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Results:
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Results: 22
Authors:
Heller, D
Schneider, U
Seifert, J
Cimander, KF
Stuhrmann, M
Citation: D. Heller et al., The cannabinoid receptor gene (CNR1) is not affected in German i.v. drug users, ADDICT BIOL, 6(2), 2001, pp. 183-187
Authors:
Ahmed, M
Stuhrmann, M
Bashawri, L
Kuhnau, W
El-Harith, EHA
Citation: M. Ahmed et al., The beta-globin genotype E121Q/W15X (cd121GAA -> CAA/cd15TGG -> TGA) underlines Hb D/beta-(0) thalassaemia marked by domination of haemoglobin D, ANN HEMATOL, 80(11), 2001, pp. 629-633
Authors:
Stuhrmann, M
Schwarz, T
Schietzel, M
Citation: M. Stuhrmann et al., Scar versus recurrence in breast cancer: Differentiation by contrast enhanced colour Doppler ultrasound, ULTRASC MED, 22(1), 2001, pp. 2-6
Authors:
Ockenga, J
Dork, T
Stuhrmann, M
Citation: J. Ockenga et al., Low prevalence of SPINK1 gene mutations in adult patients with chronic idiopathic pancreatitis, J MED GENET, 38(4), 2001, pp. 243-244
Authors:
Hughes, D
Dork, T
Stuhrmann, M
Graham, C
Citation: D. Hughes et al., Mutation and haplotype analysis of the CFTR gene in atypically mild cysticfibrosis patients from Northern Ireland, J MED GENET, 38(2), 2001, pp. 136-139
Authors:
Ockenga, J
Stuhrmann, M
Manns, MP
Citation: J. Ockenga et al., Evaluation of the role of CFTR in alcohol related pancreatic disease, GUT, 49(2), 2001, pp. 312-312
Authors:
Dork, T
Bendix, R
Bremer, M
Rades, D
Klopper, K
Nicke, M
Skawran, B
Hector, A
Yamini, P
Steinmann, D
Weise, S
Stuhrmann, M
Karstens, JH
Citation: T. Dork et al., Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patients, CANCER RES, 61(20), 2001, pp. 7608-7615
Authors:
Stuhrmann, M
Bashawri, L
Ahmed, MA
Al-Awamy, BH
Kuhnau, W
Schmidtke, J
El-Harith, EA
Citation: M. Stuhrmann et al., Familial thrombocytosis as a recessive, possibly X-linked trait in an Arabfamily, BR J HAEM, 112(3), 2001, pp. 616-620
Authors:
Langen, H
von Kietzell, D
Byrd, D
Arslan-Kirchner, M
Vester, U
Stuhrmann, M
Dork, T
Saar, K
Reis, A
Schmidtke, J
Brodehl, J
Citation: H. Langen et al., Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria, PED NEPHROL, 14(5), 2000, pp. 376-384
Authors:
Schneider, U
Muller-Vahl, KR
Stuhrmann, M
Gadzicki, D
Heller, D
Seifert, J
Emrich, HM
Citation: U. Schneider et al., The importance of the endogenous cannabinoid system in various neuropsychiatric disorders, F NEUR PSYC, 68(10), 2000, pp. 433-438
Authors:
Stuhrmann, M
Aronius, R
Schietzel, M
Citation: M. Stuhrmann et al., Tumor vascularity of breast lesions: Potentials and limits of contrast-enhanced Doppler sonography, AM J ROENTG, 175(6), 2000, pp. 1585-1589
Authors:
Dork, T
Macek, M
Mekus, F
Tummler, B
Tzountzouris, J
Casals, T
Krebsova, A
Koudova, M
Sakmaryova, I
Macek, M
Vavrova, V
Zemkova, D
Ginter, E
Petrova, NV
Ivaschenko, T
Baranov, V
Witt, M
Pogorzelski, A
Bal, J
Zekanowsky, C
Wagner, K
Stuhrmann, M
Bauer, I
Seydewitz, HH
Neumann, T
Jakubiczka, S
Kraus, C
Thamm, B
Nechiporenko, M
Livshits, L
Mosse, N
Tsukerman, G
Kadasi, L
Ravnik-Glavac, M
Glavac, D
Komel, R
Vouk, K
Kucinskas, V
Krumina, A
Teder, M
Kocheva, S
Efremov, GD
Onay, T
Kirdar, B
Malone, G
Schwarz, M
Zhou, ZQ
Friedman, KJ
Carles, S
Claustres, M
Bozon, D
Verlingue, C
Ferec, C
Tzetis, M
Kanavakis, E
Cuppens, H
Bombieri, C
Pignatti, PF
Sangiuolo, F
Jordanova, A
Kusic, J
Radojkovic, D
Sertic, J
Richter, D
Rukavina, AS
Bjorck, E
Strandvik, B
Cardoso, H
Montgomery, M
Nakielna, B
Hughes, D
Estivill, X
Aznarez, I
Tullis, E
Tsui, LC
Zielenski, J
Citation: T. Dork et al., Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe, HUM GENET, 106(3), 2000, pp. 259-268
Authors:
Stuhrmann, M
Graf, N
Dork, T
Schmidtke, J
Citation: M. Stuhrmann et al., Mutation screening for prenatal and presymptomatic diagnosis: cystic fibrosis and haemochromatosis, EUR J PED, 159, 2000, pp. S186-S191
Authors:
Stuhrmann, M
Dork, T
Citation: M. Stuhrmann et T. Dork, CFTR gene mutations and male infertility, ANDROLOGIA, 32(2), 2000, pp. 71-83
Authors:
Ockenga, J
Stuhrmann, M
Ballmann, M
Teich, N
Keim, V
Dork, T
Manns, MP
Citation: J. Ockenga et al., Mutations of the cystic fibrosis gene, but not cationic trypsinogen gene, are associated with recurrent or chronic idiopathic pancreatitis, AM J GASTRO, 95(8), 2000, pp. 2061-2067
Authors:
Sandoval, N
Platzer, M
Rosenthal, A
Dork, T
Bendix, R
Skawran, B
Stuhrmann, M
Wegner, RD
Sperling, K
Banin, S
Shiloh, Y
Baumer, A
Bernthaler, U
Sennefelder, H
Brohm, M
Weber, BHF
Schindler, D
Citation: N. Sandoval et al., Characterization of ATM gene mutations in 66 ataxia telangiectasia families, HUM MOL GEN, 8(1), 1999, pp. 69-79
Authors:
Gadzicki, D
Muller-Vahl, K
Stuhrmann, M
Citation: D. Gadzicki et al., A frequent polymorphism in the coding exon of the human cannabinoid receptor (CNR1) gene, MOL CELL PR, 13(4), 1999, pp. 321-323
Authors:
El-Harith, EA
Al-Kharasani, M
Ahmed, MA
Stuhrmann, M
Citation: Ea. El-harith et al., Hereditary hemorrhagic telangiectasia: A case report, SAUDI MED J, 20(10), 1999, pp. 797-799
Authors:
Backe, J
Hofferbert, S
Skawran, B
Dork, T
Stuhrmann, M
Karstens, JH
Untch, M
Meindl, A
Burgemeister, R
Chang-Claude, J
Weber, BHF
Citation: J. Backe et al., Frequency of BRCA1 mutation 5382insC in German breast cancer patients, GYNECOL ONC, 72(3), 1999, pp. 402-406
Authors:
Dork, T
Skawran, B
Stuhrmann, M
Bremer, M
Karstens, JH
Citation: T. Dork et al., BRCA1 expression is not affected by the intronic 12 bp duplication, J MED GENET, 36(3), 1999, pp. 262-263
Authors:
El-Harith, EA
Kuhnau, W
Schmidtke, J
Stuhrmann, M
Nasserallah, Z
Al-Shahri, A
Citation: Ea. El-harith et al., Identification and clinical presentation of beta thalassaemia mutations inthe eastern region of Saudi Arabia, J MED GENET, 36(12), 1999, pp. 935-937
Authors:
Stuhrmann, M
von der Hardt, H
Fabel, H
Citation: M. Stuhrmann et al., Cystic fibrosis - Also a disease in adults, INTERNIST, 40(5), 1999, pp. 476-485
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