Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Laurence Newrick"'
Publikováno v:
Cerebellum & Ataxias, Vol 8, Iss 1, Pp 1-6 (2021)
Cerebellum & Ataxias
Cerebellum & Ataxias
Background Most immune-mediated cerebellar ataxias, including those associated with gluten sensitivity (Gluten Ataxia), tend to present subacutely and usually progress gradually. Acute presentations with rapid progression outside the context of paran
Autor:
Nathan Rugg, N R Lewis, Alan Kelsall, David S Sanders, Stefanie N. Winfield, Marios Hadjivassiliou, Imran Aziz, Laurence Newrick
Publikováno v:
European Journal of Gastroenterology & Hepatology. 26:33-39
Reports suggest that gluten sensitivity (GS) exists in the absence of coeliac disease (CD). This clinical entity has been termed noncoeliac gluten sensitivity (NCGS).To determine the population prevalence of self-reported GS and referral characterist
Publikováno v:
Progress in Neurology and Psychiatry. 21:11-12
Frontotemporal dementia (FTD) is a heterogeneous neurodegenerative disease whose early behavioural and emotional symptoms often mimic psychiatric disorders. Here, the authors highlight the challenges of diagnosis with the reassessment of an elderly p
Publikováno v:
Progress in Neurology and Psychiatry. 21:24-25
Autoimmune encephalitis may present with prominent neuropsychiatric symptoms, and is increasingly considered in the differential diagnosis of patients with altered mental state. Here, the authors navigate the muddy waters between neurology and psychi
Ataxia telangiectasia (AT) is a rare autosomal-recessive disorder caused by mutations in the AT-mutated ( ATM ) gene (chromosome 11q 22-23) with absent or aberrant ATM protein kinase.1 It is usually characterized by childhood-onset cerebellar ataxia,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b60b12c3083541acb47b48dc50fb3e91
https://europepmc.org/articles/PMC5764536/
https://europepmc.org/articles/PMC5764536/
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 84:e2.48-e2
Ataxia telangiectasia (AT) is a multisystem autosomal recessive disorder caused by mutations in the ATM gene found on the large arm of chromosome 11 (11q 22–23). The ATM gene encodes the protein kinase ATM, which is the key regulator of cellular re
Autor:
S Winfield, N Rugg, A Kelsall, Imran Aziz, David S Sanders, Marios Hadjivassiliou, Laurence Newrick
Publikováno v:
Gut. 62:A128.2-A129
Introduction Healthcare professionals commonly encounter patients complaining of gluten sensitivity (GS) in the absence of serological and histological markers for coeliac disease (CD). This clinical entity has recently been termed non-coeliac gluten
Publikováno v:
Gut. 61:A250.2-A250
Introduction Many unselected patients presenting to gastrointestinal (GI) clinics self-report that they have symptoms related to the ingestion of gluten. For this reason we undertook a prospective and systematic evaluation of this group of patients t
Publikováno v:
Cerebellum & Ataxias
We report a mother and daughter with autosomal recessive ataxia with occulomotor apraxia in whom sequence analysis of senataxin revealed a dignosis of AOA2 (ataxia with occulomotor apraxia type 2) in both individuals. The apparent dominant inheritanc