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)

  • 41. Brain white matter involvement in hereditary spastic paraplegias: analysis with multiple diffusion tensor indices.
    Aghakhanyan G; Martinuzzi A; Frijia F; Vavla M; Hlavata H; Baratto A; Martino N; Paparella G; Montanaro D
    AJNR Am J Neuroradiol; 2014 Aug; 35(8):1533-8. PubMed ID: 24788132
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Novel insights into the genetic profile of hereditary spastic paraplegia in India.
    Narendiran S; Debnath M; Shivaram S; Kannan R; Sharma S; Christopher R; Seshagiri DV; Jain S; Purushottam M; Mangalore S; Bharath RD; Bindu PS; Sinha S; Taly AB; Nagappa M
    J Neurogenet; 2022 Mar; 36(1):21-31. PubMed ID: 35499206
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A novel homozygous variant in the
    Eriksen KO; Wigers AR; Wedding IM; Erichsen AK; Barøy T; Søberg K; Jørstad ØK
    Am J Ophthalmol Case Rep; 2022 Jun; 26():101400. PubMed ID: 35243150
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Genetic background of the hereditary spastic paraplegia phenotypes in Hungary - An analysis of 58 probands.
    Balicza P; Grosz Z; Gonzalez MA; Bencsik R; Pentelenyi K; Gal A; Varga E; Klivenyi P; Koller J; Züchner S; Molnar JM
    J Neurol Sci; 2016 May; 364():116-21. PubMed ID: 27084228
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Novel SPG 11 Mutations in Hereditary Spastic Paraplegia With Thin Corpus Callosum in a Chinese Family.
    Tian X; Wang M; Zhang K; Zhang X
    Can J Neurol Sci; 2016 Nov; 43(6):833-840. PubMed ID: 27018819
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Investigating ZFYVE26 mutations in a Taiwanese cohort with hereditary spastic paraplegia.
    Hsu SL; Lu YJ; Tsai YS; Chao HC; Fuh JL; Liao YC; Lee YC
    J Formos Med Assoc; 2022 Jan; 121(1 Pt 1):126-133. PubMed ID: 33637369
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Identification of a Mutation in SPG11 in an Iranian Patient with Spastic Paraplegia and Ears of the Lynx Sign.
    Sayad A; Akbari MT; Hesami O; Ghafouri-Fard S; Taheri M
    J Mol Neurosci; 2020 Jun; 70(6):959-961. PubMed ID: 32040826
    [TBL] [Abstract][Full Text] [Related]  

  • 48. VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesis.
    Hausman-Kedem M; Ben-Shachar S; Menascu S; Geva K; Sagie L; Fattal-Valevski A
    Neurogenetics; 2019 Oct; 20(4):187-195. PubMed ID: 31418091
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A novel mutation in the
    Nakamura-Shindo K; Ono K; Koh K; Ishiura H; Tsuji S; Takiyama Y; Yamada M
    eNeurologicalSci; 2020 Jun; 19():100238. PubMed ID: 32280793
    [TBL] [Abstract][Full Text] [Related]  

  • 50. CYP7B1: novel mutations and magnetic resonance spectroscopy abnormalities in hereditary spastic paraplegia type 5A.
    Roos P; Svenstrup K; Danielsen ER; Thomsen C; Nielsen JE
    Acta Neurol Scand; 2014 May; 129(5):330-4. PubMed ID: 24117163
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A novel compound heterozygous SPG7 variant is associated with progressive spastic ataxia and persecutory delusions found in Chinese patients: two case reports.
    Wang S; Wang Y; Wu Y; Zhang J; Zhang W; Li C; Song X
    BMC Neurol; 2022 May; 22(1):200. PubMed ID: 35637455
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A new locus (SPG47) maps to 1p13.2-1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum.
    Blumkin L; Lerman-Sagie T; Lev D; Yosovich K; Leshinsky-Silver E
    J Neurol Sci; 2011 Jun; 305(1-2):67-70. PubMed ID: 21440262
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Movement disorders in hereditary spastic paraplegia (HSP): a systematic review and individual participant data meta-analysis.
    Fereshtehnejad SM; Saleh PA; Oliveira LM; Patel N; Bhowmick S; Saranza G; Kalia LV
    Neurol Sci; 2023 Mar; 44(3):947-959. PubMed ID: 36441344
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A case of spastic paraplegia-15 with a novel pathogenic variant in
    Özdemir TR; Gençpınar P; Arıcan P; Öztekin Ö; Dündar NO; Özyılmaz B
    Int J Neurosci; 2019 Dec; 129(12):1198-1202. PubMed ID: 31385551
    [TBL] [Abstract][Full Text] [Related]  

  • 55. An atypical case of SPG56/CYP2U1-related spastic paraplegia presenting with delayed myelination.
    Minase G; Miyatake S; Nabatame S; Arai H; Koshimizu E; Mizuguchi T; Nakashima M; Miyake N; Saitsu H; Miyamoto T; Sengoku K; Matsumoto N
    J Hum Genet; 2017 Nov; 62(11):997-1000. PubMed ID: 28725025
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Neuroimaging patterns in paediatric onset hereditary spastic paraplegias.
    Dosi C; Pasquariello R; Ticci C; Astrea G; Trovato R; Rubegni A; Tessa A; Cioni G; Santorelli FM; Battini R
    J Neurol Sci; 2021 Jun; 425():117441. PubMed ID: 33866115
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Childhood-Onset Hereditary Spastic Paraplegia (HSP): A Case Series and Review of Literature.
    Panwala TF; Garcia-Santibanez R; Vizcarra JA; Garcia AG; Verma S
    Pediatr Neurol; 2022 May; 130():7-13. PubMed ID: 35303589
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Hereditary spastic paraplegia: new insights into clinical variability and spasticity-ataxia phenotype, and novel mutations.
    Sahin I; Saat H
    Acta Neurol Belg; 2022 Dec; 122(6):1529-1535. PubMed ID: 34420199
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Impaired mitochondrial dynamics underlie axonal defects in hereditary spastic paraplegias.
    Denton K; Mou Y; Xu CC; Shah D; Chang J; Blackstone C; Li XJ
    Hum Mol Genet; 2018 Jul; 27(14):2517-2530. PubMed ID: 29726929
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [A novel mutation of SPAST gene in a hereditary spastic paraplegia type 4 family].
    Zhang LP; Wang YF
    Zhonghua Nei Ke Za Zhi; 2022 Dec; 61(12):1343-1350. PubMed ID: 36456515
    [No Abstract]   [Full Text] [Related]  

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