International Pediatric Otolaryngology Group (IPOG): Juvenile-onset recurrent respiratory papillomatosis consensus recommendations
Claire M. Lawlor(Tufts University), Roger C. Nuss(Boston Children's Hospital), Seth M. Pransky(Rady Children's Hospital-San Diego), John Carter(The University of Sydney), Richard J. Smith(University of Iowa), Marlene Soma(Sydney Children's Hospital), Karen B. Zur(Children's Hospital of Philadelphia), Alan Cheng(The University of Sydney), Karthik Balakrishnan(Mayo Clinic), Dana M. Thompson(Lurie Children's Hospital), Éric Moreddu(Assistance Publique Hôpitaux de Marseille), Douglas R. Sidell(Lucile Packard Children's Hospital), George H. Zalzal(Children's National), John Russell(Children's Health Ireland at Crumlin), Sergio Bottero(Bambino Gesù Children's Hospital), Marilena Trozzi(Bambino Gesù Children's Hospital), Alejandro Cocciaglia(Garrahan Hospital), Christopher J. Hartnick(Massachusetts Eye and Ear Infirmary), Reza Rahbar(Boston Children's Hospital), Julie E. Strychowsky(Western University), Jean‐Michel Triglia(Hôpital de la Timone), Riaz Y. Seedat(Nelson Mandela Academic Hospital), Catherine K. Hart(Cincinnati Children's Hospital Medical Center), P. Fayoux(Université de Lille), Shazia Peer(University of Cape Town), Michael J. Rutter(Cincinnati Children's Hospital Medical Center), Craig S. Derkay(Sentara Norfolk General Hospital), Paolo Campisi(Hospital for Sick Children), Nicolas Leboulanger(Hôpital Necker-Enfants Malades), An Boudewyns(University of Antwerp), R. Nicollas(Hôpital de la Timone), Harlan Muntz(University of Utah), Alessandro deAlarcón(Cincinnati Children's Hospital Medical Center)
International Journal of Pediatric Otorhinolaryngology
September 28, 2019
Cited by 40
Related Papers
A common haplotype in the complement regulatory gene factor H ( <i>HF1/CFH</i> ) predisposes individuals to age-related macular degeneration
|Proceedings of the National Academy of Sciences|2005|2k
Clinical Practice Guideline: Hoarseness (Dysphonia)
|Otolaryngology|2009|446
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1–SIX1–DNA complexes
|Proceedings of the National Academy of Sciences|2004|420
Clinical diagnosis of the Usher syndromes
|American Journal of Medical Genetics|1994|343
On Using Gait in Forensic Biometrics
|Journal of Forensic Sciences|2011|245