Search Results - "Guðmundsson, Grétar"

No association between VAPB mutations and familial or sporadic ALS in Sweden, Portugal and Iceland by Ingre, Caroline, Pinto, Susana, Birve, Anna, Press, Rayomand, Danielsson, Olof, de Carvalho, Mamede, Gu mundsson, Grétar, Andersen, Peter M.

“…Abstract Linkage analysis in Brazilian families with amyotrophic lateral sclerosis (ALS) revealed that a missense mutation p.Pro56Ser in a conserved gene…”
Get full text

Case–control studies on ceruloplasmin and superoxide dismutase (SOD1) in neurodegenerative diseases: A short review by Torsdottir, Gudlaug, Kristinsson, Jakob, Snaedal, Jón, Sveinbjörnsdóttir, Sigurlaug, Gudmundsson, Grétar, Hreidarsson, Stefán, Jóhannesson, Torkell

“…Abstract This short review describes a series of case–control studies on the concentration and oxidative activity of ceruloplasmin (CP) in serum and the…”
Get full text

Ceruloplasmin and superoxide dismutase (SOD1) in heterozygotes for Wilson disease: A case control study by Tórsdóttir, Gudlaug, Gudmundsson, Grétar, Kristinsson, Jakob, Snaedal, Jón, Jóhannesson, Torkell

“…At the time of this study, there were five known patients with Wilson disease (WD) in Iceland. The mutation, a 7-bp deletion in exon 7 on chromosome 13 for WD,…”
Get full text

Familial Aggregation of Parkinson's Disease in Iceland by Sveinbjörnsdóttir, Sigurlaug, Hicks, Andrew A, Jónsson, Thorlákur, Pétursson, Hjörvar, Guðmundsson, Grétar, Frigge, Michael L, Kong, Augustine, Gulcher, Jeffrey R, Stefánsson, Kári

“…Parkinson's disease is an important neurodegenerative disorder affecting middle-aged and elderly persons. Its causes are largely unknown, but there is evidence…”
Get full text

Localization of a Gene for Migraine without Aura to Chromosome 4q21 by Björnsson, Ásgeir, Gudmundsson, Grétar, Gudfinnsson, Einar, Hrafnsdóttir, María, Benedikz, John, Skúladóttir, Svanhildur, Kristjánsson, Kristleifur, Frigge, Michael L., Kong, Augustine, Stefánsson, Kári, Gulcher, Jeffrey R.

“…Migraine is a common form of headache and has a significant genetic component. Here, we report linkage results from a study in Iceland of migraine without aura…”
Get full text

Incidence and prevalence of multiple system atrophy: a nationwide study in Iceland by Bjornsdottir, Anna, Gudmundsson, Gretar, Blondal, Hannes, Olafsson, Elias

“…Background Multiple system atrophy (MSA) is a neurodegenerative disorder characterised by autonomic dysfunction with parkinsonism (MSAp) or cerebellar (MSAc)…”
Get full text

Copper, Ceruloplasmin and Superoxide Dismutase (SOD) in Amyotrophic Lateral Sclerosis by Torsdottir, Gudlaug, Kristinsson, Jakob, Gudmundsson, Gretar, Snaedal, Jon, Johannesson, Torkell

“…Abstract only…”
Get full text

Copper, Ceruloplasmin and Superoxide Dismutase (SOD) in Amyotrophic Lateral Sclerosis by Tórsdóttir, Gudlaug, Kristinsson, Jakob, Gudmundsson, Grétar, Snaedal, Jón, Jóhannesson, Torkell

“…: In two previous studies we found copper dyshomeostasis in patients with Alzheimer's disease and in patients with Parkinson's disease. In this study, the…”
Get full text

Progressive dementia and leucoencephalopathy as the initial presentation of late onset hereditary cystatin-C amyloidosis Clinicopathological presentation of two cases by Sveinbjörnsdóttir, Sigurlaug, Blöndal, Hannes, Gudmundsson, Gretar, Kjartansson, Ólafur, Jónsdóttir, Sif, Gudmundsson, Gunnar

“…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…”
Get full text

Whooping Cough and Parkinson's Disease by DE PEDRO-CUESTA, JESÚS, GUDMUNDSSON, GRETAR, ABRAIRA, VICTOR, GUDMUNDSSON, GUNNAR, LŌVE, ARTHUR, TULINIUS, HRAFN, VEIGA, JORGE, ALMAZÁN, JAVIER, PETERSEN, INGOLF J

“…de Pedro-Cuesta J (Instituto de Salud Carlos III, Centro Nacional de Epidemiología, Departamento de Epidemiología Aplicada, c/ Sinesio Delgado, 6, 28029…”
Get full text