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Edythe Wiggs

Showing results (21-30 of 28) with videos related to

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DNA Repair|October 29, 2008
XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptomsSikandar G Khan, Kyu-Seon Oh, Steffen Emmert, et al.
Epilepsia|February 12, 2019
fMRI prediction of naming change after adult temporal lobe epilepsy surgery: Activation mattersXiaozhen You, Ashley N Zachery, Eleanor J Fanto, et al.
Brain : a Journal of Neurology|February 1, 2013
Auditory analysis of xeroderma pigmentosum 1971-2012: hearing function, sun sensitivity and DNA repair predict neurological degenerationMariam B Totonchy, Deborah Tamura, Matthew S Pantell, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
Neuropsychological phenotypes of 76 individuals with Joubert syndrome evaluated at a single centerAngela C Summers, Joseph Snow, Edythe Wiggs, et al.
JCI Insight|January 25, 2019
One-year pilot study on the effects of nitisinone on melanin in patients with OCA-1BDavid R Adams, Supriya Menezes, Ramon Jauregui, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
In-depth investigations of adolescents and adults with holoprosencephaly identify unique characteristicsKarin Weiss, Paul Kruszka, Maria J Guillen Sacoto, et al.
The New England Journal of Medicine|August 11, 2006
Neonatal-onset multisystem inflammatory disease responsive to interleukin-1beta inhibitionRaphaela Goldbach-Mansky, Natalie J Dailey, Scott W Canna, et al.
Science Translational Medicine|March 31, 2017
Poly(GP) proteins are a useful pharmacodynamic marker for <i>C9ORF72</i>-associated amyotrophic lateral sclerosisTania F Gendron, Jeannie Chew, Jeannette N Stankowski, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
DNA Repair|October 29, 2008
XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptomsSikandar G Khan, Kyu-Seon Oh, Steffen Emmert, et al.
Epilepsia|February 12, 2019
fMRI prediction of naming change after adult temporal lobe epilepsy surgery: Activation mattersXiaozhen You, Ashley N Zachery, Eleanor J Fanto, et al.
Brain : a Journal of Neurology|February 1, 2013
Auditory analysis of xeroderma pigmentosum 1971-2012: hearing function, sun sensitivity and DNA repair predict neurological degenerationMariam B Totonchy, Deborah Tamura, Matthew S Pantell, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
Neuropsychological phenotypes of 76 individuals with Joubert syndrome evaluated at a single centerAngela C Summers, Joseph Snow, Edythe Wiggs, et al.
JCI Insight|January 25, 2019
One-year pilot study on the effects of nitisinone on melanin in patients with OCA-1BDavid R Adams, Supriya Menezes, Ramon Jauregui, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
In-depth investigations of adolescents and adults with holoprosencephaly identify unique characteristicsKarin Weiss, Paul Kruszka, Maria J Guillen Sacoto, et al.
The New England Journal of Medicine|August 11, 2006
Neonatal-onset multisystem inflammatory disease responsive to interleukin-1beta inhibitionRaphaela Goldbach-Mansky, Natalie J Dailey, Scott W Canna, et al.
Science Translational Medicine|March 31, 2017
Poly(GP) proteins are a useful pharmacodynamic marker for <i>C9ORF72</i>-associated amyotrophic lateral sclerosisTania F Gendron, Jeannie Chew, Jeannette N Stankowski, et al.
Pageof 3