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Marianna Bugiani

Showing results (41-50 of 152) with videos related to

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Neuropediatrics|November 28, 2017
4H Leukodystrophy: Lessons from 3T ImagingFerdy K Cayami, Marianna Bugiani, Petra J W Pouwels, et al.
Acta Neuropathologica|August 10, 2025
A focus on the normal-appearing white and gray matter within the multiple sclerosis brain: a link to smoldering progressionGema Muñoz González, Bert A T Hart, Marianna Bugiani, et al.
Annals of Neurology|September 5, 2002
X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8Alberto Bizzi, Marianna Bugiani, Gajja S Salomons, et al.
Neuropediatrics|December 1, 2015
Absent Thalami Caused by a Homozygous EARS2 Mutation: Expanding Disease Spectrum of LTBLSietske H Kevelam, Femke C C Klouwer, Johanna M Fock, et al.
Brain : a Journal of Neurology|February 1, 2013
Hyaluronan accumulation and arrested oligodendrocyte progenitor maturation in vanishing white matter diseaseMarianna Bugiani, Nienke Postma, Emiel Polder, et al.
American Journal of Respiratory and Critical Care Medicine|March 8, 2023
Rapid On-Site Pathology Visualization of COVID-19 Characteristics Using Higher Harmonic Generation MicroscopyLaura M G van Huizen, Kirsten A Kalverda, Marianna Bugiani, et al.
Brain : a Journal of Neurology|February 2, 2023
Cortical interneuron development is affected in 4H leukodystrophyStephanie Dooves, Liza M L Kok, Dwayne B Holmes, et al.
Human Molecular Genetics|April 4, 2007
Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathyErika Fernandez-Vizarra, Marianna Bugiani, Paola Goffrini, et al.
Annals of Clinical and Translational Neurology|August 15, 2015
Interferon-α and the calcifying microangiopathy in Aicardi-Goutières syndromeMelanie D Klok, Hannah S Bakels, Nienke L Postma, et al.
Frontiers in Pediatrics|January 8, 2015
Severe Neonatal Epileptic Encephalopathy and KCNQ2 Mutation: Neuropathological Substrate?Charlotte Dalen Meurs-van der Schoor, Mirjam van Weissenbruch, Marjan van Kempen, et al.
Pageof 16

Showing results (41-50 of 152) with videos related to

Sort By:
Pageof 16
Neuropediatrics|November 28, 2017
4H Leukodystrophy: Lessons from 3T ImagingFerdy K Cayami, Marianna Bugiani, Petra J W Pouwels, et al.
Acta Neuropathologica|August 10, 2025
A focus on the normal-appearing white and gray matter within the multiple sclerosis brain: a link to smoldering progressionGema Muñoz González, Bert A T Hart, Marianna Bugiani, et al.
Annals of Neurology|September 5, 2002
X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8Alberto Bizzi, Marianna Bugiani, Gajja S Salomons, et al.
Neuropediatrics|December 1, 2015
Absent Thalami Caused by a Homozygous EARS2 Mutation: Expanding Disease Spectrum of LTBLSietske H Kevelam, Femke C C Klouwer, Johanna M Fock, et al.
Brain : a Journal of Neurology|February 1, 2013
Hyaluronan accumulation and arrested oligodendrocyte progenitor maturation in vanishing white matter diseaseMarianna Bugiani, Nienke Postma, Emiel Polder, et al.
American Journal of Respiratory and Critical Care Medicine|March 8, 2023
Rapid On-Site Pathology Visualization of COVID-19 Characteristics Using Higher Harmonic Generation MicroscopyLaura M G van Huizen, Kirsten A Kalverda, Marianna Bugiani, et al.
Brain : a Journal of Neurology|February 2, 2023
Cortical interneuron development is affected in 4H leukodystrophyStephanie Dooves, Liza M L Kok, Dwayne B Holmes, et al.
Human Molecular Genetics|April 4, 2007
Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathyErika Fernandez-Vizarra, Marianna Bugiani, Paola Goffrini, et al.
Annals of Clinical and Translational Neurology|August 15, 2015
Interferon-α and the calcifying microangiopathy in Aicardi-Goutières syndromeMelanie D Klok, Hannah S Bakels, Nienke L Postma, et al.
Frontiers in Pediatrics|January 8, 2015
Severe Neonatal Epileptic Encephalopathy and KCNQ2 Mutation: Neuropathological Substrate?Charlotte Dalen Meurs-van der Schoor, Mirjam van Weissenbruch, Marjan van Kempen, et al.
Pageof 16