Title: 2008
Subtitle:
Author:



Publikationen 2008

Baek, R. C., J. L. Kasperzyk, F. M. Platt and T. N. Seyfried (2008). "N-butyldeoxygalactonojirimycin reduces brain ganglioside and GM2 content in neonatal Sandhoff disease mice." Neurochem Int 52(6): 1125-33.Biology Department, Boston College, 140 Commonwealth Avenue, Chestnut Hill, MA 02467, USA. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Becker, I., L. Wang-Eckhardt, A. Yaghootfam, V. Gieselmann and M. Eckhardt (2008). "Differential expression of (dihydro)ceramide synthases in mouse brain: oligodendrocyte-specific expression of CerS2/Lass2." Histochem Cell Biol 129(2): 233-41.Institute of Physiological Chemistry, University of Bonn, 53115 , Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Beetz, C., R. Schule, S. Klebe, S. Klimpe, T. Klopstock, A. Lacour, S. Otto, A. D. Sperfeld, B. van de Warrenburg, L. Schols and T. Deufel (2008). "Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspots." J Neurol Sci 268(1-2): 131-5.Institut fur Klinische Chemie und Laboratoriumsdiagnostik, Universitatsklinikum, 07747 Jena, Germany. christian.beetz@med.uni-jena.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Begemann, M., D. Sargin, M. J. Rossner, C. Bartels, F. Theis, S. P. Wichert, N. Stender, B. Fischer, S. Sperling, S. Stawicki, A. Wiedl, P. Falkai, K. A. Nave and H. Ehrenreich (2008). "Episode-specific differential gene expression of peripheral blood mononuclear cells in rapid cycling supports novel treatment approaches." Mol Med 14(9-10): 546-52.Division of Clinical Neuroscience, Max Planck Institute of Experimental Medicine, Gottingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Bennati, A. M., G. Schiavoni, S. Franken, D. Piobbico, M. A. Della Fazia, D. Caruso, E. De Fabiani, L. Benedetti, M. G. Cusella De Angelis, V. Gieselmann, G. Servillo, T. Beccari and R. Roberti (2008). "Disruption of the gene encoding 3beta-hydroxysterol Delta-reductase (Tm7sf2) in mice does not impair cholesterol biosynthesis." FEBS J 275(20): 5034-47.Department of Internal Medicine, University of Perugia, Italy. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Birchmeier, C. and K. A. Nave (2008). "Neuregulin-1, a key axonal signal that drives Schwann cell growth and differentiation." Glia 56(14): 1491-7.Max-Delbrueck-Centrum, Robert-Roessle-Strasse 10, Berlin-Buch, Germany. cbirch@mdc-berlin.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Brinkmann, B. G., A. Agarwal, M. W. Sereda, A. N. Garratt, T. Muller, H. Wende, R. M. Stassart, S. Nawaz, C. Humml, V. Velanac, K. Radyushkin, S. Goebbels, T. M. Fischer, R. J. Franklin, C. Lai, H. Ehrenreich, C. Birchmeier, M. H. Schwab and K. A. Nave (2008). "Neuregulin-1/ErbB signaling serves distinct functions in myelination of the peripheral and central nervous system." Neuron 59(4): 581-95.Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Goettingen 37075, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Brockmann, K., S. Dreha-Kulaczewski, P. Dechent, C. Bonnemann, G. Helms, M. Kyllerman, W. Bruck, J. Frahm, K. Huehne, J. Gartner and B. Rautenstrauss (2008). "Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations." J Neurol 255(7): 1049-58.Dept. of Pediatrics and Pediatric Neurology, Georg August University, Robert-Koch-Str. 40, 37075 Gottingen, Germany. kbrock@med.uni-goettingen.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Brohl, D., M. Strehle, H. Wende, K. Hori, I. Bormuth, K. A. Nave, T. Muller and C. Birchmeier (2008). "A transcriptional network coordinately determines transmitter and peptidergic fate in the dorsal spinal cord." Dev Biol 322(2): 381-93.Department of Neuroscience, Max-Delbruck-Centrum for Molecular Medicine, Berlin, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Charnas, L., F. Eichler, A. Kohlschuetter, J. Tolar and P. J. Orchard (2008). "Reply to: Reduced intensity conditioning haematopoietic stem cell transplantation with mesenchymal stromal cells infusion for the treatment of metachromatic leukodystrophy: a case report. Haematologica 2008; 93:e11-13." Haematologica 93(5): e47; author reply e48 www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Chatterjee, N., J. Stegmuller, P. Schatzle, K. Karram, M. Koroll, H. B. Werner, K. A. Nave and J. Trotter (2008). "Interaction of syntenin-1 and the NG2 proteoglycan in migratory oligodendrocyte precursor cells." J Biol Chem 283(13): 8310-7.Molecular Cell Biology, Department of Biology, Johannes Gutenberg University of Mainz, Mainz, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Delaunay, D., K. Heydon, A. Cumano, M. H. Schwab, J. L. Thomas, U. Suter, K. A. Nave, B. Zalc and N. Spassky (2008). "Early neuronal and glial fate restriction of embryonic neural stem cells." J Neurosci 28(10): 2551-62.Inserm, Unite 711, 75013 Paris, France. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Dreha-Kulaczewski, S. F., P. Dechent, J. Finsterbusch, K. Brockmann, J. Gartner, J. Frahm and F. A. Hanefeld (2008). "Early reduction of total N-acetyl-aspartate-compounds in patients with classical vanishing white matter disease. A long-term follow-up MRS study." Pediatr Res 63(4): 444-9.Department of Pediatrics and Pediatric Neurology, Georg August University, 37075 Gottingen, Germany. sdreha@gwdg.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Ebbing, B., K. Mann, A. Starosta, J. Jaud, L. Schols, R. Schule and G. Woehlke (2008). "Effect of spastic paraplegia mutations in KIF5A kinesin on transport activity." Hum Mol Genet 17(9): 1245-52.Institute for Cell Biology, University of Munich, Schillerstr. 42, D-80336 Munich, Germany. bettina.ebbing@lrz.uni-muenchen.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Eckhardt, M. (2008). "The role and metabolism of sulfatide in the nervous system." Mol Neurobiol 37(2-3): 93-103.Institute of Physiological Chemistry, University of Bonn, Nussallee 11, 53115 Bonn, Germany. eckhardt@institut.physiochem.uni-bonn.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Frese, M. A., S. Schulz and T. Dierks (2008). "Arylsulfatase G, a novel lysosomal sulfatase." J Biol Chem 283(17): 11388-95.Fakultat fur Chemie, Biochemie I, Universitat Bielefeld, 33615 Bielefeld, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Gallitzendoerfer, R., M. M. Abouzied, D. Hartmann, R. Dobrowolski, V. Gieselmann and S. Franken (2008). "Hepatoma-derived growth factor (HDGF) is dispensable for normal mouse development." Dev Dyn 237(7): 1875-85.Institute of Physiological Chemistry, University of Bonn, Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Gieselmann, V. (2008). "Metachromatic leukodystrophy: genetics, pathogenesis and therapeutic options." Acta Paediatr Suppl 97(457): 15-21.Institut fur Physiologische Chemie, Rheinische-Friedrich-Wilhems Universitat Bonn, Bonn, Germany. gieselmann@institut.physiochem.uni-bonn.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Globas, C., S. T. du Montcel, L. Baliko, S. Boesch, C. Depondt, S. DiDonato, A. Durr, A. Filla, T. Klockgether, C. Mariotti, B. Melegh, M. Rakowicz, P. Ribai, R. Rola, T. Schmitz-Hubsch, S. Szymanski, D. Timmann, B. P. Van de Warrenburg, P. Bauer and L. Schols (2008). "Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6." Mov Disord 23(15): 2232-8.Department of Neurology and Hertie-Institute for Clinical Brain Research, University of Tubingen, Tubingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Hattermann, K., A. Ludwig, V. Gieselmann, J. Held-Feindt and R. Mentlein (2008). "The chemokine CXCL16 induces migration and invasion of glial precursor cells via its receptor CXCR6." Mol Cell Neurosci 39(1): 133-41.Department of Anatomy, University of Kiel, Olshausenstrasse 40, 24098 Kiel, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Henneke, M., P. Combes, S. Diekmann, E. Bertini, K. Brockmann, A. P. Burlina, J. Kaiser, A. Ohlenbusch, B. Plecko, D. Rodriguez, O. Boespflug-Tanguy and J. Gartner (2008). "GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease." Neurology 70(10): 748-54.Department of Pediatrics and Pediatric Neurology, Georg August University, Faculty of Medicine, Robert-Koch-Strasse 40, 37075 Gottingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Huppke, P., W. Stark, C. Zurcher, B. Huppke, W. Bruck and J. Gartner (2008). "Natalizumab use in pediatric multiple sclerosis." Arch Neurol 65(12): 1655-8.Department of Pediatrics and Pediatric Neurology, Faculty of Medicine, Georg August University, Robert-Koch-Strasse 40, D-37075 Gottingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Ip, C. W., B. Kohl, C. Kleinschnitz, B. Reuss, K. A. Nave, A. Kroner and R. Martini (2008). "Origin of CD11b+ macrophage-like cells in the CNS of PLP-overexpressing mice: low influx of haematogenous macrophages and unchanged blood-brain-barrier in the optic nerve." Mol Cell Neurosci 38(4): 489-94.Department of Neurology, Developmental Neurobiology, University of Wuerzburg, Josef-Schneider Str. 11, D-97080 Wuerzburg, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Kalus, I., B. Salmen, C. Viebahn, K. von Figura, D. Schmitz, R. D'Hooge and T. Dierks (2008). "Differential Involvement of the Extracellular 6-O-Endosulfatases Sulf1 and Sulf2 in Brain Development and Neuronal and Behavioral Plasticity." J Cell Mol Med.Department of Chemistry, Biochemistry I, Bielefeld University, Bielefeld, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Kaminski, T., J. P. Siebrasse, V. Gieselmann, U. Kubitscheck and J. Kappler (2008). "Imaging and tracking of single hyaluronan molecules diffusing in solution." Glycoconj J.Institut fur Physiologische Chemie, Rheinische Friedrich-Wilhelms-Universitat Bonn, Nussallee 11, 53115, Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Karram, K., S. Goebbels, M. Schwab, K. Jennissen, G. Seifert, C. Steinhauser, K. A. Nave and J. Trotter (2008). "NG2-expressing cells in the nervous system revealed by the NG2-EYFP-knockin mouse." Genesis 46(12): 743-57.Molecular Cell Biology, Department of Biology, Johannes Gutenberg University of Mainz, 55128 Mainz, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Kassmann, C. M. and K. A. Nave (2008). "Oligodendroglial impact on axonal function and survival - a hypothesis." Curr Opin Neurol 21(3): 235-41.Department of Neurogenetics, Max Planck Institute of Experimental Medicine, Goettingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Koehler, K., K. Brockmann, M. Krumbholz, B. Kind, C. Bonnemann, J. Gartner and A. Huebner (2008). "Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430Phe." Eur J Hum Genet 16(12): 1499-506.Children's Hospital, Technical University Dresden, Dresden, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Kohler, W. (2008). "Diagnostic algorithm for the differentiation of leukodystrophies in early MS." J Neurol 255 Suppl 6: 123-6.Chefarzt der Klinik fur Neurologie und neurologische Intensivmedizin, Fachkrankenhaus Hubertusburg, An der Hubertusburg, 04779, Wermsdorf, Germany. wolfgang.koehler@kh-hubertusburg.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Krone, B., D. Pohl, K. Rostasy, E. Kahler, E. Brunner, F. Oeffner, J. M. Grange, J. Gartner and F. Hanefeld (2008). "Common infectious agents in multiple sclerosis: a case-control study in children." Mult Scler 14(1): 136-9.Department of Virology, Georg August University Goettingen,Germany. bkrone@gwdg.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Lamanna, W. C., M. A. Frese, M. Balleininger and T. Dierks (2008). "Sulf loss influences N-, 2-O-, and 6-O-sulfation of multiple heparan sulfate proteoglycans and modulates fibroblast growth factor signaling." J Biol Chem 283(41): 27724-35.Fakultat fur Chemie, Biochemie I, Universitat Bielefeld, 33615 Bielefeld, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Lunemann, J. D., P. Huppke, S. Roberts, W. Bruck, J. Gartner and C. Munz (2008). "Broadened and elevated humoral immune response to EBNA1 in pediatric multiple sclerosis." Neurology 71(13): 1033-5.Laboratory of Viral Immunobiology, Christopher H. Browne Center for Immunology and Immune Diseases, Rockefeller University, New York, NY 10021-6399, USA. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Maier, E. M., P. U. Mayerhofer, M. Asheuer, W. Kohler, M. Rothe, A. C. Muntau, A. A. Roscher, A. Holzinger, P. Aubourg and J. Berger (2008). "X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype." Biochem Biophys Res Commun 377(1): 176-80.Department of Biochemical Genetics and Molecular Biology, Dr von Hauner Children's Hospital, Research Center, Ludwig-Maximilians-University, Munich, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Matzner, U., F. Matthes, C. Weigelt, C. Andersson, C. Eistrup, J. Fogh and V. Gieselmann (2008). "Non-inhibitory antibodies impede lysosomal storage reduction during enzyme replacement therapy of a lysosomal storage disease." J Mol Med.Institut fur Physiologische Chemie, Rheinische Friedrich-Wilhelms-Universitat, Nussallee 11, D-53115, Bonn, Germany, matzner@institut.physiochem.uni-bonn.de. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Mobius, W., J. Patzig, K. A. Nave and H. B. Werner (2008). "Phylogeny of proteolipid proteins: divergence, constraints, and the evolution of novel functions in myelination and neuroprotection." Neuron Glia Biol 4(2): 111-27.Department of Neurogenetics, Max-Planck Institute of Experimental Medicine, Gottingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Morath, M. A., J. G. Okun, I. B. Muller, S. W. Sauer, F. Horster, G. F. Hoffmann and S. Kolker (2008). "Neurodegeneration and chronic renal failure in methylmalonic aciduria--a pathophysiological approach." J Inherit Metab Dis 31(1): 35-43.Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital Heidelberg, Im Neuenheimer Feld 150, 69120, Heidelberg, Germany. marina.morath@med.uni-heidelberg.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Muller, I., S. Kordowich, C. Holzwarth, G. Isensee, P. Lang, F. Neunhoeffer, M. Dominici, J. Greil and R. Handgretinger (2008). "Application of multipotent mesenchymal stromal cells in pediatric patients following allogeneic stem cell transplantation." Blood Cells Mol Dis 40(1): 25-32.Department of General Pediatrics, Hematology and Oncology, University Children's Hospital Tubingen, Hoppe-Seyler-St. 1, 72076, Tubigen, Germany. Ingo.Mueller@med.uni-tuebingen.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Muller, I., S. Lymperi and F. Dazzi (2008). "Mesenchymal stem cell therapy for degenerative inflammatory disorders." Curr Opin Organ Transplant 13(6): 639-44.Department of General Pediatrics, Hematology and Oncology, University Children's Hospital Tubingen, Tubingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Nave, K. A. (2008). "Neuroscience: An ageing view of myelin repair." Nature 455(7212): 478-9 www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Nave, K. A. and B. D. Trapp (2008). "Axon-glial signaling and the glial support of axon function." Annu Rev Neurosci 31: 535-61.Department of Neurogenetics, Max Planck Institute of Experimental Medicine, D-37075 Gottingen, Germany. nave@em.mpg.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Ratzka, A., I. Kalus, M. Moser, T. Dierks, S. Mundlos and A. Vortkamp (2008). "Redundant function of the heparan sulfate 6-O-endosulfatases Sulf1 and Sulf2 during skeletal development." Dev Dyn 237(2): 339-53.Center for Medical Biotechnology, University of Duisburg-Essen, Essen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Riess, O., U. Rub, A. Pastore, P. Bauer and L. Schols (2008). "SCA3: neurological features, pathogenesis and animal models." Cerebellum 7(2): 125-37.Department of Medical Genetics, University of Tuebingen, Calwerstrasse 7, D-72076 Tuebingen, Germany. olaf.riess@med.uni-tuebingen.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Rossner, M. J., H. Oster, S. P. Wichert, L. Reinecke, M. C. Wehr, J. Reinecke, G. Eichele, R. Taneja and K. A. Nave (2008). "Disturbed clockwork resetting in Sharp-1 and Sharp-2 single and double mutant mice." PLoS One 3(7): e2762.Max-Planck-Institute of Experimental Medicine, Gottingen, Germany. rossner@em.mpg.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Rub, U., E. R. Brunt, K. Seidel, K. Gierga, C. M. Mooy, M. Kettner, C. Van Broeckhoven, I. Bechmann, A. R. La Spada, L. Schols, W. den Dunnen, R. A. de Vos and T. Deller (2008). "Spinocerebellar ataxia type 7 (SCA7): widespread brain damage in an adult-onset patient with progressive visual impairments in comparison with an adult-onset patient without visual impairments." Neuropathol Appl Neurobiol 34(2): 155-68.Institute for Clinical Neuroanatomy, J. W. Goethe-University, Frankfurt/Main, Germany. u.rueb@em.uni-frankfurt.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Schlotawa, L., R. Steinfeld, K. von Figura, T. Dierks and J. Gartner (2008). "Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency." Hum Mutat 29(1): 205.Department of Pediatrics and Pediatric Neurology, Georg August University Gottingen, Gottingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Schmitz-Hubsch, T., M. Coudert, P. Bauer, P. Giunti, C. Globas, L. Baliko, A. Filla, C. Mariotti, M. Rakowicz, P. Charles, P. Ribai, S. Szymanski, J. Infante, B. P. van de Warrenburg, A. Durr, D. Timmann, S. Boesch, R. Fancellu, R. Rola, C. Depondt, L. Schols, E. Zdienicka, J. S. Kang, S. Dohlinger, B. Kremer, D. A. Stephenson, B. Melegh, M. Pandolfo, S. di Donato, S. T. du Montcel and T. Klockgether (2008). "Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms." Neurology 71(13): 982-9.Department of Neurology, University Hospital of Bonn, Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Schmitz-Hubsch, T., P. Giunti, D. A. Stephenson, C. Globas, L. Baliko, F. Sacca, C. Mariotti, M. Rakowicz, S. Szymanski, J. Infante, B. P. van de Warrenburg, D. Timmann, R. Fancellu, R. Rola, C. Depondt, L. Schols, E. Zdzienicka, J. S. Kang, S. Dohlinger, B. Kremer, B. Melegh, A. Filla and T. Klockgether (2008). "SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia." Neurology 71(7): 486-92.Department of Neurology, University Hospital of Bonn, Sigmund-Freud-Str 25, D-53105 Bonn, Germany. tanja.schmitz-huebsch@ukb.uni-bonn.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Schols, L., L. Arning, R. Schule, J. T. Epplen and D. Timmann (2008). ""Pseudodominant inheritance" of ataxia with ocular apraxia type 2 (AOA2)." J Neurol 255(4): 495-501.Hertie-Institute for Clinical Brain Research and Department of Neurology, Eberhard Karls-University Tubingen, Hoppe-Seyler-Str. 3, 72076 Tubingen, Germany. Ludger.Schoels@uni-tuebingen.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Schule, R., B. P. Kremer, J. Kassubek, M. Auer-Grumbach, V. Kostic, T. Klopstock, S. Klimpe, S. Otto, S. Boesch, B. P. van de Warrenburg and L. Schols (2008). "SPG10 is a rare cause of spastic paraplegia in European families." J Neurol Neurosurg Psychiatry 79(5): 584-7.Department of Neurology and Hertie Institute for Clinical Brain Research, University of Tubingen, Hoppe-Seyler-Str 3, D-72076 Tubingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Semmler, A., W. Kohler, H. H. Jung, M. Weller and M. Linnebank (2008). "Therapy of X-linked adrenoleukodystrophy." Expert Rev Neurother 8(9): 1367-79.University Hospital Zurich, Department of Neurology, Frauenklinikstr. 26, CH-8091 Zurich, Switzerland. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

 

Stam, A. H., K. R. Vanmolkot, H. P. Kremer, J. Gartner, J. Brown, E. Leshinsky-Silver, R. Gilad, E. E. Kors, W. S. Frankhuizen, H. B. Ginjaar, J. Haan, R. R. Frants, M. D. Ferrari, A. M. van den Maagdenberg and G. M. Terwindt (2008). "CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine." Clin Genet 74(5): 481-5.Department of Neurology and Clinical Genetic, Erasmus Medical Centre, Leiden, The Netherlands. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Stark, W., P. Huppke and J. Gartner (2008). "Paediatric multiple sclerosis: the experience of the German Centre for Multiple Sclerosis in Childhood and Adolescence." J Neurol 255 Suppl 6: 119-22.Department of Paediatrics and Paediatric Neurology, Georg August University, University Medical Centre Gottingen (UMG), Robert-Koch-Strasse 40, 37075 Gottingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Staudt, M., L. F. Ticini, W. Grodd, I. Krageloh-Mann and H. O. Karnath (2008). "Functional topography of early periventricular brain lesions in relation to cytoarchitectonic probabilistic maps." Brain Lang 106(3): 177-83.Department of Pediatric Neurology and Developmental Medicine, University Children's Hospital, Hoppe-Seyler-Str. 1, D-72076 Tubingen, Germany. martin.staudt@med.uni-tuebingen.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Stettner, G. M., P. Huppke, J. Gartner, D. W. Richter and M. Dutschmann (2008). "Disturbances of breathing in Rett syndrome: results from patients and animal models." Adv Exp Med Biol 605: 503-7.Department of Pediatrics and Pediatric Neurology, Georg August University, Robert-Koch-Str. 40, 37075 Gottingen, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Stroobants, S., T. Leroy, M. Eckhardt, J. M. Aerts, D. Berckmans and R. D'Hooge (2008). "Early signs of neurolipidosis-related behavioural alterations in a murine model of metachromatic leukodystrophy." Behav Brain Res 189(2): 306-16.Laboratory of Biological Psychology, Department of Psychology, University of Leuven, Leuven, Belgium. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Trapp, B. D. and K. A. Nave (2008). "Multiple sclerosis: an immune or neurodegenerative disorder?" Annu Rev Neurosci 31: 247-69.Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA. trappb@ccf.org www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Weber, Y. G., A. Storch, T. V. Wuttke, K. Brockmann, J. Kempfle, S. Maljevic, L. Margari, C. Kamm, S. A. Schneider, S. M. Huber, A. Pekrun, R. Roebling, G. Seebohm, S. Koka, C. Lang, E. Kraft, D. Blazevic, A. Salvo-Vargas, M. Fauler, F. M. Mottaghy, A. Munchau, M. J. Edwards, A. Presicci, F. Margari, T. Gasser, F. Lang, K. P. Bhatia, F. Lehmann-Horn and H. Lerche (2008). "GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak." J Clin Invest 118(6): 2157-68.Neurologische Klinik and Institut fur Anatomie und Zellbiologie, Universitat Ulm, Ulm, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Weller, S., H. Rosewich and J. Gartner (2008). "Cerebral MRI as a valuable diagnostic tool in Zellweger spectrum patients." J Inherit Metab Dis.Department of Pediatrics and Pediatric Neurology, Georg August University, Robert-Koch-Strasse 40, 37075, Gottingen, Germany, s.weller@med.uni-goettingen.de. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Wilken, B., P. Dechent, F. Hanefeld and J. Frahm (2008). "Proton MRS of a child with Sandhoff disease reveals elevated brain hexosamine." Eur J Paediatr Neurol 12(1): 56-60.Abteilung Neuropadiatrie, Department of Pediatric Neurology, Klinikum Kassel, Monchebergstr. 41-43, 34125 Kassel, Germany. wilken@klinikum-kassel.de www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Yin, X., G. J. Kidd, K. A. Nave and B. D. Trapp (2008). "P0 protein is required for and can induce formation of schmidt-lantermann incisures in myelin internodes." J Neurosci 28(28): 7068-73.Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195, USA. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 

Zoller, I., M. Meixner, D. Hartmann, H. Bussow, R. Meyer, V. Gieselmann and M. Eckhardt (2008). "Absence of 2-hydroxylated sphingolipids is compatible with normal neural development but causes late-onset axon and myelin sheath degeneration." J Neurosci 28(39): 9741-54.Institute of Physiological Chemistry, University of Bonn, 53115 Bonn, Germany. www.ncbi.nlm.nih.gov/entrez/query.fcgi

 



Go back to the regular design...