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H H Goebel

Showing results (271-280 of 323) with videos related to

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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.
Journal of Neuropathology and Experimental Neurology|December 31, 1997
Expression of different isoforms of nitric oxide synthase in experimentally denervated and reinnervated skeletal muscleD S Tews, H H Goebel, I Schneider, et al.
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.
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.
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.
Journal of Neuropathology and Experimental Neurology|October 1, 1974
Preferential induction of central or peripheral nervous system tumors in rats by nitrosourea derivativesH M Cravioto, J F Weiss, H H Goebel, et al.
European Neurology|January 1, 1977
Adult metachromatic leukodystrophy. I. Clinical manifestation in a female aged 44 years, previously diagnosed in the preclinical stateH Pilz, I Duensing, R Heipertz, et al.
Pageof 33

Showing results (271-280 of 323) with videos related to

Sort By:
Pageof 33
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.
Journal of Neuropathology and Experimental Neurology|December 31, 1997
Expression of different isoforms of nitric oxide synthase in experimentally denervated and reinnervated skeletal muscleD S Tews, H H Goebel, I Schneider, et al.
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.
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.
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.
Journal of Neuropathology and Experimental Neurology|October 1, 1974
Preferential induction of central or peripheral nervous system tumors in rats by nitrosourea derivativesH M Cravioto, J F Weiss, H H Goebel, et al.
European Neurology|January 1, 1977
Adult metachromatic leukodystrophy. I. Clinical manifestation in a female aged 44 years, previously diagnosed in the preclinical stateH Pilz, I Duensing, R Heipertz, et al.
Pageof 33