Stroke-like onset of Wilson disease associated with a novel mutation (T766R)

Stroke-like onset of Wilson disease associated with a novel mutation (T766R)

Manylion Llyfryddiaeth
Prif Awduron:	Pendlebury, S, Dalton, A, Rothwell, P
Fformat:	Conference item
Cyhoeddwyd:	2004

Eitemau Tebyg

Strokelike presentation of Wilson disease with homozygosity for a novel T766R mutation.
gan: Pendlebury, S, et al.
Cyhoeddwyd: (2004)

Prevalence, incidence, and factors associated with pre-stroke and post-stroke dementia: a systematic review and meta-analysis.
gan: Pendlebury, S, et al.
Cyhoeddwyd: (2009)

Late-Onset Wilson's Disease
gan: Miroslav Žigrai, et al.
Cyhoeddwyd: (2020-02-01)

Secondary prevention of stroke and post-stroke dementia
gan: Pendlebury, S, et al.
Cyhoeddwyd: (2008)

Truncating mutations in the Wilson disease gene ATP7B are associated with very low serum ceruloplasmin oxidase activity and an early onset of Wilson disease
gan: Tuma Sabine, et al.
Cyhoeddwyd: (2010-01-01)

Management of stroke
gan: Pendlebury, S, et al.
Cyhoeddwyd: (2006)

Stroke: Management and prevention
gan: Pendlebury, S, et al.
Cyhoeddwyd: (2004)

Risk of recurrent stroke, other vascular events and dementia after transient ischaemic attack and stroke.
gan: Pendlebury, S, et al.
Cyhoeddwyd: (2009)

Acute-Onset Optic Neuropathy in Wilson’s Disease
gan: Liyung Tiffany Chou, et al.
Cyhoeddwyd: (2019-01-01)

HAPLOTYPES IN WILSON DISEASE - IMPLICATIONS FOR MUTATIONAL ANALYSIS
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Cyhoeddwyd: (1993)

Wilson’s Disease. Onset and Complex Diagnosis: Clinical Case
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Cyhoeddwyd: (2024-12-01)

766 Novel bioluminescent bioassays for the discovery and development of T cell redirecting cancer therapies
gan: Jamison Grailer, et al.
Cyhoeddwyd: (2020-11-01)

Schizophrenia-like disorder in Wilson's disease
gan: I. D. Spirina, et al.
Cyhoeddwyd: (2019-06-01)

MoCA, ACE-R, and MMSE versus the national institute of neurological disorders and stroke-canadian stroke network vascular cognitive impairment harmonization standards neuropsychological battery after TIA and stroke
gan: Pendlebury, S, et al.
Cyhoeddwyd: (2012)

MoCA, ACE-R, and MMSE versus the National Institute of Neurological Disorders and Stroke-Canadian Stroke Network Vascular Cognitive Impairment Harmonization Standards Neuropsychological Battery after TIA and stroke.
gan: Pendlebury, S, et al.
Cyhoeddwyd: (2012)

Underfunding of stroke research across Europe
gan: Pendlebury, S, et al.
Cyhoeddwyd: (2004)

Incidence and prevalence of dementia associated with transient ischaemic attack and stroke: analysis of the population-based Oxford Vascular Study
gan: Pendlebury, S, et al.
Cyhoeddwyd: (2019)

Novel mutations in ATP7B gene of Wilson\'s disease in Iranian patients
gan: Iradj Maleki, et al.
Cyhoeddwyd: (2013-02-01)

Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutations
gan: De-Min Yu, et al.
Cyhoeddwyd: (2011-01-01)

The key role of microRNA-766 in the cancer development
gan: Jitendra Gupta, et al.
Cyhoeddwyd: (2023-05-01)

Clinical and genetic characterization of patients with late onset Wilson’s disease
gan: Wenming Yang, et al.
Cyhoeddwyd: (2024-12-01)

Wilson’s Disease with Acute Hepatic Onset: How to Diagnose and Treat It
gan: Valeria Delle Cave, et al.
Cyhoeddwyd: (2024-01-01)

Polysomnographic Findings in A Late Onset Wilson’s Disease Patient
gan: Barış Metin, et al.
Cyhoeddwyd: (2007-04-01)

Association between LRP1 C766T polymorphism and Alzheimer’s disease susceptibility: a meta-analysis
gan: Yun Wang, et al.
Cyhoeddwyd: (2017-08-01)

Age-dependent association of white matter abnormality with cognition after TIA or minor stroke.
gan: Zamboni, G, et al.
Cyhoeddwyd: (2019)

Circ_0088194 Promotes the Invasion and Migration of Rheumatoid Arthritis Fibroblast-Like Synoviocytes via the miR-766-3p/MMP2 Axis
gan: Yujie Cai, et al.
Cyhoeddwyd: (2021-02-01)

Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identified
gan: Zhongyan Xiao, et al.
Cyhoeddwyd: (2021-09-01)

P198: Mutation spectrum of Wilson disease in Taiwan
gan: Yu-Hsuan Huang, et al.
Cyhoeddwyd: (2023-01-01)

Wilson Disease: Epigenetic Factors Contribute to Genetic Mutations to Affect the Disease
gan: Som Dev, PhD, et al.
Cyhoeddwyd: (2021-01-01)

Brain atrophy, N-terminal brain natriuretic peptide and carotid disease: interconnecting relationships between cerebral perfusion, cardiovascular disease, inflammation and cognitive decline.
gan: Pendlebury, S, et al.
Cyhoeddwyd: (2016)

Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson disease
gan: Nguyen Thi Mai Huong, et al.
Cyhoeddwyd: (2018-06-01)

Novel ATPase Cu(2+) transporting beta polypeptide mutations in Chinese families with Wilson's disease.
gan: Shaojuan Gu, et al.
Cyhoeddwyd: (2013-01-01)

The mutation spectrum and ethnic distribution of Wilson disease, a review
gan: Zahra Beyzaei, et al.
Cyhoeddwyd: (2024-03-01)

Variable iron-line emission near the black hole of Markarian 766
gan: Miller, L, et al.
Cyhoeddwyd: (2006)

Specification of signalling system no 7 : recommendations Q.721 - Q.766
gan: International Telegraph and Telephone Consultative Committee, et al.
Cyhoeddwyd: (1989)

Outcomes and complications of prophylactic incisional gastropexy in 766 dogs (2009–2019).
gan: Miranda de la Vega, et al.
Cyhoeddwyd: (2023-10-01)

Transient cognitive impairment in TIA and minor stroke.
gan: Pendlebury, S, et al.
Cyhoeddwyd: (2011)

Acute reversible cognitive impairment after TIA and minor stroke: a population-based study
gan: Simoni, M, et al.
Cyhoeddwyd: (2009)

Late Onset Wilson Disease with Neurologic Involvement Without Kayser-Fleisher Ring
gan: Shree Ram Sharma, et al.
Cyhoeddwyd: (2011-12-01)

Circ_0000479 promotes proliferation, invasion, migration and inflammation and inhibits apoptosis of rheumatoid arthritis fibroblast-like synoviocytes via miR-766/FKBP5 axis
gan: Peng Zhao, et al.
Cyhoeddwyd: (2023-03-01)