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Search Results - Gjerulfsen, Cathrine E.
Search Results - Gjerulfsen, Cathrine E.
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Fenfluramine treatment in pediatric patients with Dravet syndrome reduces seizure burden and overall healthcare costs: A retrospective and observational real‐world study
by
Gjerulfsen, Cathrine E.
,
Nikanorova, Marina
,
Olofsson, Kern
,
Johannessen Landmark, Cecilie
,
Rubboli, Guido
,
Møller, Rikke S.
Published in
Epilepsia open
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Vinpocetine improved neuropsychiatric and epileptic outcomes in a patient with a GABRA1 loss‐of‐function variant
by
Gjerulfsen, Cathrine E.
,
Mieszczanek, Tomasz S.
,
Johannesen, Katrine M.
,
Liao, Vivian W. Y.
,
Chebib, Mary
,
Nørby, Helene A. J.
,
Gardella, Elena
,
Rubboli, Guido
,
Ahring, Philip
,
Møller, Rikke S.
Published in
Annals of clinical and translational neurology
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Expansion of the CCDC22 associated Ritscher-Schinzel/3C syndrome and review of the literature: Should the minimal diagnostic criteria be revised?
by
Gjerulfsen, Cathrine E.
,
Møller, Rikke S.
,
Fenger, Christina D.
,
Hammer, Trine B.
,
Bayat, Allan
Published in
European journal of medical genetics
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Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
by
Johannesen, Katrine M
,
Liu, Yuanyuan
,
Koko, Mahmoud
,
Gjerulfsen, Cathrine E
,
Sonnenberg, Lukas
,
Schubert, Julian
,
Fenger, Christina D
,
Eltokhi, Ahmed
,
Rannap, Maert
,
Koch, Nils A
,
Lauxmann, Stephan
,
Krüger, Johanna
,
Kegele, Josua
,
Canafoglia, Laura
,
Franceschetti, Silvana
,
Mayer, Thomas
,
Rebstock, Johannes
,
Zacher, Pia
,
Ruf, Susanne
,
Alber, Michael
,
Sterbova, Katalin
,
Lassuthová, Petra
,
Vlckova, Marketa
,
Lemke, Johannes R
,
Platzer, Konrad
,
Krey, Ilona
,
Heine, Constanze
,
Wieczorek, Dagmar
,
Kroell-Seger, Judith
,
Lund, Caroline
,
Klein, Karl Martin
,
Au, P Y Billie
,
Rho, Jong M
,
Ho, Alice W
,
Masnada, Silvia
,
Veggiotti, Pierangelo
,
Giordano, Lucio
,
Accorsi, Patrizia
,
Hoei-Hansen, Christina E
,
Striano, Pasquale
,
Zara, Federico
,
Verhelst, Helene
,
Verhoeven, Judith S
,
Braakman, Hilde M H
,
van der Zwaag, Bert
,
Harder, Aster V E
,
Brilstra, Eva
,
Pendziwiat, Manuela
,
Lebon, Sebastian
,
Vaccarezza, Maria
,
Le, Ngoc Minh
,
Christensen, Jakob
,
Grønborg, Sabine
,
Scherer, Stephen W
,
Howe, Jennifer
,
Fazeli, Walid
,
Howell, Katherine B
,
Leventer, Richard
,
Stutterd, Chloe
,
Walsh, Sonja
,
Gerard, Marion
,
Gerard, Bénédicte
,
Matricardi, Sara
,
Bonardi, Claudia M
,
Sartori, Stefano
,
Berger, Andrea
,
Hoffman-Zacharska, Dorota
,
Mastrangelo, Massimo
,
Darra, Francesca
,
Vøllo, Arve
,
Motazacker, M Mahdi
,
Lakeman, Phillis
,
Nizon, Mathilde
,
Betzler, Cornelia
,
Altuzarra, Cecilia
,
Caume, Roseline
,
Roubertie, Agathe
,
Gélisse, Philippe
,
Marini, Carla
,
Guerrini, Renzo
,
Bilan, Frederic
,
Tibussek, Daniel
,
Koch-Hogrebe, Margarete
,
Perry, M Scott
,
Ichikawa, Shoji
,
Dadali, Elena
,
Sharkov, Artem
,
Mishina, Irina
,
Abramov, Mikhail
,
Kanivets, Ilya
,
Korostelev, Sergey
,
Kutsev, Sergey
,
Wain, Karen E
,
Eisenhauer, Nancy
,
Wagner, Monisa
,
Savatt, Juliann M
,
Müller-Schlüter, Karen
,
Bassan, Haim
,
Borovikov, Artem
,
Nassogne, Marie Cecile
Published in
Brain (London, England : 1878)
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Clinical and molecular characterization of patients with YWHAG‐related epilepsy
by
Cetica, Valentina
,
Pisano, Tiziana
,
Lesca, Gaetan
,
Marafi, Dana
,
Licchetta, Laura
,
Riccardi, Florence
,
Mei, Davide
,
Chung, Hon‐yin B.
,
Bayat, Allan
,
Balasubramanian, Meena
,
Lowenstein, Daniel H.
,
Endzinienė, Milda
,
Alotaibi, Maha
,
Villeneuve, Nathalie
,
Jacobs, Julia
,
Isidor, Bertrand
,
Solazzi, Roberta
,
Hollander, Nicolette S.
,
Marjanovic, Dragan
,
Rougeot‐Jung, Christelle
,
Jung, Julien
,
Lesieur‐Sebellin, Marion
,
Accogli, Andrea
,
Salpietro, Vincenzo
,
Saadi, Nebal W.
,
Panagiotakaki, Eleni
,
Foiadelli, Thomas
,
Redon, Sylvia
,
Tsai, Meng‐Han
,
Bisulli, Francesca
,
Hammer, Trine B.
,
Lupski, James R.
,
Parrini, Elena
,
Guerrini, Renzo
,
Alotaibi, Lena
,
Ambrosetti, Irene
,
Bellanger, Séverine A.
,
Castellotti, Barbara
,
Cavallin, Mara
,
Chan, Joshua C. K.
,
Chatron, Nicolas
,
Chavany, Julie
,
Cogne, Benjamin
,
Fung, Jasmine L. F.
,
Gjerulfsen, Cathrine E.
,
Granata, Tiziana
,
Guimier, Anne
,
Herman, Isabella
,
Ho, Chen‐Jui
,
Mandorlini, Claudia
,
Milh, Mathieu
,
Minardi, Raffaella
,
Montanari, Francesca
,
Rosenfeld, Jill A.
,
Moller, Rikke S.
,
Operto, Francesca F.
,
Posey, Jennifer E.
,
Ruivenkamp, Claudia A. L.
,
Sacaze, Elise
,
Santi, Viola
,
Savasta, Salvatore
,
Touraine, Renaud
,
Tumiene, Birute
,
Uguen, Kevin
,
Villard, Laurent
Published in
Epilepsia (Copenhagen)
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PURA- Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum
by
Johannesen, Katrine M
,
Gardella, Elena
,
Gjerulfsen, Cathrine E
,
Bayat, Allan
,
Rouhl, Rob P W
,
Reijnders, Margot
,
Whalen, Sandra
,
Keren, Boris
,
Buratti, Julien
,
Courtin, Thomas
,
Wierenga, Klaas J
,
Isidor, Bertrand
,
Piton, Amélie
,
Faivre, Laurence
,
Garde, Aurore
,
Moutton, Sébastien
,
Tran-Mau-Them, Frédéric
,
Denommé-Pichon, Anne-Sophie
,
Coubes, Christine
,
Larson, Austin
,
Esser, Michael J
,
Appendino, Juan Pablo
,
Al-Hertani, Walla
,
Gamboni, Beatriz
,
Mampel, Alejandra
,
Mayorga, Lía
,
Orsini, Alessandro
,
Bonuccelli, Alice
,
Suppiej, Agnese
,
Van-Gils, Julien
,
Vogt, Julie
,
Damioli, Simona
,
Giordano, Lucio
,
Moortgat, Stephanie
,
Wirrell, Elaine
,
Hicks, Sarah
,
Kini, Usha
,
Noble, Nathan
,
Stewart, Helen
,
Asakar, Shailesh
,
Cohen, Julie S
,
Naidu, SakkuBai R
,
Collier, Ashley
,
Brilstra, Eva H
,
Li, Mindy H
,
Brew, Casey
,
Bigoni, Stefania
,
Ognibene, Davide
,
Ballardini, Elisa
,
Ruivenkamp, Claudia
,
Faggioli, Raffaella
,
Afenjar, Alexandra
,
Rodriguez, Diana
,
Bick, David
,
Segal, Devorah
,
Coman, David
,
Gunning, Boudewijn
,
Devinsky, Orrin
,
Demmer, Laurie A
,
Grebe, Theresa
,
Pruna, Dario
,
Cursio, Ida
,
Greenhalgh, Lynn
,
Graziano, Claudio
,
Singh, Rahul Raman
,
Cantalupo, Gaetano
,
Willems, Marjolaine
,
Yoganathan, Sangeetha
,
Góes, Fernanda
,
Leventer, Richard J
,
Colavito, Davide
,
Olivotto, Sara
,
Scelsa, Barbara
,
Andrade, Andrea V
,
Ratke, Kelly
,
Tokarz, Farha
,
Khan, Atiya S
,
Ormieres, Clothilde
,
Benko, William
,
Keough, Karen
,
Keros, Sotirios
,
Hussain, Shanawaz
,
Franques, Ashlea
,
Varsalone, Felicia
,
Grønborg, Sabine
,
Mignot, Cyril
,
Heron, Delphine
,
Nava, Caroline
,
Isapof, Arnaud
,
Borlot, Felippe
,
Whitney, Robyn
,
Ronan, Anne
,
Foulds, Nicola
,
Somorai, Marta
,
Brandsema, John
,
Helbig, Katherine L
,
Helbig, Ingo
,
Ortiz-González, Xilma R
,
Dubbs, Holly
,
Vitobello, Antonio
Published in
Neurology. Genetics
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Fenfluramine treatment in pediatric patients with Dravet syndrome reduces seizure burden and overall healthcare costs: A retrospective and observational real-world study
by
Gjerulfsen, Cathrine E
,
Nikanorova, Marina
,
Olofsson, Kern
,
Landmark, Cecilie Johannessen
,
Rubboli, Guido
,
Møller, Rikke Steensbjerre
Published in
Epilepsia Open
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Article
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8
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Vinpocetine improved neuropsychiatric and epileptic outcomes in a patient with a GABRA1 loss-of-function variant
by
Gjerulfsen, Cathrine E
,
Mieszczanek, Tomasz S
,
Johannesen, Katrine M
,
Liao, Vivian W Y
,
Chebib, Mary
,
Nørby, Helene A J
,
Gardella, Elena
,
Rubboli, Guido
,
Ahring, Philip
,
Møller, Rikke S
Published in
Annals of clinical and translational neurology
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