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L P Rowland

Showing results (101-110 of 189) with videos related to

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Neurology|October 1, 1994
Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: evidence of shared genetic susceptibilityD Majoor-Krakauer, R Ottman, W G Johnson, et al.
Archives of Neurology|October 1, 1974
Normal pressure hydrocephalus and hypertensive cerebrovascular diseaseM P Earnest, S Fahn, J H Karp, et al.
Neurology|September 1, 1996
Complications of intravenous immune globulin treatment in neurologic diseaseT H Brannagan, K J Nagle, D J Lange, et al.
Archives of Neurology|October 1, 1984
Clinical varieties of neuromuscular disease in debrancher deficiencyF Cornelio, N Bresolin, P A Singer, et al.
Archives of Neurology|January 14, 2000
Amyotrophy in prion diseasesB B Worrall, L P Rowland, S S Chin, et al.
The New England Journal of Medicine|July 6, 1972
Periodic paralysis: K levels during arrhythmiaL P Rowland, R P Lisak, L P Levitt, et al.
Archives of Neurology|May 1, 1988
Granulomatous angiitis of the brain. An inflammatory reaction of diverse etiologyD S Younger, A P Hays, J C Brust, et al.
Neurology|May 1, 1992
Dystrophinopathy in isolated cases of myopathy in femalesE P Hoffman, K Arahata, C Minetti, et al.
Neurology|August 3, 1999
A prospective study of preferences and actual treatment choices in ALSS M Albert, P L Murphy, M L Del Bene, et al.
Neurology|June 3, 2009
Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALSP H Gordon, B Cheng, I B Katz, et al.
Pageof 19

Showing results (101-110 of 189) with videos related to

Sort By:
Pageof 19
Neurology|October 1, 1994
Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: evidence of shared genetic susceptibilityD Majoor-Krakauer, R Ottman, W G Johnson, et al.
Archives of Neurology|October 1, 1974
Normal pressure hydrocephalus and hypertensive cerebrovascular diseaseM P Earnest, S Fahn, J H Karp, et al.
Neurology|September 1, 1996
Complications of intravenous immune globulin treatment in neurologic diseaseT H Brannagan, K J Nagle, D J Lange, et al.
Archives of Neurology|October 1, 1984
Clinical varieties of neuromuscular disease in debrancher deficiencyF Cornelio, N Bresolin, P A Singer, et al.
Archives of Neurology|January 14, 2000
Amyotrophy in prion diseasesB B Worrall, L P Rowland, S S Chin, et al.
The New England Journal of Medicine|July 6, 1972
Periodic paralysis: K levels during arrhythmiaL P Rowland, R P Lisak, L P Levitt, et al.
Archives of Neurology|May 1, 1988
Granulomatous angiitis of the brain. An inflammatory reaction of diverse etiologyD S Younger, A P Hays, J C Brust, et al.
Neurology|May 1, 1992
Dystrophinopathy in isolated cases of myopathy in femalesE P Hoffman, K Arahata, C Minetti, et al.
Neurology|August 3, 1999
A prospective study of preferences and actual treatment choices in ALSS M Albert, P L Murphy, M L Del Bene, et al.
Neurology|June 3, 2009
Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALSP H Gordon, B Cheng, I B Katz, et al.
Pageof 19