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Hollstein, Ronja, Parry, David A, Nalbach, Lisa, Logan, Clare V, Strom, Tim M, Hartill, Verity L, Carr, Ian M, Korenke, Georg C, Uppal, Sandeep, Ahmed, Mushtaq, Wieland, Thomas, Markham, Alexander F, Bennett, Christopher P, Gillessen-Kaesbach, Gabriele, Sheridan, Eamonn G, Kaiser, Frank J, Bonthron, David T
Published in Journal of medical genetics (01.12.2015)
Published in Journal of medical genetics (01.12.2015)
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Epilepsy in KCNH1‐related syndromes
Mastrangelo, Mario, Scheffer, Ingrid E., Bramswig, Nuria C., Nair, Lal. D.V., Myers, Candace T., Dentici, Maria Lisa, Korenke, Georg C., Schoch, Kelly, Campeau, Philippe M., White, Susan M., Shashi, Vandana, Kansagra, Sujay, Van Essen, Anthonie J., Leuzzi, Vincenzo
Published in Epileptic disorders (01.06.2016)
Published in Epileptic disorders (01.06.2016)
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Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/− mice
Pringsheim, Milka, Mitter, Diana, Schröder, Simone, Warthemann, Rita, Plümacher, Kim, Kluger, Gerhard, Baethmann, Martina, Bast, Thomas, Braun, Sarah, Büttel, Hans‐Martin, Conover, Elizabeth, Courage, Carolina, Datta, Alexandre N., Eger, Angelika, Grebe, Theresa A., Hasse‐Wittmer, Annette, Heruth, Marion, Höft, Karen, Kaindl, Angela M., Karch, Stephanie, Kautzky, Torsten, Korenke, Georg C., Kruse, Bernd, Lutz, Richard E., Omran, Heymut, Patzer, Steffi, Philippi, Heike, Ramsey, Keri, Rating, Tina, Rieß, Angelika, Schimmel, Mareike, Westman, Rachel, Zech, Frank‐Martin, Zirn, Birgit, Ulmke, Pauline A., Sokpor, Godwin, Tuoc, Tran, Leha, Andreas, Staudt, Martin, Brockmann, Knut
Published in Annals of clinical and translational neurology (01.04.2019)
Published in Annals of clinical and translational neurology (01.04.2019)
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Structural brain anomalies in patients with FOXG 1 syndrome and in Foxg1+/− mice
Pringsheim, Milka, Mitter, Diana, Schröder, Simone, Warthemann, Rita, Plümacher, Kim, Kluger, Gerhard, Baethmann, Martina, Bast, Thomas, Braun, Sarah, Büttel, Hans‐Martin, Conover, Elizabeth, Courage, Carolina, Datta, Alexandre N., Eger, Angelika, Grebe, Theresa A., Hasse‐Wittmer, Annette, Heruth, Marion, Höft, Karen, Kaindl, Angela M., Karch, Stephanie, Kautzky, Torsten, Korenke, Georg C., Kruse, Bernd, Lutz, Richard E., Omran, Heymut, Patzer, Steffi, Philippi, Heike, Ramsey, Keri, Rating, Tina, Rieß, Angelika, Schimmel, Mareike, Westman, Rachel, Zech, Frank‐Martin, Zirn, Birgit, Ulmke, Pauline A., Sokpor, Godwin, Tuoc, Tran, Leha, Andreas, Staudt, Martin, Brockmann, Knut
Published in Annals of clinical and translational neurology (01.04.2019)
Published in Annals of clinical and translational neurology (01.04.2019)
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Atypical (mild) forms of dihydropteridine reductase deficiency : neurochemical evaluation and mutation detection
BLAU, N, HEIZMANN, C. W, SPERL, W, KORENKE, G. C, HOFFMANN, G. F, SMOOKER, P. M, COTTON, R. G. H
Published in Pediatric research (01.12.1992)
Published in Pediatric research (01.12.1992)
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