Výsledky vyhledávání - "J. Lonnqvist"

Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: Clinical, biochemical, and molecular genetic features of the 1Oq-linked disease

Autor: Leena Valanne, Anders Paetau, T. Salmi, K. Setälä, Hannu Somer, Anu Suomalainen, Matti Haltia, J. Lonnqvist, Leena Peltonen, K. Kontula, M. Wallin, Anna Majander, H. Leinonen

Publikováno v: Neurology. 48:1244-1253

Autosomal dominant progressive external ophthalmoplegia (adPEO) is a mitochondrial disease characterized by accumulation of multiple large deletions of mtDNA in patients9 tissues. We previously showed that the disease is genetically heterogeneous by

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7c7da655ba8ae12e13145595b386011d
https://doi.org/10.1212/wnl.48.5.1244

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Suicide rates in the world: Update

Publikováno v: Archives of Suicide Research, 5(1), 81-89. Routledge
Schmidtke, A, Weinacker, B, Apter, A, Batt, A, Berman, A, Bille-Brahe, U, Botsis, A, De Leo, D, Doneux, A, Goldney, R, Grad, O, Haring, C, Hawton, K, Hjelmeland, H, Kelleher, M, Kerkhof, A J F M, Leenaars, A, Lonnqvist, J, Michel, K, Ostamo, A, Salander-Renberg, E, Sayil, I, Takahashi, Y, Heeringen, van, C, Varnik, A & Wasserman, D 1999, ' Suicide rates in the world: Update. ', Archives of Suicide Research, vol. 5, no. 1, pp. 81-89 . https://doi.org/10.1080/13811119908258318

(1999). Suicide rates in the world: Update. Archives of Suicide Research: Vol. 5, No. 1, pp. 81-89.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad8df9c3cf33f89f06f94ba312f303ae
https://research.vu.nl/en/publications/d8ba0dbc-ba89-4427-91aa-fe4467630fce

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Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease

Autor: A, Suomalainen, A, Majander, M, Wallin, K, Setälä, K, Kontula, H, Leinonen, T, Salmi, A, Paetau, M, Haltia, L, Valanne, J, Lonnqvist, L, Peltonen, H, Somer

Publikováno v: Neurology. 48(5)

Autosomal dominant progressive external ophthalmoplegia (adPEO) is a mitochondrial disease characterized by accumulation of multiple large deletions of mtDNA in patients' tissues. We previously showed that the disease is genetically heterogeneous by

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::30d6ba0bc03507fd87d84f90b4e7f269
https://pubmed.ncbi.nlm.nih.gov/9153451

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Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia

Autor: Matti Haltia, Leena Peltonen, Anna Majander, Anu Suomalainen, Hannu Somer, J. Lonnqvist, M L Savontaus

Publikováno v: The Journal of clinical investigation. 90(1)

Multiple deletions of mitochondrial DNA (mtDNA) have recently been reported in familial progressive external ophthalmoplegia (PEO), in a case of progressive encephalomyopathy, and in inherited recurrent myoglobinuria. The inheritance of familial PEO

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6b59dca2f37428ce8a3cf824b99d143
https://pubmed.ncbi.nlm.nih.gov/1634620

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