Bálint syndrome as the presenting manifestation of adrenoleukodystrophy by R. Ghosh, M. León-Ruiz, K. Bole, S. Bandyopadhyay, S. Dubey, J. Benito-León

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The Overlooked Transformation Mechanisms of VLCFAs: Peroxisomal β-Oxidation by Qinyue Lu, Weicheng Zong, Mingyixing Zhang, Zhi Chen, Zhangping Yang

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Optic nerve demyelination as the presenting feature of adrenoleukodystrophy in a child by Nirupama Kasturi, Sandip Sarkar, Tanmay Gokhale, Chinnaiah G Delhikumar, Midhusha R Vendoti

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Role of MRI in X-linked adrenoleukodystrophy—A case report by Sajiva Aryal, MBBS, Suraj Sharma, MBBS, MD, Saroj Poudel, MBBS, Sunita Sharma, MPH

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Application of a diagnostic methodology by quantification of 26:0 lysophosphatidylcholine in dried blood spots for Japanese newborn screening of X-linked adrenoleukodystrophy by Chen Wu, Takeo Iwamoto, Junko Igarashi, Takashi Miyajima, Mohammad Arif Hossain, Hiroko Yanagisawa, Keiko Akiyama, Haruo Shintaku, Yoshikatsu Eto

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Peroxisomal Disorders Diagnosis by J Gordon Millichap

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Reduced chain length in myelin sphingolipids and poorer motor coordination in mice deficient in the fatty acid elongase Elovl1 by Masashi Isokawa, Takayuki Sassa, Satoko Hattori, Tsuyoshi Miyakawa, Akio Kihara

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Adrenoleukodystrophy in the Differential Diagnosis of Boys Presenting with Primary Adrenal Insufficiency without Adrenal Antibodies by Michael R Ryalls, Hoong-Wei Gan, James E Davison

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A novel ABCD1 G1202A mutation in a Chinese patient with pure adrenomyeloneuropathy and literature review by Yu Zhang, Guoyong Zhang, Wenhui Chen, Zheng Pu, Lu Song, Xinghua Tang, Zhenguo Liu

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Role and Function of Peroxisomes in Neuroinflammation by Chinmoy Sarkar, Marta M. Lipinski

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Atypical MRI Findings in Cerebral Adrenoleukodystrophy: a Case Report by Koray Koç, Arzu Canan, Pınar Koç, Kamil Karaali, Özgür Duman, Utku Şenol

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Cerebello-brainstem dominant form of X-linked adrenoleukodystrophy with intrafamilial phenotypic variability by Jae-Hwan Choi, Jae-Hwan Choi, Hyun Sung Kim, Eun Hye Oh, Jae Hyeok Lee, Jae Hyeok Lee, Chong Kun Cheon, Chong Kun Cheon

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Dystonic opisthotonus: A rare phenotype of adrenoleukodystrophy by Sindhu D Mallikarjuna, Sadanandavalli R Chandra, Hansashree Padmanabha, Rita Christopher

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Reassessing very long chain fatty acids elevations: Sitosterolemia as a non-peroxisomal cause by Merve Yoldaş Çelik, Burcu Köşeci, Ezgi Burgaç, Kanay Yararbaş

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The Unique Role of the ECERIFERUM2-LIKE Clade of the BAHD Acyltransferase Superfamily in Cuticular Wax Metabolism by Tegan M. Haslam, Wesley K. Gerelle, Sean W. Graham, Ljerka Kunst

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Overwhelming sepsis in a neonate affected by Zellweger syndrome due to a compound heterozygosis in PEX 6 gene: a case report by Laura Lucaccioni, Beatrice Righi, Greta Miriam Cingolani, Licia Lugli, Elisa Della Casa, Francesco Torcetta, Lorenzo Iughetti, Alberto Berardi

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A novel HPLC-based method to diagnose peroxisomal D-bifunctional protein enoyl-CoA hydratase deficiency by Jolein Gloerich, Simone Denis, Elisabeth G. van Grunsven, Georges Dacremont, Ronald J.A. Wanders, Sacha Ferdinandusse

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Silencing of Abcd1 and Abcd2 genes sensitizes astrocytes for inflammation: implication for X-adrenoleukodystrophy* by Jaspreet Singh, Mushfiquddin Khan, Inderjit Singh

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Therapy for X-adrenoleukodystrophy: normalization of very long chain fatty acids and inhibition of induction of cytokines by cAMP by Kalipada Pahan, Mushfiquddin Khan, Inderjit Singh

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Genotoxicity evaluation of a fish oil concentrate containing Very Long Chain Fatty Acids by Derek Tobin, Harald Svensen, Iren Stoknes, Michael Dornish

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