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Natural History of Clinical Phenotypes and Their Biochemical Correlates in Adult X-Linked Adrenoleukodystrophy.

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Title: Natural History of Clinical Phenotypes and Their Biochemical Correlates in Adult X-Linked Adrenoleukodystrophy.
Authors: Lier J; Department of Neurology, University Medical Center, Leipzig, Germany., Ponleitner M; Department of Neurology, University Medical Center, Leipzig, Germany.; Department of Neurology, Medical University of Vienna; Comprehensive Center for Clinical Neurosciences and Mental Health, Vienna, Austria., Popp D; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Saxony, Germany., Schäfer L; Department of Neurology, University Medical Center, Leipzig, Germany., Küstermann F; Department of Neurology, University Medical Center, Leipzig, Germany., Meigen C; LIFE Leipzig Research Center for Civilization Diseases, Leipzig University, Leipzig, Germany.; German Center for Child and Adolescent Health (DZKJ), Partner Site Leipzig/Dresden, Leipzig, Germany., Kratzer F; Division of Neuropediatrics and Metabolic Medicine, Department of Pediatrics I, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany., Janda J; Division of Neuropediatrics and Metabolic Medicine, Department of Pediatrics I, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany., Okun J; Division of Neuropediatrics and Metabolic Medicine, Department of Pediatrics I, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany., Jamra RA; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Saxony, Germany., Köhler W; Department of Neurology, University Medical Center, Leipzig, Germany., Bergner C; Department of Neurology, University Medical Center, Leipzig, Germany.
Source: Journal of inherited metabolic disease [J Inherit Metab Dis] 2026 Mar; Vol. 49 (2), pp. e70176.
Publication Type: Journal Article
Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 7910918 Publication Model: Print Cited Medium: Internet ISSN: 1573-2665 (Electronic) Linking ISSN: 01418955 NLM ISO Abbreviation: J Inherit Metab Dis Subsets: MEDLINE
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  Data: Natural History of Clinical Phenotypes and Their Biochemical Correlates in Adult X-Linked Adrenoleukodystrophy.
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  Data: <searchLink fieldCode="AU" term="%22Lier+J%22">Lier J</searchLink>; Department of Neurology, University Medical Center, Leipzig, Germany.<br /><searchLink fieldCode="AU" term="%22Ponleitner+M%22">Ponleitner M</searchLink>; Department of Neurology, University Medical Center, Leipzig, Germany.; Department of Neurology, Medical University of Vienna; Comprehensive Center for Clinical Neurosciences and Mental Health, Vienna, Austria.<br /><searchLink fieldCode="AU" term="%22Popp+D%22">Popp D</searchLink>; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Saxony, Germany.<br /><searchLink fieldCode="AU" term="%22Schäfer+L%22">Schäfer L</searchLink>; Department of Neurology, University Medical Center, Leipzig, Germany.<br /><searchLink fieldCode="AU" term="%22Küstermann+F%22">Küstermann F</searchLink>; Department of Neurology, University Medical Center, Leipzig, Germany.<br /><searchLink fieldCode="AU" term="%22Meigen+C%22">Meigen C</searchLink>; LIFE Leipzig Research Center for Civilization Diseases, Leipzig University, Leipzig, Germany.; German Center for Child and Adolescent Health (DZKJ), Partner Site Leipzig/Dresden, Leipzig, Germany.<br /><searchLink fieldCode="AU" term="%22Kratzer+F%22">Kratzer F</searchLink>; Division of Neuropediatrics and Metabolic Medicine, Department of Pediatrics I, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.<br /><searchLink fieldCode="AU" term="%22Janda+J%22">Janda J</searchLink>; Division of Neuropediatrics and Metabolic Medicine, Department of Pediatrics I, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.<br /><searchLink fieldCode="AU" term="%22Okun+J%22">Okun J</searchLink>; Division of Neuropediatrics and Metabolic Medicine, Department of Pediatrics I, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.<br /><searchLink fieldCode="AU" term="%22Jamra+RA%22">Jamra RA</searchLink>; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Saxony, Germany.<br /><searchLink fieldCode="AU" term="%22Köhler+W%22">Köhler W</searchLink>; Department of Neurology, University Medical Center, Leipzig, Germany.<br /><searchLink fieldCode="AU" term="%22Bergner+C%22">Bergner C</searchLink>; Department of Neurology, University Medical Center, Leipzig, Germany.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley%22">Wiley </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>7910918 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1573-2665 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2201418955%22">01418955 </searchLink><i>NLM ISO Abbreviation: </i>J Inherit Metab Dis <i>Subsets: </i>MEDLINE
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        Value: 10.1002/jimd.70176
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        Text: English
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              Text: 2026 Mar
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