Dexrazoxane prevents doxorubicin‐induced long‐term cardiotoxicity and protects myocardial mitochondria from genetic and functional lesions in rats
Lebrecht, D, Geist, A, Ketelsen, U‐P, Haberstroh, J, Setzer, B, Walker, U A
Published in British journal of pharmacology (01.07.2007)
Published in British journal of pharmacology (01.07.2007)
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Journal Article
Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region
Korinthenberg, R, Sauer, M, Ketelsen, U P, Hanemann, C O, Stoll, G, Graf, M, Baborie, A, Volk, B, Wirth, B, Rudnik-Schöneborn, S, Zerres, K
Published in Annals of neurology (01.09.1997)
Published in Annals of neurology (01.09.1997)
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Journal Article
Long-term observations of patients with infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1)
Rudnik-Schöneborn, S, Stolz, P, Varon, R, Grohmann, K, Schächtele, M, Ketelsen, U-P, Stavrou, D, Kurz, H, Hübner, C, Zerres, K
Published in Neuropediatrics (01.06.2004)
Published in Neuropediatrics (01.06.2004)
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Journal Article
Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy
Rudnik-Schöneborn, S, Goebel, H H, Schlote, W, Molaian, S, Omran, H, Ketelsen, U, Korinthenberg, R, Wenzel, D, Lauffer, H, Kreiss-Nachtsheim, M, Wirth, B, Zerres, K
Published in Neurology (25.03.2003)
Published in Neurology (25.03.2003)
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Journal Article
Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients
Kley, Rudolf A., Hellenbroich, Yorck, van der Ven, Peter F. M., Fürst, Dieter O., Huebner, Angela, Bruchertseifer, Vera, Peters, Sören A., Heyer, Christoph M., Kirschner, Janbernd, Schröder, Rolf, Fischer, Dirk, Müller, Klaus, Tolksdorf, Karen, Eger, Katharina, Germing, Alfried, Brodherr, Turgut, Reum, Conny, Walter, Maggie C., Lochmüller, Hanns, Ketelsen, Uwe-Peter, Vorgerd, Matthias
Published in Brain (London, England : 1878) (01.12.2007)
Published in Brain (London, England : 1878) (01.12.2007)
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Journal Article
Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot–Marie–Tooth neuropathy type 4B2/11p15
Senderek, Jan, Bergmann, Carsten, Weber, Susanne, Ketelsen, Uwe-Peter, Schorle, Hubert, Rudnik-Schöneborn, Sabine, Büttner, Reinhard, Buchheim, Eckhard, Zerres, Klaus
Published in Human molecular genetics (01.02.2003)
Published in Human molecular genetics (01.02.2003)
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Journal Article
Homozygosity Mapping of a Gene Locus for Primary Ciliary Dyskinesia on Chromosome 5p and Identification of the Heavy Dynein Chain DNAH5 as a Candidate Gene
Omran, Heymut, Haffner, Karsten, Volkel, Alexander, Kuehr, Joachim, Ketelsen, Uwe-Peter, Ross, Uwe-Henning, Konietzko, Nikolaus, Wienker, Thomas, Brandis, Matthias, Hildebrandt, Friedhelm
Published in American journal of respiratory cell and molecular biology (01.11.2000)
Published in American journal of respiratory cell and molecular biology (01.11.2000)
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Journal Article
Identification of a novel LAMP2 mutation responsible for X-chromosomal dominant Danon disease
Horváth, J, Ketelsen, U-P, Geibel-Zehender, A, Boehm, N, Olbrich, H, Korinthenberg, R, Omran, H
Published in Neuropediatrics (01.10.2003)
Published in Neuropediatrics (01.10.2003)
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Journal Article
Genotype-phenotype correlations in PCD patients carrying DNAH5 mutations
Kispert, A, Petry, M, Olbrich, H, Volz, A, Ketelsen, U-P, Horvath, J, Melkaoui, R, Omran, H, Zariwala, M, Noone, P G, Knowles, M
Published in Thorax (01.06.2003)
Published in Thorax (01.06.2003)
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Journal Article
Congenital myopathy with arrest of myogenesis prior to formation of myotubes
Ketelsen, U-P, Brand-Saberi, B, Uhlenberg, B, Wagner, M, Laberke, H-G, Omran, H
Published in Neuropediatrics (01.08.2005)
Published in Neuropediatrics (01.08.2005)
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Journal Article
Evidence of nucleoside analogue reverse transcriptase inhibitor--associated genetic and structural defects of mitochondria in adipose tissue of HIV-infected patients
Walker, Ulrich A, Bickel, Markus, Lütke Volksbeck, Severine I, Ketelsen, Uwe-Peter, Schöfer, Helmut, Setzer, Bernhard, Venhoff, Nils, Rickerts, Volker, Staszewski, Schlomo
Published in Journal of acquired immune deficiency syndromes (1999) (01.02.2002)
Published in Journal of acquired immune deficiency syndromes (1999) (01.02.2002)
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Journal Article
Motor unit involvement in spastic paresis: Relationship between leg muscle activation and histochemistry
Dietz, V., Ketelsen, U.-P., Berger, W., Quintern, J.
Published in Journal of the neurological sciences (01.08.1986)
Published in Journal of the neurological sciences (01.08.1986)
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Journal Article
Abundant minute myotubes in a patient who later developed centronuclear myopathy
WÖCKEL, L, KETELSEN, U.-P, STÖTTER, M, LAULE, S, MEYERMANN, R, BORNEMANN, A
Published in Acta neuropathologica (01.05.1998)
Published in Acta neuropathologica (01.05.1998)
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Journal Article
Phenotypic variability in two brothers with sarcotubular myopathy
Müller-Felber, W, Schlotter, B, Töpfer, M, Ketelsen, U P, Müller-Höcker, J, Pongratz, D
Published in Journal of neurology (01.05.1999)
Published in Journal of neurology (01.05.1999)
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Journal Article
3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndrome
Klopstock, T, Bischof, F, Gerok, K, Deuschl, G, Seibel, P, Ketelsen, U P, Reichmann, H
Published in Acta neuropathologica (01.08.1995)
Published in Acta neuropathologica (01.08.1995)
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Journal Article
Rare combination of Becker muscular dystrophy and Klinefelter's syndrome in one patient
Zeitoun, Omeima, Ketelsen, Uwe-Peter, Wolff, Gerhard, Müller, Clemens R., Korinthenberg, Rudolf
Published in Brain & development (Tokyo. 1979) (01.07.1997)
Published in Brain & development (Tokyo. 1979) (01.07.1997)
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Journal Article
Conference Proceeding
Diagnosis of idiopathic myositis : value of 99mtechnetium pyrophosphate muscle scintigraphy and magnetic resonance imaging in targeted muscle biopsy
VON KEMPIS, J, KALDEN, P, PETER, H. H, GUTFLEISCH, J, GRIMBACHER, B, KRAUSE, T, UHL, M, KETELSEN, U.-P, VOLK, B, RÖTHER, E, VAITH, P
Published in Rheumatology international (1998)
Published in Rheumatology international (1998)
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