Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Edit custom filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1973 1
1974 3
1975 6
1976 14
1977 10
1978 15
1979 13
1980 25
1981 26
1982 33
1983 31
1984 36
1985 47
1986 46
1987 65
1988 55
1989 48
1990 47
1991 57
1992 49
1993 81
1994 78
1995 73
1996 69
1997 60
1998 76
1999 76
2000 79
2001 69
2002 47
2003 73
2004 57
2005 68
2006 49
2007 73
2008 70
2009 56
2010 71
2011 75
2012 76
2013 73
2014 77
2015 76
2016 68
2017 70
2018 80
2019 96
2020 95
2021 112
2022 95
2023 102
2024 104
2025 120
2026 61

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

3,009 results

Results by year

Filters applied: . Clear all
Page 1
Adrenoleukodystrophy.
Moser HW. Moser HW. Curr Opin Neurol. 1995 Jun;8(3):221-6. doi: 10.1097/00019052-199506000-00011. Curr Opin Neurol. 1995. PMID: 7551122 Review.
The main advances concerning adrenoleukodystrophy have been in the fields of genetics and therapy. Abnormalities in the 'putative gene' reported in 1993 have been confirmed. Mutations in this gene have been demonstrated in all of the 80 adrenoleukodystrophy families …
The main advances concerning adrenoleukodystrophy have been in the fields of genetics and therapy. Abnormalities in the 'putative gen …
Adrenoleukodystrophy.
Cappa M, Bizzarri C, Vollono C, Petroni A, Banni S. Cappa M, et al. Endocr Dev. 2011;20:149-160. doi: 10.1159/000321236. Epub 2010 Dec 16. Endocr Dev. 2011. PMID: 21164268 Review.
X-linked adrenoleukodystrophy (ALD) is caused by mutations in the ABCD1 gene that encodes a protein of the peroxisomal membrane named ALDP. ...
X-linked adrenoleukodystrophy (ALD) is caused by mutations in the ABCD1 gene that encodes a protein of the peroxisomal membrane named …
An update on the diagnosis and treatment of adrenoleukodystrophy.
Gujral J, Sethuram S. Gujral J, et al. Curr Opin Endocrinol Diabetes Obes. 2023 Feb 1;30(1):44-51. doi: 10.1097/MED.0000000000000782. Epub 2022 Nov 14. Curr Opin Endocrinol Diabetes Obes. 2023. PMID: 36373727 Review.
PURPOSE OF REVIEW: The present review summarizes recent advances in the diagnosis and management of patients with X-linked adrenoleukodystrophy (ALD). RECENT FINDINGS: Although ALD screening has been on the list of Recommended Uniform Screening Panel since 2016, only 30 st …
PURPOSE OF REVIEW: The present review summarizes recent advances in the diagnosis and management of patients with X-linked adrenoleukodys …
Adrenoleukodystrophy in the era of newborn screening.
Eng L, Regelmann MO. Eng L, et al. Curr Opin Endocrinol Diabetes Obes. 2020 Feb;27(1):47-55. doi: 10.1097/MED.0000000000000515. Curr Opin Endocrinol Diabetes Obes. 2020. PMID: 31789721 Review.
PURPOSE OF REVIEW: Adrenoleukodystrophy (ALD) is a peroxisomal disorder with varying clinical presentations, including adrenal insufficiency, neurologic disease, and testicular dysfunction. ...
PURPOSE OF REVIEW: Adrenoleukodystrophy (ALD) is a peroxisomal disorder with varying clinical presentations, including adrenal insuff …
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management.
Engelen M, Kemp S, de Visser M, van Geel BM, Wanders RJ, Aubourg P, Poll-The BT. Engelen M, et al. Orphanet J Rare Dis. 2012 Aug 13;7:51. doi: 10.1186/1750-1172-7-51. Orphanet J Rare Dis. 2012. PMID: 22889154 Free PMC article.
X-linked adrenoleukodystrophy (X-ALD) is the most common peroxisomal disorder. The disease is caused by mutations in the ABCD1 gene that encodes the peroxisomal membrane protein ALDP which is involved in the transmembrane transport of very long-chain fatty acids (VLCFA; …
X-linked adrenoleukodystrophy (X-ALD) is the most common peroxisomal disorder. The disease is caused by mutations in the ABCD1 gene t …
Adrenoleukodystrophy.
O'Neill BP, Moser HW. O'Neill BP, et al. Can J Neurol Sci. 1982 Nov;9(4):449-52. doi: 10.1017/s0317167100044383. Can J Neurol Sci. 1982. PMID: 6758925 Review. No abstract available.
Adrenoleukodystrophy: Current understanding of disease mechanisms, diagnosis, and therapeutic advances-a recent review.
Jain CK, Maurya S, Tripathi PK. Jain CK, et al. Brain Dev. 2025 Dec;47(6):104476. doi: 10.1016/j.braindev.2025.104476. Epub 2025 Oct 24. Brain Dev. 2025. PMID: 41138396 Review.
Adrenoleukodystrophy (ALD) is a complex and devastating X-linked neurodegenerative disorder classified as rare brain disease with profound effects on patients and their families. It can manifest in various clinical forms, ranging from adult-onset adrenomyeloneuropathy (AMN …
Adrenoleukodystrophy (ALD) is a complex and devastating X-linked neurodegenerative disorder classified as rare brain disease with pro …
[Adrenoleukodystrophy].
Shimozawa N. Shimozawa N. No To Hattatsu. 2015 Mar;47(2):117-21. No To Hattatsu. 2015. PMID: 26349369 Japanese. No abstract available.
Adrenoleukodystrophy.
Moser HW, Bergin A, Naidu S, Ladenson PW. Moser HW, et al. Endocrinol Metab Clin North Am. 1991 Jun;20(2):297-318. Endocrinol Metab Clin North Am. 1991. PMID: 1879401 Review.
X-linked adrenoleukodystrophy (ALD) is a disorder of very long chain fatty acid (VLCFA) metabolism that can be diagnosed by demonstrating increased levels of VLCFA in plasma and, prenatally, by similar assays in cultured amniocytes or chorionic vilus samples. ...
X-linked adrenoleukodystrophy (ALD) is a disorder of very long chain fatty acid (VLCFA) metabolism that can be diagnosed by demonstra …
Treatment of cerebral adrenoleukodystrophy: allogeneic transplantation and lentiviral gene therapy.
Gupta AO, Raymond G, Pierpont EI, Kemp S, McIvor RS, Rayannavar A, Miller B, Lund TC, Orchard PJ. Gupta AO, et al. Expert Opin Biol Ther. 2022 Sep;22(9):1151-1162. doi: 10.1080/14712598.2022.2124857. Epub 2022 Sep 19. Expert Opin Biol Ther. 2022. PMID: 36107226 Free article. Review.
INTRODUCTION: Adrenoleukodystrophy (ALD) is an X-linked peroxisomal disorder with an incidence of 1 in 14-17,000 male births, caused by pathogenic variants within the ABCD1 gene. ...A focused literature review was performed using the terms 'hematopoietic stem cell transpla …
INTRODUCTION: Adrenoleukodystrophy (ALD) is an X-linked peroxisomal disorder with an incidence of 1 in 14-17,000 male births, caused …
3,009 results