Reconstructions acétabulaires au moyen d’allogreffes fragmentées et d’un anneau de renforcement dans les reprises de prothèse totale de hanche avec perte de substance osseuse Papro... von Philippe, R., Gosselin, O., Sedaghatian, J., Dezaly, C., Roche, O., Sirveaux, F., Molé, D.

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Traitement arthroscopique des ruptures de la coiffe des rotateurs après 60 ans : à court terme, la réparation est préférable à la décompression–ténotomie isolée von Dezaly, C., Sirveaux, F., Philippe, R., Wein-Remy, F., Sedaghatian, J., Roche, O., Molé, D.

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À propos de l’article : « Traitement arthroscopique des ruptures de la coiffe des rotateurs après 60 ans : à court terme, la réparation est préférable à la décompression-ténotomie isolée » de C. Dezaly, F. Sirveaux, R. Philippe, F. Wein-Remy, J. Sedaghatian, O. Roche et D. Molé, publié dans Rev Chir Orthop 2011;97S:S226–32 von Goutallier, D.

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Pain after shoulder arthroscopy: A prospective study on 231 cases von Stiglitz, Y, Gosselin, O, Sedaghatian, J, Sirveaux, F, Molé, D

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Arthroscopic treatment of rotator cuff tear in the over-60s: Repair is preferable to isolated acromioplasty-tenotomy in the short term von Dezaly, C, Sirveaux, F, Philippe, R, Wein-Remy, F, Sedaghatian, J, Roche, O, Molé, D

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Acetabular reconstruction using morselized allograft and a reinforcement ring for revision arthroplasty with Paprosky type II and III bone loss: Survival analysis of 95 hips after... von Philippe, R, Gosselin, O, Sedaghatian, J, Dezaly, C, Roche, O, Sirveaux, F, Molé, D

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Comments on: “Arthroscopic treatment of rotator cuff tear in the over-60s: Repair is preferable to isolated acromioplasty-tenotomy in the short term,” by C. Dezaly, F. Sirveaux, R. Philippe, F. Wein-Remy, J. Sedaghatian, O. Roche and D. Molé, published in Orthop Traumatol Surg Res 2011;97S:S125–30 von Goutallier, D

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Douleur après arthroscopie d’épaule : à propos d’une série prospective de 231 cas von Stiglitz, Y., Gosselin, O., Sedaghatian, J., Sirveaux, F., Molé, D.

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Traitement arthroscopique des ruptures de la coiffe des rotateurs après 60ans : à court terme, la réparation est préférable à la décompression–ténotomie isolée von Dezaly, C., Sirveaux, F., Philippe, R., Wein-Remy, F., Sedaghatian, J., Roche, O., Molé, D.

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Sedaghatian spondylometaphyseal dysplasia in two siblings von Peshimam, Niha, Farah, Hani, Caswell, Richard, Ellard, Sian, Jan, Wajanat, Calder, Alistair D, Cobben, Jan, Kariholu, Ujwal, Leitch, Harry G

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Sedaghatian spondylometaphyseal dysplasia with pachygyria and absence of the corpus callosum von English, Sharon J., Gayatri, Neti, Arthur, Rosemary, Crow, Yanick J.

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Mutations in the enzyme glutathione peroxidase 4 cause Sedaghatian-type spondylometaphyseal dysplasia von Smith, Amanda C, Mears, Alan J, Bunker, Ryan, Ahmed, Afsana, MacKenzie, Malcolm, Schwartzentruber, Jeremy A, Beaulieu, Chandree L, Ferretti, Emanuela, Majewski, Jacek, Bulman, Dennis E, Celik, Fatma Cakmak, Boycott, Kym M, Graham, Gail E

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Sedaghatian-type spondylometaphyseal dysplasia: Whole exome sequencing in neonatal dry blood spots enabled identification of a novel variant in GPX4 von Fedida, Ayalla, Ben Harouch, Shani, Kalfon, Limor, Abunassar, Zahi, Omari, Hussam, Mandel, Hanna, Falik-Zaccai, Tzipora C.

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Spondylomethaphyseal dysplasia, sedaghatian type von PEEDEN, J. N, LACHMAN, R. S, DYER, M. L, GERARD, D, GRUBER, H. E

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Spondylometaphyseal dysplasia, sedaghatian type von Peeden Jr, J. N., Rimoin, D. L., Lachman, R. S., Dyer, M. L., Gerard, D., Gruber, H. E.

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Simplified gyral pattern with cerebellar hypoplasia in Sedaghatian type spondylometaphyseal dysplasia: A clinical report and review of the literature von Aygun, Canan, Celik, Fatma Cakmak, Nural, Mehmet Selim, Azak, Emine, Kucukoduk, Şukru, Ogur, Gonul, Incesu, Lutfi

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Intrauterine Growth Pattern of Live-Born Infants of Southern Iran Compared with Western Norms von Sedaghatian, M. R., Shayegan, J., Barkhordar, J.

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The Shwachman–Bodian–Diamond syndrome gene mutations cause a neonatal form of spondylometaphysial dysplasia (SMD) resembling SMD Sedaghatian type von Nishimura, Gen, Nakashima, Eiji, Hirose, Yuichiro, Cole, Trevor, Cox, Phillip, Cohn, Daniel H, Rimoin, David L, Lachman, Ralph S, Miyamoto, Yoshinari, Kerr, Bronwyn, Unger, Sheila, Ohashi, Hirofumi, Superti-Furga, Andrea, Ikegawa, Shiro

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Consequences of mutations and inborn errors of selenoprotein biosynthesis and functions von Fradejas-Villar, Noelia

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Cardiolipin drives the catalytic activity of GPX4 on membranes: Insights from the R152H mutant von Roveri, Antonella, Di Giacinto, Flavio, Rossetto, Monica, Cozza, Giorgio, Cheng, Qing, Miotto, Giovanni, Zennaro, Lucio, Di Paolo, Maria Luisa, Arnér, Elias S.J., De Spirito, Marco, Maiorino, Matilde, Ursini, Fulvio

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