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F Jerusalem

Showing results (61-70 of 85) with videos related to

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Neurology|March 1, 1983
A dominantly inherited myopathy with excessive tubular aggregatesR Rohkamm, K Boxler, K Ricker, et al.
Neurology|July 1, 1995
Cytochrome c oxidase in Alzheimer's diseaseI Maurer, S Zierz, H J Möller, et al.
The British Journal of Psychiatry : the Journal of Mental Science|October 1, 1995
Neuroleptic associated extrapyramidal symptomsI Maurer, S Zierz, H J Möller, et al.
Journal of the Neurological Sciences|March 1, 1990
Exogenous coenzyme Q (coq) fails to increase coq in skeletal muscle of two patients with mitochondrial myopathiesS Zierz, O von Wersebe, J Bleistein, et al.
Neuromuscular Disorders : NMD|March 1, 1996
An autosomal-recessive congenital myasthenic syndrome with tubular aggregates in a Libyan familyJ P Sieb, K Tolksdorf, R Dengler, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1974
[Steroid myopathy in childhood (author's transl)]H Moser, R Fiechter, H P Ludin, et al.
Transactions of the American Neurological Association|January 1, 1973
Mitochondria-lipid-glycogen (MLG) disease of muscle: a morphologically regressive congenital myopathyF Jerusalem, C Angelini, A G Engel, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Innere Medizin|April 17, 1977
[McArdle's disease (muscular phosphorylase deficiency)]P Schollmeyer, J Nolte, D Meisel, et al.
Archives of Neurology|September 1, 1973
Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathyF Jerusalem, C Angelini, A G Engel, et al.
Journal of the Neurological Sciences|September 1, 1987
Benign juvenile focal muscular atrophy of upper extremities--a familial caseU Schlegel, F Jerusalem, W Tackmann, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
Neurology|March 1, 1983
A dominantly inherited myopathy with excessive tubular aggregatesR Rohkamm, K Boxler, K Ricker, et al.
Neurology|July 1, 1995
Cytochrome c oxidase in Alzheimer's diseaseI Maurer, S Zierz, H J Möller, et al.
The British Journal of Psychiatry : the Journal of Mental Science|October 1, 1995
Neuroleptic associated extrapyramidal symptomsI Maurer, S Zierz, H J Möller, et al.
Journal of the Neurological Sciences|March 1, 1990
Exogenous coenzyme Q (coq) fails to increase coq in skeletal muscle of two patients with mitochondrial myopathiesS Zierz, O von Wersebe, J Bleistein, et al.
Neuromuscular Disorders : NMD|March 1, 1996
An autosomal-recessive congenital myasthenic syndrome with tubular aggregates in a Libyan familyJ P Sieb, K Tolksdorf, R Dengler, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1974
[Steroid myopathy in childhood (author's transl)]H Moser, R Fiechter, H P Ludin, et al.
Transactions of the American Neurological Association|January 1, 1973
Mitochondria-lipid-glycogen (MLG) disease of muscle: a morphologically regressive congenital myopathyF Jerusalem, C Angelini, A G Engel, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Innere Medizin|April 17, 1977
[McArdle's disease (muscular phosphorylase deficiency)]P Schollmeyer, J Nolte, D Meisel, et al.
Archives of Neurology|September 1, 1973
Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathyF Jerusalem, C Angelini, A G Engel, et al.
Journal of the Neurological Sciences|September 1, 1987
Benign juvenile focal muscular atrophy of upper extremities--a familial caseU Schlegel, F Jerusalem, W Tackmann, et al.
Pageof 9