Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients
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.
Published in Clinical genetics (01.01.2016)
Published in Clinical genetics (01.01.2016)
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Journal Article
Efficient nitrogen incorporation in GaAs using novel metal organic As–N precursor di-tertiary-butyl-arsano-amine (DTBAA)
Sterzer, E., Beyer, A., Duschek, L., Nattermann, L., Ringler, B., Leube, B., Stegmüller, A., Tonner, R., von Hänisch, C., Stolz, W., Volz, K.
Published in Journal of crystal growth (01.04.2016)
Published in Journal of crystal growth (01.04.2016)
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Journal Article
The ubiquitin pathway in Parkinson's disease
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
Published in Nature (London) (01.10.1998)
Published in Nature (London) (01.10.1998)
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Journal Article
STK11 genotyping and cancer risk in Peutz-Jeghers syndrome
Schumacher, V, Vogel, T, Leube, B, Driemel, C, Goecke, T, Möslein, G, Royer-Pokora, B
Published in Journal of medical genetics (01.05.2005)
Published in Journal of medical genetics (01.05.2005)
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Journal Article
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 D1S443 and D1S197
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
Published in Genomics (San Diego, Calif.) (1996)
Published in Genomics (San Diego, Calif.) (1996)
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Journal Article
Sporadic focal dystonia in northwest Germany: molecular basis on chromosome 18p
Leube, B, Hendgen, T, Kessler, K R, Knapp, M, Benecke, R, Auburger, G
Published in Annals of neurology (01.07.1997)
Published in Annals of neurology (01.07.1997)
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Journal Article
Evidence for DYT7 being a common cause of cervical dystonia (torticollis) in Central Europe
Leube, B, Hendgen, T, Kessler, K R, Knapp, M, Benecke, R, Auburger, G
Published in American journal of medical genetics (19.09.1997)
Published in American journal of medical genetics (19.09.1997)
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Journal Article
Primary torsion dystonia: the search for genes is not over
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
Published in Journal of neurology, neurosurgery and psychiatry (01.09.1999)
Published in Journal of neurology, neurosurgery and psychiatry (01.09.1999)
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Journal Article
Phenotypic variability of the DYT1 mutation in German dystonia patients
Leube, B., Kessler, K. R., Ferbert, A., Ebke, M., Schwendemann, G., Erbguth, F., Benecke, R., Auburger, G.
Published in Acta neurologica Scandinavica (01.04.1999)
Published in Acta neurologica Scandinavica (01.04.1999)
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Journal Article
Modeling gray iron solidification microstructure for prediction of mechanical properties
Leube, B., Arnberg, L.
Published in International journal of cast metals research (Online) (01.05.1999)
Published in International journal of cast metals research (Online) (01.05.1999)
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Journal Article
Satisfaction with Genital Surgery and Sexual Life of Adults with XY Disorders of Sex Development: Results from the German Clinical Evaluation Study
Köhler, Birgit, Kleinemeier, Eva, Lux, Anke, Hiort, Olaf, Grüters, Annette, Thyen, Ute, DSD Network Working Group
Published in The journal of clinical endocrinology and metabolism (01.02.2012)
Published in The journal of clinical endocrinology and metabolism (01.02.2012)
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Journal Article
Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus
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
Published in Neuromuscular disorders : NMD (2001)
Published in Neuromuscular disorders : NMD (2001)
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Journal Article
Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease
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
Published in DNA research (31.12.1998)
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Published in DNA research (31.12.1998)
Journal Article
Idiopathische intrakranielle Hypertension bei einer Patientin mit einem Turner Mosaik der Zelllinie 46,X,i(Xq)
Holtmann, N, Porn, A, Südmeyer, M, Leube, B, Hampl, M, Fehm, T
Published in Geburtshilfe und Frauenheilkunde (13.10.2016)
Published in Geburtshilfe und Frauenheilkunde (13.10.2016)
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Journal Article
Idiopathic Torsion Dystonia: Assignment of a Gene to Chromosome 18p in a German Family With Adult Onset, Autosomal Dominant Inheritance and Purely Focal Distribution
Leube, Barbara, Rudnicki, Doda, Ratzlaff, Tim, Kessler, Kirn R., Benecke, Reiner, Auburger, Georg
Published in Human molecular genetics (01.10.1996)
Published in Human molecular genetics (01.10.1996)
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Journal Article
Idiopathische intrakranielle Hypertension bei einer Patientin mit einem Turner Mosaik der Zelllinie 46,X,i(Xq)
Holtmann, N, Porn, A, Südmeyer, M, Leube, B, Hampl, M, Fehm, T
Published in Geburtshilfe und Frauenheilkunde (13.10.2016)
Published in Geburtshilfe und Frauenheilkunde (13.10.2016)
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