164 related articles for article (PubMed ID: 16087056)
1. ABCD1 gene mutations in Chinese patients with X-linked adrenoleukodystrophy.
Pan H; Xiong H; Wu Y; Zhang YH; Bao XH; Jiang YW; Wu XR
Pediatr Neurol; 2005 Aug; 33(2):114-20. PubMed ID: 16087056
[TBL] [Abstract][Full Text] [Related]
2. Eight novel mutations in the ABCD1 gene and clinical characteristics of 25 Chinese patients with X-linked adrenoleukodystrophy.
Chu SS; Ye J; Zhang HW; Han LS; Qiu WJ; Gao XL; Gu XF
World J Pediatr; 2015 Nov; 11(4):366-73. PubMed ID: 26454440
[TBL] [Abstract][Full Text] [Related]
3. [X-linked adrenoleukodystrophy ABCD1 gene mutation analysis in China].
Pan H; Xiong H; Zhang YH; Wu Y; Bao XH; Jiang YW; Wu XR
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):1-4. PubMed ID: 14767898
[TBL] [Abstract][Full Text] [Related]
4. Mutational analyses of Taiwanese kindred with X-linked adrenoleukodystrophy.
Chiu HC; Liang JS; Wang JS; Lu JF
Pediatr Neurol; 2006 Oct; 35(4):250-6. PubMed ID: 16996397
[TBL] [Abstract][Full Text] [Related]
5. Two novel multiple mutations in chinese patients with adrenoleukodystrophy.
Ke LF; Wang ZH; Huang LH; Xie HH; Lan FH
Neuropediatrics; 2010 Jun; 41(3):151-3. PubMed ID: 20859837
[TBL] [Abstract][Full Text] [Related]
6. A novel ABCD1 gene mutation in a Chinese-Taiwanese patient with adrenomyeloneuropathy.
Liu YT; Lin KH; Soong BW; Liao KK; Lin KP
Pediatr Neurol; 2007 May; 36(5):348-50. PubMed ID: 17509471
[TBL] [Abstract][Full Text] [Related]
7. A novel mutation in the ABCD1 gene of a Korean boy diagnosed with X-linked adrenoleukodystrophy.
Park JA; Jun KR; Han SH; Kim GH; Yoo HW; Hur YJ
Gene; 2012 Apr; 498(1):131-3. PubMed ID: 22326269
[TBL] [Abstract][Full Text] [Related]
8. Eight novel ABCD1 gene mutations and three polymorphisms in patients with X-linked adrenoleukodystrophy: The first polymorphism causing an amino acid exchange.
Dvoráková L; Storkánová G; Unterrainer G; Hujová J; Kmoch S; Zeman J; Hrebícek M; Berger J
Hum Mutat; 2001; 18(1):52-60. PubMed ID: 11438993
[TBL] [Abstract][Full Text] [Related]
9. [Preliminary analysis of mutations in X-linked adrenoleukodystrophy gene(ABCD1) in Chinese patients].
Xiong H; Pan H; Zhang YH; Wu XR
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Oct; 20(5):400-3. PubMed ID: 14556192
[TBL] [Abstract][Full Text] [Related]
10. ABCD1 mutations and phenotype distribution in Chinese patients with X-linked adrenoleukodystrophy.
Niu YF; Ni W; Wu ZY
Gene; 2013 Jun; 522(1):117-20. PubMed ID: 23566833
[TBL] [Abstract][Full Text] [Related]
11. Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes.
Matsukawa T; Asheuer M; Takahashi Y; Goto J; Suzuki Y; Shimozawa N; Takano H; Onodera O; Nishizawa M; Aubourg P; Tsuji S
Neurogenetics; 2011 Feb; 12(1):41-50. PubMed ID: 20661612
[TBL] [Abstract][Full Text] [Related]
12. Identification of two de novo mutations in Chinese patients with X-linked adrenoleukodystrophy.
Wang Z; Ke L; Yan A; Zhu Z; Lan F
Clin Chem Lab Med; 2008; 46(12):1702-6. PubMed ID: 18973459
[TBL] [Abstract][Full Text] [Related]
13. Mutational analyses on X-linked adrenoleukodystrophy reveal a novel cryptic splicing and three missense mutations in the ABCD1 gene.
Hung KL; Wang JS; Keng WT; Chen HJ; Liang JS; Ngu LH; Lu JF
Pediatr Neurol; 2013 Sep; 49(3):185-90. PubMed ID: 23835273
[TBL] [Abstract][Full Text] [Related]
14. Novel ABCD1 gene mutations in Iranian pedigrees with X-linked adrenoleukodystrophy.
Emamalizadeh B; Daneshmandpour Y; Tafakhori A; Ranji-Burachaloo S; Shafiee S; Ghods E; Darvish H
J Pediatr Endocrinol Metab; 2019 Nov; 32(11):1207-1215. PubMed ID: 31665121
[TBL] [Abstract][Full Text] [Related]
15. Clinical, biochemical, neuroimaging and molecular findings of X-linked Adrenoleukodystrophy patients in South China.
Jiang MY; Cai YN; Liang CL; Peng MZ; Sheng HY; Fan LP; Lin RZ; Jiang H; Huang Y; Liu L
Metab Brain Dis; 2015 Dec; 30(6):1439-44. PubMed ID: 26260157
[TBL] [Abstract][Full Text] [Related]
16. Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation.
Kallabi F; Ellouz E; Tabebi M; Ben Salah G; Kaabechi N; Keskes L; Triki C; Kamoun H
Clin Chim Acta; 2016 Jan; 453():141-6. PubMed ID: 26686776
[TBL] [Abstract][Full Text] [Related]
17. [A novel missense mutation resulting in X-linked adrenoleukodystrophy in female heterozygotes of a Chinese family].
Xie HH; Ke LF; Wang ZH; Huang LH; Lan FH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):144-8. PubMed ID: 20376793
[TBL] [Abstract][Full Text] [Related]
18. A novel mutation in the ABCD1 gene of a Chinese patient with X-linked adrenoleukodystrophy: Case report.
Wang J; Zhu Q; Liu H
Medicine (Baltimore); 2018 May; 97(21):e10837. PubMed ID: 29794777
[TBL] [Abstract][Full Text] [Related]
19. Mutational and protein analysis of patients and heterozygous women with X-linked adrenoleukodystrophy.
Feigenbaum V; Lombard-Platet G; Guidoux S; Sarde CO; Mandel JL; Aubourg P
Am J Hum Genet; 1996 Jun; 58(6):1135-44. PubMed ID: 8651290
[TBL] [Abstract][Full Text] [Related]
20. Familial skewed x chromosome inactivation in adrenoleukodystrophy manifesting heterozygotes from a Chinese pedigree.
Wang Z; Yan A; Lin Y; Xie H; Zhou C; Lan F
PLoS One; 2013; 8(3):e57977. PubMed ID: 23469258
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]