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Number of items: 2.
Journal article
Bockmayr, Michael; Harnisch, Kim; Pohl, Lara C.; Schweizer, Leonille; Mohme, Theresa; Korner, Meik; Alawi, Malik; Suwala, Abigail K.; Dorostkar, Mario M.; Monoranu, Camelia M.; Hasselblatt, Martin; Wefers, Annika K.; Capper, David; Hench, Juergen; Frank, Stephan; Richardson, Timothy E.; Tran, Ivy; Liu, Elisa; Snuderl, Matija; Engertsberger, Lara; Benesch, Martin; Deimling, Andreas von; Obrecht, Denise; Mynarek, Martin; Rutkowski, Stefan; Glatzel, Markus; Neumann, Julia E. und Schueller, Ulrich
(2022):
Comprehensive profiling of myxopapillary ependymomas identifies a distinct molecular subtype with relapsing disease.
In: Neuro-Oncology, Vol. 24, No. 10: pp. 1689-1699
Schneeberger, Pauline E.; Kortuem, Fanny; Korenke, Georg Christoph; Alawi, Malik; Santer, Rene; Woidy, Mathias; Buhas, Daniela; Fox, Stephanie; Juusola, Jane; Alfadhel, Majid; Webb, Bryn D.; Coci, Emanuele G.; Abou Jamra, Rami; Siekmeyer, Manuela; Biskup, Saskia; Heller, Corina; Maier, Esther M.; Javaher-Haghighi, Poupak; Bedeschi, Maria F.; Ajmone, Paola F.; Iascone, Maria; Peeters, Hilde; Ballon, Katleen; Jaeken, Jaak; Alonso, Aroa Rodriguez; Palomares-Bralo, Maria; Santos-Simarro, Fernando; Meuwissen, Marije E. C.; Beysen, Diane; Kooy, R. Frank; Houlden, Henry; Murphy, David; Doosti, Mohammad; Karimiani, Ehsan G.; Mojarrad, Majid; Maroofian, Reza; Noskova, Lenka; Kmoch, Stanislav; Honzik, Tomas; Cope, Heidi; Sanchez-Valle, Amarilis; Gelb, Bruce D.; Kurth, Ingo; Hempel, Maja und Kutsche, Kerstin
(2020):
Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder.
In: Brain, Vol. 143: pp. 2437-2453