1. 7‐Tesla Magnetic Resonance Imaging for Brain Iron Quantification in Homozygous and Heterozygous PANK2 Mutation Carriers. Issue 4 (23rd October 2014) Authors: Dusek, Petr; Tovar Martinez, Elena Maria; Madai, Vince Istvan; Jech, Robert; Sobesky, Jan; Paul, Friedemann; Niendorf, Thoralf; Wuerfel, Jens; Schneider, Susanne A. Journal: Movement disorders clinical practice Issue: Volume 1:Issue 4(2014) Page Start: 329 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Abnormalities of Masseteric Inhibitory Reflex in Hereditary Geniospasm: Evidence for a Brainstem Myoclonus. Issue 1 (13th October 2014) Authors: Macerollo, Antonella; Saifee, Tabish A.; Kassavetis, Panagiotis; Pilurzi, Giovanna; Schneider, Susanne A.; Edwards, Mark J.; Bhatia, Kailash P. Journal: Movement disorders clinical practice Issue: Volume 2:Issue 1(2015) Page Start: 49 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Alpha synuclein and crystallin expression in human lens in Parkinson's disease. Issue 4 (16th February 2016) Authors: Klettner, Alexa; Richert, Elisabeth; Kuhlenbäumer, Gregor; Nölle, Bernhard; Bhatia, Kailash P.; Deuschl, Günter; Roider, Johann; Schneider, Susanne A. Journal: Movement disorders Issue: Volume 31:Issue 4(2016) Page Start: 600 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Atypical Parkinsonism‐Dystonia Syndrome Caused by a Novel DJ1 Mutation. Issue 1 (April 2014) Authors: Bras, Jose M.; Guerreiro, Rita J.; Teo, James T.H.; Darwent, Lee; Vaughan, Jenny; Molloy, Sophie; Hardy, John; Schneider, Susanne A. Journal: Movement disorders clinical practice Issue: Volume 1:Issue 1(2014) Page Start: 45 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Brain iron accumulation in Wilson's disease: A longitudinal imaging case study during anticopper treatment using 7.0T MRI and transcranial sonography. Issue 1 (4th April 2017) Authors: Dusek, Petr; Skoloudik, David; Maskova, Jana; Huelnhagen, Till; Bruha, Radan; Zahorakova, Daniela; Niendorf, Thoralf; Ruzicka, Evzen; Schneider, Susanne A.; Wuerfel, Jens Journal: Journal of magnetic resonance imaging Issue: Volume 47:Issue 1(2018) Page Start: 282 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Brain Iron and Metabolic Abnormalities in C19orf12 Mutation Carriers: A 7.0 Tesla MRI Study in Mitochondrial Membrane Protein–Associated Neurodegeneration. Issue 1 (13th September 2019) Authors: Dusek, Petr; Mekle, Ralf; Skowronska, Marta; Acosta‐Cabronero, Julio; Huelnhagen, Till; Robinson, Simon Daniel; Schubert, Florian; Deschauer, Marcus; Els, Antje; Ittermann, Bernd; Schottmann, Gudrun; Madai, Vince I.; Paul, Friedemann; Klopstock, Thomas; Kmiec, Tomasz; Niendorf, Thoralf; Wuerfel, ... Journal: Movement disorders Issue: Volume 35:Issue 1(2020) Page Start: 142 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Brain iron and metabolic abnormalities in C19orf12 mutation carriers: A 7.0 tesla MRI study in mitochondrial membrane protein–associated neurodegeneration. Issue 1 (13th September 2019) Authors: Dusek, Petr; Mekle, Ralf; Skowronska, Marta; Acosta‐Cabronero, Julio; Huelnhagen, Till; Robinson, Simon Daniel; Schubert, Florian; Deschauer, Marcus; Els, Antje; Ittermann, Bernd; Schottmann, Gudrun; Madai, Vince I.; Paul, Friedemann; Klopstock, Thomas; Kmiec, Tomasz; Niendorf, Thoralf; Wuerfel, ... Journal: Movement disorders Issue: Volume 35:Issue 1(2020) Page Start: 142 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Clinical, ocular motor, and imaging profile of Niemann-Pick type C heterozygosity. (21st April 2020) Authors: Bremova-Ertl, Tatiana; Sztatecsny, Clara; Brendel, Matthias; Moser, Marlene; Möller, Bettina; Clevert, Dirk A.; Beck-Wödl, Stefanie; Kun-Rodrigues, Celia; Bras, Jose; Rominger, Axel; Ninov, Dimitar; Strupp, Michael; Schneider, Susanne A. Journal: Neurology Issue: Volume 94:Number 16(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. De Novo mutations in the β‐tubulin gene TUBB4: From DYT4 to leukoencephalopathy with hypomyelination with atrophy of the basal ganglia and cerebellum (H‐ABC syndrome). Issue 10 (6th September 2013) Authors: Alexoudi, Athanasia; Schneider, Susanne A. Journal: Movement disorders Issue: Volume 28:Issue 10(2013) Page Start: 1343 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Dissecting the Phenotype and Genotype of PLA2G6‐Related Parkinsonism. Issue 1 (8th October 2021) Authors: Magrinelli, Francesca; Mehta, Sahil; Di Lazzaro, Giulia; Latorre, Anna; Edwards, Mark J.; Balint, Bettina; Basu, Purba; Kobylecki, Christopher; Groppa, Sergiu; Hegde, Anaita; Mulroy, Eoin; Estevez‐Fraga, Carlos; Arora, Anshita; Kumar, Hrishikesh; Schneider, Susanne A.; Lewis, Patrick A.; Jaunmukt... Journal: Movement disorders Issue: Volume 37:Issue 1(2022) Page Start: 148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗