Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nöel, Garabedian"'
Autor:
null Justine Lerat, null Crystel Bonnet, null François Cartault, null Natalie Loundon, null Marie-Line Jacquemont, null Françoise Darcel, null Isabelle Rouillon, null Kheira Mezouaghi, null Agnes Guichet, null Julie Litzler, null Roselyne Gesny, null Souad Gherbi, null Ines B.E.N. Aissa, null Fabienne S.A.I.N.T.J.A.M.E.S. Digeon, null Eréa-Nöel Garabedian, null Jean-Paul Bonnefont, null Emmanuelle Genin, null Françoise Denoyelle, null Laurence Jonard, null Sandrine Marlin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61b26a6c7921fbecf13f09a7b5ec4da7
https://doi.org/10.1111/cge.13460/v2/response1
https://doi.org/10.1111/cge.13460/v2/response1
Autor:
Karthik, Balakrishnan, Douglas R, Sidell, Nancy M, Bauman, Gaston F, Bellia-Munzon, R Paul, Boesch, Matthew, Bromwich, Shelagh A, Cofer, Cori, Daines, Alessandro, de Alarcon, Nöel, Garabedian, Catherine K, Hart, Jonathan B, Ida, Nicolas, Leboulanger, Peter B, Manning, Deepak K, Mehta, Philippe, Monnier, Charles M, Myer, Jeremy D, Prager, Diego, Preciado, Evan J, Propst, Reza, Rahbar, John, Russell, Michael J, Rutter, Briac, Thierry, Dana M, Thompson, Michele, Torre, Patricio, Varela, Shyan, Vijayasekaran, David R, White, Andre M, Wineland, Robert E, Wood, Christopher T, Wootten, Karen, Zur, Robin T, Cotton
Publikováno v:
The Laryngoscope. 129(1)
Develop multidisciplinary and international consensus on patient, disease, procedural, and perioperative factors, as well as key outcome measures and complications, to be reported for pediatric airway reconstruction studies.Standard Delphi methods we
Autor:
Justine, Lerat, Laurence, Jonard, Natalie, Loundon, Sophie, Christin-Maitre, Didier, Lacombe, Cyril, Goizet, Cécile, Rouzier, Lionel, Van Maldergem, Souad, Gherbi, Eréa-Nöel, Garabedian, Jean-Paul, Bonnefont, Philippe, Touraine, Isabelle, Mosnier, Arnold, Munnich, Françoise, Denoyelle, Sandrine, Marlin
Publikováno v:
Human mutation. 37(12)
Perrault syndrome (PS) is a rare autosomal recessive condition characterized by deafness and gonadic dysgenesis. Recently, mutations in five genes have been identified: C10orf2, CLPP, HARS2, HSD17B4, and LARS2. Probands included are presented with se
Akademický článek
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Autor:
Balakrishnan, Karthik, Sidell, Douglas R., Bauman, Nancy M., Bellia‐Munzon, Gaston F., Boesch, R. Paul, Bromwich, Matthew, Cofer, Shelagh A., Daines, Cori, de Alarcon, Alessandro, Garabedian, Nöel, Hart, Catherine K., Ida, Jonathan B., Leboulanger, Nicolas, Manning, Peter B., Mehta, Deepak K., Monnier, Philippe, Myer, Charles M., Prager, Jeremy D., Preciado, Diego, Propst, Evan J.
Publikováno v:
Laryngoscope; Jan2019, Vol. 129 Issue 1, p244-255, 12p
Autor:
Lerat, Justine, Marlin, Sandrine, Mezouaghi, Kheira, Guichet, Agnes, Genin, Emmanuelle, Litzler, Julie, Gesny, Roselyne, Bonnefont, Jean‐Paul, Jonard, Laurence, Bonnet, Crystel, Cartault, François, Gherbi, Souad, Aissa, Ines Ben, Digeon, Fabienne Saint James, Loundon, Natalie, Rouillon, Isabelle, Garabedian, Eréa‐Nöel, Denoyelle, Françoise, Jacquemont, Marie‐Line, Darcel, Françoise
Publikováno v:
Clinical Genetics; Jan2019, Vol. 95 Issue 1, p177-181, 5p, 1 Diagram, 2 Charts
Cette nouvelle édition de l'ouvrage « ORL de l'enfant » rend compte des multiples avancées qui ont transformé la pratique clinique en ORL pédiatrique ces dix dernières années, qu'il s'agisse de pathologies courantes ou de tumeurs ou malformat