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Publikationen 2006


Burckhardt Helferich Prizes to K. Sandhoff, H. Kessler, F. Diederich, and K. C. Nicolaou. Angew Chem Int Ed Engl 45(9): 1346.


Aerts, J. M., C. E. Hollak, R. G. Boot, J. E. Groener, M. Maas (2006). Substrate reduction therapy of glycosphingolipid storage disorders. J Inherit Metab Dis 29(2-3): 449-56. Department of Medical Biochemistry, Academic Medical Center, University of Amsterdam, Meibergdreef 15, 1105 AZ, Amsterdam, The Netherlands.


Arfi, A., R. Zisling, E. Richard, L. Batista, L. Poenaru, A. H. Futerman, C. Caillaud (2006). Reversion of the biochemical defects in murine embryonic Sandhoff neurons using a bicistronic lentiviral vector encoding hexosaminidase alpha and beta. J Neurochem 96(6): 1572-9. Universite Paris-Descartes, Faculte de Medecine, INSERM, Centre National de la Recherche Scientifique, Institut Cochin, U567-UMR 8104, Paris, France.


Bembi, B., F. Marchetti, V. I. Guerci, G. Ciana, R. Addobbati, D. Grasso, R. Barone, R. Cariati, L. Fernandez-Guillen, T. Butters, M. G. Pittis (2006). Substrate reduction therapy in the infantile form of Tay-Sachs disease. Neurology 66(2): 278-80. Unita di Malattie Metaboliche, I.R.C.C.S. Burlo Garofolo, Trieste, Italy.


Benninger, Y., H. Colognato, T. Thurnherr, R. J. Franklin, D. P. Leone, S. Atanasoski, K. A. Nave, C. Ffrench-Constant, U. Suter, J. B. Relvas (2006). Beta1-integrin signaling mediates premyelinating oligodendrocyte survival but is not required for CNS myelination and remyelination. J Neurosci 26(29): 7665-73. Institute for Cell Biology, Department of Biology, Swiss Federal Institute of Technology, CH-8093 Zurich, Switzerland.


Brockmann, K., P. Dechent, C. Bonnemann, G. Schreiber, J. Frahm, F. Hanefeld (2006). Quantitative proton MRS of cerebral metabolites in laminin alpha2 chain deficiency. Brain Dev. Department of Paediatrics and Paediatric Neurology, Georg August University, 37075 Gottingen, Germany.


Cachon-Gonzalez, M. B., S. Z. Wang, A. Lynch, R. Ziegler, S. H. Cheng, T. M. Cox (2006). Effective gene therapy in an authentic model of Tay-Sachs-related diseases. Proc Natl Acad Sci U S A 103(27): 10373-8. Department of Medicine, University of Cambridge, Level 5, Box 157, Addenbrooke's Hospital, Hills Road, Cambridge CB2 2QQ, United Kingdom.


Cortright, R. N., K. M. Sandhoff, J. L. Basilio, J. R. Berggren, R. C. Hickner, M. W. Hulver, G. L. Dohm, J. A. Houmard (2006). Skeletal muscle fat oxidation is increased in African-American and white women after 10 days of endurance exercise training. Obesity (Silver Spring) 14(7): 1201-10. The Human Performance Laboratory, Department of Excercise and Sport Science, College of Health and Human Performance, The Brody School of Medicine, East Carolina University, Greenville, NC 27858, USA.


Denny, C. A., J. L. Kasperzyk, K. N. Gorham, R. T. Bronson, T. N. Seyfried (2006). Influence of caloric restriction on motor behavior, longevity, and brain lipid composition in Sandhoff disease mice. J Neurosci Res 83(6): 1028-38. Department of Biology, Boston College, Chestnut Hill, Massachusetts 02467, USA.


Ding, X. Q., M. Goerg, B. Eckert, A. Ohlenbusch, A. Kohlschuetter, J. Gaertner, H. Zeumer (2006). Rapidly progressive vanishing white matter disease in a child with previously inconspicuous brain MRI. Neuropediatrics 37(4): 253-6. Department of Neuroradiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.


Dreha-Kulaczewski, S., P. Dechent, G. Helms, J. Frahm, J. Gartner, K. Brockmann (2006). Cerebral metabolic and structural alterations in hereditary spastic paraplegia with thin corpus callosum assessed by MRS and DTI. Neuroradiology 48(12): 893-8. Department of Pediatrics and Pediatric Neurology, Faculty of Medicine, Georg August University, Robert-Koch-Str. 40, 37075, Gottingen, Germany,


Federspiel, A., S. Begre, C. Kiefer, G. Schroth, W. K. Strik, T. Dierks (2006). Alterations of white matter connectivity in first episode schizophrenia. Neurobiol Dis 22(3): 702-9. University Hospital of Clinical Psychiatry, Department of Psychiatric Neurophysiology, Berne, Switzerland.


Fowler, J. H., J. M. Edgar, A. Pringle, M. McLaughlin, J. McCulloch, I. R. Griffiths, J. Y. Garbern, K. A. Nave, D. Dewar (2006). Alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid-mediated excitotoxic axonal damage is attenuated in the absence of myelin proteolipid protein. J Neurosci Res 84(1): 68-77. Division of Clinical Neuroscience, University of Glasgow, Wellcome Surgical Institute, Glasgow G61 1QH, United Kingdom.


Franken, S., D. Wittke, J. E. Mansson, R. D'Hooge, P. P. De Deyn, R. Lullmann-Rauch, U. Matzner, V. Gieselmann (2006). Modest phenotypic improvements in ASA-deficient mice with only one UDP-galactose:ceramide-galactosyltransferase gene. Lipids Health Dis 5(1): 21.


Gieselmann, V. (2006). Reversibility of cellular and organ pathology in enzyme replacement trials in animal models of lysosomal storage diseases. Acta Paediatr Suppl 95(451): 93-9. Institut fur Physiologische ChemieUniversitat Bonn, Germany.


Girisha, K. M., S. R. Phadke (2006). Basal ganglia changes: a diagnostic clue to Sandhoff disease. Indian Pediatr 43(10): 919-20.


Goebell, E., J. Fiehler, X. Q. Ding, S. Paustenbach, S. Nietz, O. Heese, T. Kucinski, C. Hagel, M. Westphal, H. Zeumer (2006). Disarrangement of fiber tracts and decline of neuronal density correlate in glioma patients--a combined diffusion tensor imaging and 1H-MR spectroscopy study. AJNR Am J Neuroradiol 27(7): 1426-31. Department of Neuroradiology, University of Hamburg, Martinistrasse 52, 20246 Hamburg, Germany.


Goebell, E., S. Paustenbach, O. Vaeterlein, X. Q. Ding, O. Heese, J. Fiehler, T. Kucinski, C. Hagel, M. Westphal, H. Zeumer (2006). Low-grade and anaplastic gliomas: differences in architecture evaluated with diffusion-tensor MR imaging. Radiology 239(1): 217-22. Department of Neuroradiology, University of Hamburg, Martinistrasse 52, 20251 Hamburg, Germany.


Groeschel, S., K. Brockmann, P. Dechent, E. Wilichowski, J. Frahm, F. Hanefeld (2006). Magnetic resonance imaging and proton magnetic resonance spectroscopy of megalencephaly and dilated Virchow-Robin spaces. Pediatr Neurol 34(1): 35-40. Department of Pediatrics and Neuropediatrics, Georg-August-Universitat, Gottingen, Germany.


Hoffrogge, R., S. Mikkat, C. Scharf, S. Beyer, H. Christoph, J. Pahnke, E. Mix, M. Berth, A. Uhrmacher, I. Z. Zubrzycki, E. Miljan, U. Volker, A. Rolfs (2006). 2-DE proteome analysis of a proliferating and differentiating human neuronal stem cell line (ReNcell VM). Proteomics 6(6): 1833-47. Neurobiological Laboratory, Department of Neurology, Medical Faculty, University of Rostock, Germany.


Ip, C. W., A. Kroner, M. Bendszus, C. Leder, I. Kobsar, S. Fischer, H. Wiendl, K. A. Nave, R. Martini (2006). Immune cells contribute to myelin degeneration and axonopathic changes in mice overexpressing proteolipid protein in oligodendrocytes. J Neurosci 26(31): 8206-16. Department of Neurology, University of Wuerzburg, D-97080 Wuerzburg, Germany.


Isaac, G., Z. Pernber, V. Gieselmann, E. Hansson, J. Bergquist, J. E. Mansson (2006). Sulfatide with short fatty acid dominates in astrocytes and neurons. Febs J 273(8): 1782-90. Department of Analytical Chemistry, Uppsala University, Sweden.


Itakura, T., A. Kuroki, Y. Ishibashi, D. Tsuji, E. Kawashita, Y. Higashine, H. Sakuraba, S. Yamanaka, K. Itoh (2006). Inefficiency in GM2 ganglioside elimination by human lysosomal beta-hexosaminidase beta-subunit gene transfer to fibroblastic cell line derived from Sandhoff disease model mice. Biol Pharm Bull 29(8): 1564-9. Department of Medicinal Biotechnology, Institute for Medicinal Resources, Graduate School of Pharmaceutical Sciences, The University of Tokushima, Japan.


John, M., M. Wendeler, M. Heller, K. Sandhoff, H. Kessler (2006). Characterization of human saposins by NMR spectroscopy. Biochemistry 45(16): 5206-16. Department Chemie, Technische Universitat Munchen, Lichtenbergstrasse 4, D-85747 Garching, Germany.


Kaga, Y., W. J. Shoemaker, M. Furusho, M. Bryant, J. Rosenbluth, S. E. Pfeiffer, L. Oh, M. Rasband, C. Lappe-Siefke, K. Yu, D. M. Ornitz, K. A. Nave, R. Bansal (2006). Mice with conditional inactivation of fibroblast growth factor receptor-2 signaling in oligodendrocytes have normal myelin but display dramatic hyperactivity when combined with Cnp1 inactivation. J Neurosci 26(47): 12339-50. Department of Neuroscience, University of Connecticut Medical School, Farmington, Connecticut 06030, USA.


Klein, D., T. Schmandt, E. Muth-Kohne, A. Perez-Bouza, M. Segschneider, V. Gieselmann, O. Brustle (2006). Embryonic stem cell-based reduction of central nervous system sulfatide storage in an animal model of metachromatic leukodystrophy. Gene Ther. 1Institute of Physiological Chemistry, University of Bonn, Bonn, Germany.


Kolter, T., K. Sandhoff (2006). Sphingolipid metabolism diseases. Biochim Biophys Acta 1758(12): 2057-79. Kekule-Institut fur Organische Chemie und Biochemie der Universitat, Gerhard-Domagk-Str. 1, D-53121 Bonn, Germany.


Kramer-Albers, E. M., K. Gehrig-Burger, C. Thiele, J. Trotter, K. A. Nave (2006). Perturbed interactions of mutant proteolipid protein/DM20 with cholesterol and lipid rafts in oligodendroglia: implications for dysmyelination in spastic paraplegia. J Neurosci 26(45): 11743-52. Department of Biology, Unit of Molecular Cell Biology, University of Mainz, 55099 Mainz, Germany.


Kuliev, A., S. Rechitsky, K. Laziuk, O. Verlinsky, I. Tur-Kaspa, Y. Verlinsky (2006). Pre-embryonic diagnosis for Sandhoff disease. Reprod Biomed Online 12(3): 328-33. Reproductive Genetics Institute, Chicago, IL, USA.


Lamanna, W. C., R. J. Baldwin, M. Padva, I. Kalus, G. Ten Dam, T. H. van Kuppevelt, J. T. Gallagher, K. von Figura, T. Dierks, C. L. Merry (2006). Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity. Biochem J 400(1): 63-73. Department of Chemistry, Biochemistry I, Bielefeld University, Universitatsstrasse 25, 33615 Bielefeld, Germany.


Lasek, K., R. Lencer, C. Gaser, J. Hagenah, U. Walter, A. Wolters, N. Kock, S. Steinlechner, M. Nagel, C. Zuhlke, M. F. Nitschke, K. Brockmann, C. Klein, A. Rolfs, F. Binkofski (2006). Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17). Brain 129(Pt 9): 2341-52. Department of Neurology and NeuroImage Nord, University Hospital of Schleswig-Holstein Campus Luebeck, Luebeck, Germany.


Locatelli Hoops, S., T. Kolter, K. Sandhoff (2006). Saposin C and Other Sphingolipid Activator Proteins. Gaucher Disease. A. Futerman and A. Zimran, CRC Press, Taylor & Francis Group: 67-84.


Locatelli-Hoops, S., N. Remmel, R. Klingenstein, B. Breiden, M. Rossocha, M. Schoeniger, C. Koenigs, W. Saenger, K. Sandhoff (2006). Saposin A mobilizes lipids from low cholesterol and high bis(monoacylglycerol)phosphate-containing membranes: patient variant Saposin A lacks lipid extraction capacity. J Biol Chem 281(43): 32451-60. Kekule-Institut fur Organische Chemie und Biochemie, Gerhard-Domagk-Strasse 1, D-53121 Bonn, Germany.


Lutjohann, D., K. Harzer, V. Gieselmann, M. Eckhardt (2006). Reduced brain cholesterol content in arylsulfatase A-deficient mice. Biochem Biophys Res Commun 344(2): 647-50. Institute of Clinical Pharmacology, University of Bonn, Germany.


Maegawa, G. H., T. Stockley, M. Tropak, B. Banwell, S. Blaser, F. Kok, R. Giugliani, D. Mahuran, J. T. Clarke (2006). The natural history of juvenile or subacute GM2 gangliosidosis: 21 new cases and literature review of 134 previously reported. Pediatrics 118(5): e1550-62. Division of Clinical and Metabolic Genetics, Hospital for Sick Children, 555 University Ave, Toronto, Ontario, Canada M5G 1X8.


Meyer zu Horste, G., T. Prukop, K. A. Nave, M. W. Sereda (2006). Myelin disorders: Causes and perspectives of Charcot-Marie-Tooth neuropathy. J Mol Neurosci 28(1): 77-88. Max-Planck-Institute of Experimental Medicine, Gottingen, Germany.


Mohri, I., M. Taniike, I. Okazaki, K. Kagitani-Shimono, K. Aritake, T. Kanekiyo, T. Yagi, S. Takikita, H. S. Kim, Y. Urade, K. Suzuki (2006). Lipocalin-type prostaglandin D synthase is up-regulated in oligodendrocytes in lysosomal storage diseases and binds gangliosides. J Neurochem 97(3): 641-51. Department of Pathology and Laboratory Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.


Muller, I., B. Kustermann-Kuhn, C. Holzwarth, G. Isensee, M. Vaegler, K. Harzer, I. Krageloh-Mann, R. Handgretinger, G. Bruchelt (2006). In vitro analysis of multipotent mesenchymal stromal cells as potential cellular therapeutics in neurometabolic diseases in pediatric patients. Exp Hematol 34(10): 1413-9. University Children's Hospital, Tubingen, Germany.


Nave, K. A., J. L. Salzer (2006). Axonal regulation of myelination by neuregulin 1. Curr Opin Neurobiol 16(5): 492-500. Max Planck Institute of Experimental Medicine, D-37075 Goettingen, Germany.


Neubauer, B. A., I. Stefanova, C. A. Hubner, E. Neumaier-Probst, J. Bohl, H. C. Oppermann, H. Sto, A. Hahn, U. Stephani, A. Kohlschutter, A. Gal (2006). A new type of leukoencephalopathy with metaphyseal chondrodysplasia maps to Xq25-q27. Neurology 67(4): 587-91. Department of Pediatric Neurology, Universities of Giessen.


Nobbio, L., G. Gherardi, T. Vigo, M. Passalacqua, E. Melloni, M. Abbruzzese, G. Mancardi, K. A. Nave, A. Schenone (2006). Axonal damage and demyelination in long-term dorsal root ganglia cultures from a rat model of Charcot-Marie-Tooth type 1A disease. Eur J Neurosci 23(6): 1445-52. Department of Neurosciences, Ophthalmology and Genetics, University of Genoa, Italy, Via De Toni, 5, 16132, Genoa, Italy.


Padiath, Q. S., K. Saigoh, R. Schiffmann, H. Asahara, T. Yamada, A. Koeppen, K. Hogan, L. J. Ptacek, Y. H. Fu (2006). Lamin B1 duplications cause autosomal dominant leukodystrophy. Nat Genet 38(10): 1114-23. Department of Neurology, University of California, San Francisco, San Francisco, California, USA 94158.


Pellegrini, M., E. Zicari, M. T. Dotti, A. Federico (2006). Dysautonomic achalasia in two siblings with Sandhoff disease. J Neurol Sci 241(1-2): 107-9. Digestive Surgery Unit, Department of Surgery and Surgical Specialities, University of Siena, Italy.


Pohl, D., K. Rostasy, S. Treiber-Held, K. Brockmann, J. Gartner, F. Hanefeld (2006). Pediatric multiple sclerosis: detection of clinically silent lesions by multimodal evoked potentials. J Pediatr 149(1): 125-7. Department of Pediatrics and Pediatric Neurology, Georg August University Goettingen, Germany.


Rehring, T. F., R. S. Stolcpart, B. G. Sandhoff, J. A. Merenich, H. W. Hollis, Jr. (2006). Effect of a clinical pharmacy service on lipid control in patients with peripheral arterial disease. J Vasc Surg 43(6): 1205-10. Department of Vascular Surgery, Colorado Permanente Medical Group, University of Colorado Health Sciences Center, Denver, CO 80205, USA.


Roeser, D., A. Preusser-Kunze, B. Schmidt, K. Gasow, J. G. Wittmann, T. Dierks, K. von Figura, M. G. Rudolph (2006). A general binding mechanism for all human sulfatases by the formylglycine-generating enzyme. Proc Natl Acad Sci U S A 103(1): 81-6. Department of Molecular Structural Biology, University of Gottingen, Justus-von-Liebig-Weg 11, D-37077 Gottingen, Germany.


Rosenbluth, J., K. A. Nave, A. Mierzwa, R. Schiff (2006). Subtle myelin defects in PLP-null mice. Glia 54(3): 172-82. Department of Physiology and Neuroscience, New York University School of Medicine, New York 10016, USA.


Sakuraba, H., M. Sawada, F. Matsuzawa, S. Aikawa, Y. Chiba, Y. Jigami, K. Itoh (2006). Molecular pathologies of and enzyme replacement therapies for lysosomal diseases. CNS Neurol Disord Drug Targets 5(4): 401-13. CREST, JST, Kawaguchi, Japan.


Schultz-Heienbrok, R., N. Remmel, R. Klingenstein, M. Rossocha, K. Sandhoff, W. Saenger, T. Maier (2006). Crystallization and preliminary characterization of three different crystal forms of human saposin C heterologously expressed in Pichia pastoris. Acta Crystallograph Sect F Struct Biol Cryst Commun 62(Pt 2): 117-20. Institut fur Chemie und Biochemie/Kristallographie, Freie Universitat Berlin, Germany.


Schweitzer, J., T. Becker, M. Schachner, K. A. Nave, H. Werner (2006). Evolution of myelin proteolipid proteins: gene duplication in teleosts and expression pattern divergence. Mol Cell Neurosci 31(1): 161-77. Zentrum fuer Molekulare Neurobiologie, University of Hamburg, D-20251 Hamburg, Germany.


Sereda, M. W., K. A. Nave (2006). Animal models of Charcot-Marie-Tooth disease type 1A. Neuromolecular Med 8(1-2): 205-16. Department of Neurogenetics, Max-Planck-Institute of Experimental Medicine, Gottingen, Germany.


Sevin, C., A. Benraiss, D. Van Dam, D. Bonnin, G. Nagels, L. Verot, I. Laurendeau, M. Vidaud, V. Gieselmann, M. Vanier, P. P. De Deyn, P. Aubourg, N. Cartier (2006). Intracerebral adeno-associated virus-mediated gene transfer in rapidly progressive forms of metachromatic leukodystrophy. Hum Mol Genet 15(1): 53-64. Institut National de la Sante et de la Recherche Medicale U561, Universite Paris V, 75014 Paris, France.


Stevanin, G., G. Montagna, H. Azzedine, E. M. Valente, A. Durr, V. Scarano, N. Bouslam, D. Cassandrini, P. S. Denora, C. Criscuolo, S. Belarbi, A. Orlacchio, P. Jonveaux, G. Silvestri, A. M. Hernandez, G. De Michele, M. Tazir, C. Mariotti, K. Brockmann, A. Malandrini, M. S. van der Knapp, M. Neri, H. Tonekaboni, M. A. Melone, A. Tessa, M. T. Dotti, M. Tosetti, F. Pauri, A. Federico, C. Casali, V. T. Cruz, J. L. Loureiro, F. Zara, S. Forlani, E. Bertini, P. Coutinho, A. Filla, A. Brice, F. M. Santorelli (2006). Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity. Neurogenetics 7(3): 149-56. INSERM U679, Salpetriere Hospital, 47 Boulevard de l'Hopital, 75013 Paris, France.


Thurnherr, T., Y. Benninger, X. Wu, A. Chrostek, S. M. Krause, K. A. Nave, R. J. Franklin, C. Brakebusch, U. Suter, J. B. Relvas (2006). Cdc42 and Rac1 signaling are both required for and act synergistically in the correct formation of myelin sheaths in the CNS. J Neurosci 26(40): 10110-9. Institute for Cell Biology, Department of Biology, Federal Institute of Technology (ETH) Zurich, CH-8093 Zurich, Switzerland.


Trajkovic, K., A. S. Dhaunchak, J. T. Goncalves, D. Wenzel, A. Schneider, G. Bunt, K. A. Nave, M. Simons (2006). Neuron to glia signaling triggers myelin membrane exocytosis from endosomal storage sites. J Cell Biol 172(6): 937-48. Centre for Biochemistry and Molecular Cell Biology, University of Gottingen, 37073 Gottingen, Germany.


Wehr, M. C., R. Laage, U. Bolz, T. M. Fischer, S. Grunewald, S. Scheek, A. Bach, K. A. Nave, M. J. Rossner (2006). Monitoring regulated protein-protein interactions using split TEV. Nat Methods 3(12): 985-93. Max Planck Institute of Experimental Medicine, Hermann Rein Str. 3, D-37075 Gottingen, Germany.


Weishaupt, J. H., C. Bartels, E. Polking, J. Dietrich, G. Rohde, B. Poeggeler, N. Mertens, S. Sperling, M. Bohn, G. Huther, A. Schneider, A. Bach, A. L. Siren, R. Hardeland, M. Bahr, K. A. Nave, H. Ehrenreich (2006). Reduced oxidative damage in ALS by high-dose enteral melatonin treatment. J Pineal Res 41(4): 313-23. Department of Neurology, Georg August University, Gottingen, Germany.


Wendeler, M., N. Werth, T. Maier, G. Schwarzmann, T. Kolter, M. Schoeniger, D. Hoffmann, T. Lemm, W. Saenger, K. Sandhoff (2006). The enzyme-binding region of human GM2-activator protein. Febs J 273(5): 982-91. Kekule-Institut fur Organische Chemie und Biochemie der Universitat Bonn, Germany.


Wetzstein, V., U. Budde, F. Oyen, X. Ding, J. Herrmann, B. Liebig, R. Schneppenheim (2006). Intracranial hemorrhage in a term newborn with severe von Willebrand disease type 3 associated with sinus venous thrombosis. Haematologica 91(12 Suppl): ECR60. University Medical Center Hamburg-Eppendorf, Department of Pediatric ematology and Oncology, Martinistrasse 52, D-20246 Hamburg, Germany


Winau, F., S. Weber, S. Sad, J. de Diego, S. L. Hoops, B. Breiden, K. Sandhoff, V. Brinkmann, S. H. Kaufmann, U. E. Schaible (2006). Apoptotic vesicles crossprime CD8 T cells and protect against tuberculosis. Immunity 24(1): 105-17. Department of Immunology, Max-Planck-Institute for Infection Biology, Schumannstrasse 21-22, 10117 Berlin, Germany.


Yin, X., R. C. Baek, D. A. Kirschner, A. Peterson, Y. Fujii, K. A. Nave, W. B. Macklin, B. D. Trapp (2006). Evolution of a neuroprotective function of central nervous system myelin. J Cell Biol 172(3): 469-78. Department of Neurosciences, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.


Zu Horste, G. M., K. A. Nave (2006). Animal models of inherited neuropathies. Curr Opin Neurol 19(5): 464-73. Max-Planck-Institute of Experimental Medicine, Gottingen, Germany.


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