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H Goebel

Showing results (381-390 of 483) with videos related to

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Immunobiology|October 1, 1996
Macrophages in multiple sclerosisW Brück, N Sommermeier, M Bergmann, et al.
Neuromuscular Disorders : NMD|June 1, 1997
A European family with histidine 58 transthyretin mutation in familial amyloid polyneuropathyH H Goebel, S Seddigh, H C Hopf, et al.
Neuropediatrics|June 24, 2010
Familial reducing body myopathy with cytoplasmic bodies and rigid spine revisited: identification of a second LIM domain mutation in FHL1J Schessl, A Columbus, Y Hu, et al.
Acta Neuropathologica|March 11, 2005
The enlarging spectrum of desminopathies: new morphological findings, eastward geographic spread, novel exon 3 desmin mutationAlexandra Vrabie, Lev G Goldfarb, Alexey Shatunov, et al.
Brain Pathology (Zurich, Switzerland)|March 5, 2004
July 2003: 62-year-old female with progressive muscular weaknessAntje Bornemann, Jürgen Bohl, Hans-Michael Schneider, et al.
Zeitschrift Fur Rechtsmedizin. Journal of Legal Medicine|January 1, 1989
[Complications following cell therapy]J Bohl, H H Goebel, L Pötsch, et al.
Acta Neuropathologica|July 1, 1997
Hamartoma of the triceps surae muscleD S Tews, H H Goebel, R R Heffner, et al.
American Journal of Medical Genetics|October 12, 2002
Late infantile neuronal ceroid lipofuscinosis: quantitative description of the clinical course in patients with CLN2 mutationsRobert Steinfeld, Peter Heim, Henning von Gregory, et al.
Science Translational Medicine|September 6, 2019
Topographic modeling of early human osteoarthritis in sheepTamás Oláh, Jan Reinhard, Liang Gao, et al.
Neuropediatrics|February 6, 2010
Macrophagic myofasciitis plus (distinct types of muscular dystrophy)H D Müller, F K H van Landeghem, P F Schmidt, et al.
Pageof 49

Showing results (381-390 of 483) with videos related to

Sort By:
Pageof 49
Immunobiology|October 1, 1996
Macrophages in multiple sclerosisW Brück, N Sommermeier, M Bergmann, et al.
Neuromuscular Disorders : NMD|June 1, 1997
A European family with histidine 58 transthyretin mutation in familial amyloid polyneuropathyH H Goebel, S Seddigh, H C Hopf, et al.
Neuropediatrics|June 24, 2010
Familial reducing body myopathy with cytoplasmic bodies and rigid spine revisited: identification of a second LIM domain mutation in FHL1J Schessl, A Columbus, Y Hu, et al.
Acta Neuropathologica|March 11, 2005
The enlarging spectrum of desminopathies: new morphological findings, eastward geographic spread, novel exon 3 desmin mutationAlexandra Vrabie, Lev G Goldfarb, Alexey Shatunov, et al.
Brain Pathology (Zurich, Switzerland)|March 5, 2004
July 2003: 62-year-old female with progressive muscular weaknessAntje Bornemann, Jürgen Bohl, Hans-Michael Schneider, et al.
Zeitschrift Fur Rechtsmedizin. Journal of Legal Medicine|January 1, 1989
[Complications following cell therapy]J Bohl, H H Goebel, L Pötsch, et al.
Acta Neuropathologica|July 1, 1997
Hamartoma of the triceps surae muscleD S Tews, H H Goebel, R R Heffner, et al.
American Journal of Medical Genetics|October 12, 2002
Late infantile neuronal ceroid lipofuscinosis: quantitative description of the clinical course in patients with CLN2 mutationsRobert Steinfeld, Peter Heim, Henning von Gregory, et al.
Science Translational Medicine|September 6, 2019
Topographic modeling of early human osteoarthritis in sheepTamás Oláh, Jan Reinhard, Liang Gao, et al.
Neuropediatrics|February 6, 2010
Macrophagic myofasciitis plus (distinct types of muscular dystrophy)H D Müller, F K H van Landeghem, P F Schmidt, et al.
Pageof 49