A Korean boy with atypical X-linked adrenoleukodystrophy confirmed by an unpublished mutation of by Hye Jeong Jwa, Keon Su Lee, Gu Hwan Kim, Han Wook Yoo, Han Hyuk Lim

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A Novel Mutation of the ABCD1 Gene in Serbian X-Adrenoleukodystrophy by Grkovic S, Nikolic R, Djordjevic M, Puzigaca Z, Vujic D, Ilic P

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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

Subjects: “…ABCD1gene…”
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A case of adrenomyeloneuropathy caused by a novel point mutation in the ABCD1 gene and functional verification by Xiaoxue Shi, Xiaoxue Shi, Xiaoxue Shi, Xuelin Qi, Xuelin Qi, Jinhua Zheng, Jinhua Zheng, Jinhua Zheng, Jianjun Ma, Jianjun Ma, Jianjun Ma, Dongsheng Li, Dongsheng Li, Dongsheng Li

Subjects: “…ABCD1 gene…”
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A female adult-onset X-ALD patient with pure cerebellar symptoms:a case report by Wenjing Qi, Du Cao, Lei Hao, Xiuming Guo

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Novel ABCD1 variant causes phenotype of adrenomyeloneuropathy with cerebral involvement in Ukrainian siblings: first adult hematopoietic stem cell transplantation for ALD in Ukrain... by Khrystyna Shchubelka, Olga Herasymenko, Andrii Budzyn, Oleksandr Lysytsia, Anastasiia Rusyn, Olga Oleksyk, Svitlana Tynta, Taras Oleksyk

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Successful Pregnancy Following Preimplantation Genetic Diagnosis of Adrenoleukodystrophy by Detection of Mutation on the ABCD1 Gene by Trinh The S, Trieu Tien S, Vu Van T, Nguyen Ngoc N, Tran Ngoc Thao M, Tran Van K, Vu Nhat D, Do Nhu B

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Management of X-linked adrenoleukodystrophy in Morocco: actual situation by F. Z. Madani Benjelloun, Y. Kriouile, D. Cheillan, H. Daoud-Tetouani, L. Chabraoui

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