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May 27, 2016 (publication date) through Nov 6, 2024
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Publication Name
World Journal of Medical Genetics
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2220-3184
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Kaufman CS, Butler MG. Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndrome. World J Med Genet 2016; 6(2): 17-21 [PMID: 28344932 DOI: 10.5496/wjmg.v6.i2.17] |
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| URL: | https://www.wjgnet.com/2220-3184/full/v6/i2/17.htm |
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Ian M. Clapp, Katlynn M. Paul, Edward C. Beck, Shane J. Nho. Hypermobile Disorders and Their Effects on the Hip Joint. Frontiers in Surgery 2021; 8 doi: 10.3389/fsurg.2021.596971
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Krystal VanderJagt, Merlin G. Butler. Ehlers–Danlos syndrome and other heritable connective tissue disorders that impact pregnancies can be detected using next-generation DNA sequencing. Archives of Gynecology and Obstetrics 2019; 300(3): 491 doi: 10.1007/s00404-019-05226-5
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Komal Preet, Methma Udawatta, Courtney Duong, Quinton Gopen, Isaac Yang. Bilateral Superior Semicircular Canal Dehiscence Associated with Ehlers-Danlos Syndrome: A Report of 2 Cases. World Neurosurgery 2019; 122: 161 doi: 10.1016/j.wneu.2018.10.126
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Kathryne Holmes, Pearl Shah, Melanie Jones, Ryan Langston, Faizal Asumda, Jack Yu. Delayed Wound Healing in a Young Patient with TNXB Variants and the Role of WES. FACE 2024; doi: 10.1177/27325016241274964
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Yinjie Gao, Lin Lu, Bingqing Yu, Jiangfeng Mao, Xi Wang, Min Nie, Xueyan Wu. The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers–Danlos Syndrome with 21-Hydroxylase Deficiency. The Journal of Clinical Endocrinology & Metabolism 2020; 105(7): 2288 doi: 10.1210/clinem/dgaa199
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Vidyanand Anaparti, Prasoon Agarwal, Irene Smolik, Neeloffer Mookherjee, Hani El-Gabalawy. Whole Blood Targeted Bisulfite Sequencing and Differential Methylation in the C6ORF10 Gene of Patients with Rheumatoid Arthritis. The Journal of Rheumatology 2020; 47(11): 1614 doi: 10.3899/jrheum.190376
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Lucia Micale, Vito Guarnieri, Bartolomeo Augello, Orazio Palumbo, Emanuele Agolini, Valentina Maria Sofia, Tommaso Mazza, Antonio Novelli, Massimo Carella, Marco Castori. Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome. Genes 2019; 10(12): 967 doi: 10.3390/genes10120967
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| 10 |
Negin Yekkalam, Mehmed Novo, Anders Wänman. Treatments related to temporomandibular disorders among patients with prevalent types of Ehlers-Danlos syndrome in Sweden. CRANIO® 2024; : 1 doi: 10.1080/08869634.2024.2319565
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| 11 |
Cortney Gensemer, Randall Burks, Steven Kautz, Daniel P. Judge, Mark Lavallee, Russell A. Norris. Hypermobile Ehlers‐Danlos syndromes: Complex phenotypes, challenging diagnoses, and poorly understood causes. Developmental Dynamics 2021; 250(3): 318 doi: 10.1002/dvdy.220
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Olivia J. Veatch, Jacob Steinle, Waheeda A. Hossain, Merlin G. Butler. Clinical genetics evaluation and testing of connective tissue disorders: a cross-sectional study. BMC Medical Genomics 2022; 15(1) doi: 10.1186/s12920-022-01321-w
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| 13 |
Anne Martin. An acquired or heritable connective tissue disorder? A review of hypermobile Ehlers Danlos Syndrome. European Journal of Medical Genetics 2019; 62(7): 103672 doi: 10.1016/j.ejmg.2019.103672
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| 14 |
A. Bauer, M. de Lucia, F. Leuthard, V. Jagannathan, T. Leeb. Compound heterozygosity for TNXB genetic variants in a mixed‐breed dog with Ehlers‐Danlos syndrome. Animal Genetics 2019; 50(5): 546 doi: 10.1111/age.12830
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Talal M. Al‐Harbi, Haya Al‐Rammah, Naif Al‐Zahrani, Yichuan Liu, Patrick M. A. Sleiman, Walid Dridi, Hakon Hakonarson. Rare neurological manifestations in a Saudi Arabian patient with Ehlers–Danlos syndrome and a novel homozygous variant in the TNXB gene. American Journal of Medical Genetics Part A 2022; 188(2): 618 doi: 10.1002/ajmg.a.62539
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Merlin G Butler. Classic Ehlers-Danlos syndrome and cardiac transplantation - Is there a connection?. World Journal of Cardiology 2020; 12(8): 368-372 doi: 10.4330/wjc.v12.i8.368
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