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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

101 related articles for article (PubMed ID: 36445564)

  • 1. Novel compound heterozygous variants of SPG11 gene associated with young-adult amyotrophic lateral sclerosis.
    Santos Silva C; Oliveira Santos M; Madureira J; Reimão S; de Carvalho M
    Acta Neurol Belg; 2023 Aug; 123(4):1627-1629. PubMed ID: 36445564
    [No Abstract]   [Full Text] [Related]  

  • 2. Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions.
    Denora PS; Smets K; Zolfanelli F; Ceuterick-de Groote C; Casali C; Deconinck T; Sieben A; Gonzales M; Zuchner S; Darios F; Peeters D; Brice A; Malandrini A; De Jonghe P; Santorelli FM; Stevanin G; Martin JJ; El Hachimi KH
    Brain; 2016 Jun; 139(Pt 6):1723-34. PubMed ID: 27016404
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome sequencing reveals SPG11 mutations causing juvenile ALS.
    Daoud H; Zhou S; Noreau A; Sabbagh M; Belzil V; Dionne-Laporte A; Tranchant C; Dion P; Rouleau GA
    Neurobiol Aging; 2012 Apr; 33(4):839.e5-9. PubMed ID: 22154821
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Generation and characterization of an endogenously tagged SPG11-human iPSC line by CRISPR/Cas9 mediated knock-in.
    Krumm L; Pozner T; Kaindl J; Regensburger M; Günther C; Turan S; Asadollahi R; Rauch A; Winner B
    Stem Cell Res; 2021 Oct; 56():102520. PubMed ID: 34479069
    [TBL] [Abstract][Full Text] [Related]  

  • 5. H63D CG genotype of
    Zhang QQ; Jiang H; Li CY; Liu YL; Tian XY
    J Integr Neurosci; 2020 Sep; 19(3):495-499. PubMed ID: 33070529
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel SPG11 Mutations in a Patient with Symptoms Mimicking Multiple Sclerosis.
    Mukai M; Koh K; Ohnuki Y; Nagata E; Takiyama Y; Takizawa S
    Intern Med; 2018 Nov; 57(21):3183-3186. PubMed ID: 29877287
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The distinct manifestation of young-onset amyotrophic lateral sclerosis in China.
    Lin J; Chen W; Huang P; Xie Y; Zheng M; Yao X
    Amyotroph Lateral Scler Frontotemporal Degener; 2021 Feb; 22(1-2):30-37. PubMed ID: 32729724
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations.
    Khani M; Shamshiri H; Fatehi F; Rohani M; Haghi Ashtiani B; Akhoundi FH; Alavi A; Moazzeni H; Taheri H; Ghani MT; Javanparast L; Hashemi SS; Haji-Seyed-Javadi R; Heidari M; Nafissi S; Elahi E
    Mol Genet Genomic Med; 2020 Jul; 8(7):e1240. PubMed ID: 32383541
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two types of recessive hereditary spastic paraplegia in Roma patients in compound heterozygous state; no ethnically prevalent variant found.
    Meszarosova AU; Seeman P; Jencik J; Drabova J; Cibochova R; Stellmachova J; Safka Brozkova D
    Neurosci Lett; 2020 Mar; 721():134800. PubMed ID: 32007496
    [TBL] [Abstract][Full Text] [Related]  

  • 10. GSK3ß-dependent dysregulation of neurodevelopment in SPG11-patient induced pluripotent stem cell model.
    Mishra HK; Prots I; Havlicek S; Kohl Z; Perez-Branguli F; Boerstler T; Anneser L; Minakaki G; Wend H; Hampl M; Leone M; Brückner M; Klucken J; Reis A; Boyer L; Schuierer G; Behrens J; Lampert A; Engel FB; Gage FH; Winkler J; Winner B
    Ann Neurol; 2016 May; 79(5):826-840. PubMed ID: 26971897
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and genetic characteristics of amyotrophic lateral sclerosis patients with
    Sung W; Nahm M; Lim SM; Noh MY; Lee S; Hwang SM; Kim YH; Park J; Oh KW; Ki CS; Kim YE; Kim SH
    Brain Commun; 2022; 4(6):fcac299. PubMed ID: 36458208
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia.
    Schüle R; Schlipf N; Synofzik M; Klebe S; Klimpe S; Hehr U; Winner B; Lindig T; Dotzer A; Riess O; Winkler J; Schöls L; Bauer P
    J Neurol Neurosurg Psychiatry; 2009 Dec; 80(12):1402-4. PubMed ID: 19917823
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and genetic features of patients with amyotrophic lateral sclerosis in southern China.
    Chen W; Xie Y; Zheng M; Lin J; Huang P; Pei Z; Yao X
    Eur J Neurol; 2020 Jun; 27(6):1017-1022. PubMed ID: 32166880
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Heterozygous
    Osmanovic A; Gogol I; Martens H; Widjaja M; Müller K; Schreiber-Katz O; Feuerhake F; Langhans CD; Schmidt G; Andersen PM; Ludolph AC; Weishaupt JH; Brand F; Petri S; Weber RG
    Genes (Basel); 2021 Dec; 13(1):. PubMed ID: 35052424
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel compound heterozygous ALS2 mutation in two Italian siblings with juvenile amyotrophic lateral sclerosis.
    Luigetti M; Lattante S; Conte A; Romano A; Zollino M; Marangi G; Sabatelli M
    Amyotroph Lateral Scler Frontotemporal Degener; 2013 Sep; 14(5-6):470-2. PubMed ID: 23282280
    [No Abstract]   [Full Text] [Related]  

  • 16. Novel compound heterozygous mutations of the SPG11 gene in Korean families with hereditary spastic paraplegia with thin corpus callosum.
    Kim SM; Lee JS; Kim S; Kim HJ; Kim MH; Lee KM; Hong YH; Park KS; Sung JJ; Lee KW
    J Neurol; 2009 Oct; 256(10):1714-8. PubMed ID: 19513778
    [TBL] [Abstract][Full Text] [Related]  

  • 17. ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.
    Montecchiani C; Pedace L; Lo Giudice T; Casella A; Mearini M; Gaudiello F; Pedroso JL; Terracciano C; Caltagirone C; Massa R; St George-Hyslop PH; Barsottini OG; Kawarai T; Orlacchio A
    Brain; 2016 Jan; 139(Pt 1):73-85. PubMed ID: 26556829
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Juvenile amyotrophic lateral sclerosis with complex phenotypes associated with novel
    Naruse H; Ishiura H; Mitsui J; Takahashi Y; Matsukawa T; Toda T; Tsuji S
    Amyotroph Lateral Scler Frontotemporal Degener; 2021 Nov; 22(7-8):576-578. PubMed ID: 32870032
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region variant and known pathogenic variant in
    Yu AC; Chan AY; Au WC; Shen Y; Chan TF; Chan HE
    Cold Spring Harb Mol Case Stud; 2016 Nov; 2(6):a001248. PubMed ID: 27900367
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes.
    Cady J; Allred P; Bali T; Pestronk A; Goate A; Miller TM; Mitra RD; Ravits J; Harms MB; Baloh RH
    Ann Neurol; 2015 Jan; 77(1):100-13. PubMed ID: 25382069
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.