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Julian Curiel

Children's Hospital of Philadelphia

9

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191

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TUBB4A mutations result in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse model.

2020 eLife
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Absence of axoglial paranodal junctions in a child with CNTNAP1 mutations, hypomyelination, and arthrogryposis

2018 Journal of Child Neurology
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Loss of CLOCK Results in Dysfunction of Brain Circuits Underlying Focal Epilepsy.

2017 Neuron
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UFM1 founder mutation in the Roma population causes recessive variant of H-ABC

2017 Neurology
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X-linked adrenoleukodystrophy in a chimpanzee due to an ABCD1 mutation reported in multiple unrelated humans

2017 Molecular Genetics and Metabolism
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TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes

2017 Human Molecular Genetics
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TUBB4A-Related Leukodystrophy

2016
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The emerging role of the tubulin code: From the tubulin molecule to neuronal function and disease

2016 Cytoskeleton
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Citations (82)