Search Results - Güttsches, A.K

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  1. 1
    Generation of a human iPSC line (HIMRi001-A) from a patient with filaminopathy

    Generation of a human iPSC line (HIMRi001-A) from a patient with filaminopathy by Daya, N.M., Mavrommatis, L., Zhuge, H., Athamneh, M., Roos, A., Gläser, D., Doering, K., Zaehres, H., Vorgerd, M., Güttsches, A.K.

    Published in Stem cell research
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  2. 2
    Differential proteomic analysis of abnormal intramyoplasmic aggregates in desminopathy

    Differential proteomic analysis of abnormal intramyoplasmic aggregates in desminopathy by Maerkens, A., Kley, R.A., Olivé, M., Theis, V., van der Ven, P.F.M., Reimann, J., Milting, H., Schreiner, A., Uszkoreit, J., Eisenacher, M., Barkovits, K., Güttsches, A.K., Tonillo, J., Kuhlmann, K., Meyer, H.E., Schröder, R., Tegenthoff, M., Fürst, D.O., Müller, T., Goldfarb, L.G., Vorgerd, M., Marcus, K.

    Published in Journal of proteomics
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  3. 3
    Generation of two induced pluripotent stem cell lines (HIMRi006-A and HIMRi007-A) from Pompe patients with infantile and late disease onset

    Generation of two induced pluripotent stem cell lines (HIMRi006-A and HIMRi007-A) from Pompe patients with infantile and late disease onset by Volke, L., Daya, N.M., Döring, K., Rohm, M., Athamneh, M., Zaehres, H., Roos, A., Güttsches, A.K., Mavrommatis, L., Vorgerd, M.

    Published in Stem cell research
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  4. 4
    Generation of two hiPSCs lines of two patients carrying truncating mutations in the dimerization domain of filamin C

    Generation of two hiPSCs lines of two patients carrying truncating mutations in the dimerization domain of filamin C by Daya, N.M., Döring, K., Zhuge, H., Volke, L., Stab, V., Dietz, J., Athamneh, M., Roos, A., Zaehres, H., Güttsches, A.K., Mavrommatis, L., Vorgerd, M.

    Published in Stem cell research
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  5. 5
    Generation of two human iPSC lines (HIMRi002-A and HIMRi003-A) derived from Caveolinopathy patients with rippling muscle disease

    Generation of two human iPSC lines (HIMRi002-A and HIMRi003-A) derived from Caveolinopathy patients with rippling muscle disease by Boeing, A, Mavrommatis, L, Daya, N M, Zhuge, H, Volke, L, Kocabas, A, Kneifel, M, Athamneh, M, Krause, K, Südkamp, N, Döring, K, Theiss, C, Roos, A, Zaehres, H, Güttsches, A K, Vorgerd, M

    Published in Stem cell research
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  6. 6
    G.P.64

    G.P.64 by Krause, K, Güttsches, A.K, Maerkens, A, Brady, S, Tegenthoff, M, Holton, J, Marcus, K, Vorgerd, M, Kley, R.A

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  7. 7
    P 89 Evaluating correlations of muscle MRI derived fat fractions of leg muscles and clinical outcome measurements in patients with LGMD2A

    P 89 Evaluating correlations of muscle MRI derived fat fractions of leg muscles and clinical outcome measurements in patients with LGMD2A by Forsting, J., Rohm, M., Rehmann, R., Güttsches, A.K., Froeling, M., Tegenthoff, M., Vorgerd, M., Schlaffke, L.

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  8. 8
    G.P.64: Proteomic analysis of rimmed vacuoles in sporadic inclusion body myositis (sIBM)

    G.P.64: Proteomic analysis of rimmed vacuoles in sporadic inclusion body myositis (sIBM) by Krause, K., Güttsches, A.K., Maerkens, A., Brady, S., Tegenthoff, M., Holton, J., Marcus, K., Vorgerd, M., Kley, R.A.

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