Search Results

Evidence for mtDNA Admixture between the Finns and the Saami

by Meinilä, Maria, Finnilä, Saara, Majamaa, Kari
Published in Human Heredity (2001)

Phenotype of Patients With Charcot-Marie-Tooth With the p.His123Arg Mutation in GDAP1 in Northern Finland

by Lehtilahti, Maria, Kallio, Mika, Majamaa, Kari, Kärppä, Mikko
Published in Neurology Genetics (2021)

Mutations in the two ribosomal RNA genes in mitochondrial DNA among Finnish children with hearing impairment

by Häkli, Sanna, Luotonen, Mirja, Sorri, Martti, Majamaa, Kari
Published 2015

Phenotype of Patients With Charcot-Marie-Tooth With the p.His123Arg Mutation in GDAP1 in Northern Finland

by Lehtilahti, Maria, Kallio, Mika, Majamaa, Kari, Kärppä, Mikko
Published in Neurology Genetics (2021)

Hearing in a 54- to 66-year-old population in northern Finland

by Hannula, Samuli, Mäki-Torkko, Elina, Majamaa, Kari, Sorri, Martti
Published in International Journal of Audiology (2010)

Phylogenetic Network of the mtDNA Haplogroup U in Northern Finland Based on Sequence Analysis of the Complete Coding Region by Conformation-Sensitive Gel Electrophoresis

by Finnilä, Saara, Hassinen, Ilmo E., Ala-Kokko, Leena, Majamaa, Kari
Published 2000

Phylogenetic Network of the mtDNA Haplogroup U in Northern Finland Based on Sequence Analysis of the Complete Coding Region by Conformation-Sensitive Gel Electrophoresis

by Finnilä, Saara, Hassinen, Ilmo E., Ala-Kokko, Leena, Majamaa, Kari
Published in The American Journal of Human Genetics (2000)

Childhood hearing impairment in northern Finland, etiology and additional disabilities

by Häkli, Sanna, Luotonen, Mirja, Bloigu, Risto, Majamaa, Kari, Sorri, Martti
Published in International Journal of Pediatric Otorhinolaryngology (2014)

Prehospital and hospital delays for stroke patients treated with thrombolysis: A retrospective study from mixed rural–urban area in Northern Finland

by Varjoranta, Tuure, Raatiniemi, Lasse, Majamaa, Kari, Martikainen, Matti, Liisanantti, Janne.H.
Published in Australasian Emergency Care (2019)

Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA

by Kärppä, Mikko, Herva, Riitta, Moslemi, Ali-Reza, Oldfors, Anders, Kakko, Sakari, Majamaa, Kari
Published in Brain (2005)

Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA

by Kärppä, Mikko, Herva, Riitta, Moslemi, Ali-Reza, Oldfors, Anders, Kakko, Sakari, Majamaa, Kari
Published in Brain (2005)

Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia

by Korkiamäki, Paula, Kervinen, Marko, Karjalainen, Karoliina, Majamaa, Kari, Uusimaa, Johanna, Remes, Anne M.
Published in Acta Ophthalmologica (2012)

Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland

by Kaivorinne, Anna-Lotta, Krüger, Johanna, Kuivaniemi, Katja, Tuominen, Hannu, Moilanen, Virpi, Majamaa, Kari, Remes, Anne M
Published in BMC Neurology (2008)

Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland

by Kaivorinne, Anna-Lotta, Krüger, Johanna, Kuivaniemi, Katja, Tuominen, Hannu, Moilanen, Virpi, Majamaa, Kari, Remes, Anne M.
Published in BMC Neurology (2008)

Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland

by Tuominen Hannu, Kuivaniemi Katja, Krüger Johanna, Kaivorinne Anna-Lotta, Moilanen Virpi, Majamaa Kari, Remes Anne M
Published in BMC Neurology (2008)

Role of MAPTmutations and haplotype in frontotemporal lobar degeneration in Northern Finland

by Kaivorinne, Anna-Lotta, Krüger, Johanna, Kuivaniemi, Katja, Tuominen, Hannu, Moilanen, Virpi, Majamaa, Kari, Remes, Anne M
Published 2008

Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland

by Kaivorinne, Anna-Lotta, Krüger, Johanna, Kuivaniemi, Katja, Tuominen, Hannu, Moilanen, Virpi, Majamaa, Kari, Remes, Anne M
Published in BMC Neurology (2008)