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H Goebel

Showing results (281-290 of 483) with videos related to

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Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1987
Chemical heterogeneity of amyloid in the carpal tunnel syndromeK Stein, S Störkel, R P Linke, et al.
Journal of Pharmacokinetics and Biopharmaceutics|October 1, 1977
A pharmacokinetic model for high-dose methotrexate infusions in manS D Reich, N R Bachur, R H Goebel, et al.
Residue Reviews|January 1, 1982
Properties, effects, residues, and analytics of the insecticide endosulfanH Goebel, S Gorbach, W Knauf, et al.
Neuromuscular Disorders : NMD|May 11, 2006
Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindredDanielle E Dye, Biagio Azzarelli, Hans H Goebel, et al.
Muscle & Nerve|January 1, 1978
Autosomal dominant "spheroid body myopathy"H H Goebel, J Muller, H W Gillen, et al.
Ophthalmic Paediatrics and Genetics|February 1, 1985
Ultrastructural study of primary canine and human pigmentary retinopathyH H Goebel, K Ikeda, W Eichholtz, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiencyH Porschke, W Kress, H Reichmann, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2001
Morphological studies on CLN2H H Goebel, E Kominami, E Neuen-Jacob, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 14, 2001
[Keratopathy as a sign of multifocal congenital sensory polyneuropathy. A case report]U Kottler, O Schwenn, H H Goebel, et al.
Acta Neuropathologica|January 1, 1981
Fingerprint profiles in lymphocytic vacuoles of mucopolysaccharidoses I-H, II, III-A, and III-BH H Goebel, K Ikeda, F Schulz, et al.
Pageof 49

Showing results (281-290 of 483) with videos related to

Sort By:
Pageof 49
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1987
Chemical heterogeneity of amyloid in the carpal tunnel syndromeK Stein, S Störkel, R P Linke, et al.
Journal of Pharmacokinetics and Biopharmaceutics|October 1, 1977
A pharmacokinetic model for high-dose methotrexate infusions in manS D Reich, N R Bachur, R H Goebel, et al.
Residue Reviews|January 1, 1982
Properties, effects, residues, and analytics of the insecticide endosulfanH Goebel, S Gorbach, W Knauf, et al.
Neuromuscular Disorders : NMD|May 11, 2006
Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindredDanielle E Dye, Biagio Azzarelli, Hans H Goebel, et al.
Muscle & Nerve|January 1, 1978
Autosomal dominant "spheroid body myopathy"H H Goebel, J Muller, H W Gillen, et al.
Ophthalmic Paediatrics and Genetics|February 1, 1985
Ultrastructural study of primary canine and human pigmentary retinopathyH H Goebel, K Ikeda, W Eichholtz, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiencyH Porschke, W Kress, H Reichmann, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2001
Morphological studies on CLN2H H Goebel, E Kominami, E Neuen-Jacob, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 14, 2001
[Keratopathy as a sign of multifocal congenital sensory polyneuropathy. A case report]U Kottler, O Schwenn, H H Goebel, et al.
Acta Neuropathologica|January 1, 1981
Fingerprint profiles in lymphocytic vacuoles of mucopolysaccharidoses I-H, II, III-A, and III-BH H Goebel, K Ikeda, F Schulz, et al.
Pageof 49