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Neuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiencyH Porschke, W Kress, H Reichmann, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|January 15, 2009
Risk of valvular heart disease associated with the use of dopamine agonists in Parkinson's disease: a systematic reviewMalcolm Steiger, W Jost, F Grandas, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|January 1, 1990
[Intraspinal, extradural hemorrhage in a 7-year-old boy with hemophilia B]W Jost, N Graf, G Pindur, et al.Pflugers Archiv : European Journal of Physiology|May 1, 1985
Biochemical and ultrastructural changes of skeletal muscle mitochondria after chronic electrical stimulation in rabbitsH Reichmann, H Hoppeler, O Mathieu-Costello, et al.Der Nervenarzt|September 24, 2002
[Entacapone for treatment of motor fluctuations in idiopathic Parkinson syndrome]U Sommer, A Müller, B Herting, et al.European Journal of Neurology|August 26, 2006
Task force guidelines handbook: EFNS guidelines on diagnosis and management of fatty acid mitochondrial disordersC Angelini, A Federico, H Reichmann, et al.Nucleic Acids Research|January 11, 1995
Transfection of mitochondria: strategy towards a gene therapy of mitochondrial DNA diseasesP Seibel, J Trappe, G Villani, et al.Muscle & Nerve|December 1, 1993
Focal myositis of the temporal muscleM Naumann, K V Toyka, H H Goebel, et al.Sports Health|September 28, 2012
The ulnar collateral ligament procedure revisited: the procedure we useJames R Andrews, Patrick W Jost, E Lyle CainNeurogenetics|March 29, 2000
Adult-onset glycogen storage disease type II: phenotypic and allelic heterogeneity in German patientsM Vorgerd, B Burwinkel, H Reichmann, et al.Pageof 26