Targeting transthyretin ‐ Mechanism‐based treatment approaches and future perspectives in hereditary amyloidosis von Dohrn, Maike F., Ihne, Sandra, Hegenbart, Ute, Medina, Jessica, Züchner, Stephan L., Coelho, Teresa, Hahn, Katrin

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Clinical Reasoning: A case of bilateral foot drop in a 74-year-old man von Harada, Yohei, Zuchner, Stephan L., Herrmann, David N., Veerapandiyan, Aravindhan

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PCYT2 mutations disrupting etherlipid biosynthesis: phenotypes converging on the CDP-ethanolamine pathway von De Winter, Jonathan, Beijer, Danique, De Ridder, Willem, Synofzik, Matthis, Zuchner, Stephan L, Van Damme, Philip, Spileers, Werner, Baets, Jonathan

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The phenotypic spectrum of pathogenic ATP1A1 variants expands: the novel p.P600R substitution causes demyelinating Charcot–Marie–Tooth disease von Cinarli Yuksel, Feride, Nicolaou, Paschalis, Spontarelli, Kerri, Dohrn, Maike F., Rebelo, Adriana P., Koutsou, Pantelitsa, Georghiou, Anthi, Artigas, Pablo, Züchner, Stephan L., Kleopa, Kleopas A., Christodoulou, Kyproula

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Community genetics: Genetics boosts US-Cuban links von Isasi, Rosario, Zuchner, Stephan L, Villafranca, Roberto Cañete

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Commentary: SPTBN5, encoding the βV-spectrin protein, leads to a syndrome of intellectual disability, developmental delay, and seizures von Beijer, Danique, Züchner, Stephan L.

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Gene Distribution in Pediatric-Onset Inherited Peripheral Neuropathy: A Single Tertiary Center in Thailand von Kulsirichawaroj, Pimchanok, Suksangkharn, Yanin, Nam, Da Eun, Pho-iam, Theeraphong, Limwongse, Chanin, Chung, Ki Wha, Sanmaneechai, Oranee, Zuchner, Stephan L., Choi, Byung-Ok

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Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease von Kohli, Martin A, Cukier, Holly N, Hamilton-Nelson, Kara L, Rolati, Sophie, Kunkle, Brian W, Whitehead, Patrice L, Züchner, Stephan L, Farrer, Lindsay A, Martin, Eden R, Beecham, Gary W, Haines, Jonathan L, Vance, Jeffery M, Cuccaro, Michael L, Gilbert, John R, Schellenberg, Gerard D, Carney, Regina M, Pericak-Vance, Margaret A

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PCYT2 mutations disrupting etherlipid biosynthesis: phenotypes converging on the CDP-ethanolamine pathway von De Winter, Jonathan, Beijer, Danique, De Ridder, Willem, Synofzik, Matthis, Zuchner, Stephan L, Van Damme, Philip, Spileers, Werner, Baets, Jonathan

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Genetics boosts US–Cuban links von Isasi, Rosario, Zuchner, Stephan L., Villafranca, Roberto Cañete

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CNTF and its receptor subunits in human gliomas von Weis, J, Schönrock, L M, Züchner, S L, Lie, D C, Sure, U, Schul, C, Stögbauer, F, Ringelstein, E B, Halfter, H

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METHODS OF DETECTING AND TREATING HEREDITARY SPASTIC PARAPLEGIA von Zuchner, Stephan L, Faghihi, Mohammad A

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TREATMENT AND DETECTION OF INHERITED NEUROPATHIES AND ASSOCIATED DISORDERS von REBELO, Adriana, CORTESE, Andrea, ZHAI, Rong Grace, HERRMANN, David N, ZUCHNER, Stephan L

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Treatment and detection of inherited neuropathies and associated disorders von Zuchner, Stephan L, Rebelo, Adriana, Herrmann, David N, Cortese, Andrea, Zhai, Rong Grace

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METHODS OF DETECTING AND TREATING HEREDITARY SPASTIC PARAPLEGIA von FAGHIHI, Mohammad A, ZUCHNER, Stephan L

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TREATMENT AND DETECTION OF INHERITED NEUROPATHIES AND ASSOCIATED DISORDERS von REBELO, Adriana, CORTESE, Andrea, ZHAI, Rong Grace, HERRMANN, David N, ZUCHNER, Stephan L

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TREATMENT AND DETECTION OF INHERITED NEUROPATHIES AND ASSOCIATED DISORDERS von REBELO, Adriana, CORTESE, Andrea, ZHAI, Rong Grace, HERRMANN, David N, ZUCHNER, Stephan L

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TREATMENT OF CANCER BY ACTIVATING ENDOGENOUS CRYPTIC AMYLOIDOGENIC AGGREGATING PEPTIDES von REBELO, Adriana, ZUCHNER, Stephan, L

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TREATMENT AND DETECTION OF INHERITED NEUROPATHIES AND ASSOCIATED DISORDERS von REBELO, Adriana, CORTESE, Andrea, ZHAI, Rong Grace, HERRMANN, David N, ZUCHNER, Stephan L

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TREATMENT AND DETECTION OF INHERITED NEUROPATHIES AND ASSOCIATED DISORDERS von REBELO, Adriana, CORTESE, Andrea, ZHAI, Rong Grace, HERRMANN, David N, ZUCHNER, Stephan L

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