Kristl G. Claeys - Department of Neurology and Institute of Neuropathology, RWTH Aachen University

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论文共 299 篇作者统计合作学者相似作者

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Phenotype Variability and Therapeutic Response to Patisiran in Patients with Hereditary Transthyretin Amyloidosis: a Belgian Real-World Experience

Stephanie Delstanche,Kristl G Claeys, De Bleecker,Gauthier Remiche,Pierre Troisfontaines, Vinciane Van Parys,Antoine Bondue

Acta clinica Belgicano. 6 (2025): 393-402

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Genotype and Phenotype Spectrum of Charcot-Marie-Tooth Disease Due to Mutations in SORD

Andrea Cortese,Maike F Dohrn,Riccardo Curro, Sara Negri,Petra Lassuthova,Chiara Pisciotta,Stefano Tozza,Abdullah Al-Ajmi, Changyoung Feng,Pedro J Tomaselli,Gorka Fernandez-Eulate, Saif Haddad,Matilde Laurà,Alexander M Rossor,Elisa Vegezzi,Stefano Facchini, James N Sleigh,Adriana Rebelo,Danique Beijer,Jacquelyn Raposo,Mario Saporta, Barbora Lauerova, Helena F Pernice,Pascal Achenbach,Ulrike Schöne, Tayir Alon, Marcus Deschauer,Isabell Cordts, Carolin D Obermaier,Natalie Winter,Peter D Creigh,Janet E Sowden,Tyler Rehbein,Stefania Magri,Alessandro Bertini,Paola Saveri,Paolo Ripellino, Jingyu Huang,Aleksandra Nadaj-Pakleza, Alison Ross, James K L Holt,Kathryn M Brennan,Rivka Sukenik-Halevy,Varoona Bizaoui,Yesim Parman,Esra Battaloglu,Arman Cakar, Hadil Alrohaif,Simon Hammans,Kishore R Kumar,Marina L Kennerson,Hülya Kayserili,Defne A Amado, Katrin Hahn,Paola Valentino,Francesca Cavalcanti, Carlo Gaetano,Franco Taroni,Geir J Braathen,Henry Houlden,Tanya Stojkovic, Stojan Peric,Alessandra Bolino,Stefano C Previtali,Yi-Chung Lee, Ayşe N Başak,Sherifa A Hamed,Ricardo Rojas-Garcia,Kristl G Claeys,Wilson Marques, Teresa Sevilla,Beate Schlotter-Weigel,Fiore Manganelli,Ruxu Zhang,David N Herrmann,Steven S Scherer,Pavel Seeman,Davide Pareyson,Mary M Reilly,Michael E Shy,Stephan Züchner

Brain a journal of neurology (2025)

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ADAPT NXT: Fixed Cycles or Every-Other-Week IV Efgartigimod in Generalized Myasthenia Gravis

Ali A Habib,Kristl G Claeys,Vera Bril,Yessar Hussain,Kelly Gwathmey,Gregory Sahagian,Elena Cortés-Vicente,Edward Brauer,Deborah Gelinas, Anne Sumbul, Rosa H Jimenez, Daniela Hristova, Delphine Masschaele,Renato Mantegazza,Andreas Meisel,Shahram Attarian, ADAPT NXT Study Group

Annals of clinical and translational neurology (2025)

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Fractures in Hereditary Neuromuscular Disorders: Frequency, Risk Factors, and Implications

Matthias Opsomer, Louise Iterbeke, Herman Borghs, Tine De Cuyper,Marian Dejaeger, Patrick Dupont,Kristl G Claeys

European journal of neurologyno. 3 (2025): e70099-e70099

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Switching Enzyme Replacement Therapy for Late-Onset Pompe Disease from Alglucosidase Alfa to Cipaglucosidase Alfa Plus Miglustat: Post Hoc Effect Size Analysis of PROPEL

Hani Kushlaf,Jordi Díaz-Manera,Drago Bratkovic,Barry J Byrne,Kristl G Claeys,Paula R Clemens,Mazen M Dimachkie, Priya S Kishnani,Pascal Laforêt,Mark Roberts,Benedikt Schoser,Antonio Toscano,Jeff Castelli, Fred Holdbrook, Sheela Sitaraman Das, Mitchell Goldman,Tahseen Mozaffar, PROPEL Study Group

Muscle & nerve (2025)

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What Are the Normal Serum Creatine Kinase Values for Skeletal Muscle? A Worldwide Systematic Review

Katina Aleksovska, Theodoros Kyriakides,Corrado Angelini,Zohar Argov,Kristl G Claeys,Marianne de Visser,Massimiliano Filosto, Ivanka Jovanovic,Anna Kostera-Pruszczyk, Maria Julia Molnar,Sabrina Sacconi, Jochen Schaefer,Gabriele Siciliano,Juan J Vilchez,Antonio Toscano,Benedikt Schoser

European journal of neurologyno. 6 (2025): e70240-e70240

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Unravelling Undiagnosed Rare Disease Cases by HiFi Long-Read Genome Sequencing

Wouter Steyaert,Lydia Sagath,German Demidov,Vicente A Yépez,Anna Esteve-Codina,Julien Gagneur,Kornelia Ellwanger,Ronny Derks,Marjan Weiss,Amber den Ouden,Simone van den Heuvel,Hilde Swinkels, Nick Zomer,Marloes Steehouwer,Luke O'Gorman,Galuh Astuti,Kornelia Neveling,Rebecca Schüle,Jishu Xu,Matthis Synofzik,Danique Beijer,Holger Hengel,Ludger Schöls,Kristl G Claeys,Jonathan Baets,Liedewei Van de Vondel,Alessandra Ferlini,Rita Selvatici,Heba Morsy, Marwa Saeed Abd Elmaksoud,Volker Straub,Juliane Müller,Veronica Pini,Luke Perry,Anna Sarkozy,Irina Zaharieva,Francesco Muntoni,Enrico Bugiardini,Kiran Polavarapu,Rita Horvath,Evan Reid,Hanns Lochmüller,Marco Spinazzi,Marco Savarese, Solve-RD DITF-ITHACA, Solve-RD DITF-Euro-NMD, Solve-RD DITF-RND, Solve-RD DITF-EpiCARE,Leslie Matalonga,Steven Laurie,Han G Brunner,Holm Graessner,Sergi Beltran,Stephan Ossowski,Lisenka E L M Vissers,Christian Gilissen,Alexander Hoischen, Solve-RD consortium

Genome researchno. 4 (2025): 755-768

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Disease Spectrum and Long-Term Prognosis of Patients with BAG3-associated Neuromuscular Diseases in Europe

Gorka Fernández-Eulate,Cyril Gitiaux,Simone Thiele,Heinz Jungbluth,Anna Potulska-Chromik, Chiara Marini-Bettolo, Jean Baptiste Davion,Germán Morís, Eduard Gallardo,Montsé Olivé, Carlos Pablo de Fuenmayor-Fernández de la Hoz, Frederique Audic,Arnaud Isapof,Maggie C Walter,Corrado Angelini, Enrico Bertini, Ulrike Schara-Schmidt,Kristl G Claeys,Maike F Dohrn, Mohamed Dembele, Frederic Fer, Guy Brochier, Teresinha Evangelista,Anna Kostera-Pruszczyk,Shahram Attarian,Volker Straub, Cristina Dominguez-Gonzalez,John Vissing,Pascale Richard,Corinne Metay,Diala Khraiche,Karim Wahbi,Tanya Stojkovic

Brain a journal of neurology (2025)

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SAFETY PROFILE OF INTRAVENOUS EFGARTIGIMOD FROM CLINICAL TRIALS IN IMMUNOGLOBULIN G-MEDIATED AUTOIMMUNE DISEASES

Andreas Meisel,Kelly Gwathmey,Catherine M. Broome,Hiroyuki Murai,Adrian Newland,Peter Ulrichts,Rene Kerstens,Jeffrey Guptill, Sofiane Agha, Ming Jiang,James F. Howard,Kristl Claeys

MUSCLE & NERVEno. 3 (2024): 539-539

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