Prof. Dr. med. Michael Sinnreich

Kinter, Jochen, Stiefvater, Adeline, Osterop, Samira, & Sinnreich, Michael. (2025). ratioPCR delivers precise real-time quantification from multi-template PCR via mechanistic bias correction. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2025.11.20.686216

Furrer, Regula, Dilbaz, Sedat, Steurer, Stefan A, Santos, Gesa, Karrer-Cardel, Bettina, Ritz, Danilo, Sinnreich, Michael, & Handschin, Christoph. (2025). Metabolic dysregulation contributes to the development of dysferlinopathy [Journal-article]. Life Science Alliance, 8(5), e202402991. https://doi.org/10.26508/lsa.202402991

Kesenheimer, Eva Maria, Wendebourg, Maria Janina, Weidensteiner, Claudia, Sander, Laura, Weigel, Matthias, Haas, Tanja, Fischer, Dirk, Neuwirth, Christoph, Braun, Nathalie, Weber, Markus, Granziera, Cristina, Sinnreich, Michael, Bieri, Oliver, & Schlaeger, Regina. (2025). Spinal cord gray matter atrophy is associated with disability in spinal muscular atrophy. Journal of Neurology, 272. https://doi.org/10.1007/s00415-024-12740-3

Nagy, Sara, Kubassova, Olga, Hafner, Patricia, Schädelin, Sabine, Schmidt, Simone, Sinnreich, Michael, Schröder, Jonas, Bieri, Oliver, Boesen, Mikael, & Fischer, Dirk. (2025). Automated analysis of quantitative muscle MRI and its reliability in patients with Duchenne muscular dystrophy. Journal of Neuromuscular Diseases. https://doi.org/10.1177/22143602251319184

Falcetta, Denis, Quirim, Sandrine, Cocchiararo, Ilaria, Chabry, Florent, Théodore, Marine, Stiefvater, Adeline, Lin, Shuo, Tintignac, Lionel, Ivanek, Robert, Kinter, Jochen, Rüegg, Markus A., Sinnreich, Michael, & Castets, Perrine. (2024). CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I [Journal-article]. Skeletal Muscle, 14(1). https://doi.org/10.1186/s13395-024-00345-3

Mittal, Nitish, Ataman, Meric, Tintignac, Lionel, Ham, Daniel J., Jörin, Lena, Schmidt, Alexander, Sinnreich, Michael, Ruegg, Markus A., & Zavolan, Mihaela. (2024). Calorie restriction and rapamycin distinctly restore non-canonical ORF translation in the muscles of aging mice [Journal-article]. Npj Regenerative Medicine, 9(1). https://doi.org/10.1038/s41536-024-00369-9

Wendebourg, Maria Janina, Weigel, Matthias, Weidensteiner, Claudia, Sander, Laura, Kesenheimer, Eva, Naumann, Nicole, Haas, Tanja, Madoerin, Philipp, Braun, Nathalie, Neuwirth, Christoph, Weber, Markus, Jahn, Kathleen, Kappos, Ludwig, Granziera, Cristina, Schweikert, Kathi, Sinnreich, Michael, Bieri, Oliver, & Schlaeger, Regina. (2024). Cervical and thoracic spinal cord gray matter atrophy is associated with disability in patients with amyotrophic lateral sclerosis. European Journal of Neurology, 31. https://doi.org/10.1111/ene.16268

Du Fay De Lavallaz, Jeanne, Prepoudis, Alexandra, Wendebourg, Maria Janina, Kesenheimer, Eva, Kyburz, Diego, Daikeler, Thomas, Haaf, Philip, Wanschitz, Julia, Löscher, Wolfgang N., Schreiner, Bettina, Katan, Mira, Jung, Hans H., Maurer, Britta, Hammerer-Lercher, Angelika, Mayr, Agnes, Gualandro, Danielle M., Acket, Annemarie, Puelacher, Christian, Boeddinghaus, Jasper, et al. (2022). Skeletal Muscle Disorders: A Noncardiac Source of Cardiac Troponin T. Circulation, 145(24), 1764–1779. https://doi.org/10.1161/circulationaha.121.058489

Ham DJ, Börsch A, Chojnowska K, Lin S, Leuchtmann AB, Ham AS, Thürkauf M, Delezie J, Furrer R, Burri D, Sinnreich M, Handschin C, Tintignac LA, Zavolan M, Mittal N, & Rüegg MA. (2022). Author Correction: Distinct and additive effects of calorie restriction and rapamycin in aging skeletal muscle. (Patent No. 1). 13(1), Article 1. https://doi.org/10.1038/s41467-022-30189-8

Bachmann C, Franchini M, Van den Bersselaar LR, Kruijt N, Voermans NC, Bouman K, Kamsteeg EJ, Knop KC, Ruggiero L, Santoro L, Nevo Y, Wilmshurst J, Vissing J, Sinnreich M, Zorzato D, Muntoni F, Jungbluth H, Zorzato F, & Treves S. (2022). Targeted transcript analysis in muscles from patients with genetically diverse congenital myopathies. Brain Communications, 4(5), fcac224. https://doi.org/10.1093/braincomms/fcac224

Ham, Daniel J., Börsch, Anastasiya, Chojnowska, Kathrin, Lin, Shuo, Leuchtmann, Aurel B., Ham, Alexander S., Thürkauf, Marco, Delezie, Julien, Furrer, Regula, Burri, Dominik, Sinnreich, Michael, Handschin, Christoph, Tintignac, Lionel A., Zavolan, Mihaela, Mittal, Nitish, & Rüegg, Markus A. (2022). Distinct and additive effects of calorie restriction and rapamycin in aging skeletal muscle. Nature Communications, 13(1), 2025. https://doi.org/10.1038/s41467-022-29714-6

Yahya F, Kesenheimer E, Decard BF, Sinnreich M, Wand D, & Goldblum D. (2021). Gelsolin-Amyloidosis - An Exceptional Cause of Blepharochalasis. Klinische Monatsblatter Fur Augenheilkunde, 238(4), 349–352. https://doi.org/10.1055/a-1386-3051

Ham, Daniel J., Börsch, Anastasyia, Chojnowska, Kathrin, Lin, Shuo, Leuchtmann, Aurel B., Ham, Alexander S., Thürkauf, Marco, Delezie, Julien, Furrer, Regula, Burri, Dominik, Sinnreich, Michael, Handschin, Christoph, Tintignac, Lionel A., Zavolan, Mihaela, Mittal, Nitish, & Rüegg, Markus A. (2021). Distinct and additive effects of calorie restriction and rapamycin in aging skeletal muscle. bioRxiv. https://doi.org/10.1101/2021.05.28.446097

Reinhold, Simona, Yeginsoy, Desirée, Hollinger, Alexa, Todorov, Atanas, Tintignac, Lionel, Sinnreich, Michael, Kiss, Caroline, Gebhard, Caroline E., Kovács, Balázs, Gysi, Bianca, Imwinkelried, Lara, & Siegemund, Martin. (2020). Protein delivery in intermittent and continuous enteral nutrition with a protein-rich formula in critically ill patients - A protocol for the prospective randomized controlled proof-of-concept Protein Bolus Nutrition (Pro BoNo) study. Trials, 21. https://doi.org/10.1186/s13063-020-04635-1

Bouquier, Nathalie, Moutin, Enora, Tintignac, Lionel A., Reverbel, Amandine, Jublanc, Elodie, Sinnreich, Michael, Chastagnier, Yan, Averous, Julien, Fafournoux, Pierre, Verpelli, Chiara, Boeckers, Tobias, Carnac, Gilles, Perroy, Julie, & Ollendorff, Vincent. (2020). AIMTOR, a BRET biosensor for live imaging, reveals subcellular mTOR signaling and dysfunctions. BMC Biology, 18(1). https://doi.org/10.1186/s12915-020-00790-8

Klingler C, Ashley J, Shi K, Stiefvater A, Kyba M, Sinnreich M, Aihara H, & Kinter J. (2020). DNA aptamers against the DUX4 protein reveal novel therapeutic implications for FSHD. FASEB Journal, 34(3), 4573–4590. https://doi.org/10.1096/fj.201902696

Ham, Alexander S., Chojnowska, Kathrin, Tintignac, Lionel A., Lin, Shuo, Schmidt, Alexander, Ham, Daniel J., Sinnreich, Michael, & Rüegg, Markus A. (2020). mTORC1 signalling is not essential for the maintenance of muscle mass and function in adult sedentary mice. Journal of Cachexia, Sarcopenia and Muscle, 11(1), 259–273. https://doi.org/10.1002/jcsm.12505

Ham, Daniel J., Börsch, Anastasiya, Lin, Shuo, Thürkauf, Marco, Weihrauch, Martin, Reinhard, Judith R., Delezie, Julien, Battilana, Fabienne, Wang, Xueyong, Kaiser, Marco S., Guridi, Maitea, Sinnreich, Michael, Rich, Mark M., Mittal, Nitish, Tintignac, Lionel A., Handschin, Christoph, Zavolan, Mihaela, & Rüegg, Markus A. (2020). The neuromuscular junction is a focal point of mTORC1 signaling in sarcopenia. Nature Communications, 11(1), 4510. https://doi.org/10.1038/s41467-020-18140-1

Sinnecker, Tim, Andelova, Michaela, Mayr, Michael, Rüegg, Stephan, Sinnreich, Michael, Hench, Juergen, Frank, Stephan, Schaller, André, Stippich, Christoph, Wuerfel, Jens, & Bonati, Leo H. (2019). Diagnosis of adult-onset MELAS syndrome in a 63-year-old patient with suspected recurrent strokes - A case report. BMC Neurology, 19. https://doi.org/10.1186/s12883-019-1306-6

Castets, Perrine, Rion, Nathalie, Théodore, Marine, Falcetta, Denis, Lin, Shuo, Reischl, Markus, Wild, Franziska, Guérard, Laurent, Eickhorst, Christopher, Brockhoff, Marielle, Guridi, Maitea, Ibebunjo, Chikwendu, Cruz, Joseph, Sinnreich, Michael, Rudolf, Rüdiger, Glass, David J., & Rüegg, Markus A. (2019). mTORC1 and PKB/Akt control the muscle response to denervation by regulating autophagy and HDAC4. Nature Communications, 10(1), 3187. https://doi.org/10.1038/s41467-019-11227-4

Azakir BA, Di Fulvio S, Kinter J, & Sinnreich M. (2017). Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells. The Journal of Biological Chemistry, 292(30), 12542. https://doi.org/10.1074/jbc.a111.329078

Brockhoff, Marielle, Rion, Nathalie, Chojnowska, Kathrin, Wiktorowicz, Tatiana, Eickhorst, Christopher, Erne, Beat, Frank, Stephan, Angelini, Corrado, Furling, Denis, Rüegg, Markus A., Sinnreich, Michael, & Castets, Perrine. (2017). Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I. Journal of Clinical Investigation, 127(2), 549–563. https://doi.org/10.1172/jci89616

Athanasopoulou, I. M., Rasenack, M., Grimm, C., Axer, H., Sinnreich, M., Decard, B. F., & Grimm, A. (2016). Ultrasound of the nerves - An appropriate addition to nerve conduction studies to differentiate paraproteinemic neuropathies. Journal of the Neurological Sciences, 362, 188–195. https://doi.org/10.1016/j.jns.2016.01.055

Castets, Perrine, Frank, Stephan, Sinnreich, Michael, & Rüegg, Markus A. (2016). “Get the Balance Right”: Pathological Significance of Autophagy Perturbation in Neuromuscular Disorders. Journal of Neuromuscular Diseases, 3(2), 127–155. https://doi.org/10.3233/jnd-160153

Hafner, P., Bonati, U., Erne, B., Schmid, M., Rubino, D., Pohlman, U., Peters, T., Rutz, E., Frank, S., Neuhaus, C., Deuster, S., Gloor, M., Bieri, O., Fischmann, A., Sinnreich, M., Gueven, N., & Fischer, D. (2016). Improved Muscle Function in Duchenne Muscular Dystrophy through L-Arginine and Metformin: An Investigator-Initiated, Open-Label, Single-Center, Proof-Of-Concept-Study. PLoS ONE, 11(1), e0147634. https://doi.org/10.1371/journal.pone.0147634

Herrendorff, R., Faleschini, M. T., Stiefvater, A., Erne, B., Wiktorowicz, T., Kern, F., Hamburger, M., Potterat, O., Kinter, J., & Sinnreich, M. (2016). Identification of plant-derived alkaloids with therapeutic potential for myotonic dystrophy type I. Journal of Biological Chemistry, 291(33), 17165–17177. https://doi.org/10.1074/jbc.m115.710616

Probstel, A. K., Schaller, A., Lieb, J., Hench, J., Frank, S., Fuhr, P., Kappos, L., & Sinnreich, M. (2016). Mitochondrial cytopathy with common MELAS mutation presenting as multiple system atrophy mimic. Neurol Genet, 2(6), e121. https://doi.org/10.1212/nxg.0000000000000121

Sunderkotter, C., Nast, A., Worm, M., Dengler, R., Dorner, T., Ganter, H., Hohlfeld, R., Melms, A., Melzer, N., Rosler, K., Schmidt, J., Sinnreich, M., Walter, M. C., Wanschitz, J., & Wiendl, H. (2016). Guidelines on dermatomyositis-excerpt from the interdisciplinary S2k guidelines on myositis syndromes by the German Society of Neurology. J Dtsch Dermatol Ges, 14(3), 321–333. https://doi.org/10.1111/ddg.12909

Sinnreich M. (2015). [Muscle pain: what should you think?]. Revue medicale suisse, 11(459), 319–320.

Bonati, Ulrike, Hafner, Patricia, Schadelin, Sabine, Schmid, Maurice, Naduvilekoot Devasia, Arjith, Schroeder, Jonas, Zuesli, Stephanie, Pohlman, Urs, Neuhaus, Cornelia, Klein, Andrea, Sinnreich, Michael, Haas, Tanja, Gloor, Monika, Bieri, Oliver, Fischmann, Arne, & Fischer, Dirk. (2015). Quantitative muscle MRI: A powerful surrogate outcome measure in Duchenne muscular dystrophy. Neuromuscular Disorders, 25(9), 679–685. https://doi.org/10.1016/j.nmd.2015.05.006

Grimm, Alexander, Decard, Bernhard F., Athanasopoulou, Ioanna, Schweikert, Kathi, Sinnreich, Michael, & Axer, Hubertus. (2015). Nerve ultrasound for differentiation between amyotrophic lateral sclerosis and multifocal motor neuropathy. Journal of Neurology, 262(4), 870–880. https://doi.org/10.1007/s00415-015-7648-0

Petersen, Jens A., Kuntzer, Thierry, Fischer, Dirk, von der Hagen, Maja, Huebner, Angela, Kana, Veronika, Lobrinus, Johannes A., Kress, Wolfram, Rushing, Elisabeth J., Sinnreich, Michael, & Jung, Hans H. (2015). Dysferlinopathy in Switzerland: clinical phenotypes and potential founder effects. BMC Neurology, 15, 182. https://doi.org/10.1186/s12883-015-0449-3

Sinnreich, Michael. (2015). [Muscle pain: what should you think?]. Revue Médicale Suisse, 11(459), 319–320. https://www.ncbi.nlm.nih.gov/pubmed/25845194

Wiktorowicz, Tatiana, Kinter, Jochen, Kobuke, Kazuhiro, Campbell, Kevin P., & Sinnreich, Michael. (2015). Genetic characterization and improved genotyping of the dysferlin-deficient mouse strain Dysf (tm1Kcam). Skeletal Muscle, 5, 32. https://doi.org/10.1186/s13395-015-0057-3

Azakir BA, Erne B, Di Fulvio S, Stirnimann G, & Sinnreich M. (2014). Proteasome inhibitors increase missense mutated dysferlin in patients with muscular dystrophy (Patent No. 250). Science Translational Medicine, 6(250), Article 250. https://doi.org/10.1126/scitranslmed.3009612

Kinter, Jochen, & Sinnreich, Michael. (2014). Molecular targets to treat muscular dystrophies. Swiss Medical Weekly, 144, w13916. https://doi.org/10.4414/smw.2014.13916

Castets, Perrine, Lin, Shuo, Rion, Nathalie, Di Fulvio, Sabrina, Romanino, Klaas, Guridi, Maitea, Frank, Stephan, Tintignac, Lionel A., Sinnreich, Michael, & Ruegg, Markus A. (2013). Sustained activation of mTORC1 in skeletal muscle inhibits constitutive and starvation-induced autophagy and causes a severe, late-onset myopathy. Cell metabolism, 17(5), 731–744. https://doi.org/10.1016/j.cmet.2013.03.015

O’Ferrall, Erin K, Gendron, Daniel, Guiot, Marie-Christine, Hall, Jeffery, & Sinnreich, Michael. (2013). Lower motor neuron syndrome due to cauda equina hypertrophy with onion bulbs. Muscle & Nerve, 48(2), 301–305. https://doi.org/10.1002/mus.23816

Ozcelik, S., Fraser, G., Castets, P., Schaeffer, V., Skachokova, Z., Breu, K., Clavaguera, F., Sinnreich, M., Kappos, L., Goedert, M., Tolnay, M., & Winkler, D. T. (2013). Rapamycin attenuates the progression of tau pathology in P301S tau transgenic mice. PLoS ONE, 8(5), e62459. https://doi.org/10.1371/journal.pone.0062459

Peyer, Anne-Kathrin, Abicht, Angela, Heinimann, Karl, Sinnreich, Michael, & Fischer, Dirk. (2013). Quinine sulfate as a therapeutic option in a patient with slow channel congenital myasthenic syndrome. Neuromuscular Disorders, 23(7), 571–574. https://doi.org/10.1016/j.nmd.2013.04.001

Peyer, Anne-Kathrin, Kinter, Jochen, Hench, Jürgen, Frank, Stephan, Fuhr, Peter, Thomann, Sandra, Fischmann, Arne, Kneifel, Stefan, Camaño, Pilar, López de Munain, Adolfo, Sinnreich, Michael, & Renaud, Susanne. (2013). Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia. Neuromuscular Disorders, 23(2), 149–154. https://doi.org/10.1016/j.nmd.2012.09.009

Azakir, Bilal A, Di Fulvio, Sabrina, Kinter, Jochen, & Sinnreich, Michael. (2012). Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells. Journal of Biological Chemistry, 287(13), 10344–10354. https://doi.org/10.1074/jbc.m111.329078

Azakir, Bilal A, Di Fulvio, Sabrina, Salomon, Steven, Brockhoff, Marielle, Therrien, Christian, & Sinnreich, Michael. (2012). Modular dispensability of dysferlin C2 domains reveals rational design for mini-dysferlin molecules. Journal of Biological Chemistry, 287(33), 27629–27636. https://doi.org/10.1074/jbc.m112.391722

Di Fulvio, S., Azakir, B. A., Therrien, C., & Sinnreich, M. (2011). Dysferlin interacts with histone deacetylase 6 and increases alpha-tubulin acetylation. PLoS ONE, 6(12), e28563. https://doi.org/10.1371/journal.pone.0028563

Azakir, Bilal A., Di Fulvio, Sabrina, Therrien, Christian, & Sinnreich, Michael. (2010). Dysferlin interacts with tubulin and microtubules in mouse skeletal muscle. PLoS ONE, 5(4), e10122. https://doi.org/10.1371/journal.pone.0010122

Geddes, Maiya R., Sinnreich, Michael, & Chalk, Colin. (2010). Minocycline-induced dermatomyositis. Muscle & Nerve, 41(4), 547–549. https://doi.org/10.1002/mus.21487

Kinter, Jochen, Broglio, Laura, Steck, Andreas J, Tolnay, Markus, Fuhr, Peter, Latov, Norman, Kalbermatten, Daniel, Sinnreich, Michael, Schaeren-Wiemers, Nicole, & Renaud, Susanne. (2010). Gene expression profiling in nerve biopsy of vasculitic neuropathy. Journal of Neuroimmunology, 225(1-2), 184–189. https://doi.org/10.1016/j.jneuroim.2010.05.023

O’Ferrall, Erin K, & Sinnreich, Michael. (2009). The role of muscle biopsy in the age of genetic testing. Current Opinion in Neurology, 22(5), 543–553. https://doi.org/10.1097/wco.0b013e32832ffc60

Therrien, Christian, Di Fulvio, Sabrina, Pickles, Sarah, & Sinnreich, Michael. (2009). Characterization of lipid binding specificities of dysferlin C2 domains reveals novel interactions with phosphoinositides. Biochemistry : A Biweekly Publication of the American Chemical Society, 48(11), 2377–2384. https://doi.org/10.1021/bi802242r

Nadeau, Amelie, Therrien, Christian, Karpati, George, & Sinnreich, Michael. (2008). Danon disease due to a novel splice mutation in the LAMP2 gene. Muscle & Nerve, 37(3), 338–342. https://doi.org/10.1002/mus.20930

Picard, Martin, Godin, Richard, Sinnreich, Michael, Baril, Jacinthe, Bourbeau, Jean, Perrault, Hélène, Taivassalo, Tanja, & Burelle, Yan. (2008). The mitochondrial phenotype of peripheral muscle in chronic obstructive pulmonary disease : disuse or dysfunction? American Journal of Respiratory and Critical Care Medicine, 178(10), 1040–1047. https://doi.org/10.1164/rccm.200807-1005oc

Therrien C, Dodig D, Karpati G, & Sinnreich M. (2006). Mutation impact on dysferlin inferred from database analysis and computer-based structural predictions. Journal of the Neurological Sciences, 250(1-2), 71–78. https://doi.org/10.1016/j.jns.2006.07.004

Kuntzer T, Bader CR, & Sinnreich M. (2006). [Mechanisms leading to muscle degeneration: molecular mechanisms and therapeutical forecasts]. Revue medicale suisse, 2(64), 1174–1177.

Sinnreich M, Therrien C, & Karpati G. (2006). Lariat branch point mutation in the dysferlin gene with mild limb-girdle muscular dystrophy. Neurology, 66(7), 1114–1116. https://doi.org/10.1212/01.wnl.0000204358.89303.81

Sinnreich M, Shaw CA, Pari G, Nalbantoglu J, Holland PC, & Karpati G. (2005). Localization of coxsackie virus and adenovirus receptor (CAR) in normal and regenerating human muscle. Neuromuscular Disorders, 15(8), 541–548. https://doi.org/10.1016/j.nmd.2005.05.007

Sinnreich M, Taylor BV, & Dyck PJ. (2005). Diabetic neuropathies: Classification, clinical features, and pathophysiological basis. Neurologist, 11(2), 63–79. https://doi.org/10.1097/01.nrl.0000156314.24508.ed

Sinnreich M, Klein CJ, Daube JR, Engelstad J, Spinner RJ, & Dyck PJ. (2004). Chronic immune sensory polyradiculopathy: A possibly treatable sensory ataxia. Neurology, 63(9), 1662–1669. https://doi.org/10.1212/01.wnl.0000142507.12763.58

Shaw CA, Holland PC, Sinnreich M, Allen C, Sollerbrant K, Karpati G, & Nalbantoglu J. (2004). Isoform-specific expression of the Coxsackie and adenovirus receptor (CAR) in neuromuscular junction and cardiac intercalated discs. BMC Cell Biology, 5(1), 42. https://doi.org/10.1186/1471-2121-5-42

Sinnreich M, & Klein CJ. (2004). Bulbospinal muscular atrophy: Kennedy’s disease. Archives of Neurology, 61(8), 1324–1326. https://doi.org/10.1001/archneur.61.8.1324

Karpati G, & Sinnreich M. (2004). A clever road from myopathology to genes: The myotilin story (Patent No. 8). Neurology, 62(8), Article 8. https://doi.org/10.1212/01.wnl.0000126179.90958.94

Sinnreich M, Meins M, Niclou SP, Suidan HS, & Monard D. (2004). Prothrombin overexpressed in post-natal neurones requires blood factors for activation in the mouse brain. Journal of Neurochemistry, 88(6), 1380–1388. https://doi.org/10.1046/j.1471-4159.2003.02268.x

Sinnreich M, Sorenson EJ, & Klein CJ. (2004). Neurologic course, endocrine dysfunction and triplet repeat size in spinal bulbar muscular atrophy. Canadian Journal of Neurological Sciences, 31(3), 378–382. https://doi.org/10.1017/s0317167100003486

Sinnreich M, Rossillion B, Landis T, Burkhard PR, & Sztajzel R. (2003). Bilateral optic ischemic neuropathy related to chronic hepatitis C-associated anticardiolipin antibodies. European Neurology, 49(4), 243–245. https://doi.org/10.1159/000070195

Klein CJ, Sinnreich M, & Dyck PJ. (2003). Indifference rather than insensitivity to pain. (Patent No. 3). 53(3), Article 3. https://doi.org/10.1002/ana.10469

Truffert A, Lalive PH, Janssens JP, Sinnreich M, & Magistris MR. (2003). Endplate dysfunction causing respiratory failure in a patient with prior paralytic poliomyelitis. Journal of Neurology Neurosurgery and Psychiatry, 74(3), 370–372. https://doi.org/10.1136/jnnp.74.3.370

Burkhard PR, Masouyé I, Sinnreich M, & Harms M. (2003). [Quiz case]. Revue medicale de la Suisse romande, 123(1), 75–76.

Du Pasquier RA, Blanc Y, Sinnreich M, Landis T, Burkhard P, & Vingerhoets FJ. (2003). The effect of aging on postural stability: A cross sectional and longitudinal study. Neurophysiologie Clinique, 33(5), 213–218. https://doi.org/10.1016/j.neucli.2003.09.001

Karpati G, & Sinnreich M. (2003). The Molecular Era of Myology. Journal of Neuropathology and Experimental Neurology, 62(12), 1203–1210. https://doi.org/10.1093/jnen/62.12.1203

Sinnreich M, Assal F, Hefft S, Magistris MR, Chizzolini C, Landis T, & Burkhard PR. (2001). Anti-GAD antibodies and breast cancer in a patient with stiff-person syndrome: A puzzling association. European Neurology, 46(1), 51–52. https://doi.org/10.1159/000050758

Sztajzel R, Coeytaux A, Dehdashti AR, Delavelle J, & Sinnreich M. (2001). Subarachnoid hemorrhage: A rare presentation of cerebral venous thrombosis. Headache, 41(9), 889–892. https://doi.org/10.1046/j.1526-4610.2001.041009889.x

Occhiodoro T, Bernheim L, Liu JH, Bijlenga P, Sinnreich M, Bader CR, & Fischer-Lougheed J. (1998). Cloning of a human ether-a-go-go potassium channel expressed in myoblasts at the onset of fusion. FEBS Letters, 434(1-2), 177–182. https://doi.org/10.1016/s0014-5793(98)00973-9