Moser, Ann B.; Kreiter, Nancy; Bezman, Lena; Lu, Shou-En; Raymond, Gerald V.; Naidu, Sakkubai; Moser, Hugo W. (January 1999). "Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls". Annals of Neurology. 45 (1): 100–110. doi:10.1002/1531-8249(199901)45:1<100::aid-art16>3.0.co;2-u. PMID9894883. S2CID24516921.
Sandlers, Yana; Moser, Ann B.; Hubbard, Walter C.; Kratz, Lisa E.; Jones, Richard O.; Raymond, Gerald V. (March 2012). "Combined extraction of acyl carnitines and 26:0 lysophosphatidylcholine from dried blood spots: Prospective newborn screening for X-linked adrenoleukodystrophy". Molecular Genetics and Metabolism. 105 (3): 416–420. doi:10.1016/j.ymgme.2011.11.195. PMID22197596.
Hubbard, Walter C.; Moser, Ann B.; Liu, Anita C.; Jones, Richard O.; Steinberg, Steven J.; Lorey, Fred; Panny, Susan R.; Vogt Jr., Robert F.; Macaya, Daniela; Turgeon, Coleman T.; Tortorelli, S; Raymond, GV (July 2009). "Newborn screening for X-linked adrenoleukodystrophy (X-ALD): Validation of a combined liquid chromatography–tandem mass spectrometric (LC–MS/MS) method". Molecular Genetics and Metabolism. 97 (3): 212–220. doi:10.1016/j.ymgme.2009.03.010. PMID19423374.
Raymond, Gerald V.; Jones, Richard O.; Moser, Ann B. (16 August 2012). "Newborn Screening for Adrenoleukodystrophy". Molecular Diagnosis & Therapy. 11 (6): 381–384. doi:10.1007/BF03256261. PMID18078355. S2CID21323198.
Moser, Hugo W.; Moser, Ann B.; Hollandsworth, Kim; Brereton, N. Hong; Raymond, Gerald V. (24 August 2007). "'Lorenzo's Oil' Therapy for X-linked Adrenoleukodystrophy: Rationale and Current Assessment of Efficacy". Journal of Molecular Neuroscience. 33 (1): 105–113. doi:10.1007/s12031-007-0041-4. PMID17901554. S2CID21333247.
Raymond GV, Moser AB, Fatemi A (6 April 2023) [Originally published 26 March 1999]. "X-Linked Adrenoleukodystrophy". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya A (eds.). GeneReviews. Seattle: University of Washington, Seattle. ISSN2372-0697. PMID20301491. National Library of Medicine Bookshelf ID NBK1315.
Hung, Kun-Long; Wang, Jinn-Shyan; Keng, Wee Teik; Chen, Hui-Ju; Liang, Jao-Shwann; Ngu, Lock Hock; Lu, Jyh-Feng (September 2013). "Mutational Analyses on X-Linked Adrenoleukodystrophy Reveal a Novel Cryptic Splicing and Three Missense Mutations in the ABCD1 Gene". Pediatric Neurology. 49 (3): 185–190. doi:10.1016/j.pediatrneurol.2013.04.021. PMID23835273.
Smith, Kirby D.; Kemp, Stephan; Braiterman, Lelita T.; Lu, Jyh-Feng; Wei, He-Ming; Geraghty, Michael; Stetten, Gail; Bergin, James S.; Pevsner, Jonathan; Watkins, Paul A. (1999). "X-linked adrenoleukodystrophy: Genes, mutations, and phenotypes". Neurochemical Research. 24 (4): 521–535. doi:10.1023/a:1022535930009. PMID10227685. S2CID38326524.
Moser, Ann B.; Kreiter, Nancy; Bezman, Lena; Lu, Shou-En; Raymond, Gerald V.; Naidu, Sakkubai; Moser, Hugo W. (January 1999). "Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls". Annals of Neurology. 45 (1): 100–110. doi:10.1002/1531-8249(199901)45:1<100::aid-art16>3.0.co;2-u. PMID9894883. S2CID24516921.
Sandlers, Yana; Moser, Ann B.; Hubbard, Walter C.; Kratz, Lisa E.; Jones, Richard O.; Raymond, Gerald V. (March 2012). "Combined extraction of acyl carnitines and 26:0 lysophosphatidylcholine from dried blood spots: Prospective newborn screening for X-linked adrenoleukodystrophy". Molecular Genetics and Metabolism. 105 (3): 416–420. doi:10.1016/j.ymgme.2011.11.195. PMID22197596.
Hubbard, Walter C.; Moser, Ann B.; Liu, Anita C.; Jones, Richard O.; Steinberg, Steven J.; Lorey, Fred; Panny, Susan R.; Vogt Jr., Robert F.; Macaya, Daniela; Turgeon, Coleman T.; Tortorelli, S; Raymond, GV (July 2009). "Newborn screening for X-linked adrenoleukodystrophy (X-ALD): Validation of a combined liquid chromatography–tandem mass spectrometric (LC–MS/MS) method". Molecular Genetics and Metabolism. 97 (3): 212–220. doi:10.1016/j.ymgme.2009.03.010. PMID19423374.
Raymond, Gerald V.; Jones, Richard O.; Moser, Ann B. (16 August 2012). "Newborn Screening for Adrenoleukodystrophy". Molecular Diagnosis & Therapy. 11 (6): 381–384. doi:10.1007/BF03256261. PMID18078355. S2CID21323198.
Moser, Hugo W.; Moser, Ann B.; Hollandsworth, Kim; Brereton, N. Hong; Raymond, Gerald V. (24 August 2007). "'Lorenzo's Oil' Therapy for X-linked Adrenoleukodystrophy: Rationale and Current Assessment of Efficacy". Journal of Molecular Neuroscience. 33 (1): 105–113. doi:10.1007/s12031-007-0041-4. PMID17901554. S2CID21333247.
Moser, Ann B.; Kreiter, Nancy; Bezman, Lena; Lu, Shou-En; Raymond, Gerald V.; Naidu, Sakkubai; Moser, Hugo W. (January 1999). "Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls". Annals of Neurology. 45 (1): 100–110. doi:10.1002/1531-8249(199901)45:1<100::aid-art16>3.0.co;2-u. PMID9894883. S2CID24516921.
Raymond, Gerald V.; Jones, Richard O.; Moser, Ann B. (16 August 2012). "Newborn Screening for Adrenoleukodystrophy". Molecular Diagnosis & Therapy. 11 (6): 381–384. doi:10.1007/BF03256261. PMID18078355. S2CID21323198.
Moser, Hugo W.; Moser, Ann B.; Hollandsworth, Kim; Brereton, N. Hong; Raymond, Gerald V. (24 August 2007). "'Lorenzo's Oil' Therapy for X-linked Adrenoleukodystrophy: Rationale and Current Assessment of Efficacy". Journal of Molecular Neuroscience. 33 (1): 105–113. doi:10.1007/s12031-007-0041-4. PMID17901554. S2CID21333247.
Raymond GV, Moser AB, Fatemi A (6 April 2023) [Originally published 26 March 1999]. "X-Linked Adrenoleukodystrophy". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya A (eds.). GeneReviews. Seattle: University of Washington, Seattle. ISSN2372-0697. PMID20301491. National Library of Medicine Bookshelf ID NBK1315.