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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Volume 20, 2019 - Issue 3-4
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FUS-ALS presenting with myoclonic jerks in a 17-year-old man

Katherine Claire DoddDepartment of Neurology, Greater Manchester Neurosciences Centre, Salford Royal Foundation Trust, Salford, UK,Correspondence[email protected]
ORCID Iconhttp://orcid.org/0000-0002-0491-7030
ORCID Icon,
Rachael PowerDepartment of Neurology, Greater Manchester Neurosciences Centre, Salford Royal Foundation Trust, Salford, UK,
,
John EalingDepartment of Neurology, Greater Manchester Neurosciences Centre, Salford Royal Foundation Trust, Salford, UK,;Institute of Brain, Behaviour and Mental Health, University of Manchester, Manchester, UK
&
Hisham HamdallaDepartment of Neurology, Greater Manchester Neurosciences Centre, Salford Royal Foundation Trust, Salford, UK,;Institute of Brain, Behaviour and Mental Health, University of Manchester, Manchester, UK
Pages 278-280 | Received 29 Aug 2018, Accepted 03 Feb 2019, Published online: 18 Mar 2019

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Cristiano Schaffer Aguzzoli, Petronilla Battista, Rafi Hadad, Yuri Ferreira Felloni Borges, Lucas Porcello Schilling & Bruce L Miller. (2022) Very early-onset behavioral variant frontotemporal dementia in a patient with a variant of uncertain significance of a FUS gene mutation. Neurocase 28:4, pages 403-409.
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Articles from other publishers (8)

Zeinab Ali, Juan M. Godoy-Corchuelo, Aurea B. Martins-Bach, Irene Garcia-Toledo, Luis C. Fernández-Beltrán, Remya R. Nair, Shoshana Spring, Brian J. Nieman, Irene Jimenez-Coca, Rasneer S. Bains, Hamish Forrest, Jason P. Lerch, Karla L. Miller, Elizabeth M. C. Fisher, Thomas J. Cunningham & Silvia Corrochano. (2023) Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations. Disease Models & Mechanisms 16:10.
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Xiaole Liu, Xinyue Zhao, Jinhan He, Sishi Wang, Xinfei Shen, Qingfeng Liu & Shenlin Wang. (2023) Advances in the Structure of GGGGCC Repeat RNA Sequence and Its Interaction with Small Molecules and Protein Partners. Molecules 28:15, pages 5801.
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Alberto A Zambon, Veronica Pini, Luca Bosco, Yuri M Falzone, Pinki Munot, Francesco Muntoni & Stefano C Previtali. (2023) Early onset hereditary neuronopathies: an update on non- 5q motor neuron diseases . Brain 146:3, pages 806-822.
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Peishan WangQiao WeiHongfu LiZhi-Ying Wu. (2023) Clinical feature difference between juvenile amyotrophic lateral sclerosis with SPTLC1 and FUS mutations. Chinese Medical Journal 136:2, pages 176-183.
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Tanya Lehky & Christopher Grunseich. (2021) Juvenile Amyotrophic Lateral Sclerosis: A Review. Genes 12:12, pages 1935.
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L. Chen. (2021) FUS mutation is probably the most common pathogenic gene for JALS, especially sporadic JALS. Revue Neurologique 177:4, pages 333-340.
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Pedro Fraiman, Mario Emilio Dourado & Clecio Godeiro‐Junior. (2021) Amyotrophic Lateral Sclerosis and Palatal Myoclonus: An Uncommon Association. Movement Disorders Clinical Practice 8:2, pages 288-289.
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Vincent Picher-Martel, Francis BrunetNicolas Dupré & Nicolas Chrestian. (2020) The Occurrence of FUS Mutations in Pediatric Amyotrophic Lateral Sclerosis: A Case Report and Review of the Literature. Journal of Child Neurology 35:8, pages 556-562.
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