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10 results on '"Kleveland, Grethe"'

1. Repeat expansions in AR, ATXN1, ATXN2 and HTT in Norwegian patients diagnosed with amyotrophic lateral sclerosis

Author

Novy, Camilla, primary, Busk, Øyvind L, additional, Tysnes, Ole-Bjørn, additional, Landa, Sigve S, additional, Aanjesen, Tori N, additional, Alstadhaug, Karl B, additional, Bjerknes, Tale L, additional, Bjørnå, Ingrid K, additional, Bråthen, Geir, additional, Dahl, Elin, additional, Demic, Natasha, additional, Fahlström, Maria, additional, Flemmen, Heidi Ø, additional, Hallerstig, Erika, additional, HogenEsch, Ineke, additional, Kampman, Margitta T, additional, Kleveland, Grethe, additional, Kvernmo, Helene B, additional, Ljøstad, Unn, additional, Maniaol, Angelina, additional, Morsund, Aase Hagen, additional, Nakken, Ola, additional, Olsen, Cathrine G, additional, Schlüter, Katrin, additional, Utvik, May-Sissel, additional, Yaseen, Ryaz, additional, Holla, Øystein L, additional, Holmøy, Trygve, additional, and Høyer, Helle, additional

Published
2024
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2. The Effect of Smoking on Long-term Gray Matter Atrophy and Clinical Disability in Patients with Relapsing-Remitting Multiple Sclerosis

Author

Lie, Ingrid Anne, primary, Wesnes, Kristin, additional, Kvistad, Silje S., additional, Brouwer, Iman, additional, Wergeland, Stig, additional, Holmøy, Trygve, additional, Midgard, Rune, additional, Bru, Alla, additional, Edland, Astrid, additional, Eikeland, Randi, additional, Gosal, Sonia, additional, Harbo, Hanne F., additional, Kleveland, Grethe, additional, Sørenes, Yvonne S., additional, Øksendal, Nina, additional, Barkhof, Frederik, additional, Vrenken, Hugo, additional, Myhr, Kjell-Morten, additional, Bø, Lars, additional, and Torkildsen, Øivind, additional

Published
2022
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3. Serum neurofilament as a predictor of 10-year grey matter atrophy and clinical disability in multiple sclerosis: a longitudinal study

Author

Lie, Ingrid Anne, primary, Kaçar, Sezgi, additional, Wesnes, Kristin, additional, Brouwer, Iman, additional, Kvistad, Silje S, additional, Wergeland, Stig, additional, Holmøy, Trygve, additional, Midgard, Rune, additional, Bru, Alla, additional, Edland, Astrid, additional, Eikeland, Randi, additional, Gosal, Sonia, additional, Harbo, Hanne F, additional, Kleveland, Grethe, additional, Sørenes, Yvonne S, additional, Øksendal, Nina, additional, Varhaug, Kristin N, additional, Vedeler, Christian A, additional, Barkhof, Frederik, additional, Teunissen, Charlotte E, additional, Bø, Lars, additional, Torkildsen, Øivind, additional, Myhr, Kjell-Morten, additional, and Vrenken, Hugo, additional

Published
2022
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4. Genetic Epidemiology of Amyotrophic Lateral Sclerosis in Norway: A 2-Year Population-Based Study

Author

Olsen, Cathrine Goberg, primary, Busk, Øyvind Løvold, additional, Aanjesen, Tori Navestad, additional, Alstadhaug, Karl Bjørnar, additional, Bjørnå, Ingrid Kristine, additional, Braathen, Geir Julius, additional, Breivik, Kristin Lif, additional, Demic, Natasha, additional, Flemmen, Heidi Øyen, additional, Hallerstig, Erika, additional, HogenEsch, Ineke, additional, Holla, Øystein Lunde, additional, Jøntvedt, Anne Berit, additional, Kampman, Margitta T., additional, Kleveland, Grethe, additional, Kvernmo, Helene Ballo, additional, Ljøstad, Unn, additional, Maniaol, Angelina, additional, Morsund, Åse Hagen, additional, Nakken, Ola, additional, Novy, Camilla, additional, Rekand, Tiina, additional, Schlüter, Katrin, additional, Schüler, Stephan, additional, Tveten, Kristian, additional, Tysnes, Ole-Bjørn, additional, Holmøy, Trygve, additional, and Høyer, Helle, additional

Published
2022
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5. Low vitamin D, but not tobacco use or high BMI, is associated with long-term disability progression in multiple sclerosis

Author

Wesnes, Kristin, primary, Myhr, Kjell-Morten, additional, Riise, Trond, additional, Kvistad, Silje Stokke, additional, Torkildsen, Øivind, additional, Wergeland, Stig, additional, Holmøy, Trygve, additional, Midgard, Rune, additional, Bru, Alla, additional, Edland, Astrid, additional, Eikeland, Randi, additional, Gosal, Sonia, additional, Harbo, Hanne F., additional, Kleveland, Grethe, additional, Sørenes, Yvonne S., additional, Øksendal, Nina, additional, and Bjørnevik, Kjetil, additional

Published
2021
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7. July 2017 ENCALS statement on edaravone

Author

Al-Chalabi, Ammar, Andersen, Peter M., Chandran, Siddharthan, Chio, Adriano, Corcia, Philippe, Couratier, Philippe, Danielsson, Olof, de Carvalho, Mamede, Desnuelle, Claude, Grehl, Torsten, Grosskreutz, Julian, Holmoy, Trygve, Ingre, Caroline, Karlsborg, Merete, Kleveland, Grethe, Christoph Koch, Jan, Koritnik, Blaz, KuzmaKozakiewicz, Magdalena, Laaksovirta, Hannu, Ludolph, Albert, McDermott, Christopher, Meyer, Thomas, Ropero, Bernardo Mitre, Pardina, Jesus Mora, Nygren, Ingela, Petri, Susanne, Povedano Panades, Monica, Salachas, Francois, Shaw, Pamela, Silani, Vincenzo, Staaf, Gert, Svenstrup, Kirsten, Talbot, Kevin, Tysnes, Ole-Bjorn, Van Damme, Philip, van der Kooi, Anneke, Weber, Markus, Weydt, Patrick, Wolf, Joachim, Hardiman, Orla, van den Berg, Leonard H., Al-Chalabi, Ammar, Andersen, Peter M., Chandran, Siddharthan, Chio, Adriano, Corcia, Philippe, Couratier, Philippe, Danielsson, Olof, de Carvalho, Mamede, Desnuelle, Claude, Grehl, Torsten, Grosskreutz, Julian, Holmoy, Trygve, Ingre, Caroline, Karlsborg, Merete, Kleveland, Grethe, Christoph Koch, Jan, Koritnik, Blaz, KuzmaKozakiewicz, Magdalena, Laaksovirta, Hannu, Ludolph, Albert, McDermott, Christopher, Meyer, Thomas, Ropero, Bernardo Mitre, Pardina, Jesus Mora, Nygren, Ingela, Petri, Susanne, Povedano Panades, Monica, Salachas, Francois, Shaw, Pamela, Silani, Vincenzo, Staaf, Gert, Svenstrup, Kirsten, Talbot, Kevin, Tysnes, Ole-Bjorn, Van Damme, Philip, van der Kooi, Anneke, Weber, Markus, Weydt, Patrick, Wolf, Joachim, Hardiman, Orla, and van den Berg, Leonard H.

Published
2017
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8. July 2017 ENCALS statement on edaravone

Author

Al-Chalabi, Ammar, primary, Andersen, Peter M., additional, Chandran, Siddharthan, additional, Chio, Adriano, additional, Corcia, Philippe, additional, Couratier, Philippe, additional, Danielsson, Olof, additional, de Carvalho, Mamede, additional, Desnuelle, Claude, additional, Grehl, Torsten, additional, Grosskreutz, Julian, additional, Holmøy, Trygve, additional, Ingre, Caroline, additional, Karlsborg, Merete, additional, Kleveland, Grethe, additional, Christoph Koch, Jan, additional, Koritnik, Blaz, additional, KuzmaKozakiewicz, Magdalena, additional, Laaksovirta, Hannu, additional, Ludolph, Albert, additional, McDermott, Christopher, additional, Meyer, Thomas, additional, Mitre Ropero, Bernardo, additional, Mora Pardina, Jesus, additional, Nygren, Ingela, additional, Petri, Susanne, additional, Povedano Panades, Mónica, additional, Salachas, Francois, additional, Shaw, Pamela, additional, Silani, Vincenzo, additional, Staaf, Gert, additional, Svenstrup, Kirsten, additional, Talbot, Kevin, additional, Tysnes, Ole-Bjørn, additional, Van Damme, Philip, additional, van der Kooi, Anneke, additional, Weber, Markus, additional, Weydt, Patrick, additional, Wolf, Joachim, additional, Hardiman, Orla, additional, and van den Berg, Leonard H., additional

Published
2017
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10. Amyotrophic lateral sclerosis caused by the <italic>C9orf72</italic> expansion in Norway – prevalence, ancestry, clinical characteristics and sociodemographic status.

Author

Olsen, Cathrine Goberg, Malmberg, Vetle Nilsen, Fahlström, Maria, Alstadhaug, Karl Bjørnar, Bjørnå, Ingrid Kristine, Braathen, Geir Julius, Bråthen, Geir, Demic, Natasha, Hallerstig, Erika, Hogenesch, Ineke, Horn, Morten Andreas, Kampman, Margitta T., Kleveland, Grethe, Ljøstad, Unn, Maniaol, Angelina, Morsund, Åse Hagen, Nakken, Ola, Schlüter, Katrin, Schuler, Stephan, and Seim, Elin

Subjects
*AMYOTROPHIC lateral sclerosis, *SURVIVAL rate, *FAMILY history (Genealogy), *NEURODEGENERATION, *GENETIC testing
Abstract

AbstractObjectiveMethodsResultsConclusionThe most common genetic cause of amyotrophic lateral sclerosis (ALS) is the C9orf72 expansion. A high incidence of this expansion has been detected in Sweden and Finland. This Norwegian population-based study aimed to identify the prevalence, geographic distribution, ancestry, and relatedness of ALS patients with a C9orf72 expansion (C9pos). Further, we compared C9pos and C9neg patients’ clinical presentation, family history of ALS and other neurodegenerative disorders, and sociodemographic status.We recruited ALS patients from all 17 Departments of neurology in Norway. Blood samples and questionnaires regarding clinical characteristics, sociodemographic status and family history of ALS, and other neurodegenerative disorders were collected. The C9orf72 expansion was examined for all patients.The study enrolled 500 ALS patients, 8.8% of whom were C9pos, with half being sporadic ALS cases. The proportion of C9pos cases differed between regions, ranging from 17.9% in the Northern region to 1.9% in the Western region. The majority of C9pos patients had non-Finnish European descent and were not closely related. C9pos patients exhibited a significantly shorter mean survival time, had a higher frequency of relatives with ALS or dementia, and were more often unmarried/single and childless than C9neg patients.C9pos patients constitute a large portion of the Norwegian ALS population. Ancestry and relatedness do not adequately explain regional differences. Relying on clinical information to identify C9pos patients has proven to be challenging. Half of C9pos patients were reported as having sporadic ALS, underlining the importance of carefully assessing family history and the need for genetic testing. [ABSTRACT FROM AUTHOR]

Published
2024
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