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Sarah Woidill

Showing results (11-20 of 32) with videos related to

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Journal of Child Neurology|May 14, 2025
Exploration Into Lived Experiences of Multiple Sulfatase Deficiency-Affected Individuals and Their FamiliesFrancesco Gavazzi, Emily Yu, Zarrin Tashnim, et al.
Journal of Child Neurology|September 28, 2019
Developmental Outcomes of Aicardi Goutières SyndromeLaura Adang, Francesco Gavazzi, Micaela De Simone, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 22, 2026
Therapeutic suppression of Tubb4a rescues H-ABC leukodystrophySunetra Sase, Julia L Hacker, Prabhat R Napit, et al.
Journal of Child Neurology|March 27, 2024
Characterization of Fine Motor and Visual Motor Skills in Aicardi-Goutières SyndromeStacy V Cusack, Francesco Gavazzi, Isabella Peixoto de Barcelos, et al.
Molecular Genetics and Metabolism|November 5, 2022
SARS-CoV-2 mRNA-based vaccines in the Aicardi Goutières SyndromeAsako Takanohashi, Mohamad-Gabriel Alameh, Sarah Woidill, et al.
Molecular Genetics and Metabolism|March 5, 2026
Design of a Pediatric Low Motor Function Item Battery in leukodystrophiesFrancesco Gavazzi, Sarah Woidill, Anjana Sevagamoorthy, et al.
Molecular Genetics and Metabolism|October 16, 2025
Functional ability profiles in beta-propeller protein-associated neurodegeneration (BPAN)Francesco Gavazzi, Samuel R Pierce, Vanessa Smith, et al.
Human Mutation|March 4, 2020
Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoformGuy Helman, Asako Takanohashi, Tracy L Hagemann, et al.
Human Mutation|August 3, 2022
Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoformGuy Helman, Asako Takanohashi, Tracy L Hagemann, et al.
Pediatric Neurology|October 23, 2025
Critical Functional Domains in Pediatric Onset TUBB4A-Related Leukodystrophy: A Clinical and Caregiver's PerspectiveFrancesco Gavazzi, Virali Patel, Jacqueline A Erler, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Journal of Child Neurology|May 14, 2025
Exploration Into Lived Experiences of Multiple Sulfatase Deficiency-Affected Individuals and Their FamiliesFrancesco Gavazzi, Emily Yu, Zarrin Tashnim, et al.
Journal of Child Neurology|September 28, 2019
Developmental Outcomes of Aicardi Goutières SyndromeLaura Adang, Francesco Gavazzi, Micaela De Simone, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 22, 2026
Therapeutic suppression of Tubb4a rescues H-ABC leukodystrophySunetra Sase, Julia L Hacker, Prabhat R Napit, et al.
Journal of Child Neurology|March 27, 2024
Characterization of Fine Motor and Visual Motor Skills in Aicardi-Goutières SyndromeStacy V Cusack, Francesco Gavazzi, Isabella Peixoto de Barcelos, et al.
Molecular Genetics and Metabolism|November 5, 2022
SARS-CoV-2 mRNA-based vaccines in the Aicardi Goutières SyndromeAsako Takanohashi, Mohamad-Gabriel Alameh, Sarah Woidill, et al.
Molecular Genetics and Metabolism|March 5, 2026
Design of a Pediatric Low Motor Function Item Battery in leukodystrophiesFrancesco Gavazzi, Sarah Woidill, Anjana Sevagamoorthy, et al.
Molecular Genetics and Metabolism|October 16, 2025
Functional ability profiles in beta-propeller protein-associated neurodegeneration (BPAN)Francesco Gavazzi, Samuel R Pierce, Vanessa Smith, et al.
Human Mutation|March 4, 2020
Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoformGuy Helman, Asako Takanohashi, Tracy L Hagemann, et al.
Human Mutation|August 3, 2022
Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoformGuy Helman, Asako Takanohashi, Tracy L Hagemann, et al.
Pediatric Neurology|October 23, 2025
Critical Functional Domains in Pediatric Onset TUBB4A-Related Leukodystrophy: A Clinical and Caregiver's PerspectiveFrancesco Gavazzi, Virali Patel, Jacqueline A Erler, et al.
Pageof 4