Search Results - "Harno, H."

Sensory profiles in women with neuropathic pain after breast cancer surgery by Mustonen, L., Vollert, J., Rice, A. S. C., Kalso, E., Harno, H.

“…Purpose We performed a detailed analysis of sensory function in patients with chronic post-surgical neuropathic pain (NP) after breast cancer treatments by…”
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Depression, anxiety, and cognitive functioning after intracerebral hemorrhage by Koivunen, R.-J., Harno, H., Tatlisumak, T., Putaala, J.

“…Background and Purpose Post‐stroke depression (PSD) is an important complication of stroke. We studied long‐term PSD after intracerebral hemorrhage (ICH) at…”
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Patients with complex regional pain syndrome overestimate applied force in observed hand actions by Hotta, J., Harno, H., Nummenmaa, L., Kalso, E., Hari, R., Forss, N.

“…Background Movement accuracy is ensured by interaction between motor, somatosensory, and visual systems. In complex regional pain syndrome (CRPS), this…”
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Subclinical vestibulocerebellar dysfunction in migraine with and without aura by HARNO, H, HIRVONEN, T, FÄRKKILÄ, M, KAUNISTO, M. A, AALTO, H, LEVO, H, ISOTALO, E, KALLELA, M, KAPRIO, J, PALOTIE, A, WESSMAN, M

“…In patients with migraine, neurotologic symptoms and signs occur commonly. The authors' aim was to determine whether neurotologic findings are in accordance…”
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Testing of variants of the MTHFR and ESR1 genes in 1798 Finnish individuals fails to confirm the association with migraine with aura by Kaunisto, M A, Kallela, M, Hämäläinen, E, Kilpikari, R, Havanka, H, Harno, H, Nissilä, M, Säkö, E, Ilmavirta, M, Liukkonen, J, Teirmaa, H, Törnwall, O, Jussila, M, Terwilliger, J, Färkkilä, M, Kaprio, J, Palotie, A, Wessman, M

“…Among the few independently replicated genetic associations in migraine are polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) and oestrogen…”
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A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2 by KAUNISTO, M. A, HARNO, H, FÄRKKILÄ, M, PALOTIE, A, WESSMAN, M, VANMOLKOT, K. R. J, GARGUS, J. J, SUN, G, HÄMÄLÄINEN, E, LIUKKONEN, E, KALLELA, M, VAN DEN MAAGDENBERG, A. M. J. M, FRANTS, R. R

“…Familial hemiplegic migraine (FHM), a rare autosomal dominant subtype of migraine with aura, has been linked to two chromosomal loci, 19p13 and 1q23. Mutations…”
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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families by Gormley, Padhraig, Kurki, Mitja I., Hiekkala, Marjo Eveliina, Häppölä, Paavo, Mitchell, Adele A., Lal, Dennis, Palta, Priit, Surakka, Ida, Kaunisto, Mari Anneli, Hämäläinen, Eija, Vepsäläinen, Salli, Havanka, Hannele, Harno, Hanna, Ilmavirta, Matti, Sumelahti, Marja-Liisa, Sillanpää, Matti, Metsähonkala, Liisa, Koskinen, Seppo, Raitakari, Olli, Jousilahti, Pekka, Anttila, Verneri, Salomaa, Veikko, Artto, Ville, Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K., Elson, Sarah L., Furlotte, Nicholas A., Huber, Karen E., Kleinman, Aaron, Litterman, Nadia K., McCreight, Jennifer C., McIntyre, Matthew H., Mountain, Joanna L., Pitts, Steven J., Sathirapongsasuti, J. Fah, Shelton, Janie F., Shringarpure, Suyash, Tian, Chao, Vacic, Vladimir, Wilson, Catherine H., Anttila, Verneri, Artto, Ville, Belin, Andrea Carmine, Børte, Sigrid, Cherkas, Lynn, Christensen, Anne Francke, Cuenca-Leon, Ester, Dichgans, Martin, van Duijn, Cornelia, Esko, Tonu, Esserlind, Ann-Louise, Frants, Rune R., Freilinger, Tobias, Furlotte, Nick, Gormley, Padhraig, Hansen, Thomas Folkmann, Hiekkala, Marjo, Ikram, M Arfan, Ingason, Andres, Kajanne, Risto, Kallela, Mikko, Kaprio, Jaakko, Kaunisto, Mari, Kubisch, Christian, Kurth, Tobias, Launer, Lenore, Lehtimaki, Terho, Lessel, Davor, Ligthart, Lannie, Litterman, Nadia, van den Maagdenberg, Arn, Macaya, Alfons, Malik, Rainer, Muller-Myhsok, Bertram, Neale, Benjamin M., Northover, Carrie, Palta, Priit, Pedersen, Nancy, Posthuma, Danielle, Pressman, Alice, Quaye, Lydia, Raitakari, Olli, Schürks, Markus, Sintas, Celia, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Strachan, David, Terwindt, Gisela, Vila-Pueyo, Marta, Winsvold, Bendik S., Wrenthal, William, Daly, Mark J., Neale, Benjamin M., Ripatti, Samuli, Kallela, Mikko, Wessman, Maija, Palotie, Aarno

“…Complex traits, including migraine, often aggregate in families, but the underlying genetic architecture behind this is not well understood. The aggregation…”
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Long-term safety and efficacy of teriflunomide: Nine-year follow-up of the randomized TEMSO study by OʼConnor, Paul, Comi, Giancarlo, Freedman, Mark S, Miller, Aaron E, Kappos, Ludwig, Bouchard, Jean-Pierre, Lebrun-Frenay, Christine, Mares, Jan, Benamor, Myriam, Thangavelu, Karthinathan, Liang, Jinjun, Truffinet, Philippe, Lawson, Victoria J, Wolinsky, Jerry S

“…OBJECTIVE:To report safety and efficacy outcomes from up to 9 years of treatment with teriflunomide in an extension (NCT00803049) of the pivotal phase 3…”
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Novel splice site CACNA1A mutation causing episodic ataxia type 2 by KAUNISTO, M. A, HARNO, H, FÄRKKILÄ, M, WESSMAN, M, KALLELA, M, SOMER, H, SALLINEN, R, HÄMÄLÄINEN, E, MIETTINEN, P. J, VESA, J, ORPANA, A, PALOTIE, A

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Complex regional pain syndrome: The matter of white matter? by Hotta, Jaakko, Zhou, Guangyu, Harno, Hanna, Forss, Nina, Hari, Riitta

“…Introduction Many central pathophysiological aspects of complex regional pain syndrome (CRPS) are still unknown. Although brain‐imaging studies are…”
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Symptom reduction and improved function in chronic CRPS type 1 after 12-week integrated, interdisciplinary therapy by Elomaa, Minna, Hotta, Jaakko, de C Williams, Amanda C, Forss, Nina, Äyräpää, Anni, Kalso, Eija, Harno, Hanno

“…Background and aims Complex Regional Pain Syndrome (CRPS) often recovers spontaneously within the first year, but when it becomes chronic, available…”
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Decreased cerebellar total creatine in episodic ataxia type 2: A 1 H MRS study by Harno, H., Heikkinen, S., Kaunisto, M. A., Kallela, M., Häkkinen, A-M., Wessman, M., Färkkilä, M., Lundbom, N.

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Decreased cerebellar total creatine in episodic ataxia type 2: A 1H MRS study by HARNO, H, HEIKKINEN, S, KAUNISTO, M. A, KALLELA, M, HÄKKINEN, A-M, WESSMAN, M, FÄRKKILÄ, M, LUNDBOM, N

“…Episodic ataxia type 2 (EA2) affects mainly the cerebellum via mutations in the CACNA1A gene. The authors used proton MR spectroscopy to examine cerebellar and…”
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Comorbidity in Finnish migraine families by ARTTO, Ville, WESSMAN, Maija, FÄRKKILÄ, Markus, KALLELA, Mikko, RUSSELL, Michael Bjørn, NISSILÄ, Markku, SÄKÖ, Erkki, LIUKKONEN, Jarmo, TEIRMAA, Heikki, HARNO, Hanna, HAVANKA, Hannele, ILMAVIRTA, Matti, PALOTIE, Aarno

“…The objective of the study was to investigate comorbidity of migraine in Finnish migraine families. One thousand consecutive participants in the Finnish…”
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Chromosome 19p13 loci in Finnish migraine with aura families by Kaunisto, Mari A., Tikka, Päivi J., Kallela, Mikko, Leal, Suzanne M., Papp, Jeanette C., Korhonen, Arja, Hämäläinen, Eija, Harno, Hanna, Havanka, Hannele, Nissilä, Markku, Säkö, Erkki, Ilmavirta, Matti, Kaprio, Jaakko, Färkkilä, Markus, Ophoff, Roel A., Palotie, Aarno, Wessman, Maija

“…Chromosomal area 19p13 contains two migraine associated genes: a Cav2.1 (P/Q‐type) calcium channel α1 subunit gene, CACNA1A, and an insulin receptor gene,…”
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Acetazolamide improves neurotological abnormalities in a family with episodic ataxia type 2 (EA-2) by Harno, Hanna, Hirvonen, Timo, Kaunisto, Mari A, Aalto, Heikki, Levo, Hilla, Isotalo, Elina, Somer, Hannu, Kallela, Mikko, Palotie, Aarno, Wessman, Maija, Färkkilä, Markus

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Novel splice site CACNA1A mutation causing episodic ataxia type 2 by Kaunisto, M A, Harno, H, Kallela, M, Somer, H, Sallinen, R, Hämäläinen, E, Miettinen, P J, Vesa, J, Orpana, A, Palotie, A, Färkkilä, M, Wessman, M

“…Episodic ataxia type 2 (EA-2) is an autosomal dominant neurological disorder, characterized by episodes of ataxia, vertigo, nausea, nystagmus, and fatigue,…”
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Coherent control of linear quantum systems: A differential evolution approach by Harno, H G, Petersen, I R

“…In this paper, we propose a new method to construct an optimal coherent quantum controller, which is required to be physically realizable. This method is based…”
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Decentralized coherent robust H∞ control of a class of large-scale uncertain linear complex quantum stochastic systems by Harno, H G, Petersen, I R

“…This paper presents a procedure to synthesize a decentralized coherent robust H ∞ quantum controller for a class of large-scale uncertain linear complex…”
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Report of the Medico-Legal Committee by Harno, Albert H.

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