Diagnostic and prognostic value of in vivo proton MR spectroscopy for Zellweger syndrome spectrum patients von Rosewich, H., Dechent, P., Krause, C., Ohlenbusch, A., Brockmann, K., Gärtner, J.

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GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease von HENNEKE, M, COMBES, P, BOESPFLUG-TANGUY, O, GÄRTNER, J, DIEKMANN, S, BERTINI, E, BROCKMANN, K, BURLINA, A. P, KAISER, J, OHIENBUSCH, A, PLECKO, B, RODRIGUEZ, D

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An unusual mutation in the XPG gene leads to an internal in-frame deletion and a XP/CS complex phenotype von Lehmann, J., Schubert, S., Schäfer, A., Apel, A., Laspe, P., Schiller, S., Ohlenbusch, A., Gratchev, A., Emmert, S.

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A novel mutation in the XPA gene results in two truncated protein variants and leads to a severe XP/neurological symptoms phenotype von Lehmann, J., Schubert, S., Schäfer, A., Laspe, P., Haenssle, H.A., Ohlenbusch, A., Gratchev, A., Emmert, S.

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Genetic and clinical aspects of Zellweger spectrum patients with PEX1 mutations von Rosewich, H, Ohlenbusch, A, Gärtner, J

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Chlamydia pneumoniae in children with MS: Frequency and quantity of intrathecal antibodies von ROSTASY, K, REIBER, H, POHL, D, LANGE, P, OHLENBUSCH, A, EIFFERT, H, MAASS, M, HANEFELD, F

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Maternal Segmental Disomy in Leigh Syndrome with Cytochrome c Oxidase Deficiency Caused by Homozygous SURF1 Mutation von van Riesen, A. K. J., Antonicka, H., Ohlenbusch, A., Shoubridge, E. A., Wilichowski, E. K. G.

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Acute Peripheral Facial Palsy in Lyme Disease - A Distal Neuritis at the Infection Site von Eiffert, H., Karsten, A., Schlott, T., Ohlenbusch, A., Laskawi, R., Hoppert, M., Christen, H.-J.

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Rapidly Progressive Vanishing White Matter Disease in a Child with Previously Inconspicuous Brain MRI von Ding, X.-Q., Goerg, M., Eckert, B., Ohlenbusch, A., Kohlschuetter, A., Gaertner, J., Zeumer, H.

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Autoantibodies to Human Manganese Superoxide Dismutase (MnSOD) in Children with Facial Palsy due to Neuroborreliosis von Eiffert, H., Karsten, A., Ritter, K., Ohlenbusch, A., Schlott, T., Laskawi, R., Christen, H.-J.

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Risk of Urban Lyme Disease Enhanced by the Presence of Rats von Matuschka, Franz-Rainer, Endepols, Stefan, Richter, Dania, Ohlenbusch, Andreas, Eiffert, Helmut, Spielman, Andrew

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Characterization of the Mitochondrial Genome in Childhood Multiple Sclerosis. - I. Optic Neuritis and LHON Mutations von Ohlenbusch, A., Wilichowski, E., Hanefeld, F.

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Characterization of the mitochondrial genome in childhood multiple sclerosis : II. Multiple sclerosis without optic neuritis and LHON-associated genes von WILICHOWSKI, E, OHLENBUSCH, A, HANEFELD, F

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Etiology of the Acrodermatitis Chronica Atrophicans Lesion in Lyme Disease von Ohlenbusch, Andreas, Matuschka, Franz-Rainer, Richter, Dania, Christen, Hans-Jürgen, Thomssen, Reiner, Spielman, Andrew, Eiffert, Helmut

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Characteristics of Lyme Disease Spirochetes in Archived European Ticks von Matuschka, Franz-Rainer, Ohlenbusch, Andreas, Eiffert, Helmut, Richter, Dania, Spielman, Andrew

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Characterization of the mitochondrial genome in childhood multiple sclerosis : III. Multiple sclerosis without optic neuritis and the non-LHON-associated genes von OHLENBUSCH, A, WILICHOWSKI, E, HANEFELD, F

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Amplifying Role of Edible Dormice in Lyme Disease Transmission in Central Europe von Matuschka, Franz-Rainer, Eiffert, Helmut, Ohlenbusch, Andreas, Spielman, Andrew

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Evaluation of the polymerase chain reaction for the detection of Borrelia burgdorferi in cerebrospinal fluid of children with acute peripheral facial palsy von CHRISTEN, H. J, EIFFERT, H, OHLENBUSCH, A, HANEFELD, F

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Nucleotide sequence of the ospAB operon of a Borrelia burgdorferi strain expressing OspA but not OspB von EIFFERT, H, OHLENBUSCH, A, FEHLING, W, LOTTER, H, THOMSSEN, R

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Identical mitochondrial DNA in monozygotic twins with discordant adrenoleukodystrophy phenotype von Wilichowski, Ekkehard, Ohlenbusch, Andreas, Korenke, G. Christoph, Hunneman, Donald H., Hanefeld, Folker

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