نتایج جستجو برای: diabetic arteriopathy

تعداد نتایج: 112195  

Journal: :Stroke 2013
Poneh Adib-Samii Natalia Rost Matthew Traylor William Devan Alessandro Biffi Silvia Lanfranconi Kaitlin Fitzpatrick Steve Bevan Allison Kanakis Valerie Valant Andreas Gschwendtner Rainer Malik Alexa Richie Dale Gamble Helen Segal Eugenio A Parati Emilio Ciusani Elizabeth G Holliday Jane Maguire Joanna Wardlaw Bradford Worrall Joshua Bis Kerri L Wiggins Will Longstreth Steve J Kittner Yu-Ching Cheng Thomas Mosley Guido J Falcone Karen L Furie Carlos Leiva-Salinas Benison C Lau Muhammed Saleem Khan Pankaj Sharma Myriam Fornage Braxton D Mitchell Bruce M Psaty Cathie Sudlow Christopher Levi Giorgio B Boncoraglio Peter M Rothwell James Meschia Martin Dichgans Jonathan Rosand Hugh S Markus

BACKGROUND AND PURPOSE Recently, a novel locus at 17q25 was associated with white matter hyperintensities (WMH) on MRI in stroke-free individuals. We aimed to replicate the association with WMH volume (WMHV) in patients with ischemic stroke. If the association acts by promoting a small vessel arteriopathy, it might be expected to also associate with lacunar stroke. METHODS We quantified WMH o...

Journal: :Stroke 1994
W I Schievink J Björnsson D G Piepgras

BACKGROUND A primary arteriopathy is suspected in most patients with spontaneous dissections of the carotid artery, although the nature of this arteriopathy usually remains elusive. Angiographic changes of fibromuscular dysplasia (FMD), however, are found in 10% to 20% of patients with carotid dissections. CASE DESCRIPTION A 26-year-old woman with Marfan's syndrome presented with bilateral am...

Journal: :AJNR. American journal of neuroradiology 1995
S J Skehan M Hutchinson D P MacErlaine

PURPOSE To describe the MR appearances of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. METHODS MR examinations were performed on 15 family members (both symptomatic and asymptomatic). The phenotype was defined by the presence of abnormalities on MR scanning in genetically susceptible individuals. RESULTS There were 10 abnormal and 5 normal MR s...

Journal: :The Journal of biological chemistry 2002
Wenli Wang Chengyu Z Prince Yongshan Mou Matthew J Pollman

Mutations in the Notch3 receptor result in the cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephelopathy (CADASIL) syndrome, a heritable arteriopathy predisposing to early onset stroke. Based upon clinical evidence that CADASIL arteriopathy results in degeneration and loss of vascular smooth muscle cells (VSMC) from the arterial wall, we postulated that Notch3 s...

Journal: :British heart journal 1987
D Heath P Smith J Gosney D Mulcahy K Fox M Yacoub P Harris

During the course of a case of primary pulmonary hypertension occurring in a 24 year old man lung tissue became available at heart-lung transplantation in 1986 and from a lung biopsy carried out in 1981. In 1986 the sections showed classic plexogenic pulmonary arteriopathy. In 1981 they revealed migration of myofibroblasts into the intima and lumen of pulmonary arteries and arterioles, the iden...

2015
Wei-Tsun Kao Wei-Chen Lin Yong-Hao Tseng Tai-Heng Chen

Vascular wall injuries account for up to 80% of childhood strokes, excluding emboli of cardiac origin. Transient cerebral arteriopathy is a recently described entity that is increasingly recognized as an important cause. The cerebral arterial wall is thought to be affected by an inflammatory process related to certain infections. The authors report a 2.5-year-old girl with sudden left hemiplegi...

2012
Julio Cesar Vasconcelos da Silva Emerson L. Gasparetto Eliasz Engelhardt

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a hereditary cerebral arteriopathy caused by mutations in the Notch-3 gene. The diagnosis is reached by skin biopsy revealing presence of granular osmiophílic material (GOM), and/or by genetic testing for Notch-3. We report a case of a 52-year-old man with recurrent transient ischemic attacks...

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