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28. X-linked adrenoleukodystrophy is a frequent cause of idiopathic Addison's disease in young adult male patients. Laureti S; Casucci G; Santeusanio F; Angeletti G; Aubourg P; Brunetti P J Clin Endocrinol Metab; 1996 Feb; 81(2):470-4. PubMed ID: 8636252 [TBL] [Abstract][Full Text] [Related]
29. Predominance of the adrenomyeloneuropathy phenotype of X-linked adrenoleukodystrophy in The Netherlands: a survey of 30 kindreds. van Geel BM; Assies J; Weverling GJ; Barth PG Neurology; 1994 Dec; 44(12):2343-6. PubMed ID: 7991123 [TBL] [Abstract][Full Text] [Related]
30. [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]
31. X-linked adrenoleukodystrophy phenotype is independent of ABCD2 genotype. Maier EM; Mayerhofer PU; Asheuer M; Köhler W; Rothe M; Muntau AC; Roscher AA; Holzinger A; Aubourg P; Berger J Biochem Biophys Res Commun; 2008 Dec; 377(1):176-80. PubMed ID: 18834860 [TBL] [Abstract][Full Text] [Related]
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33. A missense point mutation (Ser515Phe) in the adrenoleukodystrophy gene in a family with adrenomyeloneuropathy: a clinical, biochemical, and genetic study. Vorgerd M; Fuchs S; Tegenthoff M; Malin JP J Neurol Neurosurg Psychiatry; 1995 Feb; 58(2):229-31. PubMed ID: 7876858 [TBL] [Abstract][Full Text] [Related]
34. Mutations, clinical findings and survival estimates in South American patients with X-linked adrenoleukodystrophy. Pereira Fdos S; Matte U; Habekost CT; de Castilhos RM; El Husny AS; Lourenço CM; Vianna-Morgante AM; Giuliani L; Galera MF; Honjo R; Kim CA; Politei J; Vargas CR; Jardim LB PLoS One; 2012; 7(3):e34195. PubMed ID: 22479560 [TBL] [Abstract][Full Text] [Related]
35. Adult onset cerebral form of X-linked adrenoleukodystrophy with dementia of frontal lobe type with new L160P mutation in ABCD1 gene. Sutovský S; Petrovic R; Chandoga J; Turcáni P J Neurol Sci; 2007 Dec; 263(1-2):149-53. PubMed ID: 17662307 [TBL] [Abstract][Full Text] [Related]
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37. X-linked adrenoleukodystrophy: genes, mutations, and phenotypes. Smith KD; Kemp S; Braiterman LT; Lu JF; Wei HM; Geraghty M; Stetten G; Bergin JS; Pevsner J; Watkins PA Neurochem Res; 1999 Apr; 24(4):521-35. PubMed ID: 10227685 [TBL] [Abstract][Full Text] [Related]
38. Identification of new mutations in Israeli patients with X-linked adrenoleukodystrophy. Neumann S; Topper A; Mandel H; Shapira I; Golan O; Gazit E; Loewenthal R Genet Test; 2001; 5(1):65-8. PubMed ID: 11336405 [TBL] [Abstract][Full Text] [Related]
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