Results 131 to 140 of about 29,741 (152)
ABCD1-Related Disease Presenting as an Upper Motor Neuron-Predominant Amyotrophic Lateral Sclerosis Mimic in a Colombian Female Heterozygote: A Case Report. [PDF]
CureusCorrea-Arrieta C +5 more
europepmc +1 more source
Evolution of the lipidome uncovers early changes in adrenoleukodystrophy human cortical and spinal organoids. [PDF]
iScienceFerrer RM +11 more
europepmc +1 more source
The X-Linked Adrenoleukodystrophy (X-ALD) and Oxidative Stress
Journal of Herbal Pharmacotherapy: Innovations in Clinical and Applied Evidence-based Herbal Medicinals, 2006 Most of the studies indicate that there is as yet no complete cure for X-ALD. However, methods of the treatment seem to slow rather than treat the disease.
Mohamed A Al-Omar
exaly +2 more sources
Human Molecular Genetics, 2004 X-linked adrenoleukodystrophy (X-ALD) is a severe neurodegenerative disease caused by loss of function of the peroxisomal transporter ABCD1 (ALD), which results in accumulation of very long chain fatty acids (VLCFAs) in organs and serum, central ...
Isidro Ferrer +2 more
exaly +2 more sources
Treatment of cerebral adrenoleukodystrophy: allogeneic transplantation and lentiviral gene therapy
Expert Opinion on Biological Therapy, 2022 Introduction: Adrenoleukodystrophy (ALD) is an X-linked peroxisomal disorder with an incidence of 1 in 14–17,000 male births, caused by pathogenic variants within the ABCD1 gene.
Ashish Gupta +2 more
exaly +2 more sources
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Mutation analysis of the ALD gene in seven Japanese families with X-linked adrenoleukodystrophy
Journal of Human Genetics, 2003Akira Tsuru, Tatsuro Kondoh, K Tamagawa
exaly