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Acute onset of anti-IgLON5 disease with meningeal enhancement: a case report.

• Authors : Huang H; Department of Neurology, Liuzhou People's Hospital Affiliated to Guangxi Medical University, No.8 Rd.wenchang Liuzhou, Liuzhou, Guangxi Province, 545000, China.; Wei Y

Subjects: Cell Adhesion Molecules, Neuronal*/Cell Adhesion Molecules, Neuronal*/Cell Adhesion Molecules, Neuronal*/immunology ; Meninges*/Meninges*/Meninges*/pathology ; Autoantibodies*/Autoantibodies*/Autoantibodies*/blood

• Source: BMC neurology [BMC Neurol] 2025 Mar 05; Vol. 25 (1), pp. 86. Date of Electronic Publication: 2025 Mar 05.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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A fatal familial insomnia patient initially misdiagnosed as Alzheimer's disease: a case report.

• Authors : Qiao M; Department of Neurology, The Affiliated Brain Hospital of Nanjing Medical University, No.264, Guangzhou Road, Gulou District, Nanjing, Jiangsu, 210029, China.; Wu H

Subjects: Insomnia, Fatal Familial*/Insomnia, Fatal Familial*/Insomnia, Fatal Familial*/diagnosis ; Insomnia, Fatal Familial*/Insomnia, Fatal Familial*/Insomnia, Fatal Familial*/genetics ; Alzheimer Disease*/Alzheimer Disease*/Alzheimer Disease*/diagnosis

• Source: BMC neurology [BMC Neurol] 2024 Dec 23; Vol. 24 (1), pp. 489. Date of Electronic Publication: 2024 Dec 23.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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A case report of an individual with Creutzfeldt-Jakob disease characterized by prolonged isolated thalamic lesions and rare MM2-cortical-type pathology.

• Authors : Kunii M; Department of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, 236-0004, Japan.; Department of Neurology, Yokohama City University Medical Center, Yokohama, Japan.

Subjects: Creutzfeldt-Jakob Syndrome*/Creutzfeldt-Jakob Syndrome*/Creutzfeldt-Jakob Syndrome*/genetics ; Creutzfeldt-Jakob Syndrome*/Creutzfeldt-Jakob Syndrome*/Creutzfeldt-Jakob Syndrome*/pathology ; Creutzfeldt-Jakob Syndrome*/Creutzfeldt-Jakob Syndrome*/Creutzfeldt-Jakob Syndrome*/diagnosis Creutzfeldt-Jakob Disease, Sporadic

• Source: BMC neurology [BMC Neurol] 2024 Nov 22; Vol. 24 (1), pp. 456. Date of Electronic Publication: 2024 Nov 22.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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Correlated levels of cerebrospinal fluid pathogenic proteins in drug-naïve Parkinson's disease.

• Authors : Murakami H; Department of Neurology, School of Medicine, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8666, Japan.; Tokuda T

Subjects: Amyloid beta-Peptides/Amyloid beta-Peptides/Amyloid beta-Peptides/*cerebrospinal fluid ; Biomarkers/Biomarkers/Biomarkers/*cerebrospinal fluid ; Parkinson Disease/Parkinson Disease/Parkinson Disease/*cerebrospinal fluid

• Source: BMC neurology [BMC Neurol] 2019 Jun 04; Vol. 19 (1), pp. 113. Date of Electronic Publication: 2019 Jun 04.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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[ 18 F]THK-5351 PET imaging in early-stage semantic variant primary progressive aphasia: a report of two cases and a literature review.

• Authors : Kobayashi R; Department of Psychiatry, Yamagata University School of Medicine, 2-2-2 Iidanishi, Yamagata City, Yamagata, 990-9585, Japan. .; Hayashi H

Subjects: Positron-Emission Tomography*; Aminopyridines/Aminopyridines/Aminopyridines/*metabolism ; Aphasia, Primary Progressive/Aphasia, Primary Progressive/Aphasia, Primary Progressive/*diagnostic imaging

• Source: BMC neurology [BMC Neurol] 2018 Aug 08; Vol. 18 (1), pp. 109. Date of Electronic Publication: 2018 Aug 08.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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[18F]THK-5351 PET imaging in early-stage semantic variant primary progressive aphasia: a report of two cases and a literature review.

• Authors : Kobayashi, Ryota; Hayashi, Hiroshi; Otani, Koichi

Subjects: CEREBRAL circulation; MAGNETIC resonance imaging; SINGLE-photon emission computed tomography

• Source: BMC Neurology; 8/8/2018, Vol. 18 Issue 1, pN.PAG-N.PAG, 1p, 2 Charts, 2 Graphs

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Case series of Creutzfeldt-Jakob disease in a third-level hospital in Quito.

• Authors : Torres Herrán GE; Hospital Carlos Andrade Marín, Av. 18 de Septiembre y Ayacucho, Quito, Ecuador.; Ortega Heredia AD

Subjects: Creutzfeldt-Jakob Syndrome/Creutzfeldt-Jakob Syndrome/Creutzfeldt-Jakob Syndrome/*diagnosis ; Creutzfeldt-Jakob Syndrome/Creutzfeldt-Jakob Syndrome/Creutzfeldt-Jakob Syndrome/*pathology; 14-3-3 Proteins/14-3-3 Proteins/14-3-3 Proteins/cerebrospinal fluid

• Source: BMC neurology [BMC Neurol] 2018 Apr 27; Vol. 18 (1), pp. 55. Date of Electronic Publication: 2018 Apr 27.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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A novel frameshift GRN mutation results in frontotemporal lobar degeneration with a distinct clinical phenotype in two siblings: case report and literature review.

• Authors : Hosaka T; Department of the Neurology, Division of Clinical Medicine, Faculty of Medicine, University of Tsukuba, 1-1-1 Ten'noudai, Tsukuba, Ibaraki, 305-8575, Japan.; Ishii K

Subjects: Frontotemporal Dementia/Frontotemporal Dementia/Frontotemporal Dementia/*genetics ; Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/Frontotemporal Lobar Degeneration/*genetics ; Intercellular Signaling Peptides and Proteins/Intercellular Signaling Peptides and Proteins/Intercellular Signaling Peptides and Proteins/*genetics

• Source: BMC neurology [BMC Neurol] 2017 Sep 15; Vol. 17 (1), pp. 182. Date of Electronic Publication: 2017 Sep 15.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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A novel frameshift GRN mutation results in frontotemporal lobar degeneration with a distinct clinical phenotype in two siblings: case report and literature review.

• Authors : Takashi Hosaka; Kazuhiro Ishii; Takeshi Miura

Subjects: FRAMESHIFT mutation; FRONTOTEMPORAL lobar degeneration; PROGRANULINJAPAN

• Source: BMC Neurology; 9/15/2017, Vol. 17, p1-6, 6p, 1 Black and White Photograph, 1 Diagram, 1 Chart

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Proteinase-activated receptor 2 and disease biomarkers in cerebrospinal fluid in cases with autopsy-confirmed prion diseases and other neurodegenerative diseases.

• Authors : Rohan, Zdenek^1,2; Smetakova, Magdalena^1,2; Kukal, Jaromir³

• Source: BMC Neurology. 2015, Vol. 15 Issue 1, p1-5. 5p. 1 Chart, 1 Graph.

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