Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease
Gromadzka, G., Schmidt, H.H.-J., Genschel, J., Bochow, B., Rodo, M., Tarnacka, B., Litwin, T., Chabik, G., Członkowska, A.
Published in Clinical genetics (01.12.2005)
Published in Clinical genetics (01.12.2005)
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Journal Article
Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperation
Büning, C., Genschel, J., Bühner, S., Krüger, S., Kling, K., Dignass, A., Baier, P., Bochow, B., Ockenga, J., Schmidt, H. H.‐J., Lochs, H.
Published in Alimentary pharmacology & therapeutics (15.05.2004)
Published in Alimentary pharmacology & therapeutics (15.05.2004)
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Journal Article
Wilson Disease: High Prevalence in a Mountaineous Area of Crete
Dedoussis, G. V. Z., Genschel, J., Sialvera, T‐E., Bochow, B., Manolaki, N., Manios, Y., Tsafantakis, E., Schmidt, H.
Published in Annals of human genetics (01.05.2005)
Published in Annals of human genetics (01.05.2005)
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Journal Article
A R644C mutation within lamin A extends the mutations causing dilated cardiomyopathy
Genschel, Janine, Bochow, Bettina, Kuepferling, Susanne, Ewert, Ralf, Hetzer, Roland, Lochs, Herbert, Schmidt, Hartmut H-J.
Published in Human mutation (01.02.2001)
Published in Human mutation (01.02.2001)
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Journal Article
Three novel mutations (P760L, L1305P, Q1351Stop) causing Wilson disease
Genschel, Janine, Czlonkowska, Anna, Sommer, Grit, Buettner, Carsten, Bochow, Bettina, Lochs, Herbert, Schmidt, Hartmut H-J.
Published in Human mutation (01.02.2001)
Published in Human mutation (01.02.2001)
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Journal Article
Three novel mutations, c314C>A, C778insC, and c1285+2T>A, in exon 2 of the Wilson disease gene
Genschel, Janine, Sommer, Grit, Haas, Regina, Buettner, Carsten, Bochow, Bettina, Manns, Michael, Lochs, Herbert, Schmidt, Hartmut H.-J.
Published in Human mutation (01.09.2000)
Published in Human mutation (01.09.2000)
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Journal Article
p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's disease
Gromadzka, Graznya, Schmidt, Harmut H.J., Genschel, Janine, Bochow, Bettina, Rodo, M., Tarnacka, Beatek, Litwin, Thomas, Chabik, Grzegorz, Członkowska, Anna
Published in Movement disorders (01.02.2006)
Published in Movement disorders (01.02.2006)
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Journal Article
Cooperative and Self-Growing Energy-Aware Networks
Alonistioti, N, Schulz, E, Merentitis, A, Stamatelatos, M, Bochow, B, Ballon, P, Mueck, M, Van der Perre, L, Lewis, T, Chochliouros, I
Published in 2010 7th Annual IEEE Communications Society Conference on Sensor, Mesh and Ad Hoc Communications and Networks (SECON) (01.06.2010)
Published in 2010 7th Annual IEEE Communications Society Conference on Sensor, Mesh and Ad Hoc Communications and Networks (SECON) (01.06.2010)
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Conference Proceeding
Molecular characterization of familial hypercholesterolemia in German and Greek patients
Dedoussis, George V. Z., Genschel, Janine, Bochow, Bettina, Pitsavos, Christos, Skoumas, John, Prassa, Margarita, Lkhagvasuren, Sodnomtsogt, Toutouzas, Pavlos, Vogt, Anja, Kassner, Ursula, Thomas, Hans-P., Schmidt, Hartmut
Published in Human mutation (01.03.2004)
Published in Human mutation (01.03.2004)
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Journal Article
Flexible architecture for spectrum and resource management in the whitespace
Celentano, U., Bochow, B., Herrero, J., Cendon, B., Lange, C., Noack, F., Grondalen, O., Merat, V., Rosik, C.
Published in 2011 The 14th International Symposium on Wireless Personal Multimedia Communications (WPMC) (01.10.2011)
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Published in 2011 The 14th International Symposium on Wireless Personal Multimedia Communications (WPMC) (01.10.2011)
Conference Proceeding
Short Report: Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease
Gromadzka, G, H.H.-J. Schmidt, Genschel, J, Bochow, B, Rodo, M, Tarnacka, B, Litwin, T, Chabik, G, Czlonkowska, A
Published in Clinical genetics (01.12.2005)
Published in Clinical genetics (01.12.2005)
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Journal Article
Wilson disease: high prevalence in a mountainous area of Crete
Dedoussis, G V Z, Genschel, J, Sialvera, T-E, Bochow, B, Manolaki, N, Manios, Y, Tsafantakis, E, Schmidt, H
Published in Annals of human genetics (01.05.2005)
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Published in Annals of human genetics (01.05.2005)
Journal Article
Heterogene Mutationen im ALK1 und ENG Gen verursachen Hereditäre Hämorrhagische Telangiektasie
Ocran, K, Büttner, J, Bochow, B, Wermke, W, Lochs, H, Schmidt, H
Published in Zeitschrift für Gastroenterologie (05.09.2007)
Published in Zeitschrift für Gastroenterologie (05.09.2007)
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Conference Proceeding
Einfluss von Polymorphismen des MDR1-Gens auf Ausbruch und Verlauf chronisch entzündlicher Darmerkrankungen
Fiedler, T, Büning, C, Schmidt, HHJ, Reuter, W, Pitre, G, Genschel, J, Bochow, B, Ockenga, J, Meisel, C, Lochs, H, Roots, I, Koepke, K, Johne, A
Published in Zeitschrift für Gastroenterologie (10.04.2006)
Published in Zeitschrift für Gastroenterologie (10.04.2006)
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Conference Proceeding
The self-growing concept as a design principle of cognitive self-organization
Emmelmann, M., Bochow, B., Makris, A., Kaloxylos, A., Koudouridis, G. P.
Published in 2012 IEEE Globecom Workshops (01.12.2012)
Published in 2012 IEEE Globecom Workshops (01.12.2012)
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Conference Proceeding
Genotypen des Multi-Drug-Resistance-Gens MDR1: Prädiktoren für das Steroidansprechen bei chronisch entzündlichen Darmerkrankungen?
Fiedler, T, Büning, C, Reuter, W, Köpke, K, Bochow, B, Schmidt, H, Genschel, J, Lochs, H, Meisel, C
Published in Zeitschrift für Gastroenterologie (18.08.2004)
Published in Zeitschrift für Gastroenterologie (18.08.2004)
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Conference Proceeding
Multiprocessor implementation of an ATC audio codec
Bochow, B., Czyrnik, B.
Published in International Conference on Acoustics, Speech, and Signal Processing (1989)
Published in International Conference on Acoustics, Speech, and Signal Processing (1989)
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Conference Proceeding