Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients.
about
PGC-1alpha down-regulation affects the antioxidant response in Friedreich's ataxia.Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus.Friedreich ataxia: molecular mechanisms, redox considerations, and therapeutic opportunities.Progression of brain atrophy in spinocerebellar ataxia type 2: a longitudinal tensor-based morphometry study.Friedreich ataxia in Norway - an epidemiological, molecular and clinical studyClinical aspects of hereditary ataxias.Central role and mechanisms of β-cell dysfunction and death in friedreich ataxia-associated diabetes.Serum versus Imaging Biomarkers in Friedreich Ataxia to Indicate Left Ventricular Remodeling and OutcomesFunctional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARgamma pathway as a therapeutic target in Friedreich's ataxia.Friedreich's Ataxia: a review from a cardiology perspective.Clinical features of Friedreich's ataxia: classical and atypical phenotypes.Friedreich Ataxia: current status and future prospects.Unveiling a common mechanism of apoptosis in β-cells and neurons in Friedreich's ataxia.Urinary, bowel and sexual symptoms in a cohort of patients with Friedreich's ataxia.The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia.Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population.Reduced striatal [123 I]FP-CIT binding in SCA2 patients without parkinsonism.Supratentorial and infratentorial damage in spinocerebellar ataxia 2: a diffusion-weighted MRI study.Lower medulla hypoplasia in Friedreich ataxia: MR Imaging confirmation 140 years later.Progression of microstructural damage in spinocerebellar ataxia type 2: a longitudinal DTI study.Long-term effect of epoetin alfa on clinical and biochemical markers in friedreich ataxia.Regional Cerebral Disease Progression in Friedreich's Ataxia: A Longitudinal Diffusion Tensor Imaging Study.Histogram analysis of DTI-derived indices reveals pontocerebellar degeneration and its progression in SCA2.Emerging therapeutics for the treatment of Friedreich’s ataxiaEarly-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the friedreich's ataxia locus on chromosome 9q
P2860
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P2860
Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients.
description
1990 nî lūn-bûn
@nan
1990 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients.
@ast
Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients.
@en
Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients.
@nl
type
label
Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients.
@ast
Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients.
@en
Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients.
@nl
prefLabel
Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients.
@ast
Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients.
@en
Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients.
@nl
P2093
P356
P1433
P1476
Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients.
@en
P2093
P2888
P304
P356
10.1007/BF00315657
P577
1990-10-01T00:00:00Z
P6179
1023404372