Cargando…

Young adult-onset, very slowly progressive cognitive decline with spastic paraparesis in Alzheimer’s disease with cotton wool plaques due to a novel presenilin1 G417S mutation

Detalles Bibliográficos
Autores principales:	Miki, Tomoko, Yokota, Osamu, Haraguchi, Takashi, Ikeuchi, Takeshi, Zhu, Bin, Takenoshita, Shintaro, Terada, Seishi, Yamada, Norihito
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2019
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371429/ https://www.ncbi.nlm.nih.gov/pubmed/30755281 http://dx.doi.org/10.1186/s40478-019-0672-z

Ejemplares similares

Factors associated with development and distribution of granular/fuzzy astrocytes in neurodegenerative diseases
por: Miki, Tomoko, et al.
Publicado: (2020)

Reversible Spastic Paraparesis
por: Kasinathan, Ananthanarayanan, et al.
Publicado: (2019)

Amygdala granular fuzzy astrocytes are independently associated with both LATE neuropathologic change and argyrophilic grains: a study of Japanese series with a low to moderate Braak stage
por: Yokota, Osamu, et al.
Publicado: (2023)

Wool or Cotton?
Publicado: (1911)

Cotton Wool Sign in Paget Disease of Bone
por: Horino, Taro, et al.
Publicado: (2019)

Cotton-Wool Sandwiches
Publicado: (1902)

Spastic Paraparesis Following Cocaine Inhalation
por: Savage, Henry Oluwasefunmi, et al.
Publicado: (2009)

Intrathecal Baclofen in Hereditary Spastic Paraparesis
por: Pucks-Faes, Elke, et al.
Publicado: (2019)

Validation of Addenbrooke’s cognitive examination III for detecting mild cognitive impairment and dementia in Japan
por: Takenoshita, Shintaro, et al.
Publicado: (2019)

Verbal or Visual Memory Score and Regional Cerebral Blood Flow in Alzheimer Disease
por: Hayashi, Satoshi, et al.
Publicado: (2018)

Mania associated with complicated hereditary spastic paraparesis
por: Nayak, Raghavendra B, et al.
Publicado: (2011)

Gait Patterns in Patients with Hereditary Spastic Paraparesis
por: Serrao, Mariano, et al.
Publicado: (2016)

Adrenoleukodystrophy as a Cause of Spastic Paraparesis and Hyperpigmentation
por: Chary, Priyanka Kesavan, et al.
Publicado: (2021)

Gastrointestinal and urinary complaints in adults with hereditary spastic paraparesis
por: Kanavin, Øivind J., et al.
Publicado: (2018)

An epidemic of spastic paraparesis of unknown aetiology in Northern Mozambique
por: Taibo, Cátia Luciana Abdulfattáhe, et al.
Publicado: (2017)

A Rare Patient with Hereditary Spastic Paraparesis with Parkinsonism
por: Onder, Halil, et al.
Publicado: (2023)

Prevalence and modifiable risk factors for dementia in persons with intellectual disabilities
por: Takenoshita, Shintaro, et al.
Publicado: (2023)

The Coexistence of Multiple Sclerosis and Hereditary Spastic Paraparesis in a Patient
por: Yazıcı, Işıl, et al.
Publicado: (2013)

Biotinidase deficiency: A treatable cause of hereditary spastic paraparesis
por: Radelfahr, Florentine, et al.
Publicado: (2020)

Oculo-dento-digital Dysplasia Presenting as Spastic Paraparesis Which Was Successfully Treated by Intrathecal Baclofen Therapy
por: Shinya, Akiko, et al.
Publicado: (2021)

Secondary autoimmune hypothalamitis with severe memory impairment 7 years after the onset of diabetes insipidus due to lymphocytic hypophysitis: a case report
por: Asada, Takahiro, et al.
Publicado: (2022)

Pigmented Villonodular Synovitis of the Thoracic Vertebra Presenting with Progressive Spastic Paraparesis
por: Celiktas, Mustafa, et al.
Publicado: (2013)

Familial Clusters of HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis
por: Nozuma, Satoshi, et al.
Publicado: (2014)

Novel OPA1 mutation featuring spastic paraparesis and intestinal dysmotility
por: Kazamel, Mohamed, et al.
Publicado: (2014)

Early-Onset HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis
por: Schwalb, Alvaro, et al.
Publicado: (2020)

Balance assessment in HTLV-1 associated myelopathy or tropical spastic paraparesis
por: Patrício, Naiane Araújo, et al.
Publicado: (2020)

Predominant Spastic Paraparesis Associated With the D178N Mutation in PRNP
por: Thams, Sebastian, et al.
Publicado: (2021)

Three plasma biomarkers of HTLV-1-associated myelopathy/tropical spastic paraparesis
por: Kirk, Paul, et al.
Publicado: (2011)

Plasma proteome analysis in HTLV-1-associated myelopathy/tropical spastic paraparesis
por: Kirk, Paul DW, et al.
Publicado: (2011)

Correction: Familial Clusters of HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis
por: Nozuma, Satoshi, et al.
Publicado: (2016)

Health survey of adults with hereditary spastic paraparesis compared to population study controls
por: Fjermestad, Krister W., et al.
Publicado: (2016)

Study of Knowledge, Attitude, and Practice in Participants with Regular Intake of Lathyrus, But No Spastic Paraparesis
por: Chaurasia, Rameshwar Nath, et al.
Publicado: (2018)

Potential oligogenic disease of mental retardation, short stature, spastic paraparesis, and osteopetrosis
por: Alsemari, Abdulaziz, et al.
Publicado: (2018)

An Unexplained Case of Progressive Spastic Paraparesis in an Individual with Known DiGeorge Syndrome
por: Dhoot, Roshni, et al.
Publicado: (2020)

Factors Involved in Pain Perception and Quality of Life in Patients with Tropical Spastic Paraparesis
por: Criado-Martinez, Sebastian, et al.
Publicado: (2022)

A Ball of Cotton Wool Masquerading as a Conjunctiva Mass
por: Komolafe, O. O., et al.
Publicado: (2011)

Isolated retinal cotton wool spot after coronary angiography
por: Kopsachilis, Nikolaos, et al.
Publicado: (2013)

Antiphosphospholipid syndrome presenting with amaurosis fugax and cotton wool spots
por: Tran, Kimberly D., et al.
Publicado: (2017)

Bilateral cotton wool spots after ambulatory COVID-19
por: Chan, Alison X., et al.
Publicado: (2021)

Giant Cell Arteritis Presenting as Bilateral Cotton Wool Spots
por: Fu, Lanxing, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_5hu1egrairmenl2ptm2f388mhm