Torthaí cuardaigh - Gerald Pfeffer

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  1. 1
    Diagnosis and treatment of mitochondrial myopathies

    Diagnosis and treatment of mitochondrial myopathies de réir Gerald Pfeffer, Patrick F. Chinnery

    Foilsithe / Cruthaithe 2011
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  2. 2
    The Role of Vitamin D in Neuroprotection in Multiple Sclerosis: An Update

    The Role of Vitamin D in Neuroprotection in Multiple Sclerosis: An Update de réir Amarpreet Sangha, Michaela Quon, Gerald Pfeffer, Sarah-Michelle Orton

    Foilsithe / Cruthaithe 2023
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  3. 3
    Diagnosis of muscle diseases presenting with early respiratory failure

    Diagnosis of muscle diseases presenting with early respiratory failure de réir Gerald Pfeffer, Marcus Povitz, G J Gibson, Patrick F. Chinnery

    Foilsithe / Cruthaithe 2014
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  4. 4
    Multisystem Disorder in Late-Onset Chronic Progressive External Ophthalmoplegia

    Multisystem Disorder in Late-Onset Chronic Progressive External Ophthalmoplegia de réir Gerald Pfeffer, Sandra Sirrs, N. Kevin Wade, Michelle M. Mezei

    Foilsithe / Cruthaithe 2011
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  5. 5
    Emerging therapies for mitochondrial disorders

    Emerging therapies for mitochondrial disorders de réir Helen Nightingale, Gerald Pfeffer, David Bargiela, Rita Horváth, Patrick F. Chinnery

    Foilsithe / Cruthaithe 2016
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  6. 6
    Treatment for mitochondrial disorders

    Treatment for mitochondrial disorders de réir Gerald Pfeffer, Kari Majamaa, Douglass M. Turnbull, David R. Thorburn, Patrick F. Chinnery

    Foilsithe / Cruthaithe 2012
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  7. 7
    Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations

    Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutations de réir Gerald Pfeffer, Ailbhe Burke, Patrick Yu‐Wai‐Man, D. A. S. Compston, Patrick F. Chinnery

    Foilsithe / Cruthaithe 2013
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  8. 8
    Multisystem Proteinopathy Due to VCP Mutations: A Review of Clinical Heterogeneity and Genetic Diagnosis

    Multisystem Proteinopathy Due to VCP Mutations: A Review of Clinical Heterogeneity and Genetic Diagnosis de réir Gerald Pfeffer, Grace Lee, Carly Sabine Pontifex, Roberto D. Fanganiello, Allison Peck, Conrad C. Weihl, Virginia Kimonis

    Foilsithe / Cruthaithe 2022
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  9. 9
    Fibroblast Growth Factor (FGF) 18 Signals through FGF Receptor 3 to Promote Chondrogenesis

    Fibroblast Growth Factor (FGF) 18 Signals through FGF Receptor 3 to Promote Chondrogenesis de réir David Davidson, Antoine Blanc, Dominic Filion, Huifen Wang, Paul Plut, Gerald Pfeffer, Michael D. Buschmann, Janet E. Henderson

    Foilsithe / Cruthaithe 2005
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  10. 10
    Longitudinal analysis of glymphatic function in amyotrophic lateral sclerosis and primary lateral sclerosis

    Longitudinal analysis of glymphatic function in amyotrophic lateral sclerosis and primary lateral sclerosis de réir Rachel Sharkey, Filomeno Cortese, Bradley G. Goodyear, Lawrence Korngut, Sarah Jacob, Keith A. Sharkey, Sanjay Kalra, Minh Dang Nguyen, Richard Frayne, Gerald Pfeffer

    Foilsithe / Cruthaithe 2024
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  11. 11
    The MFN2 Q367H variant reveals a novel pathomechanism connected to mtDNA-mediated inflammation

    The MFN2 Q367H variant reveals a novel pathomechanism connected to mtDNA-mediated inflammation de réir Mashiat Zaman, Govinda Sharma, Walaa Almutawa, Tyler Soule, Rasha Sabouny, Matthew Joel, A Mohan, Cole Chute, Jeffrey T. Joseph, Gerald Pfeffer, Timothy E. Shutt

    Foilsithe / Cruthaithe 2025
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  12. 12
    <i>SPG7</i> mutations are a common cause of undiagnosed ataxia

    <i>SPG7</i> mutations are a common cause of undiagnosed ataxia de réir Gerald Pfeffer, Angela Pyle, Helen Griffin, Jack W. Miller, Valerie Wilson, Lisa Turnbull, Katherine A. Fawcett, David Sims, Gail Eglon, Marios Hadjivassiliou, Rita Horváth, Andrea H. Németh, Patrick F. Chinnery

    Foilsithe / Cruthaithe 2015
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  13. 13
    Identification of a mosaic <i>MTOR</i> variant in purified neuronal <scp>DNA</scp> in a patient with focal cortical dysplasia using a novel depth electrode harvesting technique

    Identification of a mosaic <i>MTOR</i> variant in purified neuronal <scp>DNA</scp> in a patient with focal cortical dysplasia using a novel depth electrode harvesting technique de réir Karl Martin Klein, Rumika Mascarenhas, Daria Merrikh, Maryam Khanbabaei, Tatiana Maroilley, Navprabhjot Kaur, Yiping Liu, Tyler Soule, Minette Manalo, Goichiro Tamura, Julia Jacobs, Walter Hader, Gerald Pfeffer, Maja Tarailo‐Graovac

    Foilsithe / Cruthaithe 2024
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  14. 14
    Exome sequencing in undiagnosed inherited and sporadic ataxias

    Exome sequencing in undiagnosed inherited and sporadic ataxias de réir Angela Pyle, Tania Smertenko, David Bargiela, Helen Griffin, Jennifer Duff, Marie Appleton, Konstantinos Douroudis, Gerald Pfeffer, Mauro Santibanez‐Koref, Gail Eglon, Patrick Yu‐Wai‐Man, Venkateswaran Ramesh, Rita Horváth, Patrick F. Chinnery

    Foilsithe / Cruthaithe 2014
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  15. 15
    Detecting somatic variants in purified brain <scp>DNA</scp> obtained from surgically implanted depth electrodes in epilepsy

    Detecting somatic variants in purified brain <scp>DNA</scp> obtained from surgically implanted depth electrodes in epilepsy de réir Rumika Mascarenhas, Daria Merrikh, Maryam Khanbabaei, Navprabhjot Kaur, Navid Ghaderi, Tatiana Maroilley, Yiping Liu, Tyler Soule, Juan Pablo Appendino, Julia Jacobs, Samuel Wiebe, Walter Hader, Gerald Pfeffer, Maja Tarailo‐Graovac, Karl Martin Klein

    Foilsithe / Cruthaithe 2025
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  16. 16
    Titin mutation segregates with hereditary myopathy with early respiratory failure

    Titin mutation segregates with hereditary myopathy with early respiratory failure de réir Gerald Pfeffer, Hannah R. Elliott, Helen Griffin, Rita Barresi, James Miller, Julie Marsh, Anni Evilä, Anna Vihola, Peter Hackman, Volker Straub, D J Dick, Rita Horváth, Mauro Santibanez‐Koref, Bjarne Udd, Patrick F. Chinnery

    Foilsithe / Cruthaithe 2012
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  17. 17
    Clonal Expansion of Secondary Mitochondrial DNA Deletions Associated With Spinocerebellar Ataxia Type 28

    Clonal Expansion of Secondary Mitochondrial DNA Deletions Associated With Spinocerebellar Ataxia Type 28 de réir Gráinne S. Gorman, Gerald Pfeffer, Helen Griffin, Emma L. Blakely, Marzena Kurzawa‐Akanbi, Jessica Gabriel, Kamil S. Sitarz, M. Roberts, Benedikt Schoser, Angela Pyle, Andrew M. Schaefer, Robert McFarland, Douglass M. Turnbull, Rita Horváth, Patrick F. Chinnery, Robert W. Taylor

    Foilsithe / Cruthaithe 2014
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  18. 18
    The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy

    The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy de réir Walaa Almutawa, Christopher Smith, Rasha Sabouny, Ryan B. Smit, Tian Zhao, Rachel Wong, Laurie Lee-Glover, Justine Desrochers-Goyette, Hema Saranya Ilamathi, Oksana Suchowersky, Marc Germain, Paul E. Mains, Jillian S. Parboosingh, Gerald Pfeffer, A. Micheil Innes, Timothy E. Shutt

    Foilsithe / Cruthaithe 2019
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  19. 19
    New treatments for mitochondrial disease—no time to drop our standards

    New treatments for mitochondrial disease—no time to drop our standards de réir Gerald Pfeffer, Rita Horváth, Thomas Klopstock, Vamsi K. Mootha, Anu Suomalainen, Saskia Koene, Michio Hirano, Massimo Zeviani, Laurence A. Bindoff, Patrick Yu‐Wai‐Man, Michael G. Hanna, Valério Carelli, Robert McFarland, Kari Majamaa, Douglass M. Turnbull, Jan Smeitink, Patrick F. Chinnery

    Foilsithe / Cruthaithe 2013
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  20. 20
    Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure

    Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure de réir Gerald Pfeffer, Rita Barresi, Ian Wilson, Steven Hardy, Helen Griffin, Judith A. Hudson, Hannah R. Elliott, Aravind Ramesh, Aleksandar Radunović, J. Winer, S. Vaidya, Ayush T. Raman, Mark Busby, Maria Elena Farrugia, and Xie Ming, C. M. Everett, Hedley Emsley, Rita Horváth, Volker Straub, K. Bushby, Hanns Lochmüller, Patrick F. Chinnery, Andrea Sarkozy

    Foilsithe / Cruthaithe 2013
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