Surgical management of congenital thoracic kyphosis and multilevel bilateral thoracic pedicle aplasia: case report

Autor: Peter P. Sun, Kenneth W. Martin, James F Policy, Darryl Lau, Cecilia L Dalle Ore

Publikováno v: Journal of Neurosurgery: Pediatrics. 23:16-21

Pedicle aplasia is an uncommon congenital anomaly most frequently involving the absence of a single pedicle at a single vertebral level. Bilateral pedicle aplasia at multiple levels is exceedingly rare and has only been described once previously in t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef2fe5e75f1610f67e4f69d5e7d065d0
https://doi.org/10.3171/2018.7.peds18222

Graph Simplification for Infrastructure Network Design

Autor: Sean Yaw, Richard S. Middleton, Brendan Hoover

Publikováno v: Combinatorial Optimization and Applications ISBN: 9783030364113
COCOA

Network design problems often involve scenarios where there exist many possible routes between fixed vertex locations (e.g. building new roads between cities, deploying communications and power lines). Many possible routes in a network result in grap

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3c69166248afcb27c7ea7460bf6ad20e
https://doi.org/10.1007/978-3-030-36412-0_47

Using the well plan™ software model to determine the optimal hole cleaning to reduce mechanical pipe sticking in a Southern Iraqi oil field.

Autor: Issa, Muntadher Adil, Alrazzaq, Ayad A. Alhaleem A.

Publikováno v: AIP Conference Proceedings; 2023, Vol. 2839 Issue 1, p1-9, 9p

Current insights in ultra-rare adenylosuccinate synthetase 1 myopathy – meeting report on the First Clinical and Scientific Conference. 3 June 2024, National Centre for Advancing Translational Science, Rockville, Maryland, the United States of America

Autor: Rybalka, Emma^1,2 (AUTHOR) emma.rybalka@vu.edu.au, Park, Hyung Jun³ (AUTHOR), Nalini, Atchayaram⁴ (AUTHOR), Baskar, Dipti⁴ (AUTHOR), Polavarapu, Kiran⁵ (AUTHOR), Durmus, Hacer⁶ (AUTHOR), Xia, Yang⁷ (AUTHOR), Wan, Linlin⁸ (AUTHOR), Shieh, Perry B.⁹ (AUTHOR), Moghadaszadeh, Behzad¹⁰ (AUTHOR), Beggs, Alan H.¹⁰ (AUTHOR), Mack, David L.¹¹ (AUTHOR), Smith, Alec S. T.¹¹ (AUTHOR), Hanna-Rose, Wendy¹² (AUTHOR), Jinnah, Hyder A.¹³ (AUTHOR), Timpani, Cara A.^1,2 (AUTHOR), Shen, Min¹⁴ (AUTHOR), Upadhyay, Jaymin^15,16 (AUTHOR), Brault, Jeffrey J.¹⁷ (AUTHOR), Hall, Matthew D.¹⁴ (AUTHOR)

Publikováno v: Orphanet Journal of Rare Diseases. 11/26/2024, Vol. 19 Issue 1, p1-18. 18p.

Elucidating the roles of SOD3 correlated genes and reactive oxygen species in rare human diseases using a bioinformatic-ontology approach.

Autor: Stanworth, Mark¹ (AUTHOR) Stanworth-M@ulster.ac.uk, Zhang, Shu-Dong¹ (AUTHOR) Stanworth-M@ulster.ac.uk

Publikováno v: PLoS ONE. 10/31/2024, Vol. 19 Issue 10, p1-31. 31p.