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Значения термина friedreich ataxia на английском

русский
атаксия фридрейха
португальский
ataxia de friedreich
испанский
ataxia de friedreich
каталонский
atàxia familiar

Human disease.

атаксия фридрейха
Синонимы
Examples for "fa"
Examples for "fa"
1
Peridal hasn't even had a chance to live in a fa'lodge yet.
The Shelters of Stone
2
When Qudiya-fa-Kana heard these lines, she made her disapproval plain to see.
The Arabian Nights: Tales of 1,001 Nights. Vol. 1
3
Here comes Neil, and we'll let the question fa' to the ground.
The Bow of Orange Ribbon: A Romance of New York
4
It was an old Breguet watch of her fa-ther's, from the fifties.
Safe harbour
5
It hasn't seen a true repeat since Graham's 2005 FA until today.
Climbing Magazine
1
Nevertheless, inadequacy of existing FRDA-cardiac cellular models limited cardiomyopathy studies.
Pubmed
2
Conclusions: DFP modulated iron homeostasis in FRDA-hiPSC-cardiomyocytes and effectively relieved stress-stimulation related to cardiomyopathy.
Pubmed
3
Linkage data indicate that FRDA is at less than 1 cM from both markers.
Pubmed
4
FRDA is also associated with cognitive impairments.
Pubmed
5
Methods: Healthy control and FRDA patient-specific hPSC-hvCMs were derived by directed differentiation using a small molecule-based protocol reported previously.
Pubmed
1
The preservation of tendon reflexes distinguishes this disorder from Friedreich's ataxia.
Pubmed
2
He has used a wheelchair since Friedreich's ataxia, a muscle-wasting disease, made walking impossible.
The Guardian
3
Other important differences from Friedreich's ataxia are absence of optic atrophy, diabetes mellitus, cardiomyopathy and severe skeletal deformity.
Pubmed
4
A cluster of Friedreich's ataxia patients has been previously investigated in two neighbouring villages of the Paphos district of Cyprus.
Pubmed
5
Unexpectedly, the genes responsible for Friedreich's ataxia and a form of autosomal recessive spastic paraplegia place these diseases in the category of mitochondrial disorders.
Pubmed
Использование термина friedreich ataxia на английском
1
The Friedreich ataxia phenotype is the most frequent clinical presentation.
Pubmed
2
Friedreich ataxia (FA) is an autosomal recessive degenerative disease of the nervous system of unknown biochemical cause.
Pubmed
3
Reduced expression of a mitochondrial protein called frataxin causes a neurodegenerative disorder named Friedreich Ataxia, which decreases life span in humans.
Pubmed
4
We present a linkage study of three large Friedreich ataxia families of Tunisian origin, with several multiallelic markers around D9S5 and D9S15.
Pubmed
5
Precise linkage mapping of the Friedreich ataxia locus (FRDA) in 9q13-q21 should lead to the isolation of the defective gene by positional cloning.
Pubmed