Universidade Federal de São Paulo (UNIFESP) Department of Neurology and NeurosurgeryUNIFESP, Department of Neurology and NeurosurgerySciEL
Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia due to muta...
Introduction Ataxia with oculomotor apraxia type 2 (AOA2) is an autosomal recessive disorder due to ...
Alpha-fetoprotein (AFP) is present in fetal serum in concentrations up to 5,000,000 mu g/l. After bi...
International audiencealpha-Fetoprotein (AFP) is a biomarker of several autosomal recessive cerebell...
Background: Ataxias represent a challenging group of disorders due to significant clinical overlap. ...
International audienceAtaxia with oculomotor apraxia type 2 (AOA2) is an autosomal recessive disease...
Ataxia with oculomotor apraxia type 2 (AOA2) is an autosomal recessive disease due to mutations in t...
International audienceWhether the recessive ataxias, Ataxia with oculomotor apraxia type 1 (AOA1) an...
BACKGROUND: Ataxia with oculomotor apraxia type 2 (AOA2) is characterized by onset between age 10 an...
We describe three patients from two families with progressive spinocerebellar ataxia, peripheral neu...
A 23-year-old woman had presented initially to a podiatrist complaining of poorly fitting shoes duri...
Hereditary autosomal-recessive cerebellar ataxias are a genetically and clinically heterogeneous gro...
Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia due to muta...
Introduction Ataxia with oculomotor apraxia type 2 (AOA2) is an autosomal recessive disorder due to ...
Alpha-fetoprotein (AFP) is present in fetal serum in concentrations up to 5,000,000 mu g/l. After bi...
International audiencealpha-Fetoprotein (AFP) is a biomarker of several autosomal recessive cerebell...
Background: Ataxias represent a challenging group of disorders due to significant clinical overlap. ...
International audienceAtaxia with oculomotor apraxia type 2 (AOA2) is an autosomal recessive disease...
Ataxia with oculomotor apraxia type 2 (AOA2) is an autosomal recessive disease due to mutations in t...
International audienceWhether the recessive ataxias, Ataxia with oculomotor apraxia type 1 (AOA1) an...
BACKGROUND: Ataxia with oculomotor apraxia type 2 (AOA2) is characterized by onset between age 10 an...
We describe three patients from two families with progressive spinocerebellar ataxia, peripheral neu...
A 23-year-old woman had presented initially to a podiatrist complaining of poorly fitting shoes duri...
Hereditary autosomal-recessive cerebellar ataxias are a genetically and clinically heterogeneous gro...
Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia due to muta...
Introduction Ataxia with oculomotor apraxia type 2 (AOA2) is an autosomal recessive disorder due to ...
Alpha-fetoprotein (AFP) is present in fetal serum in concentrations up to 5,000,000 mu g/l. After bi...