U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from MedGen

Items: 1 to 20 of 46

1.
A case study on the pitfalls in prenatal ultrasonic detection of butterfly vertebra
Jia-Qi Hu, Yu-Guo Zhang, Wei Feng, Hua Shi
Heliyon. 2023 Nov; 9(11): e21754. Published online 2023 Oct 29. doi: 10.1016/j.heliyon.2023.e21754
PMCID:
PMC10660013
AbstractArticlePDF–2.2M
2.
Don't Play It by Ear: Technical Considerations to Optimize Outcome and Procedural Safety of Congenital Microtia Reconstruction in a Dextrocardia Patient With Situs Inversus Totalis, Butterfly Vertebra, and Hemivertebra
Shivangi Saha, Amiteshwar Singh, Arbab Mohammad, Shashank Chauhan, Kavya Chinta, Maneesh Singhal
Eplasty. 2023; 23: e57. Published online 2023 Aug 31.
PMCID:
PMC10517671
AbstractArticlePDF–15M
3.
An Incidental Finding of Butterfly Vertebrae in a Case of Vertebral Defects, Anal Atresia, Cardiac Defects, Tracheo-Esophageal Fistula, Renal Anomalies, and Limb Abnormalities (VACTERL)
Ashritha Rao, Sarika Gaikwad, Amar Taksande, Mayur B Wanjari
Cureus. 2023 Jan; 15(1): e33401. Published online 2023 Jan 5. doi: 10.7759/cureus.33401
PMCID:
PMC9899095
AbstractArticlePDF–589K
4.
A rare incidental finding of an isolated S1 butterfly vertebra: A case report
Vikash Bhattarai, Sanjeev Kharel, Sandeep Mahat, Sandip Kuikel, Amir Joshi, Amit Sharma, Sulav Acharya
Radiol Case Rep. 2022 Dec; 17(12): 4761–4765. Published online 2022 Oct 5. doi: 10.1016/j.radcr.2022.09.028
PMCID:
PMC9535292
AbstractArticlePDF–1.0M
5.
Spinal cord injury in an adult patient with thoracic butterfly vertebra: a case report and review of the literature
Ai-Bing Huang, Meng Bai, Huan Liu, Zhi-Yong Zhou, Jia-Xu Wei
BMC Musculoskelet Disord. 2020; 21: 392. Published online 2020 Jun 22. doi: 10.1186/s12891-020-03433-9
PMCID:
PMC7310430
AbstractArticlePDF–849K
6.
Butterfly Vertebrae: A Systematic Review of the Literature and Analysis
Yoshihiro Katsuura, Han Jo Kim
Global Spine J. 2019 Sep; 9(6): 666–679. Published online 2018 Sep 18. doi: 10.1177/2192568218801016
PMCID:
PMC6693069
AbstractArticlePDF–1014K
7.
Sacral butterfly vertebrae in the setting of a sacral fracture and unstable pelvic ring injury: A case report and review of the literature
Yoshihiro Katsuura, Dirk Kiner
Trauma Case Rep. 2019 Feb; 19: 7–10. Published online 2018 Dec 6. doi: 10.1016/j.tcr.2018.11.011
PMCID:
PMC6289954
AbstractArticlePDF–850K
8.
Differential diagnosis of multiple vertebral compression: butterfly vertebrae
Nihal Ozaras, Kevser Gumussu, Saliha Eroglu Demir, Aylin Rezvani
J Phys Ther Sci. 2015 Nov; 27(11): 3601–3603. Published online 2015 Nov 30. doi: 10.1589/jpts.27.3601
PMCID:
PMC4681953
AbstractArticlePDF–710K
9.
Differentiating between Traumatic Pathology and Congenital Variant: A Case Report of Butterfly Vertebra
Orestis Karargyris, Kalliopi Lampropoulou-Adamidou, Lampros-Guiseppe Morassi, Ioannis P. Stathopoulos, Sofia N. Chatziioannou, Spyros G. Pneumaticos
Clin Orthop Surg. 2015 Sep; 7(3): 406–409. Published online 2015 Aug 13. doi: 10.4055/cios.2015.7.3.406
PMCID:
PMC4553293
AbstractArticlePDF–993K
10.
Congenital ‘butterfly vertebra’ associated with low back pain: a case report
Rachael M Hopkins, Abbott JH
J Man Manip Ther. 2015 May; 23(2): 93–100. doi: 10.1179/2042618613Y.0000000057
PMCID:
PMC4461719
AbstractArticlePDF–724K
11.
The early origin of vertebral anomalies, as illustrated by a 'butterfly vertebra'.
F Müller, R O'Rahilly, D R Benson
J Anat. 1986 Dec; 149: 157–169.
PMCID:
PMC1261641
SummaryPage BrowsePDF–2.9M
12.
Clinical Characterization of Alagille Syndrome in Patients with Cholestatic Liver Disease
Natalia Semenova, Elena Kamenets, Eleonora Annenkova, Andrey Marakhonov, Elena Gusarova, Nina Demina, Daria Guseva, Inga Anisimova, Anna Degtyareva, Natalia Taran, Tatiana Strokova, Ekaterina Zakharova
Int J Mol Sci. 2023 Jul; 24(14): 11758. Published online 2023 Jul 21. doi: 10.3390/ijms241411758
PMCID:
PMC10380973
AbstractArticlePDF–2.1M
13.
Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population
Mohammad AlMuhaizea, Omar Dabbagh, Hanan AlQudairy, Aljouhra AlHargan, Wafa Alotaibi, Ruba Sami, Rahaf AlOtaibi, Mariam Mahmoud Ali, Hindi AlHindi, Dilek Colak, Namik Kaya
Genes (Basel) 2021 Nov; 12(11): 1783. Published online 2021 Nov 10. doi: 10.3390/genes12111783
PMCID:
PMC8620084
AbstractArticlePDF–2.1M
14.
Precise breakpoint detection in a patient with 9p– syndrome
Jeffrey Ng, Eleanor Sams, Dustin Baldridge, Milinn Kremitzki, Daniel J. Wegner, Tina Lindsay, Robert Fulton, F. Sessions Cole, Tychele N. Turner
Cold Spring Harb Mol Case Stud. 2020 Jun; 6(3): a005348. doi: 10.1101/mcs.a005348
PMCID:
PMC7304358
AbstractArticlePDF–2.2M
15.
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model
Jiaqi Liu, Nan Wu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Nan Yang, Kazuki Takeda, Weisheng Chen, Weiyu Li, Renqian Du, Sen Liu, Yangzhong Zhou, Ling Zhang, Zhenlei Liu, Yuzhi Zuo, Sen Zhao, Robert Blank, Davut Pehlivan, Shuangshuang Dong, Jianguo Zhang, Jianxiong Shen, Nuo Si, Yipeng Wang, Gang Liu, Shugang Li, Yanxue Zhao, Hong Zhao, Yixin Chen, Yu Zhao, Xiaofei Song, Jianhua Hu, Mao Lin, Ye Tian, Bo Yuan, Keyi Yu, Yuchen Niu, Bin Yu, Xiaoxin Li, Jia Chen, Zihui Yan, Qiankun Zhu, Xiaolu Meng, Xiaoli Chen, Jianzhong Su, Xiuli Zhao, Xiaoyue Wang, Yue Ming, Xiao Li, Cathleen L. Raggio, Baozhong Zhang, Xisheng Weng, Shuyang Zhang, Xue Zhang, Kota Watanabe, Japan Early Onset Scoliosis Research Group, Li Jin, Yiping Shen, Nara L. Sobreira, Jennifer E. Posey, Philip Giampietro, Baylor-Hopkins Center for Mendelian Genomics, Pengfei Liu, Zhihong Wu, Shiro Ikegawa, James R. Lupski, Feng Zhang, Guixing Qiu
Genet Med. Author manuscript; available in PMC 2020 Jul 1.
Published in final edited form as: Genet Med. 2019 Jul; 21(7): 1548–1558. Published online 2019 Jan 14. doi: 10.1038/s41436-018-0377-x
PMCID:
PMC6659397
AbstractArticlePDF–1.0M
16.
Screening of known disease genes in congenital scoliosis
Kazuki Takeda, Ikuyo Kou, Shuji Mizumoto, Shuhei Yamada, Noriaki Kawakami, Masahiro Nakajima, Nao Otomo, Yoji Ogura, Noriko Miyake, Naomichi Matsumoto, Toshiaki Kotani, Hideki Sudo, Ikuho Yonezawa, Koki Uno, Hiroshi Taneichi, Kei Watanabe, Hideki Shigematsu, Ryo Sugawara, Yuki Taniguchi, Shohei Minami, Masaya Nakamura, Morio Matsumoto, Japan Early Onset Scoliosis Research Group, Kota Watanabe, Shiro Ikegawa
Mol Genet Genomic Med. 2018 Nov; 6(6): 966–974. Published online 2018 Sep 9. doi: 10.1002/mgg3.466
PMCID:
PMC6305645
AbstractArticlePDF–1.2M
17.
JAGGED1 gene variations in Chinese twin sisters with Alagille syndrome
Xinbao Xie, Yi Lu, Xiaohong Wang, Bingbing Wu, Hui Yu
Int J Clin Exp Pathol. 2015; 8(7): 8506–8511. Published online 2015 Jul 1.
PMCID:
PMC4555753
AbstractArticlePDF–238K
18.
Notch gain of function inhibits chondrocyte differentiation via Rbpj-dependent suppression of Sox9
Shan Chen, Jianning Tao, Yangjin Bae, Ming-Ming Jiang, Terry Bertin, Yuqing Chen, Tao Yang, Brendan Lee
J Bone Miner Res. 2013 Mar; 28(3): 649–659. Published online 2013 Feb 15. doi: 10.1002/jbmr.1770
PMCID:
PMC3548081
AbstractArticlePDF–568K
19.
Alagille syndrome.
I D Krantz, D A Piccoli, N B Spinner
J Med Genet. 1997 Feb; 34(2): 152–157. doi: 10.1136/jmg.34.2.152
PMCID:
PMC1050871
SummaryPage BrowsePDF–1.5M
20.
Tetralogy of Fallot with vertebral defect and left aberrant subclavian artery: a rare occurrence
Marya Hameed, Muhammad Fazal Hussain Qureshi
Egypt Heart J. 2024 Dec; 76: 23. Published online 2024 Feb 20. doi: 10.1186/s43044-024-00454-w
PMCID:
PMC10879043
AbstractArticlePDF–923K

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI > Literature > PubMed Central (PMC)
Support Center