These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Predictive genetic testing for amyotrophic lateral sclerosis and frontotemporal dementia: genetic counselling considerations. Crook A; Williams K; Adams L; Blair I; Rowe DB Amyotroph Lateral Scler Frontotemporal Degener; 2017 Nov; 18(7-8):475-485. PubMed ID: 28585888 [TBL] [Abstract][Full Text] [Related]
4. Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotype. Synofzik M; Maetzler W; Grehl T; Prudlo J; Vom Hagen JM; Haack T; Rebassoo P; Munz M; Schöls L; Biskup S Neurobiol Aging; 2012 Dec; 33(12):2949.e13-7. PubMed ID: 22892309 [TBL] [Abstract][Full Text] [Related]
11. [Amyotrophic lateral sclerosis, a heterogeneous disorder]. van Es MA; Kruitwagen-van Reenen ET; Schröder CD; Pasterkamp RJ; Veldink JH; van den Berg LH Ned Tijdschr Geneeskd; 2016; 160():A9658. PubMed ID: 26860749 [TBL] [Abstract][Full Text] [Related]
12. Patient and Relative Experiences and Decision-making About Genetic Testing and Counseling for Familial ALS and FTD: A Systematic Scoping Review. Crook A; Jacobs C; Newton-John T; Richardson E; McEwen A Alzheimer Dis Assoc Disord; 2021 Oct-Dec 01; 35(4):374-385. PubMed ID: 34054018 [TBL] [Abstract][Full Text] [Related]
13. Genetic testing and genetic counseling for amyotrophic lateral sclerosis: an update for clinicians. Roggenbuck J; Quick A; Kolb SJ Genet Med; 2017 Mar; 19(3):267-274. PubMed ID: 27537704 [TBL] [Abstract][Full Text] [Related]
14. Clinical variability and female penetrance in X-linked familial FTD/ALS caused by a P506S mutation in UBQLN2. Vengoechea J; David MP; Yaghi SR; Carpenter L; Rudnicki SA Amyotroph Lateral Scler Frontotemporal Degener; 2013 Dec; 14(7-8):615-9. PubMed ID: 23944734 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Co-occurrence of the C9ORF72 expansion and a novel GRN mutation in a family with alternative expression of frontotemporal dementia and amyotrophic lateral sclerosis. Testi S; Tamburin S; Zanette G; Fabrizi GM J Alzheimers Dis; 2015; 44(1):49-56. PubMed ID: 25182743 [TBL] [Abstract][Full Text] [Related]
17. The Role of APOE in the Occurrence of Frontotemporal Dementia in Amyotrophic Lateral Sclerosis. Chiò A; Brunetti M; Barberis M; Iazzolino B; Montuschi A; Ilardi A; Cammarosano S; Canosa A; Moglia C; Calvo A JAMA Neurol; 2016 Apr; 73(4):425-30. PubMed ID: 26903389 [TBL] [Abstract][Full Text] [Related]
18. One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated with myopathy with rimmed vacuoles, amyotrophic lateral sclerosis and frontotemporal dementia. Abrahao A; Abath Neto O; Kok F; Zanoteli E; Santos B; Pinto WB; Barsottini OG; Oliveira AS; Pedroso JL J Neurol Sci; 2016 Sep; 368():352-8. PubMed ID: 27538664 [TBL] [Abstract][Full Text] [Related]
19. Tale of two diseases: amyotrophic lateral sclerosis and frontotemporal dementia. Verma A Neurol India; 2014; 62(4):347-51. PubMed ID: 25237937 [TBL] [Abstract][Full Text] [Related]
20. [A Pair of Siblings with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis and a Novel Thr462Lysfs Mutation in the TBK1 Gene]. Schönecker S; Brendel M; van der Zee J; van Broeckhoven C; Rominger A; Danek A; Levin J Fortschr Neurol Psychiatr; 2016 Aug; 84(8):494-8. PubMed ID: 27570907 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]