Add to ORKGAmong 300 patients affected by hereditary ataxia, 94 received the diagnosis of Friedreich's disease, 12 of Late Onset Friedreich's disease, 27 of Early Onset Cerebellar Ataxia with retained tendon reflexes, 10 of Progressive Myoclonic Ataxia, 4 of Ataxia with hypogonadism and 2 of Ataxia with hearing loss. Only Friedreich's disease appears clinically homogeneous, whereas the others are not specific entities and each of them probably includes different diseases
Friedreich ataxia (FRDA) is a rare autosomal recessive hereditary disorder caused by expansion of a ...
PubMed ID: 3407387ABSTRACT— The authors report the clinical review of 20 childhood cases with Friedr...
Friedreich ataxia is the commonest of the inherited ataxias, accounting for at least 50 % in most la...
Among 300 patients affected by hereditary ataxia, 94 received the diagnosis of Friedreich's disease,...
The classifications of hereditary ataxias (HA) proposed from 1907 to 1984 are reviewed. An analysis ...
Friedreich's ataxia, a hereditary disorder of the nervous system, is characterized by the onset...
Friedreich ataxia (FRDA) is a rare autosomal recessive hereditary disorder that affects approximatel...
Objective To provide a systematic evaluation of the broad clinical variability in Friedreich ataxia ...
Atypical Friedreich's ataxia was diagnosed by DNA-analysis in 4 patients, 2 men aged 70 and 67 and 2...
Friedreich was the fast person to gave chemical description of ataxia. Three types of Ataxias are o...
OBJECTIVE: To provide a systematic evaluation of the broad clinical variability in Friedreich ataxia...
Objective To provide a systematic evaluation of the broad clinical variability in Friedreich ataxia ...
The clinical and genetic features of 80 patients with Friedreich's disease from 64 families are desc...
SUMMARY A family is described in which Friedreich's ataxia occurred in two generations. It is p...
The accuracy of the diagnostic criteria for Friedreich's ataxia proposed by Harding and by the Quebe...
Friedreich ataxia (FRDA) is a rare autosomal recessive hereditary disorder caused by expansion of a ...
PubMed ID: 3407387ABSTRACT— The authors report the clinical review of 20 childhood cases with Friedr...
Friedreich ataxia is the commonest of the inherited ataxias, accounting for at least 50 % in most la...
Among 300 patients affected by hereditary ataxia, 94 received the diagnosis of Friedreich's disease,...
The classifications of hereditary ataxias (HA) proposed from 1907 to 1984 are reviewed. An analysis ...
Friedreich's ataxia, a hereditary disorder of the nervous system, is characterized by the onset...
Friedreich ataxia (FRDA) is a rare autosomal recessive hereditary disorder that affects approximatel...
Objective To provide a systematic evaluation of the broad clinical variability in Friedreich ataxia ...
Atypical Friedreich's ataxia was diagnosed by DNA-analysis in 4 patients, 2 men aged 70 and 67 and 2...
Friedreich was the fast person to gave chemical description of ataxia. Three types of Ataxias are o...
OBJECTIVE: To provide a systematic evaluation of the broad clinical variability in Friedreich ataxia...
Objective To provide a systematic evaluation of the broad clinical variability in Friedreich ataxia ...
The clinical and genetic features of 80 patients with Friedreich's disease from 64 families are desc...
SUMMARY A family is described in which Friedreich's ataxia occurred in two generations. It is p...
The accuracy of the diagnostic criteria for Friedreich's ataxia proposed by Harding and by the Quebe...
Friedreich ataxia (FRDA) is a rare autosomal recessive hereditary disorder caused by expansion of a ...
PubMed ID: 3407387ABSTRACT— The authors report the clinical review of 20 childhood cases with Friedr...
Friedreich ataxia is the commonest of the inherited ataxias, accounting for at least 50 % in most la...