Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients von Rudnik-Schöneborn, S., Tölle, D., Senderek, J., Eggermann, K., Elbracht, M., Kornak, U., von der Hagen, M., Kirschner, J., Leube, B., Müller-Felber, W., Schara, U., von Au, K., Wieczorek, D., Bußmann, C., Zerres, K.

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Efficient nitrogen incorporation in GaAs using novel metal organic As–N precursor di-tertiary-butyl-arsano-amine (DTBAA) von Sterzer, E., Beyer, A., Duschek, L., Nattermann, L., Ringler, B., Leube, B., Stegmüller, A., Tonner, R., von Hänisch, C., Stolz, W., Volz, K.

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The ubiquitin pathway in Parkinson's disease von Leroy, Elisabeth, Boyer, Rebecca, Auburger, Georg, Leube, Barbara, Ulm, Gudrun, Mezey, Eva, Harta, Gyongyi, Brownstein, Michael J, Jonnalagada, Sobhanadditya, Chernova, Tanya, Dehejia, Anindya, Lavedan, Christian, Gasser, Thomas, Steinbach, Peter J, Wilkinson, Keith D, Polymeropoulos, Mihael H

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STK11 genotyping and cancer risk in Peutz-Jeghers syndrome von Schumacher, V, Vogel, T, Leube, B, Driemel, C, Goecke, T, Möslein, G, Royer-Pokora, B

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A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1... von AUBURGER, G, RATZLAFF, T, WITTE, O. W, VOIT, T, LUNKES, A, NELLES, H. W, LEUBE, B, BINKOFSKI, F, KUGEL, H, HEINDEL, W, SEITZ, R, BENECKE, R

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Sporadic focal dystonia in Northwest Germany: Molecular basis on chromosome 18p von Leube, B., Hendgen, T., Kessler, K. R., Knapp, M., Benecke, R., Auburger, G.

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Satisfaction with Genital Surgery and Sexual Life of Adults with XY Disorders of Sex Development: Results from the German Clinical Evaluation Study von Köhler, Birgit, Kleinemeier, Eva, Lux, Anke, Hiort, Olaf, Grüters, Annette, Thyen, Ute, DSD Network Working Group

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Questionable role of adult-onset focal dystonia among sporadic dystonia patients von Leube, B., Auburger, G.

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Evidence for DYT7 being a common cause of cervical dystonia (torticollis) in Central Europe von Leube, B., Hendgen, T., Kessler, K.R., Knapp, M., Benecke, R., Auburger, G.

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Primary torsion dystonia: the search for genes is not over von Jarman, P R, del Grosso, N, Valente, E M, Leube, B, Cassetta, E, Bentivoglio, A R, Waddy, H M, Uitti, R J, Maraganore, D M, Albanese, A, Frontali, M, Auburger, G, Bressman, S B, Wood, N W, Nygaard, T G

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Cloning and tissue expression of two putative steroid membrane receptors von Gerdes, D, Wehling, M, Leube, B, Falkenstein, E

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Idiopathische intrakranielle Hypertension bei einer Patientin mit einem Turner Mosaik der Zelllinie 46,X,i(Xq) von Holtmann, N, Porn, A, Südmeyer, M, Leube, B, Hampl, M, Fehm, T

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Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation von Voit, T, Cohn, R.D, Sperner, J, Leube, B, Sorokin, L, Toda, T, Herrmann, R

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Idiopathic Torsion Dystonia: Assignment of a Gene to Chromosome 18p in a German Family With Adult Onset, Autosomal Dominant Inheritance and Purely Focal Distribution von Leube, Barbara, Rudnicki, Doda, Ratzlaff, Tim, Kessler, Kirn R., Benecke, Reiner, Auburger, Georg

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Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus von Voit, T, Kutz, P, Leube, B, Neuen-Jacob, E, Schröder, J.M, Cavallotti, D, Vaccario, M.L, Schaper, J, Broich, P, Cohn, R, Baethmann, M, Göhlich-Ratmann, G, Scoppetta, C, Herrmann, R

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Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease von Lavedan, C, Buchholtz, S, Auburger, G, Albin, R L, Athanassiadou, A, Blancato, J, Burguera, J A, Ferrell, R E, Kostic, V, Leroy, E, Leube, B, Mota-Vieira, L, Papapetropoulos, T, Pericak-Vance, M A, Pinkus, J, Scott, W K, Ulm, G, Vasconcelos, J, Vilchez, J J, Nussbaum, R L, Polymeropoulos, M H

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Idiopathische intrakranielle Hypertension bei einer Patientin mit einem Turner Mosaik der Zelllinie 46,X,i(Xq) von Holtmann, N, Porn, A, Südmeyer, M, Leube, B, Hampl, M, Fehm, T

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Clinical, cytogenetic, and molecular observations in a patient with Pallister‐Killian‐syndrome with an unusual karyotype von Leube, Barbara, Majewski, Frank, Gebauer, Jürgen, Royer‐Pokora, Brigitte

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Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family von Leube, Barbara, Kessler, Kirn R., Goecke, Timm, Auburger, Georg, Benecke, Reiner

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Refined mapping of allele loss at chromosome 10q23-26 in prostate cancer von Leube, Barbara, Drechsler, Matthias, Mühlmann, Kristina, Schäfer, Reinhold, Schulz, Wolfgang A., Santourlidis, Simon, Anastasiadis, Aristoteles, Ackermann, Rolf, Visakorpi, Tapio, Müller, Wolfram, Royer-Pokora, Brigitte

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