To characterize epileptic phenotype, electroencephalography (EEG) features, and epileptic evolution in patients with ring 14 r(14) syndrome
Ring chromosomes are rare abnormalities caused by the fusion of the telomeric regions. Three-ring ch...
Objectives: To evaluate the spectral and spatial features of the cortical rhythms in patients affect...
Ring chromosome 20 [r(20)] syndrome is a rare condition characterized by a non-supernumerary ring ch...
The ring 14 syndrome is a rare condition, whose precise clinical and genetic characterization is sti...
PubMedID: 24382541Ring chromosome 14 syndrome is a rare genetic disorder. Typically, children with t...
International audienceWe report four infants (two males, two females) with ring 14 chromosome presen...
Abstract Background Ring chromosome 14 syndrome is a rare chromosomal disorder characterized by earl...
The syndrome “ring of chromosome 14 ” is a rare pathology which reveals itself mainly by mental and ...
Objective: Ring chromosome 20 syndrome is characterized by severe, drug resistant childhood onset ep...
This study aimed to assess the communicative skills of children and young adults with ring 14 syndro...
To identify the brain networks that are involved in the different electroencephalography (EEG) abnor...
To identify the brain networks that are involved in the different electroencephalography (EEG) abnor...
Objective To identify the brain networks that are involved in the different electroencephalography (...
Objective To identify the brain networks that are involved in the different electroencephalography ...
Ring chromosome 20 [r(20)] syndrome is an underdiagnosed chromosomal anomaly characterized by severe...
Ring chromosomes are rare abnormalities caused by the fusion of the telomeric regions. Three-ring ch...
Objectives: To evaluate the spectral and spatial features of the cortical rhythms in patients affect...
Ring chromosome 20 [r(20)] syndrome is a rare condition characterized by a non-supernumerary ring ch...
The ring 14 syndrome is a rare condition, whose precise clinical and genetic characterization is sti...
PubMedID: 24382541Ring chromosome 14 syndrome is a rare genetic disorder. Typically, children with t...
International audienceWe report four infants (two males, two females) with ring 14 chromosome presen...
Abstract Background Ring chromosome 14 syndrome is a rare chromosomal disorder characterized by earl...
The syndrome “ring of chromosome 14 ” is a rare pathology which reveals itself mainly by mental and ...
Objective: Ring chromosome 20 syndrome is characterized by severe, drug resistant childhood onset ep...
This study aimed to assess the communicative skills of children and young adults with ring 14 syndro...
To identify the brain networks that are involved in the different electroencephalography (EEG) abnor...
To identify the brain networks that are involved in the different electroencephalography (EEG) abnor...
Objective To identify the brain networks that are involved in the different electroencephalography (...
Objective To identify the brain networks that are involved in the different electroencephalography ...
Ring chromosome 20 [r(20)] syndrome is an underdiagnosed chromosomal anomaly characterized by severe...
Ring chromosomes are rare abnormalities caused by the fusion of the telomeric regions. Three-ring ch...
Objectives: To evaluate the spectral and spatial features of the cortical rhythms in patients affect...
Ring chromosome 20 [r(20)] syndrome is a rare condition characterized by a non-supernumerary ring ch...
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