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Julian Curiel

Showing results (1-10 of 9) with videos related to

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Nature Reviews. Neurology|January 6, 2018
Adulthood leukodystrophiesWolfgang Köhler, Julian Curiel, Adeline Vanderver
Cytoskeleton (Hoboken, N.J.)|March 3, 2016
The emerging role of the tubulin code: From the tubulin molecule to neuronal function and diseaseSoumyananda Chakraborti, Kathiresan Natarajan, Julian Curiel, et al.
Community Mental Health Journal|January 20, 2020
Medical Comorbidities and Medication Use Among Homeless Adults Seeking Mental Health TreatmentElizabeth Mayfield Arnold, Chance R Strenth, Luke P Hedrick, et al.
Molecular Genetics and Metabolism|September 19, 2017
X-linked adrenoleukodystrophy in a chimpanzee due to an ABCD1 mutation reported in multiple unrelated humansJulian Curiel, Steven Jeffrey Steinberg, Sarah Bright, et al.
Journal of Child Neurology|June 9, 2018
Absence of Axoglial Paranodal Junctions in a Child With CNTNAP1 Mutations, Hypomyelination, and ArthrogryposisAlexander Conant, Julian Curiel, Amy Pizzino, et al.
Human Molecular Genetics|October 4, 2017
TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypesJulian Curiel, Guillermo Rodríguez Bey, Asako Takanohashi, et al.
Elife|May 29, 2020
<i>TUBB4A</i> mutations result in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse modelSunetra Sase, Akshata A Almad, C Alexander Boecker, et al.
Neurology|September 22, 2017
<i>UFM1</i> founder mutation in the Roma population causes recessive variant of H-ABCEline M C Hamilton, Enrico Bertini, Luba Kalaydjieva, et al.
Neuron|October 13, 2017
Loss of CLOCK Results in Dysfunction of Brain Circuits Underlying Focal EpilepsyPeijun Li, Xiaoqin Fu, Nathan A Smith, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Nature Reviews. Neurology|January 6, 2018
Adulthood leukodystrophiesWolfgang Köhler, Julian Curiel, Adeline Vanderver
Cytoskeleton (Hoboken, N.J.)|March 3, 2016
The emerging role of the tubulin code: From the tubulin molecule to neuronal function and diseaseSoumyananda Chakraborti, Kathiresan Natarajan, Julian Curiel, et al.
Community Mental Health Journal|January 20, 2020
Medical Comorbidities and Medication Use Among Homeless Adults Seeking Mental Health TreatmentElizabeth Mayfield Arnold, Chance R Strenth, Luke P Hedrick, et al.
Molecular Genetics and Metabolism|September 19, 2017
X-linked adrenoleukodystrophy in a chimpanzee due to an ABCD1 mutation reported in multiple unrelated humansJulian Curiel, Steven Jeffrey Steinberg, Sarah Bright, et al.
Journal of Child Neurology|June 9, 2018
Absence of Axoglial Paranodal Junctions in a Child With CNTNAP1 Mutations, Hypomyelination, and ArthrogryposisAlexander Conant, Julian Curiel, Amy Pizzino, et al.
Human Molecular Genetics|October 4, 2017
TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypesJulian Curiel, Guillermo Rodríguez Bey, Asako Takanohashi, et al.
Elife|May 29, 2020
<i>TUBB4A</i> mutations result in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse modelSunetra Sase, Akshata A Almad, C Alexander Boecker, et al.
Neurology|September 22, 2017
<i>UFM1</i> founder mutation in the Roma population causes recessive variant of H-ABCEline M C Hamilton, Enrico Bertini, Luba Kalaydjieva, et al.
Neuron|October 13, 2017
Loss of CLOCK Results in Dysfunction of Brain Circuits Underlying Focal EpilepsyPeijun Li, Xiaoqin Fu, Nathan A Smith, et al.
Pageof 1