نتایج جستجو برای: sporadic

تعداد نتایج: 21803  

2004
Evangelia Charmandari Tomoshige Kino George P. Chrousos Sebastiano Filetti

2011
Harsha Bhatia Fawzi Babtain

Hemiplegic migraines are characterised by attacks of migraine with aura accompanied by transient motor weakness. There are both familial and sporadic subtypes, which are now recognised as separate entities by the International Classification of Headache Disorders, edition II (ICHD-II). Sporadic hemiplegic migraine is a rare variant of migraine, We report a case of sporadic hemiplegic migraine a...

Journal: :The British journal of oral & maxillofacial surgery 2014
Elliot Shevel

My aim was to report for the first time (to my knowledge) the successful treatment of 3 patients with sporadic hemiplegic migraine by surgical cautery of terminal branches of the external carotid artery under conscious sedation. Since the operations (between 1 and 2 years) none of the patients have had further attacks of migraine or hemiplegia. This preliminary report suggests that for patients...

Journal: :Brain : a journal of neurology 2014
Mitsuru Shinohara Shinsuke Fujioka Melissa E Murray Aleksandra Wojtas Matthew Baker Anne Rovelet-Lecrux Rosa Rademakers Pritam Das Joseph E Parisi Neill R Graff-Radford Ronald C Petersen Dennis W Dickson Guojun Bu

Recent studies suggest that subcortical structures, including striatum, are vulnerable to amyloid-β accumulation and other neuropathological features in familial Alzheimer's disease due to autosomal dominant mutations. We explored differences between familial and sporadic Alzheimer's disease that might shed light on their respective pathogenic mechanisms. To this end, we analysed 12 brain regio...

2017
Sadanandavalli Retnaswami Chandra Chetan Vekhande Lakshminarayanapuram Gopal Viswanathan Pooja Mailankody Karru Venkata Ravi Teja

A disorder of infants and children with pathological startle response, features of other system involvement, falls, and stiffness with retained consciousness. It should be differentiated from conditions such as myoclonic epilepsy, psychogenic movement disorder, Isaac syndrome, Schwartz-Jampel syndrome, Gilles de la Tourette, and culture-specific startle syndromes such as jumping Frenchman of Ma...

2011
Roberto E.P. Sica Alejandro F. De Nicola María C. González Deniselle Gabriel Rodriguez Gisella M. Gargiulo Monachelli Liliana Martinez Mariela Bettini

This article briefly describes the already known clinical features and pathogenic mechanisms underlying sporadic amyotrophic lateral sclerosis, namely excitoxicity, oxidative stress, protein damage, inflammation, genetic abnormalities and neuronal death. Thereafter, it puts forward the hypothesis that astrocytes may be the cells which serve as targets for the harmful action of a still unknown e...

Journal: :Discrete & Computational Geometry 2013
Kevin G. Hare Michael J. Mossinghoff

Let n be a positive integer, not a power of two. A Reinhardt polygon is a convex n-gon that is optimal in three different geometric optimization problems: it has maximal perimeter relative to its diameter, maximal width relative to its diameter, and maximal width relative to its perimeter. For almost all n, there are many Reinhardt polygons with n sides, and many of them exhibit a particular pe...

Journal: :avicenna journal of medical biotechnology 0

breast cancer is the most common cancer among women in developed countries. the prevalence of the disease is increasing in the world. its annual incidence among iranian women is about 7000 cases. rap1a, a tumor suppressor gene, is located at 1p13.3 and plays an important role in the cellular adhesion pathway and is involved in the pathogenesis of breast cancer. the dock4 gene, which is located ...

2011
Els Robanus-Maandag Cathy Bosch Saeid Amini-Nik Jeroen Knijnenburg Karoly Szuhai Pascale Cervera Raymond Poon Diana Eccles Paolo Radice Marco Giovannini Benjamin A. Alman Sabine Tejpar Peter Devilee Riccardo Fodde

Desmoid tumours (also called deep or aggressive fibromatoses) are potentially life-threatening fibromatous lesions. Hereditary desmoid tumours arise in individuals affected by either familial adenomatous polyposis (FAP) or hereditary desmoid disease (HDD) carrying germline mutations in APC. Most sporadic desmoids carry somatic mutations in CTNNB1. Previous studies identified losses on 5q and 6q...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2005
David G Cox Susan E Hankinson David J Hunter

Truncation mutations in the BRCA2 gene cause a substantial increase in risk of breast cancer. However, these mutations are rare in the general population and account for little of the overall incidence of sporadic breast cancer. Recently, an intronic single-nucleotide polymorphism (G/A at bp 30,763,310) was also found associated with breast cancer risk (1). One nonsynonymous polymorphism, N372H...

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