AAAAAA
Results:
1-14
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Results: 14
Authors:
Niemann, S
Becker-Follmann, J
Nurnberg, G
Ruschendorf, F
Sieweke, N
Hugens-Penzel, M
Traupe, H
Wienker, TF
Reis, A
Muller, U
Citation: S. Niemann et al., Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma, AM J MED G, 98(1), 2001, pp. 32-36
Authors:
Laske, C
Oschmann, P
Tofighi, J
Kuhne, BS
Diehl, H
Bregenzer, T
Kraus, J
Chatzimanolis, N
Bauer, R
Traupe, H
Kaps, M
Citation: C. Laske et al., Prognostic value of soluble tumor necrosis factor receptors 1 and 2 in multiple sclerosis patients treated with interferon beta-1b, EUR NEUROL, 46(4), 2001, pp. 210-214
Authors:
Laske, C
Oschmann, P
Tofighi, J
Kuehne, SB
Diehl, H
Bregenzer, T
Kraus, J
Bauer, R
Chatzimanolis, N
Kern, A
Traupe, H
Kaps, M
Citation: C. Laske et al., Induction of sTNF-R1 and sTNF-R2 by interferon beta-1b in correlation withclinical and MRI activity, ACT NEUR SC, 103(2), 2001, pp. 105-113
Authors:
Schmitt-Egenolf, M
Windemuth, C
Hennies, HC
Albis-Camps, M
von Engelhardt, B
Wienker, T
Reis, A
Traupe, H
Blasczyk, R
Citation: M. Schmitt-egenolf et al., Comparative association analysis reveals that corneodesmosin is more closely associated with psoriasis than HLA-Cw0602-B*5701 in German families, TISSUE ANTI, 57(5), 2001, pp. 440-446
Authors:
Traupe, H
Has, C
Citation: H. Traupe et C. Has, The Conradi-Hunermann-Happle syndrome is caused by mutations in the gene that encodes a Delta 8-Delta 7 sterol isomerase and is biochemically relatedto the CHILD syndrome, EUR J DERM, 10(6), 2000, pp. 425-428
Authors:
Has, C
Bruckner-Tuderman, L
Muller, D
Floeth, M
Folkers, E
Donnai, D
Traupe, H
Citation: C. Has et al., The Conradi-Hunermann-Happle syndrome (CDPX2) and emopamil binding protein: novel mutations, and somatic and gonadal mosaicism, HUM MOL GEN, 9(13), 2000, pp. 1951-1955
Authors:
Bork, K
Barnstedt, SE
Koch, P
Traupe, H
Citation: K. Bork et al., Hereditary angioedema and normal C1-inhibitor activity in women - Reply, LANCET, 356(9239), 2000, pp. 1440-1441
Authors:
Bork, K
Barnstedt, SE
Koch, P
Traupe, H
Citation: K. Bork et al., Hereditary angioedema with normal C1-inhibitor activity in women, LANCET, 356(9225), 2000, pp. 213-217
Authors:
Lee, YA
Ruschendorf, F
Windemuth, C
Schmitt-Egenolf, M
Stadelmann, A
Nurnberg, G
Stander, M
Wienker, TF
Reis, A
Traupe, H
Citation: Ya. Lee et al., Genomewide scan in German families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13, AM J HU GEN, 67(4), 2000, pp. 1020-1024
Authors:
Kraus, J
Oschmann, P
Engelhardt, B
Stolz, E
Kuehne, BS
Laske, C
Schaefer, C
Traupe, H
Kaps, M
Citation: J. Kraus et al., CD45RA(+) ICAM-3(+) lymphocytes in cerebrospinal fluid and blood as markers of disease activity in patients with multiple sclerosis, ACT NEUR SC, 102(5), 2000, pp. 326-332
Authors:
Severin, E
Nave, B
Stander, M
Ott, R
Traupe, H
Citation: E. Severin et al., Total antioxidative capacity is normal in sera from psoriasis patients despite elevated bilirubin, tocopherol and urate levels, DERMATOLOGY, 198(4), 1999, pp. 336-339
Authors:
Traupe, H
Citation: H. Traupe, Functional X-chromosomal mosaicism of the skin: Rudolf Happle and the lines of Alfred Blaschko, AM J MED G, 85(4), 1999, pp. 324-329
Authors:
Korge, BP
Hamm, H
Jury, CS
Traupe, H
Irvine, AD
Healy, E
Birch-Machin, M
Rees, JL
Messenger, AG
Holmes, SC
Parry, DAD
Munro, CS
Citation: Bp. Korge et al., Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: Implications for protein structure and clinical phenotype, J INVES DER, 113(4), 1999, pp. 607-612
Authors:
Jacob, N
Ruschendorf, F
Schmitt-Egenolf, M
Hennies, HC
Friedl, G
Stander, M
Wienker, TF
Reis, A
Traupe, H
Citation: N. Jacob et al., Promoter polymorphism at -238 of the tumor necrosis factor alpha gene is not associated with early onset psoriasis when tested by the transmission disequilibrium test, J INVES DER, 112(4), 1999, pp. 514-515
Risultati:
1-14
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