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F Busch

Showing results (171-180 of 191) with videos related to

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International Journal of Rehabilitation Research. Internationale Zeitschrift Fur Rehabilitationsforschung. Revue Internationale De Recherches De Readaptation|October 23, 1997
Vocational perspectives and neuromuscular disordersF Andries, C W Wevers, A R Wintzen, et al.
The Journal of Infectious Diseases|September 1, 1993
A randomized, controlled study of intravenous ganciclovir therapy for cytomegalovirus peripheral retinitis in patients with AIDS. AIDS Clinical Trials Group and Cytomegalovirus Cooperative Study GroupS A Spector, T Weingeist, R B Pollard, et al.
Radiation Protection Dosimetry|March 19, 2014
Albedo neutron dosimetry in Germany: regulations and performanceM Luszik-Bhadra, A Zimbal, F Busch, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 2020
Calibrating the coevolution of Ediacaran life and environmentAlan D Rooney, Marjorie D Cantine, Kristin D Bergmann, et al.
Annals of Neurology|May 1, 1996
A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvementA J van der Kooi, T M Ledderhof, W G de Voogt, et al.
Clinical Genetics|January 1, 1981
Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency)M C Loonen, A W Schram, J F Koster, et al.
Journal of the Neurological Sciences|May 1, 1995
Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspectsG J Jöbsis, E S Louwerse, M de Visser, et al.
The Journal of Infectious Diseases|April 11, 1991
Prevalence of resistance in patients receiving ganciclovir for serious cytomegalovirus infectionW L Drew, R C Miner, D F Busch, et al.
Neurology|October 1, 1981
A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studiesM C Loonen, H F Busch, J F Koster, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotypeH R Scholte, R N Van Coster, P C de Jonge, et al.
Pageof 20

Showing results (171-180 of 191) with videos related to

Sort By:
Pageof 20
International Journal of Rehabilitation Research. Internationale Zeitschrift Fur Rehabilitationsforschung. Revue Internationale De Recherches De Readaptation|October 23, 1997
Vocational perspectives and neuromuscular disordersF Andries, C W Wevers, A R Wintzen, et al.
The Journal of Infectious Diseases|September 1, 1993
A randomized, controlled study of intravenous ganciclovir therapy for cytomegalovirus peripheral retinitis in patients with AIDS. AIDS Clinical Trials Group and Cytomegalovirus Cooperative Study GroupS A Spector, T Weingeist, R B Pollard, et al.
Radiation Protection Dosimetry|March 19, 2014
Albedo neutron dosimetry in Germany: regulations and performanceM Luszik-Bhadra, A Zimbal, F Busch, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 2020
Calibrating the coevolution of Ediacaran life and environmentAlan D Rooney, Marjorie D Cantine, Kristin D Bergmann, et al.
Annals of Neurology|May 1, 1996
A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvementA J van der Kooi, T M Ledderhof, W G de Voogt, et al.
Clinical Genetics|January 1, 1981
Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency)M C Loonen, A W Schram, J F Koster, et al.
Journal of the Neurological Sciences|May 1, 1995
Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspectsG J Jöbsis, E S Louwerse, M de Visser, et al.
The Journal of Infectious Diseases|April 11, 1991
Prevalence of resistance in patients receiving ganciclovir for serious cytomegalovirus infectionW L Drew, R C Miner, D F Busch, et al.
Neurology|October 1, 1981
A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studiesM C Loonen, H F Busch, J F Koster, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotypeH R Scholte, R N Van Coster, P C de Jonge, et al.
Pageof 20