Publications by authors named "Faisal Fecto"

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Myasthenia gravis: Mechanisms, clinical syndromes, and diagnosis.
Faisal Fecto

Dis Mon· August 2025

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Identification of TMEM230 mutations in familial Parkinson's disease.
Han-Xiang Deng, Yong Shi, Yi Yang, Kreshnik B Ahmeti, Nimrod Miller, Faisal Fecto

Nat Genet· July 2016

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Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy.
Senda Ajroud-Driss, Faisal Fecto, Kaouther Ajroud, Irfan Lalani, Sarah E Calvo

Neurogenetics· January 2015

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Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2.
George H Gorrie, Faisal Fecto, Daniel Radzicki, Craig Weiss, Yong Shi

Proc Natl Acad Sci U S A· October 2014

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Protein recycling pathways in neurodegenerative diseases.
Faisal Fecto, Y Taylan Esengul, Teepu Siddique

Alzheimers Res Ther· July 2014

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UBQLN2/P62 cellular recycling pathways in amyotrophic lateral sclerosis and frontotemporal dementia.
Faisal Fecto, Teepu Siddique

Muscle Nerve· February 2012

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What is repeated in ALS and FTLD.
Faisal Fecto, Teepu Siddique

Lancet Neurol· January 2012

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SIGMAR1 mutations, genetic heterogeneity at the chromosome 9p locus, and the expanding etiological diversity of amyotrophic lateral sclerosis.
Faisal Fecto, Teepu Siddique

Ann Neurol· December 2011

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Making connections: pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia.
Faisal Fecto, Teepu Siddique

J Mol Neurosci· November 2011

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SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis.
Faisal Fecto, Jianhua Yan, S Pavan Vemula, Erdong Liu, Yi Yang

Arch Neurol· November 2011

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Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutations.
Han-Xiang Deng, Eileen H Bigio, Hong Zhai, Faisal Fecto, Kaouther Ajroud

Arch Neurol· August 2011

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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.
Han-Xiang Deng, Wenjie Chen, Seong-Tshool Hong, Kym M Boycott, George H Gorrie, Faisal Fecto

Nature· August 2011

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Mutant TRPV4-mediated toxicity is linked to increased constitutive function in axonal neuropathies.
Faisal Fecto, Yong Shi, Rafiq Huda, Marco Martina, Teepu Siddique

J Biol Chem· May 2011

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An unusual case of familial ALS and cerebellar ataxia.
Sadia Yasser, Faisal Fecto, Teepu Siddique, Kazim A Sheikh, Parveen Athar

Amyotroph Lateral Scler· December 2010

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FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis.
Han-Xiang Deng, Hong Zhai, Eileen H Bigio, Jianhua Yan, Faisal Fecto

Ann Neurol· June 2010

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Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4.
Han-Xiang Deng, Christopher J Klein, Jianhua Yan, Yong Shi, Yanhong Wu, Faisal Fecto

Nat Genet· February 2010

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Signaling mechanisms mediated by G-protein coupled receptors in human platelets.
Sheikh Arshad Saeed, Huma Rasheed, Faisal A Wahed Fecto, Mohammad Ilyas Achakzai, Rahmat Ali

Acta Pharmacol Sin· July 2004

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