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Results: 1-25/62
Authors:
Voit, T
Kutz, P
Leube, B
Neuen-Jacob, E
Schroder, JM
Cavallotti, D
Vaccario, ML
Schaper, J
Broich, P
Cohn, R
Baethmann, M
Gohlich-Ratmann, G
Scoppetta, C
Herrmann, R
Citation: T. Voit et al., Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus, NEUROMUSC D, 11(1), 2001, pp. 11-19
Authors:
Mrowietz, U
Koch, WA
Zhu, K
Wiedow, O
Bartels, J
Christophers, E
Schroder, JM
Citation: U. Mrowietz et al., Psoriasis scales contain C5a as the predominant chemotaxin for monocyte-derived dendritic cells, EXP DERMATO, 10(4), 2001, pp. 238-245
Authors:
Dunsche, A
Acil, Y
Siebert, R
Harder, J
Schroder, JM
Jepsen, S
Citation: A. Dunsche et al., Expression profile of human defensins and antimicrobial proteins in oral tissues, J ORAL PATH, 30(3), 2001, pp. 154-158
Authors:
Droste, S
Jorg, J
Lux, G
Sellhaus, B
Schroder, JM
Citation: S. Droste et al., Immunomediated interstitial myositis and aplastic anemia accompanying a benign thymoma, AKT NEUROL, 28(6), 2001, pp. 281-284
Authors:
Bergmann, C
Schroder, JM
Rudnik-Schneborn, S
Zerres, K
Senderek, J
Citation: C. Bergmann et al., A point mutation in the human connexin32 promoter P2 does not correlate with X-linked dominant Charcot-Marie-Tooth neuropathy in Germany, MOL BRAIN R, 88(1-2), 2001, pp. 183-185
Authors:
Paulsen, FP
Pufe, T
Schaudig, U
Held-Feindt, J
Lehmann, J
Schroder, JM
Tillmann, BN
Citation: Fp. Paulsen et al., Detection of natural peptide antibiotics in human nasolacrimal ducts, INV OPHTH V, 42(10), 2001, pp. 2157-2163
Authors:
Senderek, J
Ramaekers, VT
Zerres, K
Rudnik-Schoneborn, S
Schroder, JM
Bergmann, C
Citation: J. Senderek et al., Phenotypic variation of a novel nonsense mutation in the P0 intracellular domain, J NEUR SCI, 192(1-2), 2001, pp. 49-51
Authors:
Sindern, E
Schroder, JM
Krismann, M
Malin, JP
Citation: E. Sindern et al., Inflammatory polyradiculoneuropathy with spinal cord involvement and letaloutcome after hepatitis B vaccination, J NEUR SCI, 186(1-2), 2001, pp. 81-85
Authors:
Vielhaber, S
Schroder, R
Winkler, K
Weis, S
Sailer, M
Feistner, H
Heinze, HJ
Schroder, JM
Kunz, WS
Citation: S. Vielhaber et al., Defective mitochondrial oxidative phosphorylation in myopathies with tubular aggregates originating from sarcoplasmic reticulum, J NE EXP NE, 60(11), 2001, pp. 1032-1040
Authors:
Harder, J
Bartels, J
Christophers, E
Schroder, JM
Citation: J. Harder et al., Isolation and characterization of human beta-defensin-3, a novel human inducible peptide antibiotic, J BIOL CHEM, 276(8), 2001, pp. 5707-5713
Authors:
Mawrin, C
Schutz, G
Schroder, JM
Citation: C. Mawrin et al., Correlation between the number of epineurial and endoneurial blood vesselsin diseased human sural nerves, ACT NEUROP, 102(4), 2001, pp. 364-372
Authors:
Muller, HD
Vielhaber, S
Brunn, A
Schroder, JM
Citation: Hd. Muller et al., Dominantly inherited myopathy with novel tubular aggregates containing 1-21 tubulofilamentous structures, ACT NEUROP, 102(1), 2001, pp. 27-35
Authors:
De Bleecker, JL
Meire, VI
Van Walleghem, IE
Groessens, IM
Schroder, JM
Citation: Jl. De Bleecker et al., Immunolocalization of FAS and FAS ligand in inflammatory myopathies, ACT NEUROP, 101(6), 2001, pp. 572-578
Authors:
Meyer, JE
Harder, J
Gorogh, T
Schroder, JM
Maune, S
Citation: Je. Meyer et al., hBD-2-gene expression in nasal mucosa., LARY RH OTO, 79(7), 2000, pp. 400-403
Authors:
Schroder, JM
Wiegand, S
Citation: Jm. Schroder et S. Wiegand, Experimental suppression of multiple scattering: Effect on dynamic and static scattering data, PHYS CHEM P, 2(7), 2000, pp. 1493-1495
Authors:
Muller, HD
Mugler, M
Ramaekers, VT
Schroder, JM
Citation: Hd. Muller et al., Hereditary motor and sensory neuropathy with absence of large myelinated fibers due to absence of large neurons in dorsal root ganglia and anterior horns, clinically associated with deafness, mental retardation, and epilepsy(HMSN-ADM), J PERIPH N, 5(3), 2000, pp. 147-157
Authors:
Harder, J
Meyer-Hoffert, U
Teran, LM
Schwichtenberg, L
Bartels, J
Maune, S
Schroder, JM
Citation: J. Harder et al., Mucoid Pseudomonas aeruginosa, TNF-alpha, and IL-1 beta, but not IL-6, induce human beta-defensin-2 in respiratory epithelia, AM J RESP C, 22(6), 2000, pp. 714-721
Authors:
Zimpfer, U
Dichmann, S
Termeer, CC
Simon, JC
Schroder, JM
Norgauer, J
Citation: U. Zimpfer et al., Human dendritic cells are a physiological source of the chemotactic arachidonic acid metabolite 5-oxo-eicosatetraenoic acid, INFLAMM RES, 49(11), 2000, pp. 633-638
Authors:
Senderek, J
Hermanns, B
Lehmann, U
Bergmann, C
Marx, G
Kabus, C
Timmerman, V
Stoltenburg-Didinger, G
Schroder, JM
Citation: J. Senderek et al., Charcot-Marie-Tooth neuropathy type 2 and P0 point mutations: Two novel amino acid substitutions (Asp61Gly; Tyr119Cys) and a possible "hotspot" on Thr124Met, BRAIN PATH, 10(2), 2000, pp. 235-248
Authors:
Nickoloff, BJ
Schroder, JM
von den Driesch, P
Raychaudhuri, SP
Farber, EM
Boehncke, WH
Morhenn, VB
Rosenberg, EW
Schon, MP
Holick, MF
Citation: Bj. Nickoloff et al., Is psoriasis a T-cell disease?, EXP DERMATO, 9(5), 2000, pp. 359-363
Authors:
Schroder, JM
Citation: Jm. Schroder, Is psoriasis a T-cell disease? Viewpoint 2, EXP DERMATO, 9(5), 2000, pp. 363-366
Authors:
Schroder, JM
Citation: Jm. Schroder, Chemoattractants as mediators of neutrophilic tissue recruitment, CLIN DERMAT, 18(3), 2000, pp. 245-263
Authors:
Beckmann, A
Schroder, JM
Citation: A. Beckmann et Jm. Schroder, Recessive PMP22 mutations: Quantitative and qualitative aspects, ANN NEUROL, 48(1), 2000, pp. 131-132
Authors:
Ziemssen, F
Sindern, E
Schroder, JM
Shin, YS
Zange, JH
Kilimann, MW
Malin, JP
Vorgerd, M
Citation: F. Ziemssen et al., Novel missense mutations in the glycogen-branching enzyme gene in adult polyglucosan body disease, ANN NEUROL, 47(4), 2000, pp. 536-540
Authors:
Thomas, PK
King, RHM
Workman, JM
Schroder, JM
Citation: Pk. Thomas et al., Hypertrophic perineurial dysplasia in multifocal and generalized peripheral neuropathies, NEUROP AP N, 26(6), 2000, pp. 536-543