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G Engel

Showing results (291-300 of 741) with videos related to

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The American Journal of Pathology|October 1, 1993
Localization of dystrophin and beta-spectrin in vacuolar myopathiesJ L De Bleecker, A G Engel, J C Winkelmann
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.
Current Psychiatry Reports|October 6, 2021
Review of Changes in the Reinforcing Effects of Alcohol in Weight Loss Surgery PatientsScott G Engel, Lauren M Schaefer, Jon Davis, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Patterns of abnormal protein expression in target formations and unstructured coresJ L De Bleecker, B B Ertl, A G Engel
Breast Cancer Research and Treatment|February 1, 1997
Distribution of stromelysin-3 mRNA transcripts and microvessels in human breast carcinomasC Linder, G Engel, G Auer, et al.
Human Molecular Genetics|October 9, 2003
A frameshifting mutation in CHRNE unmasks skipping of the preceding exonKinji Ohno, Margherita Milone, Xin-Ming Shen, et al.
Rontgenpraxis; Zeitschrift Fur Radiologische Technik|March 1, 1995
[BOOP (bronchiolitis obliterans with organizing pneumonia) syndrome: value of high-resolution CT within the scope of clinical and radiologic diagnosis]N Reutter, R Schmitt, G Engel, 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.
Annals of the New York Academy of Sciences|July 21, 1998
Congenital myasthenic syndromes. New insights from molecular genetic and patch-clamp studiesA G Engel, K Ohno, M Milone, et al.
Annals of the New York Academy of Sciences|July 21, 1998
AChR channel blockade by quinidine sulfate reduces channel open duration in the slow-channel congenital myasthenic syndromeT Fukudome, K Ohno, J M Brengman, et al.
Pageof 75

Showing results (291-300 of 741) with videos related to

Sort By:
Pageof 75
The American Journal of Pathology|October 1, 1993
Localization of dystrophin and beta-spectrin in vacuolar myopathiesJ L De Bleecker, A G Engel, J C Winkelmann
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.
Current Psychiatry Reports|October 6, 2021
Review of Changes in the Reinforcing Effects of Alcohol in Weight Loss Surgery PatientsScott G Engel, Lauren M Schaefer, Jon Davis, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Patterns of abnormal protein expression in target formations and unstructured coresJ L De Bleecker, B B Ertl, A G Engel
Breast Cancer Research and Treatment|February 1, 1997
Distribution of stromelysin-3 mRNA transcripts and microvessels in human breast carcinomasC Linder, G Engel, G Auer, et al.
Human Molecular Genetics|October 9, 2003
A frameshifting mutation in CHRNE unmasks skipping of the preceding exonKinji Ohno, Margherita Milone, Xin-Ming Shen, et al.
Rontgenpraxis; Zeitschrift Fur Radiologische Technik|March 1, 1995
[BOOP (bronchiolitis obliterans with organizing pneumonia) syndrome: value of high-resolution CT within the scope of clinical and radiologic diagnosis]N Reutter, R Schmitt, G Engel, 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.
Annals of the New York Academy of Sciences|July 21, 1998
Congenital myasthenic syndromes. New insights from molecular genetic and patch-clamp studiesA G Engel, K Ohno, M Milone, et al.
Annals of the New York Academy of Sciences|July 21, 1998
AChR channel blockade by quinidine sulfate reduces channel open duration in the slow-channel congenital myasthenic syndromeT Fukudome, K Ohno, J M Brengman, et al.
Pageof 75