Konstantin L Makridis

ORCID

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 15

Top Venues

eLife

Epilepsia open

Epilepsia

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

Publications

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)
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)
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)
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)
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)
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)
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)

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Publication Activity (10 Years)

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Konstantin L Makridis