Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Lars Olof Ronnevi"'
Autor:
Freya Kamel, Henrik Larsson, Daniela Mariosa, Weimin Ye, Rino Bellocco, Lars-Olof Ronnevi, Catarina Almqvist, Fang Fang
Publikováno v:
European Journal of Neurology. 27:1010-1016
Background: Medications that are used for treatment of metabolic disorders have been suggested to be associated with the development of amyotrophic lateral sclerosis (ALS). Methods: To examine the associations of antidiabetics and statins with the su
Autor:
Fang Fang, Honglei Chen, Karin Wirdefeldt, Lars-Olof Ronnevi, Ammar Al-Chalabi, Tracy L Peters, Freya Kamel, Weimin Ye
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e29749 (2011)
Severe infections may lead to chronic inflammation in the central nervous system (CNS) which may in turn play a role in the etiopathogenesis of amyotrophic lateral sclerosis (ALS). The relentless progression and invasive supportive treatments of ALS
Externí odkaz:
https://doaj.org/article/7de5ec47c67f474798f0e3e3e70f22e0
Autor:
Weimin Ye, Martin R Turner, Lars-Olof Ronnevi, Fang Fang, Ammar Al-Chalabi, Karin Wirdefeldt, Freya Kamel
Comorbidity of cancer with ALS has been studied previously. Detailed description of the temporal relationship between cancer and ALS is, however, lacking. We conducted a nested case-control study of ALS in Sweden during 1987-2009, including 5481 case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fc6c26f4f45f6528e1dd7659cf29127
https://doi.org/10.3109/21678421.2013.775309
https://doi.org/10.3109/21678421.2013.775309
Publikováno v:
Acta Neurologica Scandinavica. 65:203-211
Six ALS-patients were given long-term penicillamine treatment. A rapid, long-lasting increase in urinary lead was provoked, whereas whole blood and plasma lead were unchanged. In four patients, the progress did not change markedly, one patient deteri
Autor:
Sebastian Conradi, Lars-Olof Ronnevi
Publikováno v:
Journal of the Neurological Sciences. 139:60-63
The phase of rapid reduction of isometric strength in single muscle groups was identified and its slope was calculated in patients studied with the TQNE method. This parameter was studied in the extremities and in respiration in 4 ALS patients and 4
Autor:
Weimin Ye, Lars-Olof Ronnevi, Fang Fang, Tracy L. Peters, Ammar Al-Chalabi, Karin Wirdefeldt, Honglei Chen, Freya Kamel
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e29749 (2011)
PLoS ONE
PLoS ONE; Vol 6
PLoS ONE
PLoS ONE; Vol 6
Background Severe infections may lead to chronic inflammation in the central nervous system (CNS) which may in turn play a role in the etiopathogenesis of amyotrophic lateral sclerosis (ALS). The relentless progression and invasive supportive treatme
Autor:
Johan G. Eriksson, Birgitta Bergman, Ulla Rasmussen, Lars-Olof Ronnevi, Lotta Berntzon, Leopold L. Ilag, Zdenĕk Spáčil, Sara Jonasson
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 107(20)
β-methylamino-L-alanine (BMAA), a neurotoxic nonprotein amino acid produced by most cyanobacteria, has been proposed to be the causative agent of devastating neurodegenerative diseases on the island of Guam in the Pacific Ocean. Because cyanobacteri
Autor:
Fang Fang, Weimin Ye, Rino Bellocco, Unnur Valdimarsdóttir, Pär Sparén, Katja Fall, Lars-Olof Ronnevi
Publikováno v:
Archives of Neurology. 66
To investigate the temporal trend of amyotrophic lateral sclerosis (ALS) incidence in Sweden between January 1, 1991, and December 31, 2005, and to explore incidence variations according to major demographic factors.Population-based study.Academic re
Autor:
Vesa Juvonen, Christina Kölmel, Markus Weber, Lionel Van Maldergem, Bjarne Udd, Mark R. Davis, Sven Asger Sørensen, Annastiina Lund, Kristina Cederquist, Lars Olof Ronnevi, Mitsunori Watanabe, Leone Yeung, Cinzia Gellera, Marja-Liisa Savontaus, Anne D. Sperfeld, Peter M. Andersen, Lisbeth Tranebjærg
Publikováno v:
European journal of human genetics : EJHG. 9(6)
SBMA (spinal and bulbar muscular atrophy), also called Kennedy disease, is an X-chromosomal recessive adult-onset neurodegenerative disorder caused by death of the spinal and bulbar motor neurones and dorsal root ganglia. Patients may also show signs
Autor:
Sebastian Conradi, Lars-Olof Ronnevi
Publikováno v:
Journal of the neurological sciences.
Autoantibodies of the IgG and IgA types against a membrane bound AChE fraction were studied in the serum of ALS/MND patients, controls with neurological or autoimmune diseases, and normal controls. About 70% of ALS and progressive spinal muscle atrop