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Academic Journal

Dissecting the Many Faces of Frontotemporal Dementia: An Imaging Perspective.

Authors : Pengo, Marta¹ (AUTHOR); Premi, Enrico² (AUTHOR); Borroni, Barbara^3,4 (AUTHOR)

Source: International Journal of Molecular Sciences. Nov2022, Vol. 23 Issue 21, p12867. 14p.

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Academic Journal

Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementia.

Authors : Miedema, Suzanne S. M.¹ (AUTHOR) ; Mol, Merel O.² (AUTHOR); Koopmans, Frank T. W.¹ (AUTHOR)

Source: Acta Neuropathologica Communications. 7/7/2022, Vol. 10 Issue 1, p1-20. 20p.

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Academic Journal

Differential impairment of cerebrospinal fluid synaptic biomarkers in the genetic forms of frontotemporal dementia.

Authors : Sogorb-Esteve, Aitana^1,2 (AUTHOR); Nilsson, Johanna³ (AUTHOR); Swift, Imogen J.^1,2 (AUTHOR)

Source: Alzheimer's Research & Therapy. 8/31/2022, Vol. 14 Issue 1, p1-12. 12p.

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Academic Journal

Very early-onset behavioral variant frontotemporal dementia in a patient with a variant of uncertain significance of a FUS gene mutation.

Authors : Aguzzoli, Cristiano Schaffer^1,2 (AUTHOR) ; Battista, Petronilla^1,3 (AUTHOR); Hadad, Rafi^1,4 (AUTHOR)

Source: Neurocase (Taylor & Francis Ltd). Aug2022, Vol. 28 Issue 4, p403-409. 7p.

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Academic Journal

The enhanced association between mutant CHMP2B and spastin is a novel pathological link between frontotemporal dementia and hereditary spastic paraplegias.

Authors : Chen, Yongping^1,2 (AUTHOR); Krishnan, Gopinath¹ (AUTHOR); Parsi, Sepideh^3,4 (AUTHOR)

Source: Acta Neuropathologica Communications. 11/22/2022, Vol. 10 Issue 1, p1-8. 8p.

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Academic Journal

Six generations of CHMP2B‐mediated Frontotemporal Dementia: Clinical features, predictive testing, progression, and survival.

Authors : Roos, Peter¹ (AUTHOR) ; Johannsen, Peter^1,2 (AUTHOR); Lindquist, Suzanne G.^1,3 (AUTHOR)

Source: Acta Neurologica Scandinavica. May2022, Vol. 145 Issue 5, p529-540. 12p.

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Academic Journal

Genetic prion diseases presenting as frontotemporal dementia: clinical features and diagnostic challenge.

Authors : Chen, Zhongyun¹ (AUTHOR); Chu, Min¹ (AUTHOR); Liu, Li¹ (AUTHOR)

Source: Alzheimer's Research & Therapy. 6/29/2022, Vol. 14 Issue 1, p1-11. 11p.

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Academic Journal

Survival in Korean Patients with Frontotemporal Dementia Syndrome: Association with Behavioral Features and Parkinsonism.

Authors : Jung, Na-Yeon^1,2 (AUTHOR) ; Park, Kee Hyung³ (AUTHOR) ; Seo, Sang Won⁴ (AUTHOR)

Source: Journal of Clinical Medicine. Apr2022, Vol. 11 Issue 8, p2260-2260. 11p.

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Academic Journal

Novel TBK1 variant associated with Frontotemporal Dementia overlap syndrome.

Authors : Arshad, Faheem¹ (AUTHOR); Vengalil, Seena¹ (AUTHOR); Nalini, Atchayaram¹ (AUTHOR)

Source: Acta Neurologica Scandinavica. Apr2022, Vol. 145 Issue 4, p399-406. 8p.

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Academic Journal

Neurocognitive patterns across genetic levels in behavioral variant frontotemporal dementia: a multiple single cases study.

Authors : Santamaría-García, Hernando^1,2,3 (AUTHOR) ; Ogonowsky, Natalia⁴ (AUTHOR); Baez, Sandra⁵ (AUTHOR)

Source: BMC Neurology. 12/9/2022, Vol. 22 Issue 1, p1-23. 23p.

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فلترة النتائج

Dissecting the Many Faces of Frontotemporal Dementia: An Imaging Perspective.

Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementia.

Differential impairment of cerebrospinal fluid synaptic biomarkers in the genetic forms of frontotemporal dementia.

Very early-onset behavioral variant frontotemporal dementia in a patient with a variant of uncertain significance of a FUS gene mutation.

The enhanced association between mutant CHMP2B and spastin is a novel pathological link between frontotemporal dementia and hereditary spastic paraplegias.

Six generations of CHMP2B‐mediated Frontotemporal Dementia: Clinical features, predictive testing, progression, and survival.

Genetic prion diseases presenting as frontotemporal dementia: clinical features and diagnostic challenge.

Survival in Korean Patients with Frontotemporal Dementia Syndrome: Association with Behavioral Features and Parkinsonism.

Novel TBK1 variant associated with Frontotemporal Dementia overlap syndrome.

Neurocognitive patterns across genetic levels in behavioral variant frontotemporal dementia: a multiple single cases study.

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