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Journal Article
Heart, ISSN 1355-6037, 08/2003, Volume 89, Issue 8, p. 817
ObjectivesRecent advances in amyotrophic lateral sclerosis (ALS) genetics have revealed that mutations in any of more than 25 genes can cause ALS, mostly as an... 
Journal Article
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 08/2018, Volume 89, Issue 8, pp. 817 - 827
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 05/2010, Volume 81, Issue 5, pp. 572 - 577
Journal Article
Aging Cell, ISSN 1474-9718, 04/2011, Volume 10, Issue 2, pp. 239 - 254
Journal Article
Journal of Cardiovascular Magnetic Resonance, ISSN 1097-6647, 2008, Volume 10, Issue 1, pp. 50 - 50
Journal Article
by van Schaik, Ivo N and Mielke, Orell and Sabet, Arman and George, Koshy and Roberts, Leslie and Carne, Ross and Blum, Stefan and Henderson, Robert and Van Damme, Philip and Demeestere, Jelle and Larue, Sandrine and Pinard D'Amour, Catherine-Andree and Bril, Vera and Breiner, Ari and Kunc, Pavel and Valis, Martin and Sussova, Jana and Kalous, Tomas and Talab, Radomir and Bednar, Michal and Toomsoo, Toomas and Rubanovits, Inna and Gross-Paju, Katrin and Sorro, Ulvi and Saarela, Mika and Auranen, Mari and Pouget, Jean and Attarian, Shahram and Le Masson, Gwendal and Wielanek-Bachelet, Anne-Cécile and Desnuelle, Claude and Delmont, Emilien and Clavelou, Pierre and Aufauvre, Dominique and Schmidt, Jens and Zschuentssch, Jana and Sommer, Claudia and Kramer, Daniela and Hoffmann, Olaf and Goerlitz, Carsten and Haas, Judith and Chatzopoulos, Marko and Yoon, Min-Suk and Gold, Ralf and Berlit, Peter and Jaspert-Grehl, Andrea and Liebetanz, David and Kutschenko, Anna and Stangel, Martin and Trebst, Corinna and Baum, Petra and Then Bergh, Florian and Klehmet, Juliane and Meisel, Andreas and Klostermann, Fabian and Oechtering, Johanna and Lehmann, Helmar and Schroeter, Michael and Hagenacker, Tim and Mueller, Daniel and Sperfeld, Anne-Dorte and Bethke, Florian and Hartung, Hans-Peter and Drory, Vivian and Algom, Avi and Yarnitsky, David and Murinson, Beth Brianna and Di Muzio, Antonio and Ciccocioppo, Fausta and Sorbi, Sandro and Mata, Sabrina and Schenone, Angelo and Grandis, Marina and Lauria, Giuseppe and Cazzato, Daniele and Antonini, Giovanni and Morino, Stefania and Cocito, Dario and Zibetti, Maurizio and Yokota, Takanori and Ohkubo, Takuya and Kanda, Takashi and Kawai, Motoharu and Kaida, Kenichi and Onoue, Hiroyuki and Kuwabara, Satoshi and Mori, Masahiro and Iijima, Masahiro and Ohyama, Ken and Sobue, Gen and Baba, Masayuki and Tomiyama, Masahiko and Nishiyama, Kazutoshi and Akutsu, Tsugio and Yokoyama, Kazumasa and Kanai, Kazuaki and Eftimov, Filip and Notermans, Nicolette. C and Visser, Nora. A and Faber, Catharina and ... and PATH study group
The Lancet Neurology, ISSN 1474-4422, 05/2018, Volume 17, Issue 5, pp. 393 - 394
In the ICE trial (intravenous immune globulin [10% caprylate-chromatography purified] for the treatment of CIPD),2 the absolute risk reduction for relapse with... 
Administration, Intravenous | Immunoglobulins, Intravenous | Immunoglobulins | Intravenous administration
Journal Article
Journal of Neurology, ISSN 0340-5354, 8/2009, Volume 256, Issue 8, pp. 1337 - 1342
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2012, Volume 7, Issue 2, p. e30926
Background: Xeroderma pigmentosum (XP) is a rare autosomal recessive progeroid syndrome. It has recently been shown that the underlying DNA repair defect plays... 
TRICHOTHIODYSTROPHY | TRANSCRIPTION | BIOLOGY | COCKAYNE-SYNDROME | PERIPHERAL NEUROPATHY | DISORDERS | NEURODEGENERATION | DNA-REPAIR | FIBER TRACKING | BRAIN | DEFICIENCY | Xeroderma Pigmentosum - complications | Humans | Middle Aged | Child, Preschool | Male | Hippocampus - pathology | Thalamus - pathology | Sex Characteristics | Case-Control Studies | Syndrome | Diffusion Tensor Imaging | Young Adult | Xeroderma Pigmentosum - pathology | Anisotropy | Progeria - pathology | Adolescent | Adult | Female | Aged | Nutritional Status | Progeria - complications | Cerebrum - pathology | Child | Habits | Medicine, Experimental | Medical research | Neurologic manifestations of general diseases | Nervous system diseases | Neurophysiology | Neuroimaging | Brain | Neurosciences | Cognitive ability | Xeroderma pigmentosum | Systematic review | Genomes | Family medical history | Peripheral neuropathy | DNA repair | Defects | Fibers | Skin cancer | Magnetic resonance spectroscopy | Genotype & phenotype | Neurodegeneration | Spectrum analysis | Aging | Thalamus | Ataxia | Deoxyribonucleic acid--DNA | Phenotypes | Cytokines | Myelin | Dermatology | Abnormalities | Cerebral hemispheres | Pyramidal tracts | Substantia alba | Patients | Corpus callosum | Neurology | Magnetic resonance imaging | Correlation analysis | Morphology | Skin | Hippocampus | Apoptosis | Deoxyribonucleic acid | DNA
Journal Article