Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hannes Blöndal"'
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 84:136-140
Background Multiple system atrophy (MSA) is a neurodegenerative disorder characterised by autonomic dysfunction with parkinsonism (MSAp) or cerebellar (MSAc) symptoms. At autopsy, α-synuclein inclusions in glial cells of the brain are needed to conf
Publikováno v:
Læknablaðið. 2011:21-29
Wernicke's encephalopathy (WE) is caused by thiamine (vitamin B1) deficiency and most commonly found in individuals with chronic alcoholism and malnutrition. Clinically, its key features are mental status disorders and oculomotor abnormalities as wel
Autor:
Pia Davidsson, Hannes Blöndal, Finnbogi R. Thormodsson, Gunnar Gudmundsson, Maria Bjarnadottir, Veronica Lindström, Carol L. Nilsson, Anders Grubb, Ann Westman
Publikováno v:
Scopus-Elsevier
A variant of the normal extracellular cysteine protease inhibitor cystatin C (L68Q-cystatin C), is the amyloid precursor in hereditary cystatin C amyloid angiopathy (HCCAA). It has been suggested that the mutation causes cellular entrapment of L68Q-c
Autor:
Olafur Kjartansson, Hannes Blöndal, Gretar Gudmundsson, Sif Jonsdottir, Gunnar Gudmundsson, Sigurlaug Sveinbjörnsdóttir
Publikováno v:
Journal of the Neurological Sciences. 140:101-108
Hereditary Cystatin-C Amyloidosis (HCCA) is a genetic disorder in Icelandic families in which a defective cystatin-C amyloid protein is deposited in the walls of small and middle sized arteries. Cerebral vessels are most affected, resulting in recurr
Autor:
Henryk M. Wisniewski, K.S. Kim, Eirikur Benedikz, R. D. Rudelli, G Y Wen, T. Pirttilä, Hannes Blöndal, H. Frey
Publikováno v:
Acta Neuropathologica. 88:201-206
A total of 66 skin biopsies from persons with Alzheimer's disease (AD) or Down's syndrome (DS) and from persons without AD were used in this study. The age range was from 7 to 89 years. Positive immunoreactivity of skin biopsies to monoclonal antibod
Publikováno v:
Laeknabladid. 97(1)
Wernicke's encephalopathy (WE) is caused by thiamine (vitamin B1) deficiency and most commonly found in individuals with chronic alcoholism and malnutrition. Clinically, its key features are mental status disorders and oculomotor abnormalities as wel
Publikováno v:
APMIS. 100:294-300
Thirteen ependymomas reported to the Icelandic Cancer Registry during a 32-year period (1955-1986) were histologically reviewed and reclassified according to the WHO Histological Typing of Tumours of the Central Nervous System. The annual incidence r
Publikováno v:
Experimental and molecular pathology. 83(3)
Cerebral amyloid angiopathy (CAA) is characterized by the accumulation of amyloid within arteries of the cerebral cortex and leptomeninges. This condition is age related, especially prevalent in Alzheimer's disease (AD) and the main feature of certai