BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

226 related articles for article (PubMed ID: 26022168)

  • 21. The effect of genotype on the natural history of eIF2B-related leukodystrophies.
    Fogli A; Schiffmann R; Bertini E; Ughetto S; Combes P; Eymard-Pierre E; Kaneski CR; Pineda M; Troncoso M; Uziel G; Surtees R; Pugin D; Chaunu MP; Rodriguez D; Boespflug-Tanguy O
    Neurology; 2004 May; 62(9):1509-17. PubMed ID: 15136673
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Hypomyelinating leukodystrophy type 6. Clinical and neuroimaging key features in the detection of a new case].
    Otero-Dominguez E; Gomez-Lado C; Fuentes-Pita P; Dacruz D; Barros-Angueira F; Eiris-Punal J
    Rev Neurol; 2018 Nov; 67(9):339-342. PubMed ID: 30350845
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Leukodystrophies: Indian scenario.
    Singhal BS
    Indian J Pediatr; 2005 Apr; 72(4):315-8. PubMed ID: 15876760
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Diagnosing "undiagnosed" leukodystrophies: The role of molecular genetics.
    Noetzel MJ
    Neurology; 2004 Mar; 62(6):847-8. PubMed ID: 15037679
    [No Abstract]   [Full Text] [Related]  

  • 25. Imaging of adult leukodystrophies.
    Leite CC; Lucato LT; Santos GT; Kok F; Brandão AR; Castillo M
    Arq Neuropsiquiatr; 2014 Aug; 72(8):625-32. PubMed ID: 25098479
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Adult onset POLR3A leukodystrophy presenting with parkinsonism treated with pallidal deep brain stimulation.
    Kyle K; Mason X; Bordelon Y; Pouratian N; Bronstein J
    Parkinsonism Relat Disord; 2021 Apr; 85():23-25. PubMed ID: 33652360
    [No Abstract]   [Full Text] [Related]  

  • 27. Therapeutic challenge in leukodystrophies: translational and ethical research toward clinical trials (LeukoTreat).
    Hum Gene Ther Clin Dev; 2014 Jun; 25(2):66-8. PubMed ID: 24933566
    [No Abstract]   [Full Text] [Related]  

  • 28. Neuroimaging in leukodystrophies.
    Barker PB; Horská A
    J Child Neurol; 2004 Aug; 19(8):559-70. PubMed ID: 15605464
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies.
    Parikh S; Bernard G; Leventer RJ; van der Knaap MS; van Hove J; Pizzino A; McNeill NH; Helman G; Simons C; Schmidt JL; Rizzo WB; Patterson MC; Taft RJ; Vanderver A;
    Mol Genet Metab; 2015 Apr; 114(4):501-515. PubMed ID: 25655951
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Update on Leukodystrophies: A Historical Perspective and Adapted Definition.
    Kevelam SH; Steenweg ME; Srivastava S; Helman G; Naidu S; Schiffmann R; Blaser S; Vanderver A; Wolf NI; van der Knaap MS
    Neuropediatrics; 2016 Dec; 47(6):349-354. PubMed ID: 27564080
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Costs of the diagnostic odyssey in children with inherited leukodystrophies.
    Richards J; Korgenski EK; Srivastava R; Bonkowsky JL
    Neurology; 2015 Sep; 85(13):1167-70. PubMed ID: 26320197
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The burden of inherited leukodystrophies in children.
    Bonkowsky JL; Nelson C; Kingston JL; Filloux FM; Mundorff MB; Srivastava R
    Neurology; 2010 Aug; 75(8):718-25. PubMed ID: 20660364
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Leukodystrophies with late disease onset: an update.
    Köhler W
    Curr Opin Neurol; 2010 Jun; 23(3):234-41. PubMed ID: 20216214
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Autosomal dominant leukodystrophy and childhood ataxia with central nervous system hypomyelination syndrome.
    Labauge P; Gelot A; Fogli A; Boespflug-Tanguy O; Rodriguez D
    Ann Neurol; 2006 Oct; 60(4):485; author reply 485-6. PubMed ID: 16847948
    [No Abstract]   [Full Text] [Related]  

  • 35. Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adults.
    Kohlschütter A; Bley A; Brockmann K; Gärtner J; Krägeloh-Mann I; Rolfs A; Schöls L
    Brain Dev; 2010 Feb; 32(2):82-9. PubMed ID: 19427149
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genetic heterogeneity in 26 infants with a hypomyelinating leukodystrophy.
    Arai-Ichinoi N; Uematsu M; Sato R; Suzuki T; Kudo H; Kikuchi A; Hino-Fukuyo N; Matsumoto M; Igarashi K; Haginoya K; Kure S
    Hum Genet; 2016 Jan; 135(1):89-98. PubMed ID: 26597493
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prenatal diagnosis of megalencephalic leukodystrophy.
    Shukla P; Balakrishnan P; Agarwal N; Ghosh M; Kabra M; Sharma R; Deka D; Kalra V
    Prenat Diagn; 2008 Apr; 28(4):357-9. PubMed ID: 18330867
    [No Abstract]   [Full Text] [Related]  

  • 38. Inherited leukoencephalopathies.
    Renaud DL
    Semin Neurol; 2012 Feb; 32(1):3-8. PubMed ID: 22422201
    [No Abstract]   [Full Text] [Related]  

  • 39. Genes involved in leukodystrophies: a glance at glial functions.
    Boespflug-Tanguy O; Labauge P; Fogli A; Vaurs-Barriere C
    Curr Neurol Neurosci Rep; 2008 May; 8(3):217-29. PubMed ID: 18541117
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A patient with a rare leukodystrophy related to lamin B1 duplication.
    Molloy A; Cotter O; van Spaendonk R; Sistermans E; Sweeney B
    Ir Med J; 2012 Jun; 105(6):186-7. PubMed ID: 22973660
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.