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Published in European journal of human genetics : EJHG (01.06.2012)
Published in European journal of human genetics : EJHG (01.06.2012)
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Multiplex families with epilepsy: Success of clinical and molecular genetic characterization
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Depression Reduces Accuracy While Parkinsonism Slows Response Time for Processing Positive Feedback in Patients with Parkinson's Disease with Comorbid Major Depressive Disorder Tested on a Probabilistic Category-Learning Task
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Depression impairs learning whereas anticholinergics impair transfer generalization in Parkinson patients tested on dopaminergic medications
Herzallah, Mohammad M, Moustafa, Ahmed A, Misk, Adel J, Al-Dweib, Lara H, Abdelrazeq, Samer A, Myers, Catherine E, Gluck, Mark A
Published in Cognitive and behavioral neurology (01.06.2010)
Published in Cognitive and behavioral neurology (01.06.2010)
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Fe/S protein assembly gene IBA57 mutation causes hereditary spastic paraplegia
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Published in Neurology (17.02.2015)
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Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia
Damiano, John A, Afawi, Zaid, Bahlo, Melanie, Mauermann, Monika, Misk, Adel, Arsov, Todor, Oliver, Karen L, Dahl, Hans-Henrik M, Shearer, A Eliot, Smith, Richard J H, Hall, Nathan E, Mahmood, Khalid, Leventer, Richard J, Scheffer, Ingrid E, Muona, Mikko, Lehesjoki, Anna-Elina, Korczyn, Amos D, Herrmann, Harald, Berkovic, Samuel F, Hildebrand, Michael S
Published in Human molecular genetics (15.08.2015)
Published in Human molecular genetics (15.08.2015)
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Founder Effect with Variable Age at Onset in Arab Families with Lafora Disease and EPM2A Mutation
Gomez‐Abad, Cristina, Afawi, Zaid, Korczyn, Amos D., Misk, Adel, Shalev, Stavit A., Spiegel, Ronen, Lerman‐Sagie, Tally, Lev, Dorit, Kron, Katherine L., Gómez‐Garre, Pilar, Serratosa, Jose M., Berkovic, Samuel F.
Published in Epilepsia (Copenhagen) (01.05.2007)
Published in Epilepsia (Copenhagen) (01.05.2007)
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