نتائج البحث

Diversity of dopamine transporter images in frontotemporal lobar degeneration-motor neuron disease.

• Authors : Kobayashi R; Department of Psychiatry, Yamagata University School of Medicine, Yamagata, Japan.; Kawakatsu S

Subjects: Frontotemporal Lobar Degeneration*/Frontotemporal Lobar Degeneration*/Frontotemporal Lobar Degeneration*/diagnostic imaging ; Motor Neuron Disease*/Motor Neuron Disease*/Motor Neuron Disease*/diagnostic imaging ; Frontotemporal Dementia*

• Source: Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society [Psychogeriatrics] 2022 Sep; Vol. 22 (5), pp. 771. Date of Electronic Publication: 2022 Jun 05.Publisher: Blackwell Pub Country of Publication: England NLM ID: 101230058 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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ApoE and TDP-43 neuropathology in two siblings with familial FTLD-motor neuron disease.

• Authors : Vossel KA; Department of Neurology, University of California, San Francisco, CA, USA.; Bien-Ly N

Subjects: Apolipoproteins E/Apolipoproteins E/Apolipoproteins E/*genetics ; DNA-Binding Proteins/DNA-Binding Proteins/DNA-Binding Proteins/*genetics ; Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/*genetics

• Source: Neurocase [Neurocase] 2013; Vol. 19 (3), pp. 295-301. Date of Electronic Publication: 2012 Apr 18.Publisher: Routledge Country of Publication: England NLM ID: 9511374 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1465-3656

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Poly-GR dipeptide repeat polymers correlate with neurodegeneration and Clinicopathological subtypes in C9ORF72-related brain disease.

• Authors : Sakae N; Department of Neuroscience, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, USA.; Bieniek KF

Subjects: C9orf72 Protein/C9orf72 Protein/C9orf72 Protein/*genetics ; Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/*genetics ; Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/*metabolism

• Source: Acta neuropathologica communications [Acta Neuropathol Commun] 2018 Jul 20; Vol. 6 (1), pp. 63. Date of Electronic Publication: 2018 Jul 20.Publisher: BioMed Central Country of Publication: England NLM ID: 101610673 Publication Model: Electronic Cited Medium: Internet ISSN: 2051-5960

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A novel mutation P112H in the TARDBP gene associated with frontotemporal lobar degeneration without motor neuron disease and abundant neuritic amyloid plaques.

• Authors : Moreno F; Rabinovici GD; Karydas A

Subjects: Brain/Brain/Brain/*pathology ; DNA-Binding Proteins/DNA-Binding Proteins/DNA-Binding Proteins/*genetics ; Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/*genetics

• Source: Acta neuropathologica communications [Acta Neuropathol Commun] 2015 Apr 03; Vol. 3, pp. 19. Date of Electronic Publication: 2015 Apr 03.Publisher: BioMed Central Country of Publication: England NLM ID: 101610673 Publication Model: Electronic Cited Medium: Internet ISSN: 2051-5960

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Clinical features of the behavioural variant of frontotemporal dementia that are useful for predicting underlying pathological subtypes of frontotemporal lobar degeneration.

• Authors : Kobayashi Z; Department of Neurology, JA Toride Medical Center, Toride, Japan.; Dementia Research Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.

Subjects: Brain/Brain/Brain/*pathology ; Frontotemporal Dementia/Frontotemporal Dementia/Frontotemporal Dementia/*pathology ; Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/*pathology

• Source: Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society [Psychogeriatrics] 2018 Jul; Vol. 18 (4), pp. 307-312.Publisher: Blackwell Pub Country of Publication: England NLM ID: 101230058 Publication Model: Print Cited Medium: Internet ISSN: 1479-8301

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Semantic dementia with lower motor neuron disease showing FTLD-TDP type 3 pathology (sensu Mackenzie).

• Authors : Östberg P; Department of Neuroscience, Uppsala University, Uppsala, Sweden.; Bogdanović N

Subjects: Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/*complications ; Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/*pathology ; Motor Neuron Disease/Motor Neuron Disease/Motor Neuron Disease/*complications

• Source: Neuropathology : official journal of the Japanese Society of Neuropathology [Neuropathology] 2011 Jun; Vol. 31 (3), pp. 271-9. Date of Electronic Publication: 2010 Oct 05.Publisher: Blackwell Science Asia Country of Publication: Australia NLM ID: 9606526 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases.

• Authors : Rusina R; Department of Neurology, Thomayer Teaching Hospital and Institute for Postgraduate Education in Medicine, Prague, Czech Republic. ; Kovacs GG

Subjects: Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/*complications ; Motor Neuron Disease/Motor Neuron Disease/Motor Neuron Disease/*complications ; Perceptual Disorders/Perceptual Disorders/Perceptual Disorders/*complications

• Source: BMC neurology [BMC Neurol] 2011 May 10; Vol. 11, pp. 50. Date of Electronic Publication: 2011 May 10.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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Heterogeneous ribonuclear protein A3 (hnRNP A3) is present in dipeptide repeat protein containing inclusions in Frontotemporal Lobar Degeneration and Motor Neurone disease associated with expansions in C9orf72 gene.

• Authors : Davidson YS; Division of Neuroscience and Experimental Psychology, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Salford Royal Hospital, Salford, M6 8HD, UK.; Flood L

Subjects: C9orf72 Protein/C9orf72 Protein/C9orf72 Protein/*genetics ; Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/*metabolism ; Heterogeneous-Nuclear Ribonucleoprotein Group A-B/Heterogeneous-Nuclear Ribonucleoprotein Group A-B/Heterogeneous-Nuclear Ribonucleoprotein Group A-B/*metabolism

• Source: Acta neuropathologica communications [Acta Neuropathol Commun] 2017 Apr 21; Vol. 5 (1), pp. 31. Date of Electronic Publication: 2017 Apr 21.Publisher: BioMed Central Country of Publication: England NLM ID: 101610673 Publication Model: Electronic Cited Medium: Internet ISSN: 2051-5960

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Clinicopathological Correlation in Motor Neuron Disease and Frontotemporal Degeneration.

• Source: Neurology Alert. Oct2024, Vol. 44 Issue 2, p1-14. 14p.

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Review: an update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations.

• Authors : Lashley T; Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.; Rohrer JD

Subjects: Frontotemporal Dementia/Frontotemporal Dementia/Frontotemporal Dementia/*pathology ; Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/*pathology ; Motor Neuron Disease/Motor Neuron Disease/Motor Neuron Disease/*pathology

• Source: Neuropathology and applied neurobiology [Neuropathol Appl Neurobiol] 2015 Dec; Vol. 41 (7), pp. 858-81. Date of Electronic Publication: 2015 Jul 06.Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 7609829 Publication Model: Print-Electronic Cited Medium: Internet

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