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Select item 102759141.

Efficiency of non-operative management for pectus deformities in children using an X-ray-free protocol

Alexis Belgacem, Jérémy Tricard, Alexandre Dutoit, Céline Grosos, Emilie Auditeau, Mathilde Casson Masselin, Laurent Fourcade, Quentin Ballouhey

Interdiscip Cardiovasc Thorac Surg. 2023 Jun; 36(6): ivad093. Published online 2023 Jun 9. doi: 10.1093/icvts/ivad093

PMCID:: PMC10275914

Article PDF–870K

Select item 92568322.

Clinical significance of concomitant pectus deformity and adolescent idiopathic scoliosis: systematic review with best evidence synthesis

Laurian J.M. van Es, Barend J. van Royen, Matthijs W.N. Oomen

N Am Spine Soc J. 2022 Sep; 11: 100140. Published online 2022 Jun 25. doi: 10.1016/j.xnsj.2022.100140

PMCID:: PMC9256832

Article PDF–783K

Select item 89873213.

Evolution of technique and results after permanent open repair for pectus deformities

Zachary W. Sollie, Frank Gleason, James M. Donahue, Benjamin Wei

JTCVS Tech. 2022 Apr; 12: 212–219. Published online 2022 Jan 19. doi: 10.1016/j.xjtc.2021.12.008

PMCID:: PMC8987321

Article PDF–486K

Select item 86915594.

X-ray-free protocol for pectus deformities based on magnetic resonance imaging and a low-cost portable three-dimensional scanning device: a preliminary study

Marc-Samir Guillot, Aymeric Rouchaud, Charbel Mounayer, Jérémy Tricard, Alexis Belgacem, Emilie Auditeau, Olivier Omraam, Laurent Fourcade, Quentin Ballouhey

Interact Cardiovasc Thorac Surg. 2021 Jul; 33(1): 110–118. Published online 2021 Feb 28. doi: 10.1093/icvts/ivab036

PMCID:: PMC8691559

Article PDF–784K

Select item 81674625.

The 100 most-cited articles on pectus deformities: A bibliometric analysis

Hüseyin Yıldıran, Güven Sadi Sunam

Turk Gogus Kalp Damar Cerrahisi Derg. 2021 Apr; 29(2): 223–232. Published online 2021 Apr 26. doi: 10.5606/tgkdc.dergisi.2021.20295

PMCID:: PMC8167462

Article PDF–336K

Select item 72983746.

Demographic characteristics of pectus deformities across Turkey

Hakan Işık, Hasan Çaylak, Ersin Sapmaz, Okan Karataş, Kuthan Kavaklı, Merve Şengül İnan, Sedat Gürkök, Alper Gözübüyük, Onur Genç

Turk Gogus Kalp Damar Cerrahisi Derg. 2020 Jun; 28(2): 322–330. Published online 2020 Apr 22. doi: 10.5606/tgkdc.dergisi.2020.18465

PMCID:: PMC7298374

Article PDF–910K

Select item 60741107.

Repair of pectus deformities: experience and outcome in 317 cases

Onur Genc, Sedat Gurkok, Alper Gözübüyük, Mehmet Dakak, Hasan Çaylak, Orhan Yücel

Ann Saudi Med. 2006 Sep-Oct; 26(5): 370–374. doi: 10.5144/0256-4947.2006.370

PMCID:: PMC6074110

Article PDF–169K

Select item 47836688.

ORTHOPEDIC APPROACH TO PECTUS DEFORMITIES: 32 YEARS OF STUDIES

Sydney Abrão Haje, Davi de Podestá Haje

Rev Bras Ortop. 2009 Jan; 44(3): 191–198. Published online 2015 Nov 16. doi: 10.1016/S2255-4971(15)30067-7

PMCID:: PMC4783668

Article PDF–298K

Select item 25321369.

Overcorrection during treatment of pectus deformities with DCC orthoses: experience in 17 cases

S. A. Haje, D. P. Haje

Int Orthop. 2006 Aug; 30(4): 262–267. Published online 2006 Feb 11. doi: 10.1007/s00264-005-0060-0

PMCID:: PMC2532136

Article PDF–214K

Select item 157589710.

PECTUS DEFORMITIES

Ross N. Giem, George A. Paulsen, Jack Dykes

Calif Med. 1961 May; 94(5): 306–309.

PMCID:: PMC1575897

Summary Page Browse PDF–1.5M

Select item 975933211.

Natural history of KBG syndrome in a large European cohort

Lorenzo Loberti, Lucia Pia Bruno, Stefania Granata, Gabriella Doddato, Sara Resciniti, Francesca Fava, Michele Carullo, Elisa Rahikkala, Guillaume Jouret, Leonie A Menke, Damien Lederer, Pascal Vrielynck, Lukáš Ryba, Nicola Brunetti-Pierri, Amaia Lasa-Aranzasti, Anna Maria Cueto-González, Laura Trujillano, Irene Valenzuela, Eduardo F Tizzano, Alessandro Mauro Spinelli, Irene Bruno, Aurora Currò, Franco Stanzial, Francesco Benedicenti, Diego Lopergolo, Filippo Maria Santorelli, Constantia Aristidou, George A Tanteles, Isabelle Maystadt, Tinatin Tkemaladze, Tiia Reimand, Helen Lokke, Katrin Õunap, Maria K Haanpää, Andrea Holubová, Veronika Zoubková, Martin Schwarz, Riina Žordania, Kai Muru, Laura Roht, Annika Tihveräinen, Rita Teek, Ulvi Thomson, Isis Atallah, Andrea Superti-Furga, Sabrina Buoni, Roberto Canitano, Valeria Scandurra, Annalisa Rossetti, Salvatore Grosso, Roberta Battini, Margherita Baldassarri, Maria Antonietta Mencarelli, Caterina Lo Rizzo, Mirella Bruttini, Francesca Mari, Francesca Ariani, Alessandra Renieri, Anna Maria Pinto

Hum Mol Genet. 2022 Dec 15; 31(24): 4131–4142. Published online 2022 Jul 21. doi: 10.1093/hmg/ddac167

PMCID:: PMC9759332

Article PDF–1.5M

Select item 596326912.

Desmosterolosis presenting with multiple congenital anomalies

Mersedeh Rohanizadegan, Stephanie Sacharow

Eur J Med Genet. Author manuscript; available in PMC 2018 May 22.

Published in final edited form as: Eur J Med Genet. 2018 Mar; 61(3): 152–156. Published online 2017 Nov 23. doi: 10.1016/j.ejmg.2017.11.009

PMCID:: PMC5963269

Article PDF–254K

Select item 541226613.

Exome Sequencing Identified a Novel FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly

Guoling You, Bailing Zu, Bo Wang, Zhigang Wang, Yunlan Xu, Qihua Fu

Int J Mol Sci. 2017 Apr; 18(4): 626. Published online 2017 Apr 5. doi: 10.3390/ijms18040626

PMCID:: PMC5412266

Article PDF–8.4M

Select item 520731614.

Loss-of-function mutations in the X-linked biglycan gene cause a severe syndromic form of thoracic aortic aneurysms and dissections

Josephina A.N. Meester, Geert Vandeweyer, Isabel Pintelon, Martin Lammens, Lana Van Hoorick, Simon De Belder, Kathryn Waitzman, Luciana Young, Larry W. Markham, Julie Vogt, Julie Richer, Luc M. Beauchesne, Sheila Unger, Andrea Superti-Furga, Milan Prsa, Rami Dhillon, Edwin Reyniers, Harry C. Dietz, Wim Wuyts, Geert Mortier, Aline Verstraeten, Lut Van Laer, Bart L. Loeys

Genet Med. 2017 Apr; 19(4): 386–395. Published online 2016 Sep 15. doi: 10.1038/gim.2016.126

PMCID:: PMC5207316

Article PDF–2.5M

Select item 512248815.

Enlarged Dural Sac in Idiopathic Bronchiectasis Implicates Heritable Connective Tissue Gene Variants

M. Leigh Anne Daniels, Katherine R. Birchard, Jared R. Lowe, Michael V. Patrone, Peadar G. Noone, Michael R. Knowles

Ann Am Thorac Soc. 2016 Oct; 13(10): 1712–1720. doi: 10.1513/AnnalsATS.201603-161OC

PMCID:: PMC5122488

Article PDF–824K

Select item 487321716.

Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing

Hao Deng, Qian Lu, Hongbo Xu, Xiong Deng, Lamei Yuan, Zhijian Yang, Yi Guo, Qiongfen Lin, Jingjing Xiao, Liping Guan, Zhi Song

PLoS One. 2016; 11(5): e0155908. Published online 2016 May 19. doi: 10.1371/journal.pone.0155908

PMCID:: PMC4873217

Article PDF–1.1M

Select item 460701317.

Mutation in NRAS in familial Noonan syndrome – case report and review of the literature

Sara Ekvall, Maria Wilbe, Jovanna Dahlgren, Eric Legius, Arie van Haeringen, Otto Westphal, Göran Annerén, Marie-Louise Bondeson

BMC Med Genet. 2015; 16: 95. Published online 2015 Oct 14. doi: 10.1186/s12881-015-0239-1

PMCID:: PMC4607013

Article PDF–1018K

Select item 373281918.

Pulmonary Nontuberculous Mycobacterial Infection in Congenital Contractural Arachnodactyly

Michelle L. Paulson, Kenneth N. Olivier, Steven M. Holland

Int J Tuberc Lung Dis. Author manuscript; available in PMC 2013 Aug 4.

Published in final edited form as: Int J Tuberc Lung Dis. 2012 Apr; 16(4): 561–563. doi: 10.5588/ijtld.11.0301

PMCID:: PMC3732819

Article PDF–398K

Select item 173499419.

Coffin-Lowry syndrome: clinical and molecular features

A Hanauer, I Young

J Med Genet. 2002 Oct; 39(10): 705–713. doi: 10.1136/jmg.39.10.705

PMCID:: PMC1734994

Summary PDF–314K

Select item 37914220.

PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

Marco Tartaglia, Kamini Kalidas, Adam Shaw, Xiaoling Song, Dan L. Musat, Ineke van der Burgt, Han G. Brunner, Débora R. Bertola, Andrew Crosby, Andra Ion, Raju S. Kucherlapati, Steve Jeffery, Michael A. Patton, Bruce D. Gelb

Am J Hum Genet. 2002 Jun; 70(6): 1555–1563. Published online 2002 May 1. doi: 10.1086/340847

PMCID:: PMC379142

Article PDF–270K

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