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Journal of Neurology|January 13, 1977
The perifascicular atrophy factor. An aid in the histological diagnosis of polymyositisH P Baumli, M MumenthalerJournal of Neurology|February 1, 1989
Coenzyme Q in serum and muscle of 5 patients with Kearns-Sayre syndrome and 12 patients with ophthalmoplegia plusS Zierz, G Jahns, F JerusalemThe Clinical Investigator|May 1, 1993
Inclusion body myositis: clinical and histopathological features of 36 patientsS Beyenburg, S Zierz, F JerusalemArchives of Neurology|November 1, 1979
Quadriparesis and nuclear oculomotor palsy with total bilateral ptosis mimicking coma: a mesencephalic 'locked-in syndrome"?O Meienberg, M Mumenthaler, K KarbowskiThe Clinical Investigator|October 1, 1993
Inhibition of carnitine palmitoyltransferase in normal human skeletal muscle and in muscle of patients with carnitine palmitoyltransferase deficiency by long- and short-chain acylcarnitine and acyl-coenzyme AS Zierz, S Neumann-Schmidt, F JerusalemDer Nervenarzt|April 1, 1992
[Non-neoplastic Lambert-Eaton syndrome. A frequently missed diagnosis?]J P Sieb, R Dengler, F JerusalemSchweizerische Medizinische Wochenschrift|January 3, 1981
[Is myositis in chronic polyarthritis using d-penicillamine drug-induced?]U Schlumpf, H U Bussmann, F JerusalemSchweizerische Medizinische Wochenschrift|November 28, 1987
[Buccolinguofacial apraxia--a probably psychogenic speech and deglutition disorder]A Schnider, H Mattle, M MumenthalerThe Clinical Investigator|December 1, 1993
Biochemical evidence for heterozygosity in muscular carnitine palmitoyltransferase deficiencyS Zierz, R R Mundegar, F JerusalemSTAR Protocols|December 20, 2021
Multiplexed imaging and effluent analysis to monitor cancer cell intravasation using a colorectal cancer-on-chipCarly Strelez, Kimya Ghaffarian, Shannon M MumenthalerPageof 17