83 related articles for article (PubMed ID: 23356346)
1. Benign lower limb amyotrophy due to TARDBP mutation or post-polio syndrome?
Guennoc AM; Heuze-Vourc'h N; Gordon PH; Courty Y; Vourc'h P; Andres CR; Corcia P
Amyotroph Lateral Scler Frontotemporal Degener; 2013 Sep; 14(5-6):476-8. PubMed ID: 23356346
[No Abstract] [Full Text] [Related]
2. Sporadic ALS with early-onset respiratory failure is not associated with IGHMBP2 gene mutations.
Kühnlein P; Sperfeld AD; Endruhn S; Varon R; Ludolph AC; Hübner C
J Neurol Neurosurg Psychiatry; 2008 Jun; 79(6):737-8. PubMed ID: 18187479
[No Abstract] [Full Text] [Related]
3. Pro-inflammatory cytokines and motor neuron dysfunction: is there a connection in post-polio syndrome?
Dalakas MC
J Neurol Sci; 2002 Dec; 205(1):5-8. PubMed ID: 12409176
[No Abstract] [Full Text] [Related]
4. Co-occurrence of post poliomyelitis motor neuron disease and parkinsonism: chance or related association?
Nicolai A; Lazzarino LG
Ital J Neurol Sci; 1993 Dec; 14(9):652-3. PubMed ID: 8125770
[No Abstract] [Full Text] [Related]
5. Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease.
Synofzik M; Born C; Rominger A; Lummel N; Schöls L; Biskup S; Schüle C; Grasshoff U; Klopstock T; Adamczyk C
Neurobiol Aging; 2014 May; 35(5):1212.e1-5. PubMed ID: 24300238
[TBL] [Abstract][Full Text] [Related]
6. Coexistence of amyotrophic lateral sclerosis and Werdnig-Hoffmann disease within a family.
Appelbaum JS; Roos RP
Muscle Nerve; 1993 Dec; 16(12):1416. PubMed ID: 8232401
[No Abstract] [Full Text] [Related]
7. Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.
Daoud H; Valdmanis PN; Kabashi E; Dion P; Dupré N; Camu W; Meininger V; Rouleau GA
J Med Genet; 2009 Feb; 46(2):112-4. PubMed ID: 18931000
[TBL] [Abstract][Full Text] [Related]
8. Large-scale screening of TARDBP mutation in amyotrophic lateral sclerosis in Japanese.
Iida A; Kamei T; Sano M; Oshima S; Tokuda T; Nakamura Y; Ikegawa S
Neurobiol Aging; 2012 Apr; 33(4):786-90. PubMed ID: 20675015
[TBL] [Abstract][Full Text] [Related]
9. Different clinical and neuropathologic phenotypes of familial ALS with A315E TARDBP mutation.
Fujita Y; Ikeda M; Yanagisawa T; Senoo Y; Okamoto K
Neurology; 2011 Oct; 77(15):1427-31. PubMed ID: 21956716
[TBL] [Abstract][Full Text] [Related]
10. Neuropathological features of Japanese familial amyotrophic lateral sclerosis with p.N352S mutation in TARDBP.
Homma T; Nagaoka U; Kawata A; Mochizuki Y; Kawakami H; Maruyama H; Matsubara S; Komori T
Neuropathol Appl Neurobiol; 2014 Feb; 40(2):231-6. PubMed ID: 24117534
[No Abstract] [Full Text] [Related]
11. Primary lateral sclerosis: upper-motor-predominant amyotrophic lateral sclerosis with frontotemporal lobar degeneration--immunohistochemical and biochemical analyses of TDP-43.
Kosaka T; Fu YJ; Shiga A; Ishidaira H; Tan CF; Tani T; Koike R; Onodera O; Nishizawa M; Kakita A; Takahashi H
Neuropathology; 2012 Aug; 32(4):373-84. PubMed ID: 22098653
[TBL] [Abstract][Full Text] [Related]
12. High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis.
Orrù S; Manolakos E; Orrù N; Kokotas H; Mascia V; Carcassi C; Petersen MB
Clin Genet; 2012 Feb; 81(2):172-8. PubMed ID: 21418058
[TBL] [Abstract][Full Text] [Related]
13. Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations.
Corcia P; Valdmanis P; Millecamps S; Lionnet C; Blasco H; Mouzat K; Daoud H; Belzil V; Morales R; Pageot N; Danel-Brunaud V; Vandenberghe N; Pradat PF; Couratier P; Salachas F; Lumbroso S; Rouleau GA; Meininger V; Camu W
Neurology; 2012 May; 78(19):1519-26. PubMed ID: 22539580
[TBL] [Abstract][Full Text] [Related]
14. Phenotypes in Swiss patients with familial ALS carrying TARDBP mutations.
Czell D; Andersen PM; Morita M; Neuwirth C; Perren F; Weber M
Neurodegener Dis; 2013; 12(3):150-5. PubMed ID: 23327806
[TBL] [Abstract][Full Text] [Related]
15. Mutation of gene in spinal muscular atrophy respiratory distress type I.
Wong VC; Chung BH; Li S; Goh W; Lee SL
Pediatr Neurol; 2006 Jun; 34(6):474-7. PubMed ID: 16765827
[TBL] [Abstract][Full Text] [Related]
16. Lower motor neuron involvement in TAR DNA-binding protein of 43 kDa-related frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Riku Y; Watanabe H; Yoshida M; Tatsumi S; Mimuro M; Iwasaki Y; Katsuno M; Iguchi Y; Masuda M; Senda J; Ishigaki S; Udagawa T; Sobue G
JAMA Neurol; 2014 Feb; 71(2):172-9. PubMed ID: 24378564
[TBL] [Abstract][Full Text] [Related]
17. Candidate screening of the bovine and feline spinal muscular atrophy genes reveals no evidence for involvement in human motor neuron disorders.
Parkinson NJ; Baumer D; Rose-Morris A; Talbot K
Neuromuscul Disord; 2008 May; 18(5):394-7. PubMed ID: 18395445
[TBL] [Abstract][Full Text] [Related]
18. A new mutation of IGHMBP2 gene.
Guenther UP; Schuelke M; Grohmann K; Varon R
Pediatr Neurol; 2006 Feb; 34(2):168. PubMed ID: 16458836
[No Abstract] [Full Text] [Related]
19. Coexistence of amyotrophic lateral sclerosis and Werdnig-Hoffmann disease within a family.
Camu W; Billiard M
J Neurol Sci; 1994 Jul; 124 Suppl():88-9. PubMed ID: 7807154
[No Abstract] [Full Text] [Related]
20. The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13.
Brunialti AL; Poirier C; Schmalbruch H; Guénet JL
Genomics; 1995 Sep; 29(1):131-5. PubMed ID: 8530062
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]