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  1. 1
    Hematopoietic Stem Cell Transplantation in Inborn Errors of Metabolism

    Hematopoietic Stem Cell Transplantation in Inborn Errors of Metabolism by Emily Y. Tan, Jaap Jan Boelens, Simon Jones, Robert Wynn

    Published 2019
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  2. 2
    Fatty acid omega‐oxidation as a rescue pathway for fatty acid oxidation disorders in humans

    Fatty acid omega‐oxidation as a rescue pathway for fatty acid oxidation disorders in humans by Ronald J. A. Wanders, J.C. Komen, Stephan Kemp

    Published 2010
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  3. 3
    Adult-onset adrenoleukodystrophy presenting as a psychiatric disorder: MRI findings

    Adult-onset adrenoleukodystrophy presenting as a psychiatric disorder: MRI findings by Antonio Cézar Ribeiro Galvão, Gislaine Cristina Lopes Machado Porto, Fábio Henrique de Gobbi Porto, Leandro Tavares Lucato, Ricardo Nitríni

    Published 2012
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  4. 4
    Peroxisome biogenesis disorders

    Peroxisome biogenesis disorders by Stephen J. Gould, David Valle

    Published 2000
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  5. 5
    Cholestane-3β,5α,6β-triol: high levels in Niemann-Pick type C, cerebrotendinous xanthomatosis, and lysosomal acid lipase deficiency

    Cholestane-3β,5α,6β-triol: high levels in Niemann-Pick type C, cerebrotendinous xanthomatosis, and lysosomal acid lipase deficiency by Sonia Pajares, Ángela Arias, Judit García‐Villoria, Judit Macías‐Vidal, Emilio Ros, Javier de las Heras, M. Girós, María Josep Coll, Antònia Ribes

    Published 2015
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  6. 6
    Brain endothelial dysfunction in cerebral adrenoleukodystrophy

    Brain endothelial dysfunction in cerebral adrenoleukodystrophy by Patricia L. Musolino, Yi Gong, Juliet M T Snyder, Sandra Jimenez, Josephine Lok, Eng H. Lo, Ann B. Moser, Eríc F. Grabowski, Matthew P. Frosch, Florian Eichler

    Published 2015
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  7. 7
    The genetic landscape of X-linked adrenoleukodystrophy: inheritance, mutations, modifier genes, and diagnosis

    The genetic landscape of X-linked adrenoleukodystrophy: inheritance, mutations, modifier genes, and diagnosis by Johannes Berger, Christoph Wiesinger, Florian Eichler

    Published 2015
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  8. 8
    Altered glycolipid and glycerophospholipid signaling drive inflammatory cascades in adrenomyeloneuropathy

    Altered glycolipid and glycerophospholipid signaling drive inflammatory cascades in adrenomyeloneuropathy by Montserrat Ruíz, Mariona Jové, Agatha Schlüter, Carlos Casasnovas, Francesc Villarroya, Cristina Guilera, Francisco J. Ortega, Alba Naudí, Reinald Pamplona, Ramón Gimeno, Stéphane Fourcade, Manuel Portero‐Otín, Aurora Pujol

    Published 2015
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  9. 9
    General Aspects and Neuropathology of X‐Linked Adrenoleukodystrophy

    General Aspects and Neuropathology of X‐Linked Adrenoleukodystrophy by Isidró Ferrer, Patrick Aubourg, Aurora Pujol

    Published 2010
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  10. 10
    Pathomechanisms Underlying X‐Adrenoleukodystrophy: A Three‐Hit Hypothesis

    Pathomechanisms Underlying X‐Adrenoleukodystrophy: A Three‐Hit Hypothesis by Inderjit Singh, Aurora Pujol

    Published 2010
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  11. 11
    Biochemical Aspects of X‐Linked Adrenoleukodystrophy

    Biochemical Aspects of X‐Linked Adrenoleukodystrophy by Stephan Kemp, Ronald J. A. Wanders

    Published 2010
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  12. 12
    A mouse model for X-linked adrenoleukodystrophy

    A mouse model for X-linked adrenoleukodystrophy by Jyh‐Feng Lu, Ann M. Lawler, Paul A. Watkins, James M. Powers, Ann B. Moser, Hugo W. Moser, Kirby D. Smith

    Published 1997
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  13. 13
    Genotype–Phenotype Correlations in Disorders of Peroxisome Biogenesis

    Genotype–Phenotype Correlations in Disorders of Peroxisome Biogenesis by Hugo W. Moser

    Published 1999
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  14. 14
    Identification of a Fourth Half ABC Transporter in the Human Peroxisomal Membrane

    Identification of a Fourth Half ABC Transporter in the Human Peroxisomal Membrane by Noam Shani, Gerardo Jiménez‐Sánchez, Gary Steel, Michael Dean, David Valle

    Published 1997
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  15. 15
    Adrenoleukodystrophy: Impaired Oxidation of Very Long Chain Fatty Acids in White Blood Cells, Cultured Skin Fibroblasts, and Amniocytes

    Adrenoleukodystrophy: Impaired Oxidation of Very Long Chain Fatty Acids in White Blood Cells, Cultured Skin Fibroblasts, and Amniocytes by Inderjit Singh, Ann E. Moser, Hugo W. Moser, Yasuo Kishimoto

    Published 1984
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  16. 16
    Clinical diagnosis, biochemical findings and MRI spectrum of peroxisomal disorders

    Clinical diagnosis, biochemical findings and MRI spectrum of peroxisomal disorders by Bwee Tien Poll‐The, Jutta Gärtner

    Published 2012
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  17. 17
    Phenotypic variability in a family with x-linked adrenoleukodystrophy caused by the p.Trp132Ter mutation

    Phenotypic variability in a family with x-linked adrenoleukodystrophy caused by the p.Trp132Ter mutation by Fernanda Caroline Soardi, Adriana Mangue Esquiaveto‐Aun, Gil Guerra‐Júnior, Sofia Helena Valente de Lemos‐Marini, Maricilda Palandi de Mello

    Published 2010
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  18. 18
    The peroxisomal ABC transporter family

    The peroxisomal ABC transporter family by Ronald J. A. Wanders, Wouter F. Visser, Carlo W.T. van Roermund, Stephan Kemp, Hans R. Waterham

    Published 2006
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  19. 19
    Peroxisomal ABC transporters: Structure, function and role in disease

    Peroxisomal ABC transporters: Structure, function and role in disease by Masashi Morita, Tsuneo Imanaka

    Published 2012
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  20. 20
    Accurate DNA-Based Diagnostic and Carrier Testing for X-Linked Adrenoleukodystrophy

    Accurate DNA-Based Diagnostic and Carrier Testing for X-Linked Adrenoleukodystrophy by Corinne D. Boehm, Garry R. Cutting, M. Lachtermacher, Hugo W. Moser, Samuel S. Chong

    Published 1999
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