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B Reitter

Showing results (21-30 of 29) with videos related to

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Biochimica Et Biophysica Acta|October 1, 1986
Muscle adenylate kinase in Duchenne muscular dystrophyT Fröhlich, B Reitter, D Scheffner, et al.
Brain & Development|March 1, 1995
Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis: a combined electron microscopic and molecular genetic approachH H Goebel, J Vesa, B Reitter, et al.
Klinische Wochenschrift|April 1, 1980
Capping of lymphocytes in patients and carriers of Duchenne muscular dystrophyA D Ho, S Stojakowits, B Reitter, et al.
Der Anaesthesist|October 1, 1990
[The automated determination of the dibucaine number using the Greiner G450 selective analyzer. A routine parameter of significance?]M Gottardis, C Schmoigl, G Mitterschiffthaler, et al.
Acta Neuropathologica|July 1, 1997
Hamartoma of the triceps surae muscleD S Tews, H H Goebel, R R Heffner, et al.
Annals of Neurology|September 8, 2000
Severe congenital myasthenic syndrome due to homozygosity of the 1293insG epsilon-acetylcholine receptor subunit mutationJ P Sieb, S Kraner, B Schrank, et al.
Journal of Molecular Biology|August 16, 1996
Glycosyl-phosphatidylinositols of Trypanosoma congolense: two common precursors but a new protein-anchorP Gerold, B Striepen, B Reitter, et al.
Clinical Nephrology|September 1, 1984
Idiopathic de Toni-Debré-Fanconi syndrome with absence of proximal tubular brush borderF Manz, R Waldherr, H P Fritz, et al.
Neuromuscular Disorders : NMD|October 6, 2005
134th ENMC International Workshop: Outcome Measures and Treatment of Spinal Muscular Atrophy, 11-13 February 2005, Naarden, The NetherlandsE Bertini, A Burghes, K Bushby, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Biochimica Et Biophysica Acta|October 1, 1986
Muscle adenylate kinase in Duchenne muscular dystrophyT Fröhlich, B Reitter, D Scheffner, et al.
Brain & Development|March 1, 1995
Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis: a combined electron microscopic and molecular genetic approachH H Goebel, J Vesa, B Reitter, et al.
Klinische Wochenschrift|April 1, 1980
Capping of lymphocytes in patients and carriers of Duchenne muscular dystrophyA D Ho, S Stojakowits, B Reitter, et al.
Der Anaesthesist|October 1, 1990
[The automated determination of the dibucaine number using the Greiner G450 selective analyzer. A routine parameter of significance?]M Gottardis, C Schmoigl, G Mitterschiffthaler, et al.
Acta Neuropathologica|July 1, 1997
Hamartoma of the triceps surae muscleD S Tews, H H Goebel, R R Heffner, et al.
Annals of Neurology|September 8, 2000
Severe congenital myasthenic syndrome due to homozygosity of the 1293insG epsilon-acetylcholine receptor subunit mutationJ P Sieb, S Kraner, B Schrank, et al.
Journal of Molecular Biology|August 16, 1996
Glycosyl-phosphatidylinositols of Trypanosoma congolense: two common precursors but a new protein-anchorP Gerold, B Striepen, B Reitter, et al.
Clinical Nephrology|September 1, 1984
Idiopathic de Toni-Debré-Fanconi syndrome with absence of proximal tubular brush borderF Manz, R Waldherr, H P Fritz, et al.
Neuromuscular Disorders : NMD|October 6, 2005
134th ENMC International Workshop: Outcome Measures and Treatment of Spinal Muscular Atrophy, 11-13 February 2005, Naarden, The NetherlandsE Bertini, A Burghes, K Bushby, et al.
Pageof 3