Angela M Kaindl

ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 35

Top Venues

This page only lists publications with an associated author ORCID identifier.

Publications

Ingeborg Viezens, Ellen Knierim, Hedwig E Deubzer, Kathrin Hauptmann, Jessica Fassbender, Susanne Morales-Gonzalez, Angela M Kaindl, Markus Schuelke, Marc Nikolaus
Expression of mGluR5 in Pediatric Hodgkin and Non-Hodgkin lymphoma-A Comparative Analysis of Immunohistochemical and Clinical Findings Regarding the Association between Tumor and Paraneoplastic Neurological Disease. Cancers 16 (13) (2024)
Lena-Luise Becker, Konstantin L Makridis, Angela T Abad-Perez, Ulrich-Wilhelm Thomale, Anna Tietze, Christian E Elger, Denise Horn, Angela M Kaindl
The importance of routine genetic testing in pediatric epilepsy surgery. Epilepsia open (2024)
Lena-Luise Becker, Konstantin L Makridis, Angela T Abad-Perez, Ulrich-Wilhelm Thomale, Anna Tietze, Christian E Elger, Denise Horn, Angela M Kaindl
The importance of routine genetic testing in pediatric epilepsy surgery. Epilepsia open 9 (2) (2024)
Lena-Luise Becker, Konstantin L Makridis, Angela T Abad-Perez, Ulrich-Wilhelm Thomale, Anna Tietze, Christian E Elger, Denise Horn, Angela M Kaindl
The importance of routine genetic testing in pediatric epilepsy surgery. Epilepsia open 9 (2) (2024)
Ingeborg Viezens, Ellen Knierim, Hedwig E Deubzer, Kathrin Hauptmann, Jessica Fassbender, Susanne Morales-Gonzalez, Angela M Kaindl, Markus Schuelke, Marc Nikolaus
Expression of mGluR5 in Pediatric Hodgkin and Non-Hodgkin lymphoma-A Comparative Analysis of Immunohistochemical and Clinical Findings Regarding the Association between Tumor and Paraneoplastic Neurological Disease. Cancers 16 (13) (2024)
Fabian Dannenberg, Arpad Von Moers, Petra Bittigau, Jörn Lange, Sylvia Wiegand, Ferenc Török, Gabriel Stölting, Alexandra Pinggera, M Mahdi Motazacker, Marjoleine F Broekema, Markus Schuelke, Angela M Kaindl, Ute I Scholl, Nadine Jasmin Ortner
A Novel De Novo Gain-of-Function CACNA1D Variant in Neurodevelopmental Disease With Congenital Tremor, Seizures, and Hypotonia. Neurology. Genetics 10 (5) (2024)
Karen L Oliver, Marina Trivisano, Simone A Mandelstam, Angela De Dominicis, David I Francis, Timothy E Green, Alison M Muir, Apoorva Chowdhary, Christoph Hertzberg, Klaus Goldhahn, Julia Metreau, Christine Prager, Jason Pinner, Michael Cardamone, Kenneth A Myers, Richard J Leventer, Gaëtan Lesca, Melanie Bahlo, Michael S Hildebrand, Heather C Mefford, Angela M Kaindl, Nicola Specchio, Ingrid Eileen Scheffer
WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk. Epilepsia (2023)
Lydie Burglen, Evelien Van Hoeymissen, Leila Qebibo, Magalie Barth, Newell Belnap, Felix Boschann, Christel Depienne, Katrien De Clercq, Andrew G L Douglas, Mark P Fitzgerald, Nicola Foulds, Catherine Garel, Ingo Helbig, Katharina Held, Denise Horn, Annelies Janssen, Angela M Kaindl, Vinodh Narayanan, Christina Prager, Mailys Rupin-Mas, Alexandra Afenjar, Siyuan Zhao, Vincent Th Ramaekers, Sarah M Ruggiero, Simon Thomas, Stéphanie Valence, Lionel Van Maldergem, Tibor Rohacs, Diana Rodriguez, David Dyment, Thomas Voets, Joris Vriens
Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders. eLife 12 (2023)
Lydie Burglen, Evelien Van Hoeymissen, Leila Qebibo, Magalie Barth, Newell Belnap, Felix Boschann, Christel Depienne, Katrien De Clercq, Andrew G L Douglas, Mark P Fitzgerald, Nicola Foulds, Catherine Garel, Ingo Helbig, Katharina Held, Denise Horn, Annelies Janssen, Angela M Kaindl, Vinodh Narayanan, Christina Prager, Mailys Rupin-Mas, Alexandra Afenjar, Siyuan Zhao, Vincent Th Ramaekers, Sarah M Ruggiero, Simon Thomas, Stéphanie Valence, Lionel Van Maldergem, Tibor Rohacs, Diana Rodriguez, David Dyment, Thomas Voets, Joris Vriens
Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders. eLife 12 (2023)
Fabienne Kühne, Lena-Luise Becker, Thomas Bast, Astrid Bertsche, Ingo Borggraefe, Christian Malte Boßelmann, Jörg Fahrbach, Christoph Hertzberg, Nina A Herz, Martin Hirsch, Martin Holtkamp, Christine Janello, Gerhard Josef Kluger, Gerhard Kurlemann, Holger Lerche, Konstantin L Makridis, Felix von Podewils, Milka Pringsheim, Susanne Schubert-Bast, Juliane Schulz, Andreas Schulze-Bonhage, David Steinbart, Bernhard J Steinhoff, Adam Strzelczyk, Steffen Syrbe, Heike De Vries, Christiane Wagner, Johanna Wagner, Bernd Wilken, Christine Prager, Kerstin Alexandra Klotz, Angela M Kaindl
Real-world data on cannabidiol treatment of various epilepsy subtypes: A retrospective, multicenter study. Epilepsia open (2023)
Nina-Maria Wilpert, Ana Luisa de A Marcelino, Ellen Knierim, Pasquale Incoronato, Elisa Sanchez-Sendin, Olga Staudacher, Anne Drenckhahn, Petra Bittigau, Jakob Kreye, Harald Prüss, Markus Schuelke, Andrea A Kühn, Angela M Kaindl, Marc Nikolaus
Pediatric de novo movement disorders and ataxia in the context of SARS-CoV-2. Journal of neurology (2023)
Lydie Burglen, Evelien Van Hoeymissen, Leila Qebibo, Magalie Barth, Newell Belnap, Felix Boschann, Christel Depienne, Katrien De Clercq, Andrew G L Douglas, Mark P Fitzgerald, Nicola Foulds, Catherine Garel, Ingo Helbig, Katharina Held, Denise Horn, Annelies Janssen, Angela M Kaindl, Vinodh Narayanan, Christina Prager, Mailys Rupin-Mas, Alexandra Afenjar, Siyuan Zhao, Vincent Th Ramaekers, Sarah M Ruggiero, Simon Thomas, Stéphanie Valence, Lionel Van Maldergem, Tibor Rohacs, Diana Rodriguez, David Dyment, Thomas Voets, Joris Vriens
Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders. eLife 12 (2023)
Fabienne Kühne, Lena-Luise Becker, Thomas Bast, Astrid Bertsche, Ingo Borggraefe, Christian Malte Boßelmann, Jörg Fahrbach, Christoph Hertzberg, Nina A Herz, Martin Hirsch, Martin Holtkamp, Christine Janello, Gerhard Josef Kluger, Gerhard Kurlemann, Holger Lerche, Konstantin L Makridis, Felix von Podewils, Milka Pringsheim, Susanne Schubert-Bast, Juliane Schulz, Andreas Schulze-Bonhage, David Steinbart, Bernhard J Steinhoff, Adam Strzelczyk, Steffen Syrbe, Heike De Vries, Christiane Wagner, Johanna Wagner, Bernd Wilken, Christine Prager, Kerstin Alexandra Klotz, Angela M Kaindl
Real world data on cannabidiol treatment of various epilepsy subtypes: a retrospective, multicenter study. Epilepsia open (2023)
Karen L Oliver, Marina Trivisano, Simone A Mandelstam, Angela De Dominicis, David I Francis, Timothy E Green, Alison M Muir, Apoorva Chowdhary, Christoph Hertzberg, Klaus Goldhahn, Julia Metreau, Christine Prager, Jason Pinner, Michael Cardamone, Kenneth A Myers, Richard J Leventer, Gaëtan Lesca, Melanie Bahlo, Michael S Hildebrand, Heather C Mefford, Angela M Kaindl, Nicola Specchio, Ingrid Eileen Scheffer
WWOX Developmental and Epileptic Encephalopathy (WWOX-DEE): understanding the epileptology and the mortality risk. Epilepsia (2023)
Lydie Burglen, Evelien Van Hoeymissen, Leila Qebibo, Magalie Barth, Newell Belnap, Felix Boschann, Christel Depienne, Katrien De Clercq, Andrew G L Douglas, Mark P Fitzgerald, Nicola Foulds, Catherine Garel, Ingo Helbig, Katharina Held, Denise Horn, Annelies Janssen, Angela M Kaindl, Vinodh Narayanan, Christina Prager, Mailys Rupin-Mas, Alexandra Afenjar, Siyuan Zhao, Vincent Th Ramaekers, Sarah M Ruggiero, Simon Thomas, Stéphanie Valence, Lionel Van Maldergem, Tibor Rohacs, Diana Rodriguez, David Dyment, Thomas Voets, Joris Vriens
Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders. eLife 12 (2023)
Konstantin L Makridis, Kerstin Alexandra Klotz, Georgia Ramantani, Lena-Luise Becker, Victoria San Antonio-Arce, Steffen Syrbe, Kathrin Wagner, Mukesch Johannes Shah, Ulrich-Wilhelm Thomale, Anna Tietze, Christian E Elger, Ingo Borggraefe, Angela M Kaindl
Epilepsy surgery in early infancy: a retrospective, multicenter study. Epilepsia open (2023)
Lydie Burglen, Evelien Van Hoeymissen, Leila Qebibo, Magalie Barth, Newell Belnap, Felix Boschann, Christel Depienne, Katrien De Clercq, Andrew G L Douglas, Mark P Fitzgerald, Nicola Foulds, Catherine Garel, Ingo Helbig, Katharina Held, Denise Horn, Annelies Janssen, Angela M Kaindl, Vinodh Narayanan, Christina Pragner, Mailys Rupin, Alexandra Afenjar, Siyuan Zhao, Vincent Th Ramaekers, Sarah M Ruggiero, Simon Thomas, Stéphanie Valence, Lionel Van Maldergem, Tibor Rohacs, Diana Rodriguez, David Dyment, Thomas Voets, Joris Vriens
Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders. eLife 12 (2023)
Lena-Luise Becker, Denise Horn, Felix Boschann, Evelien Van Hoeymissen, Thomas Voets, Joris Vriens, Christine Prager, Angela M Kaindl
Primidone improves symptoms in TRPM3-linked DEE-SWAS. Epilepsia (2023)
Lydie Burglen, Evelien Van Hoeymissen, Leila Qebibo, Magalie Barth, Newell Belnap, Felix Boschann, Christel Depienne, Katrien De Clercq, Andrew G L Douglas, Mark P Fitzgerald, Nicola Foulds, Catherine Garel, Ingo Helbig, Katharina Held, Denise Horn, Annelies Janssen, Angela M Kaindl, Vinodh Narayanan, Christine Prager, Mailys Rupin, Alexandra Afenjar, Siyuan Zhao, Vincent Th Ramaekers, Sarah M Ruggiero, Simon Thomas, Stéphanie Valence, Lionel Van Maldergem, Tibor Rohacs, Diana Rodriguez, David Dyment, Thomas Voets, Joris Vriens
Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders. eLife 12 (2023)
Marc Nikolaus, Fabienne Kühne, Anna Tietze, Julia Thumfart, Caroline Kempf, Alexander Gratopp, Ellen Knierim, Petra Bittigau, Angela M Kaindl
Modified Zipper Method, a Promising Treatment Option in Severe Pediatric Immune-Mediated Neurologic Disorders. Journal of child neurology 37 (6) (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Payam Mohassel, Ning Chang, Kaoru Inoue, Angela Delaney, Ying Hu, Sandra Donkervoort, Dimah Saade, B Jeanne Billioux, Brooke Meader, Rita Volochayev, Chamindra G Konersman, Angela M Kaindl, Chie-Hee Cho, Bianca E Russell, Adrian Rodriguez, K Wade Foster, A Reghan Foley, Steven A Moore, Peter L Jones, Carsten G Bonnemann, Takako Jones, Natalie D Shaw
Cross-sectional Neuromuscular Phenotyping Study of Patients With Arhinia With SMCHD1 Variants. Neurology 98 (13) (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Konstantin L Makridis, Anna-Lena Friedo, Christoph Kellinghaus, Florian-Phillip Losch, Bettina Schmitz, Christian Malte Boßelmann, Angela M Kaindl
Successful treatment of adult Dravet syndrome patients with cenobamate. Epilepsia (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Christian L Görlich, Qian Sun, Viola Roggenkamp, Julian Hackler, Sebastian Mehl, Waldemar B Minich, Angela M Kaindl, Lutz Schomburg
Selenium Status in Paediatric Patients with Neurodevelopmental Diseases. Nutrients 14 (12) (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Ethiraj Ravindran, Nobuto Arashiki, Lena-Luise Becker, Kohtaro Takizawa, Jonathan Lévy, Thomas Rambaud, Konstantin L Makridis, Yoshio Goshima, Na Li, Maaike Vreeburg, Bénédicte Demeer, Achim Dickmanns, Alexander P A Stegmann, Hao Hu, Fumio Nakamura, Angela M Kaindl
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder. eLife 11 (2022)
Jakob Kreye, Sukhvir K Wright, Adriana van Casteren, Laura Stöffler, Marie-Luise Machule, S Momsen Reincke, Marc Nikolaus, Scott van Hoof, Elisa Sanchez-Sendin, Marie A Homeyer, César Cordero Gómez, Hans-Christian Kornau, Dietmar Schmitz, Angela M Kaindl, Philipp Boehm-Sturm, Susanne Müller, Max A Wilson, Manoj A Upadhya, Divya R Dhangar, Stuart D Greenhill, Gavin L Woodhall, Paul Turko, Imre Vida, Craig Curtis Garner, Jonathan Wickel, Christian Geis, Yuko Fukata, Masaki Fukata, Harald Prüss
Encephalitis patient-derived monoclonal GABAA receptor antibodies cause epileptic seizures. The Journal of experimental medicine 218 (11) (2021)
Joanna Schneider, Naomi Mohr, Niko Aliatakis, Ulrich Seidel, Rainer John, Gabriel Promnitz, Birgit Spors, Angela M Kaindl
Brain malformations and cognitive performance in spina bifida. Developmental medicine and child neurology 63 (3) (2020)
Tao Chen, Bin Zhang, Thomas Ziegenhals, Archana B Prusty, Sebastian Fröhler, Clemens Grimm, Yuhui Hu, Bernhard Schaefke, Liang Fang, Min Zhang, Nadine Kraemer, Angela M Kaindl, Utz Fischer, Wei Chen
A missense mutation in SNRPE linked to non-syndromal microcephaly interferes with U snRNP assembly and pre-mRNA splicing. PLoS genetics 15 (10) (2019)
Bianca Hartmann, Timothy Wai, Hao Hu, Thomas MacVicar, Luciana Musante, Björn Fischer-Zirnsak, Werner Stenzel, Ralph Gräf, Lambert van den Heuvel, Hans-Hilger Ropers, Thomas F Wienker, Christoph Hübner, Thomas Langer, Angela M Kaindl
Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation. eLife 5 (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Angela M Kaindl