Works by Feucht, Martha


Results: 86
    1

    Molecular EPISTOP, a comprehensive multi-omic analysis of blood from Tuberous Sclerosis Complex infants age birth to two years.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-42855-6
    By:
    • Huschner, Franz;
    • Głowacka-Walas, Jagoda;
    • Mills, James D.;
    • Klonowska, Katarzyna;
    • Lasseter, Kathryn;
    • Asara, John M.;
    • Moavero, Romina;
    • Hertzberg, Christoph;
    • Weschke, Bernhard;
    • Riney, Kate;
    • Feucht, Martha;
    • Scholl, Theresa;
    • Krsek, Pavel;
    • Nabbout, Rima;
    • Jansen, Anna C.;
    • Petrák, Bořivoj;
    • van Scheppingen, Jackelien;
    • Zamecnik, Josef;
    • Iyer, Anand;
    • Anink, Jasper J.
    Publication type:
    Article
    2
    3

    TuberOus SClerosis registry to increase disease Awareness (TOSCA) - baseline data on 2093 patients.

    Published in:
    2017
    By:
    • Kingswood, John C.;
    • d'Augères, Guillaume B.;
    • Belousova, Elena;
    • Ferreira, José C.;
    • Carter, Tom;
    • Castellana, Ramon;
    • Cottin, Vincent;
    • Curatolo, Paolo;
    • Dahlin, Maria;
    • de Vries, Petrus J.;
    • Feucht, Martha;
    • Fladrowski, Carla;
    • Gislimberti, Gabriella;
    • Hertzberg, Christoph;
    • Jozwiak, Sergiusz;
    • Lawson, John A.;
    • Macaya, Alfons;
    • Nabbout, Rima;
    • O'Callaghan, Finbar;
    • Benedik, Mirjana P.
    Publication type:
    journal article
    4
    5

    Impaired oligodendroglial turnover is associated with myelin pathology in focal cortical dysplasia and tuberous sclerosis complex.

    Published in:
    Brain Pathology, 2017, v. 27, n. 6, p. 770, doi. 10.1111/bpa.12452
    By:
    • Scholl, Theresa;
    • Mühlebner, Angelika;
    • Ricken, Gerda;
    • Gruber, Victoria;
    • Fabing, Anna;
    • Samueli, Sharon;
    • Gröppel, Gudrun;
    • Dorfer, Christian;
    • Czech, Thomas;
    • Hainfellner, Johannes A.;
    • Prabowo, Avanita S.;
    • Reinten, Roy J.;
    • Hoogendijk, Lisette;
    • Anink, Jasper J.;
    • Aronica, Eleonora;
    • Feucht, Martha
    Publication type:
    Article
    6

    Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Frontal Lobe Epilepsy: A New Clinico-Pathological Entity.

    Published in:
    Brain Pathology, 2017, v. 27, n. 1, p. 26, doi. 10.1111/bpa.12347
    By:
    • Schurr, Johannes;
    • Coras, Roland;
    • Rössler, Karl;
    • Pieper, Tom;
    • Kudernatsch, Manfred;
    • Holthausen, Hans;
    • Winkler, Peter;
    • Woermann, Friedrich;
    • Bien, Christian G.;
    • Polster, Tilman;
    • Schulz, Reinhard;
    • Kalbhenn, Thilo;
    • Urbach, Horst;
    • Becker, Albert;
    • Grunwald, Thomas;
    • Huppertz, Hans‐Juergen;
    • Gil‐Nagel, Antonio;
    • Toledano, Rafael;
    • Feucht, Martha;
    • Mühlebner, Angelika
    Publication type:
    Article
    7

    Prevention of Epilepsy in Infants with Tuberous Sclerosis Complex in the EPISTOP Trial.

    Published in:
    Annals of Neurology, 2021, v. 89, n. 2, p. 304, doi. 10.1002/ana.25956
    By:
    • Kotulska, Katarzyna;
    • Kwiatkowski, David J.;
    • Curatolo, Paolo;
    • Weschke, Bernhard;
    • Riney, Kate;
    • Jansen, Floor;
    • Feucht, Martha;
    • Krsek, Pavel;
    • Nabbout, Rima;
    • Jansen, Anna C.;
    • Wojdan, Konrad;
    • Sijko, Kamil;
    • Głowacka‐Walas, Jagoda;
    • Borkowska, Julita;
    • Sadowski, Krzysztof;
    • Domańska‐Pakieła, Dorota;
    • Moavero, Romina;
    • Hertzberg, Christoph;
    • Hulshof, Hanna;
    • Scholl, Theresa
    Publication type:
    Article
    8

    Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes.

    Published in:
    2015
    By:
    • Reinthaler, Eva M;
    • Dejanovic, Borislav;
    • Lal, Dennis;
    • Semtner, Marcus;
    • Merkler, Yvonne;
    • Reinhold, Annika;
    • Pittrich, Dorothea A;
    • Hotzy, Christoph;
    • Feucht, Martha;
    • Steinböck, Hannelore;
    • Gruber-Sedlmayr, Ursula;
    • Ronen, Gabriel M;
    • Neophytou, Birgit;
    • Geldner, Julia;
    • Haberlandt, Edda;
    • Muhle, Hiltrud;
    • Ikram, M Arfan;
    • van Duijn, Cornelia M;
    • Uitterlinden, Andre G;
    • Hofman, Albert
    Publication type:
    journal article
    9

    Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes.

    Published in:
    Annals of Neurology, 2015, v. 77, n. 6, p. 972, doi. 10.1002/ana.24395
    By:
    • Reinthaler, Eva M.;
    • Dejanovic, Borislav;
    • Lal, Dennis;
    • Semtner, Marcus;
    • Merkler, Yvonne;
    • Reinhold, Annika;
    • Pittrich, Dorothea A.;
    • Hotzy, Christoph;
    • Feucht, Martha;
    • Steinböck, Hannelore;
    • Gruber‐Sedlmayr, Ursula;
    • Ronen, Gabriel M.;
    • Neophytou, Birgit;
    • Geldner, Julia;
    • Haberlandt, Edda;
    • Muhle, Hiltrud;
    • Ikram, M. Arfan;
    • van Duijn, Cornelia M.;
    • Uitterlinden, Andre G.;
    • Hofman, Albert
    Publication type:
    Article
    10

    DEPDC5 mutations in genetic focal epilepsies of childhood.

    Published in:
    Annals of Neurology, 2014, v. 75, n. 5, p. 788, doi. 10.1002/ana.24127
    By:
    • Lal, Dennis;
    • Reinthaler, Eva M.;
    • Schubert, Julian;
    • Muhle, Hiltrud;
    • Riesch, Erik;
    • Kluger, Gerhard;
    • Jabbari, Kamel;
    • Kawalia, Amit;
    • Bäumel, Christine;
    • Holthausen, Hans;
    • Hahn, Andreas;
    • Feucht, Martha;
    • Neophytou, Birgit;
    • Haberlandt, Edda;
    • Becker, Felicitas;
    • Altmüller, Janine;
    • Thiele, Holger;
    • Lemke, Johannes R.;
    • Lerche, Holger;
    • Nürnberg, Peter
    Publication type:
    Article
    11
    12
    13

    Genomic DNA methylation distinguishes subtypes of human focal cortical dysplasia.

    Published in:
    Epilepsia (Series 4), 2019, v. 60, n. 6, p. 1091, doi. 10.1111/epi.14934
    By:
    • Kobow, Katja;
    • Coras, Roland;
    • Blümcke, Ingmar;
    • Kudernatsch, Manfred;
    • Hamer, Hajo;
    • Kasper, Burkhard S.;
    • Rössler, Karl;
    • Conti, Valerio;
    • Guerrini, Renzo;
    • Ziemann, Mark;
    • Khurana, Ishant;
    • Kaspi, Antony;
    • Kaipananickal, Harikrishnan;
    • El‐Osta, Assam;
    • Feucht, Martha;
    • Mühlebner, Angelika;
    • Aronica, Eleonora;
    • Hainfellner, Johannes A.;
    • Czech, Thomas;
    • Pieper, Tom
    Publication type:
    Article
    14
    15
    16

    Revised version of quality guidelines for presurgical epilepsy evaluation and surgical epilepsy therapy issued by the Austrian, German, and Swiss working group on presurgical epilepsy diagnosis and operative epilepsy treatment.

    Published in:
    Epilepsia (Series 4), 2016, v. 57, n. 8, p. 1215, doi. 10.1111/epi.13449
    By:
    • Rosenow, Felix;
    • Bast, Thomas;
    • Czech, Thomas;
    • Feucht, Martha;
    • Hans, Volkmar H.;
    • Helmstaedter, Christoph;
    • Huppertz, Hans‐Jürgen;
    • Noachtar, Soheyl;
    • Oltmanns, Frank;
    • Polster, Tilman;
    • Seeck, Margitta;
    • Trinka, Eugen;
    • Wagner, Kathrin;
    • Strzelczyk, Adam
    Publication type:
    Article
    17
    18

    Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy.

    Published in:
    Epilepsia (Series 4), 2014, v. 55, n. 8, p. e89, doi. 10.1111/epi.12712
    By:
    • Reinthaler, Eva M.;
    • Lal, Dennis;
    • Jurkowski, Wiktor;
    • Feucht, Martha;
    • Steinböck, Hannelore;
    • Gruber‐Sedlmayr, Ursula;
    • Ronen, Gabriel M.;
    • Geldner, Julia;
    • Haberlandt, Edda;
    • Neophytou, Birgit;
    • Hahn, Andreas;
    • Altmüller, Janine;
    • Thiele, Holger;
    • Toliat, Mohammad R.;
    • Lerche, Holger;
    • Nürnberg, Peter;
    • Sander, Thomas;
    • Neubauer, Bernd A.;
    • Zimprich, Fritz
    Publication type:
    Article
    19
    20
    21

    LETTERS/COMMENTARY.

    Published in:
    2007
    By:
    • Krämer, Günter;
    • Steinhoff, Bernhard J.;
    • Feucht, Martha;
    • Pfäfflin, Margerete;
    • May, Theodor W.
    Publication type:
    Letter
    22
    23
    24
    25

    DNA methylation-based classification of malformations of cortical development in the human brain.

    Published in:
    Acta Neuropathologica, 2022, v. 143, n. 1, p. 93, doi. 10.1007/s00401-021-02386-0
    By:
    • Jabari, Samir;
    • Kobow, Katja;
    • Pieper, Tom;
    • Hartlieb, Till;
    • Kudernatsch, Manfred;
    • Polster, Tilman;
    • Bien, Christian G.;
    • Kalbhenn, Thilo;
    • Simon, Matthias;
    • Hamer, Hajo;
    • Rössler, Karl;
    • Feucht, Martha;
    • Mühlebner, Angelika;
    • Najm, Imad;
    • Peixoto-Santos, José Eduardo;
    • Gil-Nagel, Antonio;
    • Delgado, Rafael Toledano;
    • Aledo-Serrano, Angel;
    • Hou, Yanghao;
    • Coras, Roland
    Publication type:
    Article
    26

    Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay.

    Published in:
    Acta Neuropathologica, 2020, v. 140, n. 6, p. 881, doi. 10.1007/s00401-020-02228-5
    By:
    • Kobow, Katja;
    • Jabari, Samir;
    • Pieper, Tom;
    • Kudernatsch, Manfred;
    • Polster, Tilman;
    • Woermann, Friedrich G.;
    • Kalbhenn, Thilo;
    • Hamer, Hajo;
    • Rössler, Karl;
    • Mühlebner, Angelika;
    • Spliet, Wim G. M.;
    • Feucht, Martha;
    • Hou, Yanghao;
    • Stichel, Damian;
    • Korshunov, Andrey;
    • Sahm, Felix;
    • Coras, Roland;
    • Blümcke, Ingmar;
    • von Deimling, Andreas
    Publication type:
    Article
    27

    Renal angiomyolipoma in patients with tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increase disease Awareness.

    Published in:
    Nephrology Dialysis Transplantation, 2019, v. 34, n. 3, p. 502, doi. 10.1093/ndt/gfy063
    By:
    • Kingswood, J Chris;
    • Belousova, Elena;
    • Benedik, Mirjana P;
    • Carter, Tom;
    • Cottin, Vincent;
    • Curatolo, Paolo;
    • Dahlin, Maria;
    • Amato, Lisa D';
    • d'Augères, Guillaume Beaure;
    • Vries, Petrus J de;
    • Ferreira, José C;
    • Feucht, Martha;
    • Fladrowski, Carla;
    • Hertzberg, Christoph;
    • Jozwiak, Sergiusz;
    • Lawson, John A;
    • Macaya, Alfons;
    • Marques, Ruben;
    • Nabbout, Rima;
    • O'Callaghan, Finbar
    Publication type:
    Article
    28

    miRNAs and isomiRs: Serum-Based Biomarkers for the Development of Intellectual Disability and Autism Spectrum Disorder in Tuberous Sclerosis Complex.

    Published in:
    Biomedicines, 2022, v. 10, n. 8, p. N.PAG, doi. 10.3390/biomedicines10081838
    By:
    • Scheper, Mirte;
    • Romagnolo, Alessia;
    • Besharat, Zein Mersini;
    • Iyer, Anand M.;
    • Moavero, Romina;
    • Hertzberg, Christoph;
    • Weschke, Bernhard;
    • Riney, Kate;
    • Feucht, Martha;
    • Scholl, Theresa;
    • Petrak, Borivoj;
    • Maulisova, Alice;
    • Nabbout, Rima;
    • Jansen, Anna C.;
    • Jansen, Floor E.;
    • Lagae, Lieven;
    • Urbanska, Malgorzata;
    • Ferretti, Elisabetta;
    • Tempes, Aleksandra;
    • Blazejczyk, Magdalena
    Publication type:
    Article
    29
    30

    Vigabatrin‐associated brain magnetic resonance imaging abnormalities and clinical symptoms in infants with tuberous sclerosis complex.

    Published in:
    Epilepsia (Series 4), 2025, v. 66, n. 2, p. 356, doi. 10.1111/epi.18190
    By:
    • Stevering, Carmen;
    • Lequin, Maarten;
    • Szczepaniak, Kinga;
    • Sadowski, Krzysztof;
    • Ishrat, Saba;
    • De Luca, Alberto;
    • Leemans, Alexander;
    • Otte, Willem;
    • Kwiatkowski, David J.;
    • Curatolo, Paolo;
    • Weschke, Bernhard;
    • Riney, Kate;
    • Feucht, Martha;
    • Krsek, Pavel;
    • Nabbout, Rima;
    • Jansen, Anna;
    • Wojdan, Konrad;
    • Sijko, Kamil;
    • Glowacka‐Walas, Jagoda;
    • Borkowska, Julita
    Publication type:
    Article
    31

    Perampanel as precision therapy in rare genetic epilepsies.

    Published in:
    Epilepsia (Series 4), 2023, v. 64, n. 4, p. 866, doi. 10.1111/epi.17530
    By:
    • Nissenkorn, Andreea;
    • Kluger, Gerhard;
    • Schubert‐Bast, Susanne;
    • Bayat, Allan;
    • Bobylova, Marya;
    • Bonanni, Paolo;
    • Ceulemans, Berten;
    • Coppola, Antonietta;
    • Di Bonaventura, Carlo;
    • Feucht, Martha;
    • Fuchs, Anne;
    • Gröppel, Gudrun;
    • Heimer, Gali;
    • Herdt, Brigitte;
    • Kulikova, Sviatlana;
    • Mukhin, Konstantin;
    • Nicassio, Stefania;
    • Orsini, Alessandro;
    • Panagiotou, Maria;
    • Pringsheim, Milka
    Publication type:
    Article
    32

    Increased expression of complement components in tuberous sclerosis complex and focal cortical dysplasia type 2B brain lesions.

    Published in:
    Epilepsia (Series 4), 2022, v. 63, n. 2, p. 364, doi. 10.1111/epi.17139
    By:
    • Gruber, Victoria‐Elisabeth;
    • Luinenburg, Mark J.;
    • Colleselli, Katrin;
    • Endmayr, Verena;
    • Anink, Jasper J.;
    • Zimmer, Till S.;
    • Jansen, Floor;
    • Gosselaar, Peter;
    • Coras, Roland;
    • Scholl, Theresa;
    • Blumcke, Ingmar;
    • Pimentel, José;
    • Hainfellner, Johannes A.;
    • Höftberger, Romana;
    • Rössler, Karl;
    • Feucht, Martha;
    • van Scheppingen, Jackelien;
    • Aronica, Eleonora;
    • Mühlebner, Angelika
    Publication type:
    Article
    33

    Early epileptiform EEG activity in infants with tuberous sclerosis complex predicts epilepsy and neurodevelopmental outcomes.

    Published in:
    Epilepsia (Series 4), 2021, v. 62, n. 5, p. 1208, doi. 10.1111/epi.16892
    By:
    • De Ridder, Jessie;
    • Verhelle, Birgit;
    • Vervisch, Jan;
    • Lemmens, Katrien;
    • Kotulska, Katarzyna;
    • Moavero, Romina;
    • Curatolo, Paolo;
    • Weschke, Bernhard;
    • Riney, Kate;
    • Feucht, Martha;
    • Krsek, Pavel;
    • Nabbout, Rima;
    • Jansen, Anna C.;
    • Wojdan, Konrad;
    • Domanska‐Pakieła, Dorota;
    • Kaczorowska‐Frontczak, Magdalena;
    • Hertzberg, Christoph;
    • Ferrier, Cyrille H.;
    • Samueli, Sharon;
    • Benova, Barbora
    Publication type:
    Article
    34
    35

    Impaired myelin production due to an intrinsic failure of oligodendrocytes in mTORpathies.

    Published in:
    Neuropathology & Applied Neurobiology, 2021, v. 47, n. 6, p. 812, doi. 10.1111/nan.12744
    By:
    • Gruber, Victoria‐Elisabeth;
    • Lang, Judith;
    • Endmayr, Verena;
    • Diehm, Robert;
    • Pimpel, Birgit;
    • Glatter, Sarah;
    • Anink, Jasper J.;
    • Bongaarts, Anika;
    • Luinenburg, Mark J.;
    • Reinten, Roy J.;
    • van der Wel, Nicole;
    • Larsen, Per;
    • Hainfellner, Johannes A.;
    • Rössler, Karl;
    • Aronica, Eleonora;
    • Scholl, Theresa;
    • Mühlebner, Angelika;
    • Feucht, Martha
    Publication type:
    Article
    36

    MicroRNA‐34a activation in tuberous sclerosis complex during early brain development may lead to impaired corticogenesis.

    Published in:
    Neuropathology & Applied Neurobiology, 2021, v. 47, n. 6, p. 796, doi. 10.1111/nan.12717
    By:
    • Korotkov, Anatoly;
    • Sim, Nam Suk;
    • Luinenburg, Mark J.;
    • Anink, Jasper J.;
    • van Scheppingen, Jackelien;
    • Zimmer, Till S.;
    • Bongaarts, Anika;
    • Broekaart, Diede W. M.;
    • Mijnsbergen, Caroline;
    • Jansen, Floor E.;
    • Van Hecke, Wim;
    • Spliet, Wim G. M.;
    • van Rijen, Peter C.;
    • Feucht, Martha;
    • Hainfellner, Johannes A.;
    • Kršek, Pavel;
    • Zamecnik, Josef;
    • Crino, Peter B.;
    • Kotulska, Katarzyna;
    • Lagae, Lieven
    Publication type:
    Article
    37
    38

    Historical Patterns of Diagnosis, Treatments, and Outcome of Epilepsy Associated With Tuberous Sclerosis Complex: Results From TOSCA Registry.

    Published in:
    Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.697467
    By:
    • Nabbout, Rima;
    • Belousova, Elena;
    • Benedik, Mirjana P.;
    • Carter, Tom;
    • Cottin, Vincent;
    • Curatolo, Paolo;
    • Dahlin, Maria;
    • D'Amato, Lisa;
    • Beaure d'Augères, Guillaume;
    • de Vries, Petrus J.;
    • Ferreira, José C.;
    • Feucht, Martha;
    • Fladrowski, Carla;
    • Hertzberg, Christoph;
    • Jozwiak, Sergiusz;
    • Lawson, John A.;
    • Macaya, Alfons;
    • Marques, Ruben;
    • O'Callaghan, Finbar;
    • Qin, Jiong
    Publication type:
    Article
    39
    40

    TuberOus SClerosis registry to increAse disease awareness (TOSCA) Post-Authorisation Safety Study of Everolimus in Patients With Tuberous Sclerosis Complex.

    Published in:
    Frontiers in Neurology, 2021, v. 11, p. N.PAG, doi. 10.3389/fneur.2021.630378
    By:
    • Kingswood, J. Chris;
    • Belousova, Elena;
    • Benedik, Mirjana P.;
    • Budde, Klemens;
    • Carter, Tom;
    • Cottin, Vincent;
    • Curatolo, Paolo;
    • Dahlin, Maria;
    • D'Amato, Lisa;
    • d'Augères, Guillaume B.;
    • de Vries, Petrus J.;
    • Ferreira, José C.;
    • Feucht, Martha;
    • Fladrowski, Carla;
    • Hertzberg, Christoph;
    • Jozwiak, Sergiusz;
    • Lawson, John A.;
    • Macaya, Alfons;
    • Marques, Ruben;
    • Nabbout, Rima
    Publication type:
    Article
    41

    Prediction of Neurodevelopment in Infants With Tuberous Sclerosis Complex Using Early EEG Characteristics.

    Published in:
    Frontiers in Neurology, 2020, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.582891
    By:
    • De Ridder, Jessie;
    • Lavanga, Mario;
    • Verhelle, Birgit;
    • Vervisch, Jan;
    • Lemmens, Katrien;
    • Kotulska, Katarzyna;
    • Moavero, Romina;
    • Curatolo, Paolo;
    • Weschke, Bernhard;
    • Riney, Kate;
    • Feucht, Martha;
    • Krsek, Pavel;
    • Nabbout, Rima;
    • Jansen, Anna C.;
    • Wojdan, Konrad;
    • Domanska-Pakieła, Dorota;
    • Kaczorowska-Frontczak, Magdalena;
    • Hertzberg, Christoph;
    • Ferrier, Cyrille H.;
    • Samueli, Sharon
    Publication type:
    Article
    42

    Renal Manifestations of Tuberous Sclerosis Complex: Key Findings From the Final Analysis of the TOSCA Study Focussing Mainly on Renal Angiomyolipomas.

    Published in:
    Frontiers in Neurology, 2020, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.00972
    By:
    • Kingswood, J. Chris;
    • Belousova, Elena;
    • Benedik, Mirjana P.;
    • Carter, Tom;
    • Cottin, Vincent;
    • Curatolo, Paolo;
    • Dahlin, Maria;
    • D'Amato, Lisa;
    • Beaure d'Augères, Guillaume;
    • de Vries, Petrus J.;
    • Ferreira, José C.;
    • Feucht, Martha;
    • Fladrowski, Carla;
    • Hertzberg, Christoph;
    • Jozwiak, Sergiusz;
    • Lawson, John A.;
    • Macaya, Alfons;
    • Marques, Ruben;
    • Nabbout, Rima;
    • O'Callaghan, Finbar
    Publication type:
    Article
    43
    44
    45

    Novel patients with NHLRC2 variants expand the phenotypic spectrum of FINCA disease.

    Published in:
    Frontiers in Neuroscience, 2023, p. 01, doi. 10.3389/fnins.2023.1123327
    By:
    • Tallgren, Antti;
    • Kager, Leo;
    • O'Grady, Gina;
    • Tuominen, Hannu;
    • Körkkö, Jarmo;
    • Kuismin, Outi;
    • Feucht, Martha;
    • Wilson, Callum;
    • Behunova, Jana;
    • England, Eleina;
    • Kurki, Mitja I.;
    • Palotie, Aarno;
    • Hallman, Mikko;
    • Kaarteenaho, Riitta;
    • Laccone, Franco;
    • Boztug, Kaan;
    • Hinttala, Reetta;
    • Uusimaa, Johanna
    Publication type:
    Article
    46

    The coding and non-coding transcriptional landscape of subependymal giant cell astrocytomas.

    Published in:
    2019
    By:
    • Bongaarts, Anika;
    • van Scheppingen, Jackelien;
    • Korotkov, Anatoly;
    • Mijnsbergen, Caroline;
    • Anink, Jasper J;
    • Jansen, Floor E;
    • Spliet, Wim G M;
    • den Dunnen, Wilfred F A;
    • Gruber, Victoria E;
    • Scholl, Theresa;
    • Samueli, Sharon;
    • Hainfellner, Johannes A;
    • Feucht, Martha;
    • Kotulska, Katarzyna;
    • Jozwiak, Sergiusz;
    • Grajkowska, Wieslawa;
    • Buccoliero, Anna Maria;
    • Caporalini, Chiara;
    • Giordano, Flavio;
    • Genitori, Lorenzo
    Publication type:
    journal article
    47
    48
    49

    Correction to: Implementation of a 7T Epilepsy Task Force consensus imaging protocol for routine presurgical epilepsy work-up: effect on diagnostic yield and lesion delineation.

    Published in:
    2024
    By:
    • Hangel, Gilbert;
    • Kasprian, Gregor;
    • Chambers, Stefanie;
    • Haider, Lukas;
    • Lazen, Philipp;
    • Koren, Johannes;
    • Diehm, Robert;
    • Moser, Katharina;
    • Tomschik, Matthias;
    • Wais, Jonathan;
    • Winter, Fabian;
    • Zeiser, Vitalij;
    • Gruber, Stephan;
    • Aull-Watschinger, Susanne;
    • Traub-Weidinger, Tatjana;
    • Baumgartner, Christoph;
    • Feucht, Martha;
    • Dorfer, Christian;
    • Bogner, Wolfgang;
    • Trattnig, Siegfried
    Publication type:
    Correction Notice
    50

    Implementation of a 7T Epilepsy Task Force consensus imaging protocol for routine presurgical epilepsy work-up: effect on diagnostic yield and lesion delineation.

    Published in:
    Journal of Neurology, 2024, v. 271, n. 2, p. 804, doi. 10.1007/s00415-023-11988-5
    By:
    • Hangel, Gilbert;
    • Kasprian, Gregor;
    • Chambers, Stefanie;
    • Haider, Lukas;
    • Lazen, Philipp;
    • Koren, Johannes;
    • Diehm, Robert;
    • Moser, Katharina;
    • Tomschik, Matthias;
    • Wais, Jonathan;
    • Winter, Fabian;
    • Zeiser, Vitalij;
    • Gruber, Stephan;
    • Aull-Watschinger, Susanne;
    • Traub-Weidinger, Tatjana;
    • Baumgartner, Christoph;
    • Feucht, Martha;
    • Dorfer, Christian;
    • Bogner, Wolfgang;
    • Trattnig, Siegfried
    Publication type:
    Article