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 *

829 related articles for article (PubMed ID: 24603320)

  • 1. The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
    Ruano L; Melo C; Silva MC; Coutinho P
    Neuroepidemiology; 2014; 42(3):174-83. PubMed ID: 24603320
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary ataxia and spastic paraplegia in Portugal: a population-based prevalence study.
    Coutinho P; Ruano L; Loureiro JL; Cruz VT; Barros J; Tuna A; Barbot C; Guimarães J; Alonso I; Silveira I; Sequeiros J; Marques Neves J; Serrano P; Silva MC
    JAMA Neurol; 2013 Jun; 70(6):746-55. PubMed ID: 23609960
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study.
    Erichsen AK; Koht J; Stray-Pedersen A; Abdelnoor M; Tallaksen CM
    Brain; 2009 Jun; 132(Pt 6):1577-88. PubMed ID: 19339254
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic and Epidemiological Study of Adult Ataxia and Spastic Paraplegia in Eastern Quebec.
    Haj Salem I; Beaudin M; Stumpf M; Estiar MA; Côté PO; Brunet F; Gamache PL; Rouleau GA; Mourabit-Amari K; Gan-Or Z; Dupré N
    Can J Neurol Sci; 2021 Sep; 48(5):655-665. PubMed ID: 33397523
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The global epidemiology of hereditary ataxia and spastic paraplegia: what are the messages?
    Braschinsky M
    Neuroepidemiology; 2014; 42(3):184-5. PubMed ID: 24603355
    [No Abstract]   [Full Text] [Related]  

  • 6. Epidemiology of ataxia and hereditary spastic paraplegia in Spain: A cross-sectional study.
    Ortega Suero G; Abenza Abildúa MJ; Serrano Munuera C; Rouco Axpe I; Arpa Gutiérrez FJ; Adarmes Gómez AD; Rodríguez de Rivera FJ; Quintans Castro B; Posada Rodríguez I; Vadillo Bermejo A; Domingo Santos Á; Blanco Vicente E; Infante Ceberio I; Pardo Fernández J; Costa Arpín E; Painous Martí C; Muñoz García JE; Mir Rivera P; Montón Álvarez F; Bataller Alberola L; Gascón Bayarri J; Casasnovas Pons C; Vélez Santamaría V; López de Munain A; Fernández-Eulate G; Gazulla Abío J; Sanz Gallego I; Rojas Bartolomé L; Ayo Martín Ó; Segura Martín T; González Mingot C; Baraldés Rovira M; Sivera Mascaró R; Cubo Delgado E; Echavarría Íñiguez A; Vázquez Sánchez F; Bártulos Iglesias M; Casadevall Codina MT; Martínez Fernández EM; Labandeira Guerra C; Alemany Perna B; Carvajal Hernández A; Fernández Moreno C; Palacín Larroy M; Caballol Pons N; Ávila Rivera A; Navacerrada Barrero FJ; Lobato Rodríguez R; Sobrido Gómez MJ
    Neurologia (Engl Ed); 2023; 38(6):379-386. PubMed ID: 37120112
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary ataxias and paraplegias in Valle d'Aosta, Italy: a study of prevalence and disability.
    Leone M; Bottacchi E; D'Alessandro G; Kustermann S
    Acta Neurol Scand; 1995 Mar; 91(3):183-7. PubMed ID: 7793232
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Investigating the genetic basis of hereditary spastic paraplegia and cerebellar Ataxia in Pakistani families.
    Azeem A; Ahmed AN; Khan N; Voutsina N; Ullah I; Ubeyratna N; Yasin M; Baple EL; Crosby AH; Rawlins LE; Saleha S
    BMC Neurol; 2024 Sep; 24(1):354. PubMed ID: 39304850
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15.
    Vander Stichele G; Durr A; Yoon G; Schüle R; Blackstone C; Esposito G; Buffel C; Oliveira I; Freitag C; van Rooijen S; Hoffmann S; Thielemans L; Cowling BS
    BMC Neurol; 2022 Mar; 22(1):115. PubMed ID: 35331153
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical study.
    Polo JM; Calleja J; Combarros O; Berciano J
    Brain; 1991 Apr; 114 ( Pt 2)():855-66. PubMed ID: 2043954
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey.
    Akçakaya NH; Özeş Ak B; Gonzalez MA; Züchner S; Battaloğlu E; Parman Y
    Neurol Neurochir Pol; 2020; 54(2):176-184. PubMed ID: 32242913
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic.
    Wang YG; Du J; Wang JL; Chen J; Chen C; Luo YY; Xiao ZQ; Jiang H; Yan XX; Xia K; Pan Q; Tang BS; Shen L
    J Neurol Sci; 2009 Oct; 285(1-2):121-4. PubMed ID: 19608203
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic origin of patients having spastic paraplegia with or without other neurologic manifestations.
    Chen J; Zhao Z; Shen H; Bing Q; Li N; Guo X; Hu J
    BMC Neurol; 2022 May; 22(1):180. PubMed ID: 35578252
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
    Ben Hamida M; Attia-Romdhane N; Triki CH; Oueslati S; Hentati F
    Rev Neurol (Paris); 1991; 147(12):798-808. PubMed ID: 1780608
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum.
    Boukhris A; Feki I; Elleuch N; Miladi MI; Boland-Augé A; Truchetto J; Mundwiller E; Jezequel N; Zelenika D; Mhiri C; Brice A; Stevanin G
    Neurogenetics; 2010 Oct; 11(4):441-8. PubMed ID: 20593214
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ophthalmological changes in hereditary spastic paraplegia and other genetic diseases with spastic paraplegia.
    de Freitas JL; Rezende Filho FM; Sallum JMF; França MC; Pedroso JL; Barsottini OGP
    J Neurol Sci; 2020 Feb; 409():116620. PubMed ID: 31865189
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Epidemiology of ataxia and hereditary spastic paraplegia in Spain: a cross-sectional study.
    Ortega Suero G; Abenza Abildúa MJ; Serrano Munuera C; Rouco Axpe I; Arpa Gutiérrez FJ; Adarmes Gómez AD; Rodríguez de Rivera FJ; Quintans Castro B; Posada Rodríguez I; Vadillo Bermejo A; Domingo Santos Á; Blanco Vicente E; Infante Ceberio I; Pardo Fernández J; Costa Arpín E; Painous Martí C; Muñoz JE; Mir Rivera P; Montón Álvarez F; Bataller Alberola L; Gascón Bayarri J; Casasnovas Pons C; Vélez Santamaría V; López Munain A; Fernández García Eulate G; Gazulla Abío J; Sanz Gallego I; Rojas Bartolomé L; Ayo Martín Ó; Segura Martín T; González Mingot C; Baraldés Rovira M; Sivera Mascaró R; Cubo Delgado E; Echevarría Íñiguez A; Vázquez Sánchez F; Bártulos Iglesias M; Casadevall Codina MT; Martínez Fernández EM; Labandeira Guerra C; Alemany Perna B; Carvajal Hernández A; Fernández Moreno C; Palacín Larroy M; Caballol Pons N; Ávila Rivera A; Navacerrada Barrero FJ; Lobato Rodríguez R; Sobrido Gómez MJ
    Neurologia (Engl Ed); 2021 Mar; ():. PubMed ID: 33775475
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity.
    Boukhris A; Stevanin G; Feki I; Denis E; Elleuch N; Miladi MI; Truchetto J; Denora P; Belal S; Mhiri C; Brice A
    Arch Neurol; 2008 Mar; 65(3):393-402. PubMed ID: 18332254
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic, clinical and neuroimaging profiles of sporadic and autosomal recessive hereditary spastic paraplegia cases in Chinese.
    Dong Y; Li XY; Wang XL; Xu F; Wang ZJ; Song Y; Li Q; Lin R; Wang C
    Neurosci Lett; 2021 Sep; 761():136108. PubMed ID: 34256108
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum.
    Olmez A; Uyanik G; Ozgül RK; Gross C; Cirak S; Elibol B; Anlar B; Winner B; Hehr U; Topaloglu H; Winkler J
    Neuropediatrics; 2006 Apr; 37(2):59-66. PubMed ID: 16773502
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 42.