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Hans-Peter Köhler

Leipzig University

21H指数
65论文数
1.4K被引数
收录论文 10
发表时间
A 6-week randomized-controlled field study: effect of isokinetic eccentric resistance training on strength, flexibility and muscle structure of the shoulder external rotators in male junior handball players
err2024-03-07
err0
errOAAI
errVetter, Sebastian; Witt, Maren; Hepp, Pierre; Schleichardt, Axel; Schleifenbaum, Stefan; Roth, Christian; Denecke, Timm; Henkelmann, Jeanette; Koehler, Hans-Peter
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Annular closure in lumbar microdiscectomy for prevention of reherniation: a randomized clinical trial
err2018-12-01
err65
errOAAI
errThome, Claudius; Klassen, Peter Douglas; Bouma, Gerrit Joan; Kursumovic, Adisa; Fandino, Javier; Barth, Martin; Arts, Mark; van den Brink, Wimar; Bostelmann, Richard; Hegewald, Aldemar; Heidecke, Volkmar; Vajkoczy, Peter; Froehlich, Susanne; Wolfs, Jasper; Assaker, Richard; Van de Kelft, Erik; Koehler, Hans-Peter; Jadik, Senol; Eustacchio, Sandro; Hes, Robert; Martens, Frederic
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Identification of two novel missense mutations causing severe factor XIII deficiency
err2015-03-31
err5
PREAI
errHandrkova, H.; Borhany, M.; Schroeder, V.; Fatima, N.; Hussain, A.; Shamsi, T.; Kohler, H. P.
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Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations
err2013-12-16
err14
errOAAI
errBorhany, M.; Handrkova, H.; Cairo, A.; Schroeder, V.; Fatima, N.; Naz, A.; Amanat, S.; Shamsi, T.; Peyvandi, F.; Kohler, H. P.
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Further evidence of heterogeneity of gene defects in Italian families with factor XIII deficiency
err2011-08-04
err8
PREAI
errCastaman, G.; Giacomelli, S. H.; Schroeder, V.; Sanna, S.; Valdre, L.; Morfini, M.; Banov, L.; Kohler, H. P.; Rodeghiero, F.
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Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency
err2010-06-21
err35
PREAI
errIvaskevicius, V.; Biswas, A.; Loreth, R.; Schroeder, V.; Ohlenforst, S.; Rott, H.; Krause, M.; Kohler, H. -P.; Scharrer, I.; Oldenburg, J.
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Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations
err2007-07-12
err26
PREAI
errIvaskevicius, V.; Windyga, J.; Baran, B.; Schroeder, V.; Junen, J.; Bykowska, K.; Seifried, E.; Kohler, H. P.; Oldenburg, J.
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Circulating levels of coagulation factor XIII in subjects with type 2 diabetes and in their first-degree relatives
err2000-05-01
err42
errOAAI
errMansfield, MW; Kohler, HP; Ariëns, RAS; McCormack, LJ; Grant, PJ
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