175 related articles for article (PubMed ID: 36285345)
1. Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis.
Manini A; Gagliardi D; Meneri M; Antognozzi S; Del Bo R; Scaglione C; Comi GP; Corti S; Ronchi D
Ann Clin Transl Neurol; 2022 Nov; 9(11):1820-1825. PubMed ID: 36285345
[TBL] [Abstract][Full Text] [Related]
2. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.
Dewan R; Chia R; Ding J; Hickman RA; Stein TD; Abramzon Y; Ahmed S; Sabir MS; Portley MK; Tucci A; Ibáñez K; Shankaracharya FNU; Keagle P; Rossi G; Caroppo P; Tagliavini F; Waldo ML; Johansson PM; Nilsson CF; ; ; ; ; ; ; ; ; Rowe JB; Benussi L; Binetti G; Ghidoni R; Jabbari E; Viollet C; Glass JD; Singleton AB; Silani V; Ross OA; Ryten M; Torkamani A; Tanaka T; Ferrucci L; Resnick SM; Pickering-Brown S; Brady CB; Kowal N; Hardy JA; Van Deerlin V; Vonsattel JP; Harms MB; Morris HR; Ferrari R; Landers JE; Chiò A; Gibbs JR; Dalgard CL; Scholz SW; Traynor BJ
Neuron; 2021 Feb; 109(3):448-460.e4. PubMed ID: 33242422
[TBL] [Abstract][Full Text] [Related]
3. Reduced-penetrance Huntington's disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosis.
Jih KY; Lai KL; Lin KP; Liao YC; Lee YC
J Chin Med Assoc; 2023 Jan; 86(1):47-51. PubMed ID: 36599142
[TBL] [Abstract][Full Text] [Related]
4. A mother and her daughter carrying a pathogenic expansion of the HTT gene with a phenotype encompassing motor neuron disease and Huntington's disease.
Canosa A; Cabras S; Di Pede F; Manera U; Vasta R; Moglia C; Calvo A; Gallone S; Chiò A
Clin Genet; 2024 Apr; 105(4):430-433. PubMed ID: 38092667
[TBL] [Abstract][Full Text] [Related]
5. A Novel Triplet-Primed PCR Assay to Detect the Full Range of Trinucleotide CAG Repeats in the Huntingtin Gene (
De Luca A; Morella A; Consoli F; Fanelli S; Thibert JR; Statt S; Latham GJ; Squitieri F
Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33567536
[TBL] [Abstract][Full Text] [Related]
6. Prevalence of Huntington's disease gene CAG repeat alleles in sporadic amyotrophic lateral sclerosis patients.
Ramos EM; Keagle P; Gillis T; Lowe P; Mysore JS; Leclerc AL; Ratti A; Ticozzi N; Gellera C; Gusella JF; Silani V; Alonso I; Brown RH; MacDonald ME; Landers JE
Amyotroph Lateral Scler; 2012 May; 13(3):265-9. PubMed ID: 22409360
[TBL] [Abstract][Full Text] [Related]
7. A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington's Disease Symptoms.
Chheda P; Chanekar M; Salunkhe Y; Dama T; Pais A; Pande S; Bendre R; Shah N
Mol Diagn Ther; 2018 Jun; 22(3):353-359. PubMed ID: 29619771
[TBL] [Abstract][Full Text] [Related]
8. Questioning the causality of HTT CAG-repeat expansions in FTD/ALS.
Thomas Q; Coarelli G; Heinzmann A; Le Ber I; Amador MDM; Durr A
Neuron; 2021 Jun; 109(12):1945-1946. PubMed ID: 34139183
[No Abstract] [Full Text] [Related]
9. Prevalence of Huntington's disease gene CAG trinucleotide repeat alleles in patients with bipolar disorder.
Ramos EM; Gillis T; Mysore JS; Lee JM; Alonso I; Gusella JF; Smoller JW; Sklar P; MacDonald ME; Perlis RH
Bipolar Disord; 2015 Jun; 17(4):403-8. PubMed ID: 25726852
[TBL] [Abstract][Full Text] [Related]
10. Enhanced Detection and Sizing of the HTT CAG Repeat Expansion in Huntington Disease Using an Improved Triplet-Primed PCR Assay.
Zhao M; Lee CG; Law HY; Chong SS
Neurodegener Dis; 2016; 16(5-6):348-51. PubMed ID: 27207688
[TBL] [Abstract][Full Text] [Related]
11. Loss of CAA interruption and intergenerational CAG instability in Chinese patients with Huntington's disease.
Bao YF; Li XY; Dong Y; Wu ZY
J Mol Med (Berl); 2023 Jul; 101(7):869-876. PubMed ID: 37231148
[TBL] [Abstract][Full Text] [Related]
12. Approaches to Sequence the HTT CAG Repeat Expansion and Quantify Repeat Length Variation.
Ciosi M; Cumming SA; Chatzi A; Larson E; Tottey W; Lomeikaite V; Hamilton G; Wheeler VC; Pinto RM; Kwak S; Morton AJ; Monckton DG
J Huntingtons Dis; 2021; 10(1):53-74. PubMed ID: 33579864
[TBL] [Abstract][Full Text] [Related]
13. Investigations of Huntington's Disease and Huntington's Disease-Like Syndromes in Indian Choreatic Patients.
Kaur J; Parveen S; Shamim U; Sharma P; Suroliya V; Sonkar AK; Ahmad I; Garg J; Anand KS; Laskar S; Chowdhury D; Kushwaha S; Goyal V; Srivastava AK; Singh G; Faruq M
J Huntingtons Dis; 2020; 9(3):283-289. PubMed ID: 32675418
[TBL] [Abstract][Full Text] [Related]
14. The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.
Simón-Sánchez J; Dopper EG; Cohn-Hokke PE; Hukema RK; Nicolaou N; Seelaar H; de Graaf JR; de Koning I; van Schoor NM; Deeg DJ; Smits M; Raaphorst J; van den Berg LH; Schelhaas HJ; De Die-Smulders CE; Majoor-Krakauer D; Rozemuller AJ; Willemsen R; Pijnenburg YA; Heutink P; van Swieten JC
Brain; 2012 Mar; 135(Pt 3):723-35. PubMed ID: 22300876
[TBL] [Abstract][Full Text] [Related]
15. HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease.
Menéndez-González M; Clarimón J; Rosas-Allende I; Blázquez M; San Martín ES; García-Fernández C; Lleó A; Dols-Icardo O; Illán-Gala I; Morís G; Ribacoba R; Álvarez V; Martínez C
Neurobiol Aging; 2019 Apr; 76():215.e9-215.e14. PubMed ID: 30583877
[TBL] [Abstract][Full Text] [Related]
16. Investigation of the Influence of TBP CAG/CAA Repeats in Conjunction with HTT CAG Repeats on Huntington's Disease Age at Onset in a Brazilian Sample.
da Silva IDS; Apolinário TA; de Andrade Agostinho L; Paiva CLA
J Mol Neurosci; 2022 May; 72(5):1116-1124. PubMed ID: 35275350
[TBL] [Abstract][Full Text] [Related]
17. Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic Approach.
Mariani LL; Tesson C; Charles P; Cazeneuve C; Hahn V; Youssov K; Freeman L; Grabli D; Roze E; Noël S; Peuvion JN; Bachoud-Levi AC; Brice A; Stevanin G; Durr A
JAMA Neurol; 2016 Sep; 73(9):1105-14. PubMed ID: 27400454
[TBL] [Abstract][Full Text] [Related]
18. Identification of C9orf72 repeat expansions in patients with amyotrophic lateral sclerosis and frontotemporal dementia in mainland China.
Jiao B; Tang B; Liu X; Yan X; Zhou L; Yang Y; Wang J; Xia K; Shen L
Neurobiol Aging; 2014 Apr; 35(4):936.e19-22. PubMed ID: 24269022
[TBL] [Abstract][Full Text] [Related]
19. Highlighting the clinical potential of HTT repeat expansions in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.
Dewan R; Scholz SW; Chiò A; Traynor BJ
Neuron; 2021 Jun; 109(12):1947-1948. PubMed ID: 34139184
[No Abstract] [Full Text] [Related]
20. Amyotrophic lateral sclerosis is over-represented in two Huntington's disease brain bank cohorts: further evidence to support genetic pleiotropy of pathogenic HTT gene expansion.
Hickman RA; Dewan R; Cortes E; Traynor BJ; Marder K; Vonsattel JP
Acta Neuropathol; 2022 Jan; 143(1):105-108. PubMed ID: 34800149
[No Abstract] [Full Text] [Related]
[Next] [New Search]
