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 *

134 related articles for article (PubMed ID: 16437562)

  • 21. 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]  

  • 22. TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome.
    Hoffmann LA; Lohse P; König FB; Feneberg W; Hohlfeld R; Kümpfel T
    Neurology; 2008 Mar; 70(13 Pt 2):1155-6. PubMed ID: 18287568
    [No Abstract]   [Full Text] [Related]  

  • 23. A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations.
    Brussino A; Vaula G; Cagnoli C; Panza E; Seri M; Di Gregorio E; Scappaticci S; Camanini S; Daniele D; Bradac GB; Pinessi L; Cavalieri S; Grosso E; Migone N; Brusco A
    Eur J Neurol; 2010 Apr; 17(4):541-9. PubMed ID: 19961535
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Peripheral neuropathy in vanishing white matter disease with a novel EIF2B5 mutation.
    Federico A; Scali O; Stromillo ML; Di Perri C; Bianchi S; Sicurelli F; De Stefano N; Malandrini A; Dotti MT
    Neurology; 2006 Jul; 67(2):353-5. PubMed ID: 16864840
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Decreased guanine nucleotide exchange factor activity in eIF2B-mutated patients.
    Fogli A; Schiffmann R; Hugendubler L; Combes P; Bertini E; Rodriguez D; Kimball SR; Boespflug-Tanguy O
    Eur J Hum Genet; 2004 Jul; 12(7):561-6. PubMed ID: 15054402
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Identification of ten novel mutations in patients with eIF2B-related disorders.
    Ohlenbusch A; Henneke M; Brockmann K; Goerg M; Hanefeld F; Kohlschütter A; Gärtner J
    Hum Mutat; 2005 Apr; 25(4):411. PubMed ID: 15776425
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Adult-onset autosomal dominant leukodystrophy without early autonomic dysfunctions linked to lamin B1 duplication: a phenotypic variant.
    Potic A; Pavlovic AM; Uziel G; Kozic D; Ostojic J; Rovelli A; Sternic N; Bjelan M; Sarto E; Di Bella D; Taroni F
    J Neurol; 2013 Aug; 260(8):2124-9. PubMed ID: 23681646
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Vanishing white matter disease: the first reported chinese patient.
    Wong SS; Luk DC; Wong VC; Scheper GC; van der Knaap MS
    J Child Neurol; 2008 Jun; 23(6):710-4. PubMed ID: 18539998
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Adult-onset autosomal dominant leukodystrophy: linking nuclear envelope to myelin.
    Lin ST; Ptácek LJ; Fu YH
    J Neurosci; 2011 Jan; 31(4):1163-6. PubMed ID: 21273400
    [No Abstract]   [Full Text] [Related]  

  • 31. [Leukoencephalopathy with vanishing white matter: A case report].
    San Antonio-Arce V; Martín Fernández-Mayoralas D; Muñoz-Jareño N; Fresneda-Machado C; Sáiz-Ayala A; Campos-Castelló J
    Rev Neurol; 2006 Nov 1-15; 43(9):535-40. PubMed ID: 17072809
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Adult-onset 4H leukodystrophy: a case presentation and review of the literature.
    Uygun Ö; Gündüz T; Eraksoy M; Kürtüncü M
    Acta Neurol Belg; 2020 Dec; 120(6):1461-1462. PubMed ID: 32052360
    [No Abstract]   [Full Text] [Related]  

  • 33. Vanishing white matter disease in French-Canadian patients from Quebec.
    Robinson MÈ; Rossignol E; Brais B; Rouleau G; Arbour JF; Bernard G
    Pediatr Neurol; 2014 Aug; 51(2):225-32. PubMed ID: 25079571
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Sporadic adult-onset leukoencephalopathy with neuroaxonal spheroids mimicking cerebral MS.
    Keegan BM; Giannini C; Parisi JE; Lucchinetti CF; Boeve BF; Josephs KA
    Neurology; 2008 Mar; 70(13 Pt 2):1128-33. PubMed ID: 18287567
    [TBL] [Abstract][Full Text] [Related]  

  • 35. MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS WITH HOMOZYGOUS MUTATION (C.448DELC, P.LEU150 SER FSX11) ON EXON 6 OF MLC1 GENE.
    Soysal Z; Okur M; Eroz R; Gun E; Kocabay K; Besir FH
    Genet Couns; 2015; 26(2):233-6. PubMed ID: 26349194
    [TBL] [Abstract][Full Text] [Related]  

  • 36. MR imaging characteristics and neuropathology of the spinal cord in adult-onset autosomal dominant leukodystrophy with autonomic symptoms.
    Sundblom J; Melberg A; Kalimo H; Smits A; Raininko R
    AJNR Am J Neuroradiol; 2009 Feb; 30(2):328-35. PubMed ID: 18945794
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Adulthood leukodystrophies.
    Köhler W; Curiel J; Vanderver A
    Nat Rev Neurol; 2018 Feb; 14(2):94-105. PubMed ID: 29302065
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Demyelinating disease of central and peripheral nervous systems associated with a A8344G mutation in tRNALys.
    Erol I; Alehan F; Horvath R; Schneiderat P; Talim B
    Neuromuscul Disord; 2009 Apr; 19(4):275-8. PubMed ID: 19269823
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Update on genetic disorders affecting white matter.
    Kaye EM
    Pediatr Neurol; 2001 Jan; 24(1):11-24. PubMed ID: 11182276
    [TBL] [Abstract][Full Text] [Related]  

  • 40. An adult case of leukoencephalopathy with intracranial calcifications and cysts.
    Corboy JR; Gault J; Kleinschmidt-DeMasters BK
    Neurology; 2006 Nov; 67(10):1890-2. PubMed ID: 17130435
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.