| For: | Palakuzhiyil SV, Christopher R, Chandra SR. Deciphering the modifiers for phenotypic variability of X-linked adrenoleukodystrophy. World J Biol Chem 2020; 11(3): 99-111 [PMID: 33274015 DOI: 10.4331/wjbc.v11.i3.99] |
|---|---|
| URL: | https://www.wjgnet.com/1949-8454/full/v11/i3/99.htm |
| Number | Citing Articles |
| 1 |
Khrystyna Shchubelka, Olga Herasymenko, Andrii Budzyn, Oleksandr Lysytsia, Anastasiia Rusyn, Olga Oleksyk, Svitlana Tynta, Taras Oleksyk. Novel ABCD1 variant causes phenotype of adrenomyeloneuropathy with cerebral involvement in Ukrainian siblings: first adult hematopoietic stem cell transplantation for ALD in Ukraine: a case report. Journal of Medical Case Reports 2024; 18(1) doi: 10.1186/s13256-023-04321-1
|
| 2 |
Bhavya Sharma, Yashika Gupta, Sarita Maurya, Pankaj Kumar Tripathi, Kavya Raj Thekkedathu, Chakresh Kumar Jain. Advancing Diagnosis and Therapy of Rare Monogenic Disorders through AI: Insights from Adrenoleukodystrophy. BIO Web of Conferences 2026; 233 doi: 10.1051/bioconf/202623301022
|
| 3 |
Thomas Haschka, Foudil Lamari, Fanny Mochel, Violetta Zujovic. Innovative tree-based method for sampling molecular conformations: exploring the ATP-binding cassette subfamily D member 1 (ABCD1) transporter as a case study. Frontiers in Molecular Biosciences 2024; 11 doi: 10.3389/fmolb.2024.1440529
|
| 4 |
Charles J. Billington, Arpana Rayannavar, Rebecca Tryon, Tory Kaye, Ashish Gupta, Troy C. Lund, Aida Lteif, Katherine L. Adriatico, Paul J. Orchard, Bradley S. Miller, Nishitha R. Pillai. Prognostication and Biomarker Potential of C26:0 Lysophosphatidylcholine in Adrenoleukodystrophy. JAMA Pediatrics 2025; 179(4) doi: 10.1001/jamapediatrics.2024.6774
|
| 5 |
Xinxin Zuo, Zeyu Chen. From gene to therapy: a review of deciphering the role of ABCD1 in combating X-Linked adrenoleukodystrophy. Lipids in Health and Disease 2024; 23(1) doi: 10.1186/s12944-024-02361-0
|
| 6 |
Jatinder Singh, Paramala Santosh, Uma Ramaswami. Epigenetic Mechanisms in Fabry Disease: A Thematic Analysis Linking Differential Methylation Profiles and Genetic Modifiers to Disease Phenotype. Current Issues in Molecular Biology 2025; 47(10) doi: 10.3390/cimb47100855
|
| 7 |
Qinyue Lu, Weicheng Zong, Mingyixing Zhang, Zhi Chen, Zhangping Yang. The Overlooked Transformation Mechanisms of VLCFAs: Peroxisomal β-Oxidation. Agriculture 2022; 12(7) doi: 10.3390/agriculture12070947
|
| 8 |
Katrin A. Dohr, Silvija Tokic, Magdalena Gastager-Ehgartner, Tatjana Stojakovic, Miroslav Dumic, Barbara Plecko, Katja K. Dumic. Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct Phenotypes of X-Linked Adrenoleukodystrophy. International Journal of Molecular Sciences 2023; 24(6) doi: 10.3390/ijms24065957
|
| 9 |
Peter K. Stys, Shigeki Tsutsui, Arie R. Gafson, Bert A. ‘t Hart, Shibeshih Belachew, Jeroen J. G. Geurts. New views on the complex interplay between degeneration and autoimmunity in multiple sclerosis. Frontiers in Cellular Neuroscience 2024; 18 doi: 10.3389/fncel.2024.1426231
|
| 10 |
William B. Rizzo, Craig V. Baker. Encyclopedia of Endocrine Diseases. 2026; doi: 10.1016/B978-0-443-13825-6.00109-6
|
| 11 |
Ronald J. A. Wanders, Myriam Baes, Daniela Ribeiro, Sacha Ferdinandusse, Hans R. Waterham. The physiological functions of human peroxisomes. Physiological Reviews 2023; 103(1) doi: 10.1152/physrev.00051.2021
|
| 12 |
Trevor A Leon, Steve M Nelson, Alex Gilman, Joseph Kluesner, Jon P Williams. Clinical Variation and Neuroimaging Patterns in Monozygotic Twins With Arrested X-Linked Adrenoleukodystrophy: A Case Report. Cureus 2025; doi: 10.7759/cureus.86485
|
| 13 |
Zhen Li, Guangrui Lai. X‑linked adrenoleukodystrophy caused by maternal ABCD1 mutation and paternal X chromosome inactivation. Experimental and Therapeutic Medicine 2022; 24(3) doi: 10.3892/etm.2022.11502
|
| 14 |
Mohadeseh Fathi, Sheyda Khalilian, Arezou Sayad, Parvaneh Karimzadeh, Farzad Ahmadabadi, Soudeh Ghafouri-Fard, Mohammad Miryounesi. Overview of genetic mutations causing adrenoleukodystrophy: A case-series study. Molecular Genetics and Metabolism Reports 2025; 44 doi: 10.1016/j.ymgmr.2025.101237
|
| 15 |
Jovito Chacko James, Athira Mukunda, Rhea Jacob, Antony Mosses George. Incidental diagnosis of primary adrenal insufficiency precipitated by positive ABCD1 gene mutation detected on cascade screening. BMJ Case Reports 2025; 18(8) doi: 10.1136/bcr-2025-265277
|
| 16 |
Pierre Bougnères, Catherine Le Stunff. Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy. Genes 2025; 16(5) doi: 10.3390/genes16050590
|
| 17 |
Julianne H. Tieu, Siddhee A. Sahasrabudhe, Paul J. Orchard, James C. Cloyd, Reena V. Kartha. Translational and clinical pharmacology considerations in drug repurposing for X‐linked adrenoleukodystrophy—A rare peroxisomal disorder. British Journal of Clinical Pharmacology 2022; 88(6) doi: 10.1111/bcp.15090
|
| 18 |
Rosa Campopiano, Cinzia Femiano, Maria Antonietta Chiaravalloti, Rosangela Ferese, Diego Centonze, Fabio Buttari, Stefania Zampatti, Mirco Fanelli, Stefano Amatori, Carmelo D’Alessio, Emiliano Giardina, Francesco Fornai, Francesca Biagioni, Marianna Storto, Stefano Gambardella. A Large Family with p.Arg554His Mutation in ABCD1: Clinical Features and Genotype/Phenotype Correlation in Female Carriers. Genes 2021; 12(5) doi: 10.3390/genes12050775
|
| 19 |
Olivia Elizabeth Altamirano Guerrero, Piedad Elizabeth Acurio Padilla, Mauricio Fernando Enrríquez Grijalva, Melany Yamilex Reascos Chalacán. Interpretation of fatty acids and adrenal function in Ald-X patients using PRISMA 2020 methodology. Salud, Ciencia y Tecnología - Serie de Conferencias 2023; 2 doi: 10.56294/sctconf2023753
|