BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 36470810)

  • 41. Differentiation of rare leukodystrophies by post-mortem morphological and biochemical studies: female adrenoleukodystrophy-like disease and late-onset Krabbe disease.
    Gullotta F; Hughes JL; Wittkowski W; Poulos A; Sträter R; Bernheimer H; Harzer K
    Neuropediatrics; 1996 Feb; 27(1):37-41. PubMed ID: 8677024
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Juvenile onset globoid cell leukodystrophy masquerading as XL-adrenoleukodystrophy.
    Srinivasan J; Coleman L; Kornberg AJ
    J Paediatr Child Health; 2008; 44(7-8):459-61. PubMed ID: 18638333
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [Myelin diseases affecting both the central and the peripheral nervous system].
    Hagen K; Mellgren SI; Bovim G
    Tidsskr Nor Laegeforen; 1998 Sep; 118(23):3600-2. PubMed ID: 9820004
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Hematopoietic Stem Cell Transplantation to Treat Leukodystrophies: Clinical Practice Guidelines from the Hunter's Hope Leukodystrophy Care Network.
    Page KM; Stenger EO; Connelly JA; Shyr D; West T; Wood S; Case L; Kester M; Shim S; Hammond L; Hammond M; Webb C; Biffi A; Bambach B; Fatemi A; Kurtzberg J
    Biol Blood Marrow Transplant; 2019 Dec; 25(12):e363-e374. PubMed ID: 31499213
    [TBL] [Abstract][Full Text] [Related]  

  • 45. The future for treatment by bone marrow transplantation for adrenoleukodystrophy, metachromatic leukodystrophy, globoid cell leukodystrophy and Hurler syndrome.
    Krivit W; Lockman LA; Watkins PA; Hirsch J; Shapiro EG
    J Inherit Metab Dis; 1995; 18(4):398-412. PubMed ID: 7494399
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Childhood leukodystrophies: a clinical perspective.
    Kohlschütter A; Eichler F
    Expert Rev Neurother; 2011 Oct; 11(10):1485-96. PubMed ID: 21955203
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Aicardi-Goutières syndrome may present with positive newborn screen for X-linked adrenoleukodystrophy.
    Tise CG; Morales JA; Lee AS; Velez-Bartolomei F; Floyd BJ; Levy RJ; Cusmano-Ozog KP; Feigenbaum AS; Ruzhnikov MRZ; Lee CU; Enns GM
    Am J Med Genet A; 2021 Jun; 185(6):1848-1853. PubMed ID: 33683010
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Diagnosis of metachromatic leukodystrophy, Krabbe disease, and Farber disease after uptake of fatty acid-labeled cerebroside sulfate into cultured skin fibroblasts.
    Kudoh T; Wenger DA
    J Clin Invest; 1982 Jul; 70(1):89-97. PubMed ID: 6806321
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Clinical pathological correlation.
    Singer HS; Rorke LB
    Pediatr Neurosci; 1985-1986; 12(1):31-7. PubMed ID: 3001681
    [No Abstract]   [Full Text] [Related]  

  • 50. Structural manifestations of leukodystrophies.
    Seitelberger F
    Neuropediatrics; 1984 Sep; 15 Suppl():53-61. PubMed ID: 6152813
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Hematopoietic stem cell gene therapy in Hurler syndrome, globoid cell leukodystrophy, metachromatic leukodystrophy and X-adrenoleukodystrophy.
    Cartier N; Aubourg P
    Curr Opin Mol Ther; 2008 Oct; 10(5):471-8. PubMed ID: 18830923
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Early-Onset Aicardi-Goutières Syndrome: Magnetic Resonance Imaging (MRI) Pattern Recognition.
    Vanderver A; Prust M; Kadom N; Demarest S; Crow YJ; Helman G; Orcesi S; La Piana R; Uggetti C; Wang J; Gordisch-Dressman H; van der Knaap MS; Livingston JH
    J Child Neurol; 2015 Sep; 30(10):1343-8. PubMed ID: 25535058
    [TBL] [Abstract][Full Text] [Related]  

  • 53. MRI appearances of metachromatic leukodystrophy.
    Faerber EN; Melvin J; Smergel EM
    Pediatr Radiol; 1999 Sep; 29(9):669-72. PubMed ID: 10460327
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Brainstem auditory evoked responses in leukodystrophies.
    Ochs R; Markand ON; DeMyer WE
    Neurology; 1979 Aug; 29(8):1089-93. PubMed ID: 572495
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Hereditary metabolic myelin diseases in humans.
    Martin JJ
    Bull Soc Belge Ophtalmol; 1983 Nov; 208 Pt 1():375-98. PubMed ID: 6675823
    [No Abstract]   [Full Text] [Related]  

  • 56. Adult Leukodystrophies: A Step-by-Step Diagnostic Approach.
    Resende LL; de Paiva ARB; Kok F; da Costa Leite C; Lucato LT
    Radiographics; 2019; 39(1):153-168. PubMed ID: 30620693
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Developmental Outcomes of Aicardi Goutières Syndrome.
    Adang L; Gavazzi F; De Simone M; Fazzi E; Galli J; Koh J; Kramer-Golinkoff J; De Giorgis V; Orcesi S; Peer K; Ulrick N; Woidill S; Shults J; Vanderver A
    J Child Neurol; 2020 Jan; 35(1):7-16. PubMed ID: 31559893
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Genetic leukodystrophies.
    Suzuki K
    Trans Am Neurol Assoc; 1976; 101():116-21. PubMed ID: 1028213
    [No Abstract]   [Full Text] [Related]  

  • 59. 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]  

  • 60. Some thoughts on the neurobiology of the leukodystrophies.
    Norton WT
    Neuropediatrics; 1984 Sep; 15 Suppl():28-31. PubMed ID: 6100796
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.