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103 Possible Causes for repp

  • Osteoporosis

    PLoS One. 2009, 4: e7930- PubMed Central PubMed Google Scholar Reppe S, Refvem H, Gautvik VT, Olstad OK, Hovring PI, Reinholt FP, Holden M, Frigessi A, Jemtland R, Gautvik[doi.org]

  • Glycogen Storage Disease due to Aldolase A Deficiency

    PMID 19850718 . a b c d Kreuder J, Borkhardt A, Repp R, Perkrun A, Gottsche B, Gottschalk U, Reichmann H, Schachenmayr W, Schiegel K, Lampert F (1996).[en.wikipedia.org] Journal Biochem Biophys Res Commun 168:677-82 (1990) DOI: 10.1016/0006-291X(90)92374-9 Reference PMID: 8598869 (GSD type XII) Authors Kreuder J, Borkhardt A, Repp R, Pekrun[genome.jp] ., Reinald Repp, M.D., Arnulf Pekrun, M.D., Barbara Göttsche, M.D., Urda Gottschalk, M.D., Heinz Reichmann, M.D., Walter Schachenmayr, M.D., Kurt Schlegel, M.D., and Fritz[nejm.org]

  • Eyebrow Duplication - Syndactyly Syndrome

    […] copy number at REPP and REPD in Family 2 ( Table 1 ).[nature.com] […] extending from REPP in 8p23.1 to introns 5–6 of the DLC1 gene in 8p22 ( Figure 4a ; Table 1 ).[nature.com] […] and REPD and Family 2 having corresponding ‘deletions’ at REPP and REPD using MLPA and array CGH ( Figure 4a and b ).[nature.com]

  • Glycogen Storage Disease due to Hepatic Glycogen Synthase Deficiency

    Journal Biochem Biophys Res Commun 168:677-82 (1990) DOI: 10.1016/0006-291X(90)92374-9 Reference PMID: 8598869 (GSD type XII) Authors Kreuder J, Borkhardt A, Repp R, Pekrun[genome.jp] Kreuder J, Borkhardt A, Repp R, et al. (1996) Inherited metabolic myopathy and hemolysis due to a mutation in aldolase A. New England Journal of Medicine 334: 1100–1110.[els.net] Kreuder J, Borkhardt A, Repp R et al (1996) Brief report: inherited metabolic myopathy and hemolysis due to a mutation in aldolase A.[link.springer.com]

  • Myeloproliferative Disease

    Lanska M , Link H , Ludwig L , Mahlberg R , Löffler LM , Mayer J , Neubauer A , Neuhaus T , Pflüger KH , Pfreundschuh M , Pielken HJ , Possinger K , Reichele A , Reinel HH , Repp[ncbi.nlm.nih.gov] Collaborators (91) Schulz-Abelius A , Friedrichsen K , Repp R , Helm G , Kiani A , Krost A , Thiel E , Baldus C , Possinger K , Kühnhardt D , Görner M , Probst S , Pflüger[ncbi.nlm.nih.gov]

  • Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency

    Journal Biochem Biophys Res Commun 168:677-82 (1990) DOI: 10.1016/0006-291X(90)92374-9 Reference PMID: 8598869 (GSD type XII) Authors Kreuder J, Borkhardt A, Repp R, Pekrun[genome.jp] Kreuder J, Borkhardt A, Repp R, et al. (1996) Inherited metabolic myopathy and hemolysis due to a mutation in aldolase A. New England Journal of Medicine 334: 1100–1110.[els.net] Kreuder J, Borkhardt A, Repp R, Pekrun A, Göttsche B, Gottschalk U; et al. (1996).[wikidoc.org]

  • Cerebral Lipidosis

    In AC Repp & NN Singh (Eds.), Perspectives on the use of nonaversive and aversive interventions for persons with developmental disabilities (pp. 273-286).[books.google.com]

  • Hip Sprain

    Will Repp. -------------------------------- "If it kills you, it kills you"- Bruce Lee Reg Park 3x5 Program..[forum.bodybuilding.com]

  • Glycogen Storage Disease due to Phosphoglycerate Kinase 1 Deficiency

    Journal Biochem Biophys Res Commun 168:677-82 (1990) DOI: 10.1016/0006-291X(90)92374-9 Reference PMID: 8598869 (GSD type XII) Authors Kreuder J, Borkhardt A, Repp R, Pekrun[genome.jp] Kreuder J, Borkhardt A, Repp R, Pekrun A, Göttsche B, Gottschalk U; et al. (1996).[wikidoc.org] Ann Neurol 46:274–277 PubMed Google Scholar [142] Kreuder J, Borkhardt A, Repp R et al. (1996) Inherited metabolic myopathy and hemolysis due to a mutation in aldolase A ([link.springer.com]

  • Trisomy 8q

    […] copy number at REPP and REPD in Family 2 ( Table 1 ).[nature.com] […] extending from REPP in 8p23.1 to introns 5–6 of the DLC1 gene in 8p22 ( Figure 4a ; Table 1 ).[nature.com] […] and REPD and Family 2 having corresponding ‘deletions’ at REPP and REPD using MLPA and array CGH ( Figure 4a and b ).[nature.com]

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