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 *

154 related articles for article (PubMed ID: 37077568)

  • 21. Hereditary spastic paraplegia and prominent sensorial involvement: think MAG mutations!
    Roubertie A; Charif M; Meyer P; Manes G; Meunier I; Taieb G; Junta Morales R; Guichet A; Delettre C; Sarzi E; Leboucq N; Rivier F; Lenaers G
    Ann Clin Transl Neurol; 2019 Aug; 6(8):1572-1577. PubMed ID: 31402626
    [TBL] [Abstract][Full Text] [Related]  

  • 22. CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.
    Goizet C; Boukhris A; Durr A; Beetz C; Truchetto J; Tesson C; Tsaousidou M; Forlani S; Guyant-Maréchal L; Fontaine B; Guimarães J; Isidor B; Chazouillères O; Wendum D; Grid D; Chevy F; Chinnery PF; Coutinho P; Azulay JP; Feki I; Mochel F; Wolf C; Mhiri C; Crosby A; Brice A; Stevanin G
    Brain; 2009 Jun; 132(Pt 6):1589-600. PubMed ID: 19439420
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Expansion of the mutation and phenotypic spectrum of hereditary spastic paraplegia.
    Xing F; Du J
    Neurol Sci; 2022 Aug; 43(8):4989-4996. PubMed ID: 35348942
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic and phenotypic characterization of complex hereditary spastic paraplegia.
    Kara E; Tucci A; Manzoni C; Lynch DS; Elpidorou M; Bettencourt C; Chelban V; Manole A; Hamed SA; Haridy NA; Federoff M; Preza E; Hughes D; Pittman A; Jaunmuktane Z; Brandner S; Xiromerisiou G; Wiethoff S; Schottlaender L; Proukakis C; Morris H; Warner T; Bhatia KP; Korlipara LV; Singleton AB; Hardy J; Wood NW; Lewis PA; Houlden H
    Brain; 2016 Jul; 139(Pt 7):1904-18. PubMed ID: 27217339
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Hereditary spastic paraplegia type 35 caused by a novel FA2H mutation.
    Bektaş G; Yeşil G; Yıldız EP; Aydınlı N; Çalışkan M; Özmen M
    Turk J Pediatr; 2017; 59(3):329-334. PubMed ID: 29376581
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Early onset disease, anarthria, areflexia, and dystonia can be the distinctive features of SPG64, a very rare form of hereditary spastic paraplegias.
    Ölmez A; Çetin GO; Karaer K
    Am J Med Genet A; 2022 Sep; 188(9):2712-2717. PubMed ID: 35758610
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A novel homozygous mutation in ERLIN1 gene causing spastic paraplegia 62 and literature review.
    Zhu ZY; Li ZY; Zhang C; Liu XL; Tian WT; Cao L
    Eur J Med Genet; 2022 Nov; 65(11):104608. PubMed ID: 36100157
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia.
    Hehr U; Bauer P; Winner B; Schule R; Olmez A; Koehler W; Uyanik G; Engel A; Lenz D; Seibel A; Hehr A; Ploetz S; Gamez J; Rolfs A; Weis J; Ringer TM; Bonin M; Schuierer G; Marienhagen J; Bogdahn U; Weber BH; Topaloglu H; Schols L; Riess O; Winkler J
    Ann Neurol; 2007 Dec; 62(6):656-65. PubMed ID: 18067136
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel frameshift mutation of DDHD1 in a Japanese patient with autosomal recessive spastic paraplegia.
    Miura S; Morikawa T; Fujioka R; Kosaka K; Yamada K; Hattori G; Motomura M; Taniwaki T; Shibata H
    Eur J Med Genet; 2016 Aug; 59(8):413-6. PubMed ID: 27216551
    [TBL] [Abstract][Full Text] [Related]  

  • 30.
    Garcia-Berlanga JE; Moscovich M; Palacios IJ; Banegas-Lagos A; Rojas-Martinez A; Martinez-Ramirez D
    Case Rep Neurol Med; 2019; 2019():7615605. PubMed ID: 31355030
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A novel homozygous synonymous splicing variant in SELENOI gene causes spastic paraplegia 81.
    Sarma AS; Siddardha B; T PL; Ranganath P; Dalal A
    J Gene Med; 2023 Jul; 25(7):e3501. PubMed ID: 36942482
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study.
    Criscuolo C; Filla A; Coppola G; Rinaldi C; Carbone R; Pinto S; Wang Q; de Leva MF; Salvatore E; Banfi S; Brunetti A; Quarantelli M; Geschwind DH; Pappatà S; De Michele G
    J Neurol; 2009 Aug; 256(8):1252-7. PubMed ID: 19363635
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Tremor as an early sign of hereditary spastic paraplegia due to mutations in ALDH18A1.
    Kalmár T; Maróti Z; Zimmermann A; Sztriha L
    Brain Dev; 2021 Jan; 43(1):144-151. PubMed ID: 32798076
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegia.
    Coarelli G; Romano S; Travaglini L; Ferraldeschi M; Nicita F; Spadaro M; Fornasiero A; Frontali M; Salvetti M; Bertini E; Ristori G
    Clin Neurol Neurosurg; 2018 May; 168():60-63. PubMed ID: 29524657
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset.
    Brockmann K; Simpson MA; Faber A; Bönnemann C; Crosby AH; Gärtner J
    Neuropediatrics; 2005 Aug; 36(4):274-8. PubMed ID: 16138254
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel SPAST gene mutation identified in a Chinese family with hereditary spastic paraplegia.
    Yu W; Jin H; Deng J; Nan D; Huang Y
    BMC Med Genet; 2020 Jun; 21(1):123. PubMed ID: 32493220
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel mutation in the
    Li P; Huang X; Chai S; Zhu D; Huang H; Ma F; Zhang S; Xie X
    Front Genet; 2022; 13():936292. PubMed ID: 35928447
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Stop-gain mutations in UBAP1 cause pure autosomal-dominant spastic paraplegia.
    Lin X; Su HZ; Dong EL; Lin XH; Zhao M; Yang C; Wang C; Wang J; Chen YJ; Yu H; Xu J; Ma LX; Xiong ZQ; Wang N; Chen WJ
    Brain; 2019 Aug; 142(8):2238-2252. PubMed ID: 31203368
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Spastic paraplegia 15: linkage and clinical description of three Tunisian families.
    Boukhris A; Feki I; Denis E; Miladi MI; Brice A; Mhiri C; Stevanin G
    Mov Disord; 2008 Feb; 23(3):429-33. PubMed ID: 18098276
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mutation analysis of CAPN1 in Chinese populations with spastic paraplegia and related neurodegenerative diseases.
    Xia ZC; Liu ZH; Zhou XX; Liu Z; Wang JL; Hu ZM; Tan JQ; Shen L; Jiang H; Tang BS; Lei LF
    J Neurol Sci; 2020 Apr; 411():116691. PubMed ID: 31982778
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.