Dynorphin‐based “release on demand” gene therapy for drug‐resistant temporal lobe epilepsy von Agostinho, Alexandra S, Mietzsch, Mario, Zangrandi, Luca, Kmiec, Iwona, Mutti, Anna, Kraus, Larissa, Fidzinski, Pawel, Schneider, Ulf C, Holtkamp, Martin, Heilbronn, Regine, Schwarzer, Christoph

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Is there heart disease in cases of neurodegeneration associated with mutations in C19orf12? von Skowronska, Marta, Buksinska-Lisik, Malgorzata, Kmiec, Tomasz, Litwin, Tomasz, Kurkowska-Jastrzębska, Iwona, Czlonkowska, Anna

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Eye of the tiger sign in a 23 year patient with mitochondrial membrane protein associated neurodegeneration von Skowronska, Marta, Kmiec, Tomasz, Kurkowska-Jastrzębska, Iwona, Czlonkowska, Anna

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Eye of the tiger sign in a 23year patient with mitochondrial membrane protein associated neurodegeneration von Skowronska, Marta, Kmiec, Tomasz, Kurkowska-Jastrzębska, Iwona, Czlonkowska, Anna

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Aphid-stimulated transcriptional reconfigurations of chlorophyllase-2 gene in maize (Zea mays L.) seedlings von Sytykiewicz, Hubert, Gabryś, Beata, Dancewicz, Katarzyna, Borowiak-Sobkowiak, Beata, Kmieć, Katarzyna, Łukasik, Iwona, Sprawka, Iwona, Sempruch, Cezary, Chrzanowski, Grzegorz

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Hair Concentration of Selenium in European Bison in Relation to Sex and Age, with Regard to Liver and Kidney Se Levels von Kośla, Tadeusz, Małgorzata Skibniewska, Ewa, Skibniewski, Michał, Małgorzata Kołnierzak, Marta, Lasocka, Iwona, Kmieć, Hubert

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Severe phenotypes of SMARD1 associated with novel mutations of the IGHMBP2 gene and nuclear degeneration of muscle and Schwann cells von Jędrzejowska, Maria, Madej-Pilarczyk, Agnieszka, Fidziańska, Anna, Mierzewska, Hanna, Pronicka, Ewa, Obersztyn, Ewa, Gos, Monika, Pronicki, Maciej, Kmieć, Tomasz, Migdał, Marek, Mierzewska-Schmidt, Magdalena, Walczak-Wojtkowska, Iwona, Konopka, Elżbieta, Hausmanowa-Petrusewicz, Irena

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MRI of a family with leukoencephalypathy with vanishing white matter von Jurkiewicz, Elzbieta, Mierzewska, Hanna, Bekiesińska-Figatowska, Monika, Pakua-Kościesza, Iwona, Kmieć, Tomasz, Scheper, Gert, van der Knaap, Marjo S, Pronicka, Ewa

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Homozygote for mutation c.1204 + 1G > A of the ARSA gene presents with a late-infantile form of metachromatic leukodystrophy and a rare MRI white matter lesion type von Ługowska, Agnieszka, Szymańska, Krystyna, Kmiec, Tomasz, Tarczyńska, Iwona, Czartoryska, Barbara, Tylki-Szymańska, Anna, Jurkiewicz, Elzbieta

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Eye of the tiger sign in a 23 year patient with mitochondrial membrane protein associated neurodegeneration von Skowronska, Marta, Kmiec, Tomasz, Kurkowska-Jastrzębska, Iwona, Czlonkowska, Anna

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