Results 71 to 80 of about 29,741 (152)
, 2017 X-linked Adrenoleukodystrophy (X-ALD) is a genetic disease that caused by mutations in adenosine triphosphate [ATP]-binding-cassette transporter superfamily D member 1 (ABCD1) gene. We generated an induced pluripotent stem cell (iPSC) line from a 21-year-
Young Rang You +4 more
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Asymmetric Cerebral Lesion Pattern in X-linked Adrenoleukodystrophy [PDF]
, 2006 X-linked adrenoleukodystrophy (X-ALD) is an inherited disease caused by peroxisomal dysfunction. X-ALD usually involves the cerebral white matter in an approximately symmetric way. We report a 10-year-old boy with the cerebral form of X-ALD who presented
Wang, Shuang +2 more
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Growth characteristics, optical properties, and crystallinity of thermal and plasma-enhanced ALD AlN films [PDF]
, 2014 Using real-time in-situ spectroscopic ellipsometry and ex-situ atomic force microscopy and X-ray diffraction, we have investigated the growth characteristics, especially ocusing on the initial growth (nucleation) regime, optical properties and ...
Wiggers, Frank Bert +6 more
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Easily misdiagnosed X-linked adrenoleukodystrophy
Italian Journal of PediatricsBackground Addison’s disease and X-linked adrenoleukodystrophy (X-ALD) (Addison’s-only) are two diseases that need to be identified. Addison’s disease is easy to diagnose clinically when only skin and mucosal pigmentation symptoms are present. However, X-
Qiu-Hong Wang +10 more
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Coping with the Pressure of Adrenoleukodystrophy（ALD）
, 2007 本研究的目的是想要了解Adrenoleukodystrophy（ALD）個案在面對疾病本身的壓力的影響下，對於疾病治療的期望、對於未來的計畫，以及透過哪些形式的想法與實際上的因應行為去面對疾病。希望透過這個探討，可以知道哪種因應方式有效，以之用來協助未來的個案去克服ALD這個疾病。 研究者利用個案研究法，以深度訪談及參與觀察的方式蒐集八個ALD家族中已被診斷，但是還沒發病；或是仍可以清楚自由表達自己意見的ALD患者做為研究樣本，研究內容包括進行個案病歷資料的蒐集，每次個案就診時 ...
Huang, Ai-Chu, 黃愛珠
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Journal of Lipid Research, 1998 Studies with purified subcellular organelles from rat liver indicate that nervonic acid (C24:1) is β-oxidized preferentially in peroxisomes. Lack of effect by etomoxir, inhibitor of mitochondrial β-oxidation, on β-oxidation of lignoceric acid (C24:0), a ...
Rajat Sandhir +3 more
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Peroxisomal ABC transporters and X-linked adrenoleukodystrophy
, 2012 X-linked adrenoleukodystrophy (X-ALD) is a complex neurodegenerative disease associated with mutations in the ABCD1 gene, which encodes for a peroxisomal ABC transporter.
Gondcaille, Catherine +9 more
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, 2013 International audienceX-linked adrenoleukodystrophy (X-ALD) is the most common leukodystrophy and the most frequent peroxisomal disorder, with an estimated incidence of 1:17,000. This complex neurodegenerative disorder is characterized by a huge clinical
Trompier, Doriane, Savary, Stéphane
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Adrenoleukodystrophy in a Chinese boy
, 1992 We report the first Chinese boy with adrenoleukodystrophy (ALD) who presented with hyperpigmentation, behavioral change and demyelination shown in magnetic resonance imaging of the brain.
Wong, V
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ALD of Copper and Copper Oxide Thin Films for Applications in Metallization Systems of ULSI Devices
, 2022 17 FolienAs a possible alternative for growing seed layers required for electrochemical Cu deposition of metallization systems in ULSI circuits, the atomic layer deposition (ALD) of Cu is under consideration. To avoid drawbacks related to plasma-enhanced
Waechtler, T. +5 more
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