Cryo-EM reveals structural breaks in a patient-derived amyloid fibril from systemic AL amyloidosis von Radamaker, Lynn, Baur, Julian, Huhn, Stefanie, Haupt, Christian, Hegenbart, Ute, Schönland, Stefan, Bansal, Akanksha, Schmidt, Matthias, Fändrich, Marcus

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Cryo-EM structure of a light chain-derived amyloid fibril from a patient with systemic AL amyloidosis von Radamaker, Lynn, Lin, Yin-Hsi, Annamalai, Karthikeyan, Huhn, Stefanie, Hegenbart, Ute, Schönland, Stefan O., Fritz, Günter, Schmidt, Matthias, Fändrich, Marcus

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Prognosis and Staging of AL Amyloidosis von Dittrich, Tobias, Kimmich, Christoph, Hegenbart, Ute, Schönland, Stefan O.

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Role of mutations and post-translational modifications in systemic AL amyloidosis studied by cryo-EM von Radamaker, Lynn, Karimi-Farsijani, Sara, Andreotti, Giada, Baur, Julian, Neumann, Matthias, Schreiner, Sarah, Berghaus, Natalie, Motika, Raoul, Haupt, Christian, Walther, Paul, Schmidt, Volker, Huhn, Stefanie, Hegenbart, Ute, Schönland, Stefan O., Wiese, Sebastian, Read, Clarissa, Schmidt, Matthias, Fändrich, Marcus

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Analysis of the complete lambda light chain germline usage in patients with AL amyloidosis and dominant heart or kidney involvement von Berghaus, Natalie, Schreiner, Sarah, Granzow, Martin, Müller-Tidow, Carsten, Hegenbart, Ute, Schönland, Stefan O, Huhn, Stefanie

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New Criteria for Response to Treatment in Immunoglobulin Light Chain Amyloidosis Based on Free Light Chain Measurement and Cardiac Biomarkers: Impact on Survival Outcomes von PALLADINI, Giovanni, DISPENZIERI, Angela, DIMOPOULOS, Meletios A, JACCARD, Arnaud, KLERSY, Catherine, MERLINI, Giampaolo, GERTZ, Morie A, KUMAR, Shaji, WECHALEKAR, Ashutosh, HAWKINS, Philip N, SCHÖNLAND, Stefan, HEGENBART, Ute, COMENZO, Raymond, KASTRITIS, Efstathios

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Systemic immunoglobulin light chain amyloidosis von Merlini, Giampaolo, Dispenzieri, Angela, Sanchorawala, Vaishali, Schönland, Stefan O., Palladini, Giovanni, Hawkins, Philip N., Gertz, Morie A.

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Translocation t(11;14) is associated with adverse outcome in patients with newly diagnosed AL amyloidosis when treated with bortezomib-based regimens von Bochtler, Tilmann, Hegenbart, Ute, Kunz, Christina, Granzow, Martin, Benner, Axel, Seckinger, Anja, Kimmich, Christoph, Goldschmidt, Hartmut, Ho, Anthony D, Hose, Dirk, Jauch, Anna, Schönland, Stefan O

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AL amyloidosis patients with low amyloidogenic free light chain levels at first diagnosis have an excellent prognosis von Dittrich, Tobias, Bochtler, Tilmann, Kimmich, Christoph, Becker, Natalia, Jauch, Anna, Goldschmidt, Hartmut, Ho, Anthony D., Hegenbart, Ute, Schönland, Stefan O.

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A phase 1/2 study of the oral proteasome inhibitor ixazomib in relapsed or refractory AL amyloidosis von Sanchorawala, Vaishali, Palladini, Giovanni, Kukreti, Vishal, Zonder, Jeffrey A., Cohen, Adam D., Seldin, David C., Dispenzieri, Angela, Jaccard, Arnaud, Schönland, Stefan O., Berg, Deborah, Yang, Huyuan, Gupta, Neeraj, Hui, Ai-Min, Comenzo, Raymond L., Merlini, Giampaolo

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A staging system for renal outcome and early markers of renal response to chemotherapy in AL amyloidosis von Palladini, Giovanni, Hegenbart, Ute, Milani, Paolo, Kimmich, Christoph, Foli, Andrea, Ho, Anthony D., Rosin, Marta Vidus, Albertini, Riccardo, Moratti, Remigio, Merlini, Giampaolo, Schönland, Stefan

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Venetoclax induces deep hematologic remissions in t(11;14) relapsed/refractory AL amyloidosis von Premkumar, Vikram J., Lentzsch, Suzanne, Pan, Samuel, Bhutani, Divaya, Richter, Joshua, Jagannath, Sundar, Liedtke, Michaela, Jaccard, Arnaud, Wechalekar, Ashutosh D., Comenzo, Raymond, Sanchorawala, Vaishali, Royer, Bruno, Rosenzweig, Michael, Valent, Jason, Schönland, Stefan, Fonseca, Rafael, Wong, Sandy, Kapoor, Prashant

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Clarification on the definition of complete haematologic response in light-chain (AL) amyloidosis von Palladini, Giovanni, Schoenland, Stefan O., Sanchorawala, Vaishali, Kumar, Shaji, Wechalekar, Ashutosh, Hegenbart, Ute, Milani, Paolo, Ando, Yukio, Westermark, Per, Dispenzieri, Angela, Merlini, Giampaolo

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Light chain mutations contribute to defining the fibril morphology in systemic AL amyloidosis von Karimi-Farsijani, Sara, Pfeiffer, Peter Benedikt, Banerjee, Sambhasan, Baur, Julian, Kuhn, Lukas, Kupfer, Niklas, Hegenbart, Ute, Schönland, Stefan O., Wiese, Sebastian, Haupt, Christian, Schmidt, Matthias, Fändrich, Marcus

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Common transthyretin-derived amyloid fibril structures in patients with hereditary ATTR amyloidosis von Steinebrei, Maximilian, Baur, Julian, Pradhan, Anaviggha, Kupfer, Niklas, Wiese, Sebastian, Hegenbart, Ute, Schönland, Stefan O., Schmidt, Matthias, Fändrich, Marcus

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Daratumumab for systemic AL amyloidosis: prognostic factors and adverse outcome with nephrotic-range albuminuria von Kimmich, Christoph R., Terzer, Tobias, Benner, Axel, Dittrich, Tobias, Veelken, Kaya, Carpinteiro, Alexander, Hansen, Timon, Goldschmidt, Hartmut, Seckinger, Anja, Hose, Dirk, Jauch, Anna, Wörner, Stefan, Beimler, Jörg, Müller-Tidow, Carsten, Hegenbart, Ute, Schönland, Stefan O.

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Immunohistochemistry in the classification of systemic forms of amyloidosis: a systematic investigation of 117 patients von Schönland, Stefan O., Hegenbart, Ute, Bochtler, Tilmann, Mangatter, Anja, Hansberg, Marion, Ho, Anthony D., Lohse, Peter, Röcken, Christoph

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Polymorphism of Amyloid Fibrils In Vivo von Annamalai, Karthikeyan, Gührs, Karl-Heinz, Koehler, Rolf, Schmidt, Matthias, Michel, Henri, Loos, Cornelia, Gaffney, Patricia M., Sigurdson, Christina J., Hegenbart, Ute, Schönland, Stefan, Fändrich, Marcus

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Cryo-EM structure of an ATTRwt amyloid fibril from systemic non-hereditary transthyretin amyloidosis von Steinebrei, Maximilian, Gottwald, Juliane, Baur, Julian, Röcken, Christoph, Hegenbart, Ute, Schönland, Stefan, Schmidt, Matthias

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Cryo-EM structure of a lysozyme-derived amyloid fibril from hereditary amyloidosis von Karimi-Farsijani, Sara, Sharma, Kartikay, Ugrina, Marijana, Kuhn, Lukas, Pfeiffer, Peter Benedikt, Haupt, Christian, Wiese, Sebastian, Hegenbart, Ute, Schönland, Stefan O., Schwierz, Nadine, Schmidt, Matthias, Fändrich, Marcus

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