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M C Koch

Showing results (21-30 of 59) with videos related to

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Neuromuscular Disorders : NMD|March 29, 2000
An inherited 4q35-EcoRI-DNA-fragment of 35 kb in a family with a sporadic case of facioscapulohumeral muscular dystrophy (FSHD)K Busse, J Köhler, K Stegmann, et al.
American Journal of Human Genetics|December 1, 1995
Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotoniaC Meyer-Kleine, K Steinmeyer, K Ricker, et al.
Muscle & Nerve|July 1, 1995
Proximal myotonic myopathy syndrome in the absence of trinucleotide repeat expansionsG Stoll, H J von Giesen, M C Koch, et al.
Thrombosis and Haemostasis|April 1, 1997
Hepatitis C virus type 4 in Portuguese haemophiliacsF Araújo, M C Koch, I Henriques, et al.
Neuroreport|December 20, 1994
Brain disease and molecular analysis in myotonic dystrophyM S Damian, G Bachmann, M C Koch, et al.
Journal of Human Genetics|April 20, 2001
Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German populationB Richter, K Stegmann, B Röper, et al.
Neuropediatrics|April 25, 2001
Myotonic dystrophy associated with VACTERL? A case reportS Kölker, I Degen, M C Koch, et al.
Transfusion Science|May 7, 1998
The blood bank and hepatitis GF Araújo, M C Koch, F Monteiro, et al.
Journal of the Neurological Sciences|December 1, 1996
Cardiac involvement in facio-scapulo-humeral muscular dystrophy: a family study using Thallium-201 single-photon-emission-computed tomographyP M Faustmann, J Farahati, B Rupilius, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Hepatitis E in Portuguese haemophiliacs and blood donorsF Araújo, M C Koch, F Monteiro, et al.
Pageof 6

Showing results (21-30 of 59) with videos related to

Sort By:
Pageof 6
Neuromuscular Disorders : NMD|March 29, 2000
An inherited 4q35-EcoRI-DNA-fragment of 35 kb in a family with a sporadic case of facioscapulohumeral muscular dystrophy (FSHD)K Busse, J Köhler, K Stegmann, et al.
American Journal of Human Genetics|December 1, 1995
Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotoniaC Meyer-Kleine, K Steinmeyer, K Ricker, et al.
Muscle & Nerve|July 1, 1995
Proximal myotonic myopathy syndrome in the absence of trinucleotide repeat expansionsG Stoll, H J von Giesen, M C Koch, et al.
Thrombosis and Haemostasis|April 1, 1997
Hepatitis C virus type 4 in Portuguese haemophiliacsF Araújo, M C Koch, I Henriques, et al.
Neuroreport|December 20, 1994
Brain disease and molecular analysis in myotonic dystrophyM S Damian, G Bachmann, M C Koch, et al.
Journal of Human Genetics|April 20, 2001
Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German populationB Richter, K Stegmann, B Röper, et al.
Neuropediatrics|April 25, 2001
Myotonic dystrophy associated with VACTERL? A case reportS Kölker, I Degen, M C Koch, et al.
Transfusion Science|May 7, 1998
The blood bank and hepatitis GF Araújo, M C Koch, F Monteiro, et al.
Journal of the Neurological Sciences|December 1, 1996
Cardiac involvement in facio-scapulo-humeral muscular dystrophy: a family study using Thallium-201 single-photon-emission-computed tomographyP M Faustmann, J Farahati, B Rupilius, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Hepatitis E in Portuguese haemophiliacs and blood donorsF Araújo, M C Koch, F Monteiro, et al.
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