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Mari Auranen

Showing results (1-10 of 51) with videos related to

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Duodecim; Laaketieteellinen Aikakauskirja|December 1, 2017
Myotonia in ion channel diseases of muscleJuhani Partanen, Pirjo Isohanni, Mari Auranen
Frontiers in Neurology|March 3, 2020
Beneficial Effects of Ketogenic Diet on Phosphofructokinase Deficiency (Glycogen Storage Disease Type VII)Minna E Similä, Mari Auranen, Päivi Liisa Piirilä
Duodecim; Laaketieteellinen Aikakauskirja|December 16, 2017
Adrenomyeloneuropathy due to mutation in the ABCD1 gene as underlying factor in spastic paraparesisEmil Ylikallio, Elisa Rahikkala, Riikka Keski-Filppula, et al.
Journal of the Neurological Sciences|April 3, 2026
Epidemiology, treatment practices, and societal and economic burden of Duchenne muscular dystrophy in Finland: A retrospective register and chart review studyPirjo Isohanni, Mari Auranen, Aino Vesikansa, et al.
Clinical Case Reports|May 11, 2018
Focal atrophy of the unilateral masticatory muscles caused by pure trigeminal motor neuropathy: case reportAntti Kämppi, Leena Kämppi, Pentti Kemppainen, et al.
Neuromuscular Disorders : NMD|July 23, 2014
Screening for late-onset Pompe disease in FinlandJohanna Palmio, Mari Auranen, Sari Kiuru-Enari, et al.
Neurogenetics|March 5, 2013
Dominant GDAP1 founder mutation is a common cause of axonal Charcot-Marie-Tooth disease in FinlandMari Auranen, Emil Ylikallio, Jussi Toppila, et al.
Duodecim; Laaketieteellinen Aikakauskirja|December 16, 2017
Diagnostics and current care of myasthenia gravisSari Atula, Kathrin Pfau, Tapani Salmi, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Dominant transmission of de novo KIF1A motor domain variant underlying pure spastic paraplegiaEmil Ylikallio, Doyoun Kim, Pirjo Isohanni, et al.
Clinical Physiology and Functional Imaging|March 21, 2023
Lactate and ammonia measurements during cardiopulmonary exercise testing and its recovery phase-Consideration of age and sex in its interpretationNadja Ratia, Hanna Lantto, Emmi Rotgers, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
Duodecim; Laaketieteellinen Aikakauskirja|December 1, 2017
Myotonia in ion channel diseases of muscleJuhani Partanen, Pirjo Isohanni, Mari Auranen
Frontiers in Neurology|March 3, 2020
Beneficial Effects of Ketogenic Diet on Phosphofructokinase Deficiency (Glycogen Storage Disease Type VII)Minna E Similä, Mari Auranen, Päivi Liisa Piirilä
Duodecim; Laaketieteellinen Aikakauskirja|December 16, 2017
Adrenomyeloneuropathy due to mutation in the ABCD1 gene as underlying factor in spastic paraparesisEmil Ylikallio, Elisa Rahikkala, Riikka Keski-Filppula, et al.
Journal of the Neurological Sciences|April 3, 2026
Epidemiology, treatment practices, and societal and economic burden of Duchenne muscular dystrophy in Finland: A retrospective register and chart review studyPirjo Isohanni, Mari Auranen, Aino Vesikansa, et al.
Clinical Case Reports|May 11, 2018
Focal atrophy of the unilateral masticatory muscles caused by pure trigeminal motor neuropathy: case reportAntti Kämppi, Leena Kämppi, Pentti Kemppainen, et al.
Neuromuscular Disorders : NMD|July 23, 2014
Screening for late-onset Pompe disease in FinlandJohanna Palmio, Mari Auranen, Sari Kiuru-Enari, et al.
Neurogenetics|March 5, 2013
Dominant GDAP1 founder mutation is a common cause of axonal Charcot-Marie-Tooth disease in FinlandMari Auranen, Emil Ylikallio, Jussi Toppila, et al.
Duodecim; Laaketieteellinen Aikakauskirja|December 16, 2017
Diagnostics and current care of myasthenia gravisSari Atula, Kathrin Pfau, Tapani Salmi, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Dominant transmission of de novo KIF1A motor domain variant underlying pure spastic paraplegiaEmil Ylikallio, Doyoun Kim, Pirjo Isohanni, et al.
Clinical Physiology and Functional Imaging|March 21, 2023
Lactate and ammonia measurements during cardiopulmonary exercise testing and its recovery phase-Consideration of age and sex in its interpretationNadja Ratia, Hanna Lantto, Emmi Rotgers, et al.
Pageof 6