tooth neuropathy associated with FBLN5 mutations
14. Provenance variation, genetic parameters and potential gains from selection for biomass and cineole production in three-year-old Eucalyptus loxophleba subsp. gratiae progeny trials
15. Effect of ascorbic acid in CMT1A disease: a Czech multicentre, randomized, double-blind, placebo-controlled trial: SC134
16. Clinical and in silico evidence for and against pathogenicity of 11 new mutations in the MPZ gene
17. Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease (vol 13, 155, 2018)
18. Charcot-Marie-Tooth neuropathy type 1A combined with Duchenne muscular dystrophy
19. Phenotypic expression of MFN2 gene mutations in six Czech CMT2A families: SC222
20. INHERITED ULCERO-MUTILATING NEUROPATHIES CMT2B AND HSN1 IN CZECH FAMILIES
21. TWO DISTINCTIVE PATHOLOGIES BETWEEN EARLY-AND LATE-ONSET OF CMT1B
22. A decadal multi-site study of the effects of frequency and season of harvest on biomass production from mallee eucalypts
23. Lyme neuroborreliosis without and with skin symptoms: why is the clinical picture of neuroborreliosis changing?
24. CANVAS – nově identifikovaná genetická příčina ataxie s pozdním nástupem. Popis prvních diagnostikovaných pacientů v České republice.
25. Využití rohovkové konfokální mikroskopie u neurologických onemocnění.
26. Český národní registr Guillainova-Barrého syndromu
27. Prevalence of Martin-Gruber Anastomosis – an Electrophysiological Study
28. Novel SBF2 mutations and clinical spectrum of Charcot-Marie-Tooth neuropathy type 4B2
29. Výsledky aktuálně probíhající validace českých a slovenských verzí dotazníků využívaných k monitoraci klinického stavu u pacientů s ALS -- pilotní projekt.
30. Nodo-paranodopatie s protilátkami IgG4 proti neurofascinu-155.
31. Genetic parameters and potential gains from breeding for biomass and cineole production in three-year-old Eucalyptus polybracteaprogeny trials
32. Czech national registry of facioscapulohumeral muscular dystrophy
33. Provenance variation, genetic parameters and potential gains from breeding for biomass and cineole production in three-year-old Eucalyptus loxophleba subsp. lissophloia progeny trials
34. Provenance variation, genetic parameters and potential gains from selection for biomass and cineole production in three-year-old Eucalyptus loxophlebasubsp. gratiaeprogeny trials
35. Selected items from the Charcot-Marie-Tooth (CMT) Neuropathy Score and secondary clinical outcome measures serve as sensitive clinical markers of disease severity in CMT1A patients
36. Efficacy and Safety of Lacosamide in Painful Diabetic Neuropathy
37. Muscular dystrophies and myopathies: the spectrum of mutated genes in the Czech Republic
38. HSMNR belongs to the most frequent types of hereditary neuropathy in the Czech Republic and is twice more frequent than HMSNL
39. Prevalence kardiální autonomní neuropatie u vybraných hereditárních neuropatií.
40. Zkušenosti s léčbou nusinersenem u dospělých SMA pacientů v NM centru FN Motol a role EMG v monitoraci průběhu nemoci a léčby.
41. Myotonic dystrophy in Czech Republic: data from the national registry
42. Selected items from the Charcot-Marie-Tooth (CMT) Neuropathy Score and secondary clinical outcome measures serve as sensitive clinical markers of disease severity in CMT1A patients
43. P.108 - Czech national registry of facioscapulohumeral muscular dystrophy
44. Prevalence of Martin-Gruber Anastomosis - an Electrophysiological Study.
45. Český národní registr Guil lainova-Barrého syndromu.
46. Kmenové buňky v léčbě amyotrofi cké laterální sklerózy - přehled současných klinických zkušeností.
47. Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom
48. G.P.250
49. 5. Electrophysiological features of peripheral and central nervous system in hereditary neuropathy Charcot Marie Tooth linked to X chromosome
50. Lower urinary tract functions in a series of Charcot-Marie-Tooth neuropathy patients
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