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Consensus Expert Recommendations for the Diagnosis and Management of Autosomal Recessive Polycystic Kidney Disease: Report of an International Conference

Autor: Binita M. Kamath, John J. Bissler, Karen F. Murray, Ronald D. Perrone, Stephen R. Hooper, Larissa Kerecuk, Melissa A. Cadnapaphornchai, Carsten Bergmann, Katherine MacRae Dell, Detlef Bockenhauer, Randi Streisand, Theo Heller, Sukru Emre, Kenneth J. Moise, Meral Gunay-Aygun, Jacquelyn R. Evans, Michael C. Braun, Marva Moxey-Mims, Max C. Liebau, Kristina K. Hardy, Benjamin L. Shneider, Louise Wilkins-Haug, Maria H. Alonso-Peclet, Eric E. Eichenwald, Erum A. Hartung, Roberta L. Keller, Lisa M. Guay-Woodford

Publikováno v: The Journal of pediatrics, vol 165, iss 3

Autosomal-recessive polycystic kidney disease (ARPKD; MIM 263200) is a severe, typically early-onset form of cystic disease that primarily involves the kidneys and biliary tract. Phenotypic expression and age at presentation can be quite variable. 1

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8d4d4f94eb8b50d90ef5582a1e9bf82
https://doi.org/10.1016/j.jpeds.2014.06.015

Randomized Trial of Late Surfactant Treatment in Ventilated Preterm Infants Receiving Inhaled Nitric Oxide

Autor: Roberta A. Ballard, Roberta L. Keller, Dennis M. Black, Philip L. Ballard, Jeffrey D. Merrill, Eric C. Eichenwald, William E. Truog, Mark C. Mammel, Robin H. Steinhorn, Elizabeth E. Rogers, Rita M. Ryan, David J. Durand, Jeanette M. Asselin, Catherine M. Bendel, Ellen M. Bendel-Stenzel, Sherry E. Courtney, Ramasubbareddy Dhanireddy, Mark L. Hudak, Frances R. Koch, Dennis E. Mayock, Victor J. McKay, T. Michael O'Shea, Nicolas F. Porta, Rajan Wadhawan, Lisa Palermo, S. Hamilton Strong, J. Immamura-Ching, M. Orfanos-Villalobos, C. Williams, D. Horton, L. Pacello, A. Willard, C. Gauldin, A. Holmes, P. Johnson, K. Meinert, A.M. Reynolds, J. Lucie, P. Conway, M.l. Sacilowski, M. Leadersdorff, P. Orbank, K. Wynn, M. deUngria, J. Khan, K. Hamann, M. Schau, B. Hopkins, J. Jenson, C. Garcia, J. Shariff, R. McGovern, J. Adelman, A. Combs, M. Tjersland, S. Walker, E. Howland, J. Longoria, H. Meo, G. McDavid, K. Burson, R. Hinojosa, C. Johnson, K. Miller, S. Rogers, S. Wright, K. Barnette, A. Kellum, M. Burke, C. Hayes, S. Chadwick, D. Howard, C. Kennedy, R. Prince, B. Stefanescu, J. Helderman, K. Warden, P. Brown, J. Griffin, L. Conley, M. Georgieff, B. Davern, M. Mills, S. Ritter, C. Wagner, D. Fanning, J. Roberson, A. Lampland, P. Meyers, A. Brey, C. Worwa, P. Dixon, G. Ebert, C. Hejl, M. Maxwell, K. McCullough, M.T. El Abiad, A. Talati, S. Dempsey, K. Gammage, G. Gower, K. James, P. LeNoue, S. Bell, D. Bruton, M. Beaulieu, R. Williams, R. Barron-Nelson, S. Taylor, N.C. Sikes, G. Lowe, B. Proffitt, C. Chapin, H. Horneman, S. Kelley, E. Vittinghoff, J. Hietpas, L. Denton, L. Wu, A. Jobe, A. Fanaroff, T. Clemons, L. Glantz, D. Reboussin, K. Van Meurs, M. Allen, B. Vohr, R. Ballard, P. Ballard, C. Blaisdell, D. Durand, D. Black, E. Eichenwald, R. Keller, M. Mammel, J. Merrill, E. Rogers, R. Ryan, W. Truog, J. Asselin, N. Newton

ObjectiveTo assess whether late surfactant treatment in extremely low gestational age (GA) newborn infants requiring ventilation at 7-14 days, who often have surfactant deficiency and dysfunction, safely improves survival without bronchopulmonary dys

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74f9a82c41743dd72df1d3f505ead368
https://escholarship.org/uc/item/7vc0t2c6

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