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H Reichmann

Showing results (181-190 of 273) with videos related to

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Neurology|June 1, 1996
Mitochondrial DNA in migraine with auraT Klopstock, A May, P Seibel, et al.
European Journal of Pediatrics|May 1, 1991
Myopathy in Williams-Beuren syndromeT Voit, H Kramer, C Thomas, et al.
Fortschritte Der Neurologie-Psychiatrie|February 16, 2013
[The prevalence of Parkinson's disease, associated dementia, and depression in Dresden]O Riedel, C Schneider, J Klotsche, et al.
Der Nervenarzt|April 1, 1994
[MELAS syndrome. Clinical aspects, MRI, biochemistry and molecular genetics]M S Damian, H Reichmann, P Seibel, et al.
Der Nervenarzt|March 8, 2020
[Dystonia Non-Motor Symptoms Questionnaire (DNMSQuest) for assessment of non-motor symptoms in dystonia : Intercultural adaptation in the German language]L Klingelhoefer, W Jost, P Odin, et al.
Muscle & Nerve|July 1, 1997
Mitochondrial dysfunction with myoclonus epilepsy and ragged-red fibers point mutation in nerve, muscle, and adipose tissue of a patient with multiple symmetric lipomatosisM Naumann, R Kiefer, K V Toyka, et al.
Pflugers Archiv : European Journal of Physiology|April 1, 1984
Exercise-induced fibre type transitions with regard to myosin, parvalbumin, and sarcoplasmic reticulum in muscles of the ratH J Green, G A Klug, H Reichmann, et al.
Fortschritte Der Neurologie-Psychiatrie|June 9, 2016
[The Geriatric Patient with Parkinson's Disease - a Neurological Challenge]P Lingor, I Csoti, J Koschel, et al.
Acta Neuropathologica|January 1, 1993
Progression of myopathology in Kearns-Sayre syndrome: a morphological follow-up studyH Reichmann, R Gold, B Meurers, et al.
European Neurology|January 1, 1996
Phosphorus magnetic resonance spectroscopy in the evaluation of mitochondrial myopathies: results of a 6-month therapy study with coenzyme QR Gold, P Seibel, G Reinelt, et al.
Pageof 28

Showing results (181-190 of 273) with videos related to

Sort By:
Pageof 28
Neurology|June 1, 1996
Mitochondrial DNA in migraine with auraT Klopstock, A May, P Seibel, et al.
European Journal of Pediatrics|May 1, 1991
Myopathy in Williams-Beuren syndromeT Voit, H Kramer, C Thomas, et al.
Fortschritte Der Neurologie-Psychiatrie|February 16, 2013
[The prevalence of Parkinson's disease, associated dementia, and depression in Dresden]O Riedel, C Schneider, J Klotsche, et al.
Der Nervenarzt|April 1, 1994
[MELAS syndrome. Clinical aspects, MRI, biochemistry and molecular genetics]M S Damian, H Reichmann, P Seibel, et al.
Der Nervenarzt|March 8, 2020
[Dystonia Non-Motor Symptoms Questionnaire (DNMSQuest) for assessment of non-motor symptoms in dystonia : Intercultural adaptation in the German language]L Klingelhoefer, W Jost, P Odin, et al.
Muscle & Nerve|July 1, 1997
Mitochondrial dysfunction with myoclonus epilepsy and ragged-red fibers point mutation in nerve, muscle, and adipose tissue of a patient with multiple symmetric lipomatosisM Naumann, R Kiefer, K V Toyka, et al.
Pflugers Archiv : European Journal of Physiology|April 1, 1984
Exercise-induced fibre type transitions with regard to myosin, parvalbumin, and sarcoplasmic reticulum in muscles of the ratH J Green, G A Klug, H Reichmann, et al.
Fortschritte Der Neurologie-Psychiatrie|June 9, 2016
[The Geriatric Patient with Parkinson's Disease - a Neurological Challenge]P Lingor, I Csoti, J Koschel, et al.
Acta Neuropathologica|January 1, 1993
Progression of myopathology in Kearns-Sayre syndrome: a morphological follow-up studyH Reichmann, R Gold, B Meurers, et al.
European Neurology|January 1, 1996
Phosphorus magnetic resonance spectroscopy in the evaluation of mitochondrial myopathies: results of a 6-month therapy study with coenzyme QR Gold, P Seibel, G Reinelt, et al.
Pageof 28