JP van der Voorn, PJW Pouwels… - American Journal …, 2011 - Am Soc Neuroradiology BACKGROUND AND PURPOSE: Quantitative MR imaging techniques may improve the pathologic specificity of MR imaging regarding white matter abnormalities. Our purposes were to determine whether ADC, FA, MTR, and MRS metabolites correlate with the degree of white matter ... Related articles - All 4 versions
Y Wang, R Busin, C Reeves, L Bezman… - Molecular genetics …, 2011 - ncbi.nlm.nih.gov X-linked adrenoleukodystrophy (X-ALD) is a progressive peroxisomal disorder affecting adrenal glands, testes and myelin stability that is caused by mutations in the ABCD1 (NM_000033) gene. Males with X-ALD may be diagnosed by the demonstration of elevated very long ...
[HTML] from pediatricsdigest.mobiAJ Taxter, MD Bellin… - Pediatrics, 2011 - Am Acad Pediatrics X-linked adrenoleukodystrophy is characterized by elevated levels of very long chain fatty acids in the serum, brain, and adrenal glands that can lead to neurodevelopmental impairment and decreased adrenal function. We report here the case of a pediatric patient with ... Related articles - All 4 versions
[HTML] from nih.govY Uchida, E Kimura, T Hirano, S Nishi… - Case Reports in …, 2011 - ncbi.nlm.nih.gov X-linked adrenoleukodystrophy is a severe and progressive neurodegenerative disease caused by the peroxisomal transporter ATP-binding cassette, subfamily D, member 1 gene mutations. The defect of this gene product results in accumulation of very-long-chain fatty ... Related articles - All 3 versions
WP Miller, SM Rothman, D Nascene, T Kivisto… - Blood, 2011 - ncbi.nlm.nih.gov Cerebral adrenoleukodystrophy (cALD) remains a devastating neuro-degenerative disease; only allogeneic hematopoietic cell transplant (HCT) has been shown to provide long-term disease stabilization and survival. Sixty boys undergoing HCT for cALD from 2000 to 2009 were ...
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