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Showing results (771-780 of 898) with videos related to

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Archives of Neurology|September 14, 2011
Hypomyelination and congenital cataract: broadening the clinical phenotypeRoberta Biancheri, Federico Zara, Andrea Rossi, et al.
Journal of Cancer Research and Clinical Oncology|February 17, 2020
Clinical characteristics and outcomes of SDHB-related pheochromocytoma and paraganglioma in children and adolescentsIvana Jochmanova, April Melody T Abcede, Ruby Jane S Guerrero, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 20, 2013
Drastic neofunctionalization associated with evolution of the timezyme AANAT 500 MyaJack Falcón, Steven L Coon, Laurence Besseau, et al.
Nucleic Acids Research|April 25, 2022
The tRNA discriminator base defines the mutual orthogonality of two distinct pyrrolysyl-tRNA synthetase/tRNAPyl pairs in the same organismHaolin Zhang, Xuemei Gong, Qianqian Zhao, et al.
Journal of Neuro-Oncology|July 28, 2017
A phase I/II study of gemcitabine during radiotherapy in children with newly diagnosed diffuse intrinsic pontine gliomaSophie E M Veldhuijzen van Zanten, Fatma E El-Khouly, Marc H A Jansen, 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.
Journal of Virology|December 7, 2018
Antibody-Mediated Protective Mechanisms Induced by a Trivalent Parainfluenza Virus-Vectored Ebolavirus VaccineJ Brian Kimble, Delphine C Malherbe, Michelle Meyer, et al.
Journal of Medical Genetics|September 8, 2016
SLC13A5 is the second gene associated with Kohlschütter-Tönz syndromeAnna Schossig, Agnès Bloch-Zupan, Adrian Lussi, et al.
Brain : a Journal of Neurology|May 3, 2014
Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlationEline M Hamilton, Emiel Polder, Adeline Vanderver, et al.
European Radiology|September 25, 2024
Quantitative MRI distinguishes different leukodystrophies and correlates with clinical measuresMenno D Stellingwerff, Murtadha L Al-Saady, Kwok-Shing Chan, et al.
Pageof 90

Showing results (771-780 of 898) with videos related to

Sort By:
Pageof 90
Archives of Neurology|September 14, 2011
Hypomyelination and congenital cataract: broadening the clinical phenotypeRoberta Biancheri, Federico Zara, Andrea Rossi, et al.
Journal of Cancer Research and Clinical Oncology|February 17, 2020
Clinical characteristics and outcomes of SDHB-related pheochromocytoma and paraganglioma in children and adolescentsIvana Jochmanova, April Melody T Abcede, Ruby Jane S Guerrero, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 20, 2013
Drastic neofunctionalization associated with evolution of the timezyme AANAT 500 MyaJack Falcón, Steven L Coon, Laurence Besseau, et al.
Nucleic Acids Research|April 25, 2022
The tRNA discriminator base defines the mutual orthogonality of two distinct pyrrolysyl-tRNA synthetase/tRNAPyl pairs in the same organismHaolin Zhang, Xuemei Gong, Qianqian Zhao, et al.
Journal of Neuro-Oncology|July 28, 2017
A phase I/II study of gemcitabine during radiotherapy in children with newly diagnosed diffuse intrinsic pontine gliomaSophie E M Veldhuijzen van Zanten, Fatma E El-Khouly, Marc H A Jansen, 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.
Journal of Virology|December 7, 2018
Antibody-Mediated Protective Mechanisms Induced by a Trivalent Parainfluenza Virus-Vectored Ebolavirus VaccineJ Brian Kimble, Delphine C Malherbe, Michelle Meyer, et al.
Journal of Medical Genetics|September 8, 2016
SLC13A5 is the second gene associated with Kohlschütter-Tönz syndromeAnna Schossig, Agnès Bloch-Zupan, Adrian Lussi, et al.
Brain : a Journal of Neurology|May 3, 2014
Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlationEline M Hamilton, Emiel Polder, Adeline Vanderver, et al.
European Radiology|September 25, 2024
Quantitative MRI distinguishes different leukodystrophies and correlates with clinical measuresMenno D Stellingwerff, Murtadha L Al-Saady, Kwok-Shing Chan, et al.
Pageof 90