Who gets dipyrone (metamizole) in Germany? Prescribing by age, sex and region von Hoffmann, F., Meinecke, P., Freitag, M. H., Glaeske, G., Schulze, J., Schmiemann, G.

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Concomitant Retroperitoneal and Subarachnoid Hemorrhage Due to Segmental Arterial Mediolysis: Case Report and Review of the Literature von Hellstern, V., Aguilar Pérez, M., Kohlhof-Meinecke, P., Bäzner, H., Ganslandt, O., Henkes, H.

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Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene von Nagy, R, Wang, H, Albrecht, B, Wieczorek, D, Gillessen- Kaesbach, G, Haan, E, Meinecke, P, de la Chapelle, A, Westman, JA

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Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome von Schulz, AL, Albrecht, B, Arici, C, Van Der Burgt, I, Buske, A, Gillessen-Kaesbach, G, Heller, R, Horn, D, Hübner, CA, Korenke, GC, König, R, Kress, W, Krüger, G, Meinecke, P, Mücke, J, Plecko, B, Rossier, E, Schinzel, A, Schulze, A, Seemanova, E, Seidel, H, Spranger, S, Tuysuz, B, Uhrig, S, Wieczorek, D, Kutsche, K, Zenker, M

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Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation von Morava, E, Lefeber, D J, Urban, Z, de Meirleir, L, Meinecke, P, Gillessen Kaesbach, G, Sykut-Cegielska, J, Adamowicz, M, Salafsky, I, Ranells, J, Lemyre, E, van Reeuwijk, J, Brunner, H G, Wevers, R A

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Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndrome von Seifert, W, Holder-Espinasse, M, Spranger, S, Hoeltzenbein, M, Rossier, E, Dollfus, H, Lacombe, D, Verloes, A, Chrzanowska, K H, Maegawa, G H B, Chitayat, D, Kotzot, D, Huhle, D, Meinecke, P, Albrecht, B, Mathijssen, I, Leheup, B, Raile, K, Hennies, H C, Horn, D

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Concomitant Retroperitoneal and Subarachnoid Hemorrhage Due to Segmental Arterial Mediolysis von Hellstern, V, Aguilar Pérez, M, Kohlhof-Meinecke, P, Bäzner, H, Ganslandt, O, Henkes, H

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Location and type of mutation in the LIS1 gene do not predict phenotypic severity von UYANIK, G, MORRIS-ROSENDAHL, D. J, SCHREYER, I, HERTZBERG, C, NEUMANN, T. E, BURKART, P, SPAICH, C, MENG, M, HOLTHAUSEN, H, ADES, L, SEIDEL, J, MANGOLD, E, STIEGLER, J, BUYSE, G, MEINECKE, P, SCHARA, U, ZESCHNIGK, C, MULLER, D, HELLAND, G, SCHULZE, B, WRIGHT, M. L, KORTGE-JUNG, S, HEHR, A, KLAPECKI, J, BOGDAHN, U, SCHUIERER, G, KOHLHASE, J, AIGNER, L, WOLFF, G, HEHR, U, WINKLER, J, GROSS, C, BERMAN, Y, MARTIN, P, DEY, L, SPRANGER, S, KORENKE, G. C

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Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP von Bartsch, O, Locher, K, Meinecke, P, Kress, W, Seemanová, E, Wagner, A, Ostermann, K, Rödel, G

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Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations von Zenker, Martin, Lehmann, Katarina, Schulz, Anna Leana, Barth, Helmut, Hansmann, Dagmar, Koenig, Rainer, Korinthenberg, Rudolf, Kreiss-Nachtsheim, Martina, Meinecke, Peter, Morlot, Susanne, Mundlos, Stefan, Quante, Anne S, Raskin, Salmo, Schnabel, Dirk, Wehner, Lars-Erik, Kratz, Christian P, Horn, Denise, Kutsche, Kerstin

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Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS) von WIECZOREK, DAGMAR, KRAUSE, MARIO, MAJEWSKI, FRANK, ALBRECHT, BEATE, MEINECKE, PETER, RIESS, OLAF, GILLESSEN-KAESBACH, GABRIELE

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Assignment of an autosomal sex reversa- locus ( SRA1 ) and campomelic dysplasia ( CMPD1 ) to 17q24.3-q25.1 von Schempp, W, Westvik, J, Pedersen, S, Goodpasture, C, Held, K.R, Tommerup, N, Reinwein, H, Wolf, U, Brandt, C, Scherer, G, Bolund, L, van der Hagen, C.B, Saugstad, O.D, Skjeldal, O, Meinecke, P, Guldberg, P, Toder, R

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Mutations of the Mitochondrial Holocytochrome c–Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome von Wimplinger, Isabella, Morleo, Manuela, Rosenberger, Georg, Iaconis, Daniela, Orth, Ulrike, Meinecke, Peter, Lerer, Israela, Ballabio, Andrea, Gal, Andreas, Franco, Brunella, Kutsche, Kerstin

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SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome von Zenker, Martin, Horn, Denise, Wieczorek, Dagmar, Allanson, Judith, Pauli, Silke, van der Burgt, Ineke, Doerr, Helmuth-Guenther, Gaspar, Harald, Hofbeck, Michael, Gillessen-Kaesbach, Gabriele, Koch, Andreas, Meinecke, Peter, Mundlos, Stefan, Nowka, Anja, Rauch, Anita, Reif, Silke, von Schnakenburg, Christian, Seidel, Heide, Wehner, Lars-Erik, Zweier, Christiane, Bauhuber, Susanne, Matejas, Verena, Kratz, Christian P, Thomas, Christoph, Kutsche, Kerstin

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Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions on the short arm... von BARTSCH, O, WIM WUYTS, SHAFFER, L. G, WILLEMS, P. J, VAN HUL, W, HECHT, J. T, MEINECKE, P, HOGUE, D, WERNER, W, ZABEL, B, HINKEL, G. K, POWELL, C. M

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Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination von Elledge, Stephen J, Ades, Lesley, Roessler, Erich, Massagué, Joan, Wotton, David, Edwards, Michael C, Meinecke, Peter, Gripp, Karen W, Richieri-Costa, Antonio, Zackai, Elaine H, Muenke, Maximilian

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Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I von Glöckner, Gernot, Momeni, Parastoo, Albrecht, Beate, Lüdecke, Hermann-Josef, Zabel, Bernhard, Gillessen-Kaesbach, Gabriele, Schmidt, Olaf, Meinecke, Peter, Rosenthal, André, Hennekam, Raoul, von Holtum, Diane, Horsthemke, Bernhard

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Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of Xp von Kutsche, K., Werner, W., Bartsch, O., von der Wense, A., Meinecke, P., Gal, A.

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Genes and chromosomal breakpoints in the Langer-Giedion syndrome region on human chromosome 8 von LÜDECKE, H.-J, SCHMIDT, O, NARDMANN, J, VON HOLTUM, D, MEINECKE, P, MUENKE, M, HORSTHEMKE, B

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Oculo-auriculo-vertebral spectrum (OAVS): clinical evaluation and severity scoring of 53 patients and proposal for a new classification von Tasse, Christiane, Böhringer, Stefan, Fischer, Sven, Lüdecke, Hermann-Josef, Albrecht, Beate, Horn, Denise, Janecke, Andreas, Kling, Rainer, König, Rainer, Lorenz, Birgit, Majewski, Frank, Maeyens, Elisabeth, Meinecke, Peter, Mitulla, Beate, Mohr, Christopher, Preischl, Monika, Umstadt, Horst, Kohlhase, Jürgen, Gillessen-Kaesbach, Gabriele, Wieczorek, Dagmar

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