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 *

152 related articles for article (PubMed ID: 32342562)

  • 1. Randomized Clinical Trial of First-Line Genome Sequencing in Pediatric White Matter Disorders.
    Vanderver A; Bernard G; Helman G; Sherbini O; Boeck R; Cohn J; Collins A; Demarest S; Dobbins K; Emrick L; Fraser JL; Masser-Frye D; Hayward J; Karmarkar S; Keller S; Mirrop S; Mitchell W; Pathak S; Sherr E; van Haren K; Waters E; Wilson JL; Zhorne L; Schiffmann R; van der Knaap MS; Pizzino A; Dubbs H; Shults J; Simons C; Taft RJ;
    Ann Neurol; 2020 Aug; 88(2):264-273. PubMed ID: 32342562
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole exome sequencing in patients with white matter abnormalities.
    Vanderver A; Simons C; Helman G; Crawford J; Wolf NI; Bernard G; Pizzino A; Schmidt JL; Takanohashi A; Miller D; Khouzam A; Rajan V; Ramos E; Chowdhury S; Hambuch T; Ru K; Baillie GJ; Grimmond SM; Caldovic L; Devaney J; Bloom M; Evans SH; Murphy JLP; McNeill N; Fogel BL; ; Schiffmann R; van der Knaap MS; Taft RJ
    Ann Neurol; 2016 Jun; 79(6):1031-1037. PubMed ID: 27159321
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Argentinian clinical genomics in a leukodystrophies and genetic leukoencephalopathies cohort: Diagnostic yield in our first 9 years.
    Cohen L; Manín A; Medina N; Rodríguez-Quiroga S; González-Morón D; Rosales J; Amartino H; Specola N; Córdoba M; Kauffman M; Vega P
    Ann Hum Genet; 2020 Jan; 84(1):11-28. PubMed ID: 31418856
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genome sequencing in persistently unsolved white matter disorders.
    Helman G; Lajoie BR; Crawford J; Takanohashi A; Walkiewicz M; Dolzhenko E; Gross AM; Gainullin VG; Bent SJ; Jenkinson EM; Ferdinandusse S; Waterham HR; Dorboz I; Bertini E; Miyake N; Wolf NI; Abbink TEM; Kirwin SM; Tan CM; Hobson GM; Guo L; Ikegawa S; Pizzino A; Schmidt JL; Bernard G; Schiffmann R; van der Knaap MS; Simons C; Taft RJ; Vanderver A
    Ann Clin Transl Neurol; 2020 Jan; 7(1):144-152. PubMed ID: 31912665
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 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. Practical approach to the diagnosis of adult-onset leukodystrophies: an updated guide in the genomic era.
    Lynch DS; Wade C; Paiva ARB; John N; Kinsella JA; Merwick Á; Ahmed RM; Warren JD; Mummery CJ; Schott JM; Fox NC; Houlden H; Adams ME; Davagnanam I; Murphy E; Chataway J
    J Neurol Neurosurg Psychiatry; 2019 May; 90(5):543-554. PubMed ID: 30467211
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies.
    Ashrafi MR; Amanat M; Garshasbi M; Kameli R; Nilipour Y; Heidari M; Rezaei Z; Tavasoli AR
    Expert Rev Neurother; 2020 Jan; 20(1):65-84. PubMed ID: 31829048
    [No Abstract]   [Full Text] [Related]  

  • 11. Inherited leukoencephalopathies with clinical onset in middle and old age.
    Nannucci S; Donnini I; Pantoni L
    J Neurol Sci; 2014 Dec; 347(1-2):1-13. PubMed ID: 25307983
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.
    Abul-Husn NS; Marathe PN; Kelly NR; Bonini KE; Sebastin M; Odgis JA; Abhyankar A; Brown K; Di Biase M; Gallagher KM; Guha S; Ioele N; Okur V; Ramos MA; Rodriguez JE; Rehman AU; Thomas-Wilson A; Edelmann L; Zinberg RE; Diaz GA; Greally JM; Jobanputra V; Suckiel SA; Horowitz CR; Wasserstein MP; Kenny EE; Gelb BD
    Genet Med; 2023 Sep; 25(9):100880. PubMed ID: 37158195
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Diagnosis, prognosis, and treatment of leukodystrophies.
    van der Knaap MS; Schiffmann R; Mochel F; Wolf NI
    Lancet Neurol; 2019 Oct; 18(10):962-972. PubMed ID: 31307818
    [TBL] [Abstract][Full Text] [Related]  

  • 18. White Matter Lesion Progression: Genome-Wide Search for Genetic Influences.
    Hofer E; Cavalieri M; Bis JC; DeCarli C; Fornage M; Sigurdsson S; Srikanth V; Trompet S; Verhaaren BF; Wolf C; Yang Q; Adams HH; Amouyel P; Beiser A; Buckley BM; Callisaya M; Chauhan G; de Craen AJ; Dufouil C; van Duijn CM; Ford I; Freudenberger P; Gottesman RF; Gudnason V; Heiss G; Hofman A; Lumley T; Martinez O; Mazoyer B; Moran C; Niessen WJ; Phan T; Psaty BM; Satizabal CL; Sattar N; Schilling S; Shibata DK; Slagboom PE; Smith A; Stott DJ; Taylor KD; Thomson R; Töglhofer AM; Tzourio C; van Buchem M; Wang J; Westendorp RG; Windham BG; Vernooij MW; Zijdenbos A; Beare R; Debette S; Ikram MA; Jukema JW; Launer LJ; Longstreth WT; Mosley TH; Seshadri S; Schmidt H; Schmidt R;
    Stroke; 2015 Nov; 46(11):3048-57. PubMed ID: 26451028
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Leukoencephalopathy and long-term neurobehavioural, neurocognitive, and brain imaging outcomes in survivors of childhood acute lymphoblastic leukaemia treated with chemotherapy: a longitudinal analysis.
    Cheung YT; Sabin ND; Reddick WE; Bhojwani D; Liu W; Brinkman TM; Glass JO; Hwang SN; Srivastava D; Pui CH; Robison LL; Hudson MM; Krull KR
    Lancet Haematol; 2016 Oct; 3(10):e456-e466. PubMed ID: 27658980
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Association between homozygous c.318A>GT mutation in exon 2 of the EIF2B5 gene and the infantile form of vanishing white matter leukoencephalopathy].
    Esmer C; Blanco Hernández G; Saavedra Alanís V; Reyes Vaca JG; Bravo Oro A
    Bol Med Hosp Infant Mex; 2017; 74(5):364-369. PubMed ID: 29382480
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.