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 *

160 related articles for article (PubMed ID: 33948933)

  • 1. Epidemiological, clinical, and genetic characteristics of paediatric genetic white matter disorders in Northern Finland.
    Knuutinen OA; Oikarainen JH; Suo-Palosaari MH; Kangas SM; Rahikkala EJ; Pokka TM; Moilanen JS; Hinttala RML; Vieira PM; Uusimaa JM
    Dev Med Child Neurol; 2021 Sep; 63(9):1066-1074. PubMed ID: 33948933
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Leukodystrophies and genetic leukoencephalopathies in childhood: a national epidemiological study.
    Stellitano LA; Winstone AM; van der Knaap MS; Verity CM
    Dev Med Child Neurol; 2016 Jul; 58(7):680-9. PubMed ID: 26866636
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study.
    Depienne C; Bugiani M; Dupuits C; Galanaud D; Touitou V; Postma N; van Berkel C; Polder E; Tollard E; Darios F; Brice A; de Die-Smulders CE; Vles JS; Vanderver A; Uziel G; Yalcinkaya C; Frints SG; Kalscheuer VM; Klooster J; Kamermans M; Abbink TE; Wolf NI; Sedel F; van der Knaap MS
    Lancet Neurol; 2013 Jul; 12(7):659-68. PubMed ID: 23707145
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Natural History of Vanishing White Matter.
    Hamilton EMC; van der Lei HDW; Vermeulen G; Gerver JAM; Lourenço CM; Naidu S; Mierzewska H; Gemke RJBJ; de Vet HCW; Uitdehaag BMJ; Lissenberg-Witte BI; ; van der Knaap MS
    Ann Neurol; 2018 Aug; 84(2):274-288. PubMed ID: 30014503
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?
    Bindu PS; Sonam K; Chiplunkar S; Govindaraj P; Nagappa M; Vekhande CC; Aravinda HR; Ponmalar JJ; Mahadevan A; Gayathri N; Bharath MS; Sinha S; Taly AB
    Mult Scler Relat Disord; 2018 Feb; 20():84-92. PubMed ID: 29353736
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Brain white matter abnormalities associated with copy number variants.
    Vigdorovich N; Ben-Sira L; Blumkin L; Precel R; Nezer I; Yosovich K; Cross Z; Vanderver A; Lev D; Lerman-Sagie T; Zerem A
    Am J Med Genet A; 2020 Jan; 182(1):93-103. PubMed ID: 31622028
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants.
    Mahdieh N; Soveizi M; Tavasoli AR; Rabbani A; Ashrafi MR; Kohlschütter A; Rabbani B
    Sci Rep; 2021 Feb; 11(1):3231. PubMed ID: 33547378
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients.
    Ayrignac X; Carra-Dalliere C; Menjot de Champfleur N; Denier C; Aubourg P; Bellesme C; Castelnovo G; Pelletier J; Audoin B; Kaphan E; de Seze J; Collongues N; Blanc F; Chanson JB; Magnin E; Berger E; Vukusic S; Durand-Dubief F; Camdessanche JP; Cohen M; Lebrun-Frenay C; Brassat D; Clanet M; Vermersch P; Zephir H; Outteryck O; Wiertlewski S; Laplaud DA; Ouallet JC; Brochet B; Goizet C; Debouverie M; Pittion S; Edan G; Deburghgraeve V; Le Page E; Verny C; Amati-Bonneau P; Bonneau D; Hannequin D; Guyant-Maréchal L; Derache N; Defer GL; Moreau T; Giroud M; Guennoc AM; Clavelou P; Taithe F; Mathis S; Neau JP; Magy L; Devoize JL; Bataillard M; Masliah-Planchon J; Dorboz I; Tournier-Lasserve E; Levade T; Boespflug Tanguy O; Labauge P
    Brain; 2015 Feb; 138(Pt 2):284-92. PubMed ID: 25527826
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expanded Phenotypic Definition Identifies Hundreds of Potential Causative Genes for Leukodystrophies and Leukoencephalopathies.
    Urbik VM; Schmiedel M; Soderholm H; Bonkowsky JL
    Child Neurol Open; 2020; 7():2329048X20939003. PubMed ID: 32704519
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial loss of function of colony-stimulating factor 1 receptor in a patient with white matter abnormalities.
    Konno T; Miura T; Harriott AM; Mezaki N; Edwards ES; Rademakers R; Ross OA; Meschia JF; Ikeuchi T; Wszolek ZK
    Eur J Neurol; 2018 Jun; 25(6):875-881. PubMed ID: 29509319
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The spectrum of adult-onset heritable white-matter disorders.
    Helman G; Venkateswaran S; Vanderver A
    Handb Clin Neurol; 2018; 148():669-692. PubMed ID: 29478607
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic disorders with central nervous system white matter abnormalities: An update.
    Shukla A; Kaur P; Narayanan DL; do Rosario MC; Kadavigere R; Girisha KM
    Clin Genet; 2021 Jan; 99(1):119-132. PubMed ID: 33047326
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The First Report of Relative Incidence of Inherited White Matter Disorders in an Asian Country Based on an Iranian Bioregistry System.
    Ashrafi MR; Rezaei Z; Heidari M; Nikbakht S; Malamiri RA; Mohammadi M; Zamani GR; Badv RS; Rostami P; Movahedinia M; Qorbani M; Amanat M; Tavasoli AR
    J Child Neurol; 2018 Mar; 33(4):255-259. PubMed ID: 29333903
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Radiological correlates of episodes of acute decline in the leukodystrophy vanishing white matter.
    Stellingwerff MD; van de Wiel MA; van der Knaap MS
    Neuroradiology; 2023 Apr; 65(4):855-863. PubMed ID: 36574026
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Relative incidence of inherited white matter disorders in childhood to acquired pediatric demyelinating disorders.
    Vanderver A; Hussey H; Schmidt JL; Pastor W; Hoffman HJ
    Semin Pediatr Neurol; 2012 Dec; 19(4):219-23. PubMed ID: 23245555
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotypic and phenotypic heterogeneity among Chinese pediatric genetic white matter disorders.
    Dong L; Shang L; Liu C; Mao C; Huang X; Chu S; Peng B; Cui L; Gao J
    Ital J Pediatr; 2023 Nov; 49(1):155. PubMed ID: 37981684
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Leukodystrophies and genetic leukoencephalopathies in children.
    Sarret C
    Rev Neurol (Paris); 2020; 176(1-2):10-19. PubMed ID: 31174885
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Similarities and differences between infantile and early childhood onset vanishing white matter disease.
    Zhou L; Zhang H; Chen N; Zhang Z; Liu M; Dai L; Wang J; Jiang Y; Wu Y
    J Neurol; 2018 Jun; 265(6):1410-1418. PubMed ID: 29663120
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lysosomal Leukodystrophies Lysosomal Storage Diseases Associated With White Matter Abnormalities.
    Maegawa GHB
    J Child Neurol; 2019 May; 34(6):339-358. PubMed ID: 30757954
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Implications of the International Paediatric Multiple Sclerosis Study Group consensus criteria for paediatric acute disseminated encephalomyelitis: a nationwide validation study.
    Boesen MS; Blinkenberg M; Koch-Henriksen N; Thygesen LC; Uldall PV; Magyari M; Born AP
    Dev Med Child Neurol; 2018 Nov; 60(11):1123-1131. PubMed ID: 29744874
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.