Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Alexander Allori"'
Autor:
Anne Klassen, Irene Mathijssen, Maarten Koudstaal, Saranda Ombashi, Melissa Srijanti Kurniawan, Alexander Allori, Banafsheh Sharif-Askary, Carolyn Rogers-Vizena, Marie-Christine Franken, Aebele B Mink van der Molen, Sarah Lisa Versnel
Publikováno v:
BMJ Open, Vol 13, Iss 12 (2023)
Objectives Speech problems in patients with a cleft palate are often complex and multifactorial. Finding the optimal way of monitoring these problems is challenging. The International Consortium of Health Outcomes Measurement (ICHOM) has developed a
Externí odkaz:
https://doaj.org/article/c852bd2b372547f4af4314c578f562fa
Autor:
Kristina Dunworth, BA, Amanda Del Risco, BA, Denisse Porras Fimbres, BS, Alexander Allori, MD, MPH
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 11, Iss 4S, Pp 94-94 (2023)
Externí odkaz:
https://doaj.org/article/15798c256cac42adb7ce43b8f05605ca
Autor:
Dennis O. Frank-Ito, PhD, David J. Carpenter, BS, MHS, Tracy Cheng, AB, Yash J. Avashia, MD, David A. Brown, MD, PhD, Adam Glener, MD, Alexander Allori, MD, MPH, Jeffrey R. Marcus, MD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 7, Iss 5, p e2244 (2019)
Background:. Nasal airway obstruction (NAO) due to nasal anatomic deformities is known to be more common among cleft patients than the general population, yet information is lacking regarding severity and variability of cleft-associated nasal obstruc
Externí odkaz:
https://doaj.org/article/5aca78c88f8546bcab273a50f3585dc6
Autor:
Alexander D, Suarez, Brad, Taicher, Herbert, Fuchs, Jeffery, Marcus, Matthew, Vestal, Mayumi, Homi, Alexander, Allori, Eric M, Thompson
Publikováno v:
Journal of Craniofacial Surgery. 33:1327-1330
Blood loss is a main cause of morbidity after craniofacial procedures. The purpose of this study is to identify the incidence and predictors for transfusion of blood products in the endoscopic assisted strip craniectomy population. Data was prospecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1509cca4f532248856f163b32defe95f
https://doi.org/10.1097/scs.0000000000008441
https://doi.org/10.1097/scs.0000000000008441
Autor:
Tahir N. Khan, Kamal Khan, Azita Sadeghpour, Hannah Reynolds, Yezmin Perilla, Marie T. McDonald, William B. Gallentine, Shahid M. Baig, Erica E. Davis, Nicholas Katsanis, Alexander Allori, Misha Angrist, Patricia Ashley, Margarita Bidegain, Brita Boyd, Eileen Chambers, Heidi Cope, C. Michael Cotten, Theresa Curington, Sarah Ellestad, Kimberley Fisher, Amanda French, William Gallentine, Ronald Goldberg, Kevin Hill, Sujay Kansagra, Sara Katsanis, Joanne Kurtzberg, Jeffrey Marcus, Marie McDonald, Mohammed Mikati, Stephen Miller, Amy Murtha, Carolyn Pizoli, Todd Purves, Sherry Ross, Edward Smith, John Wiener
Publikováno v:
The American Journal of Human Genetics. 104:94-111
The use of whole-exome and whole-genome sequencing has been a catalyst for a genotype-first approach to diagnostics. Under this paradigm, we have implemented systematic sequencing of neonates and young children with a suspected genetic disorder. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bff7d2b35625122fe7ddf1f6b526f5a
https://doi.org/10.1016/j.ajhg.2018.11.017
https://doi.org/10.1016/j.ajhg.2018.11.017
Autor:
Katherine L. Helbig, Robert J. Lauerer, Jacqueline C. Bahr, Ivana A. Souza, Candace T. Myers, Betül Uysal, Niklas Schwarz, Maria A. Gandini, Sun Huang, Boris Keren, Cyril Mignot, Alexandra Afenjar, Thierry Billette de Villemeur, Delphine Héron, Caroline Nava, Stéphanie Valence, Julien Buratti, Christina R. Fagerberg, Kristina P. Soerensen, Maria Kibaek, Erik-Jan Kamsteeg, David A. Koolen, Boudewijn Gunning, H. Jurgen Schelhaas, Michael C. Kruer, Jordana Fox, Somayeh Bakhtiari, Randa Jarrar, Sergio Padilla-Lopez, Kristin Lindstrom, Sheng Chih Jin, Xue Zeng, Kaya Bilguvar, Antigone Papavasileiou, Qinghe Xing, Changlian Zhu, Katja Boysen, Filippo Vairo, Brendan C. Lanpher, Eric W. Klee, Jan-Mendelt Tillema, Eric T. Payne, Margot A. Cousin, Teresa M. Kruisselbrink, Myra J. Wick, Joshua Baker, Eric Haan, Nicholas Smith, Azita Sadeghpour, Erica E. Davis, Nicholas Katsanis, Mark A. Corbett, Alastair H. MacLennan, Jozef Gecz, Saskia Biskup, Eva Goldmann, Lance H. Rodan, Elizabeth Kichula, Eric Segal, Kelly E. Jackson, Alexander Asamoah, David Dimmock, Julie McCarrier, Lorenzo D. Botto, Francis Filloux, Tatiana Tvrdik, Gregory D. Cascino, Sherry Klingerman, Catherine Neumann, Raymond Wang, Jessie C. Jacobsen, Melinda A. Nolan, Russell G. Snell, Klaus Lehnert, Lynette G. Sadleir, Britt-Marie Anderlid, Malin Kvarnung, Renzo Guerrini, Michael J. Friez, Michael J. Lyons, Jennifer Leonhard, Gabriel Kringlen, Kari Casas, Christelle M. El Achkar, Lacey A. Smith, Alexander Rotenberg, Annapurna Poduri, Alba Sanchis-Juan, Keren J. Carss, Julia Rankin, Adam Zeman, F. Lucy Raymond, Moira Blyth, Bronwyn Kerr, Karla Ruiz, Jill Urquhart, Imelda Hughes, Siddharth Banka, Ulrike B.S. Hedrich, Ingrid E. Scheffer, Ingo Helbig, Gerald W. Zamponi, Holger Lerche, Heather C. Mefford, Alexander Allori, Misha Angrist, Patricia Ashley, Margarita Bidegain, Brita Boyd, Eileen Chambers, Heidi Cope, C. Michael Cotten, Theresa Curington, Sarah Ellestad, Kimberley Fisher, Amanda French, William Gallentine, Ronald Goldberg, Kevin Hill, Sujay Kansagra, Sara Katsanis, Joanne Kurtzberg, Jeffrey Marcus, Marie McDonald, Mohammed Mikati, Stephen Miller, Amy Murtha, Yezmin Perilla, Carolyn Pizoli, Todd Purves, Sherry Ross, Edward Smith, John Wiener
Publikováno v:
American Journal of Human Genetics, 103, 666-678
Deciphering Developmental Disorders Study 2018, ' De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias ', American Journal of Human Genetics, vol. 103, no. 5, pp. 666-678 . https://doi.org/10.1016/j.ajhg.2018.09.006
American Journal of Human Genetics, 103, 5, pp. 666-678
American journal of human genetics, vol 103, iss 5
Deciphering Developmental Disorders Study 2018, ' De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias ', American Journal of Human Genetics, vol. 103, no. 5, pp. 666-678 . https://doi.org/10.1016/j.ajhg.2018.09.006
American Journal of Human Genetics, 103, 5, pp. 666-678
American journal of human genetics, vol 103, iss 5
Item does not contain fulltext Developmental and epileptic encephalopathies (DEEs) are severe neurodevelopmental disorders often beginning in infancy or early childhood that are characterized by intractable seizures, abundant epileptiform activity on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94c2ddc9d5f68e0eed9530ef99151563
http://hdl.handle.net/2066/200025
http://hdl.handle.net/2066/200025
Autor:
Dunya Atisha, Alexander Allori, David Nolen, Edward Ruane, Brian Christie, Ketan Sharma, Ryan Kellogg, Amelia Maiga, Liana Puscus, Jeffrey R. Marcus, Detlev Erdmann
Publikováno v:
Plastic and Reconstructive Surgery. 130:6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54b389f1e188f00f7f8ff6fe9a1e4539
https://doi.org/10.1097/01.prs.0000421702.36644.c0
https://doi.org/10.1097/01.prs.0000421702.36644.c0
Autor:
Ming-Huei Cheng, Eric M. Brey, Alexander Allori, William C. Satterfield, David W. Chang, Charles W. Patrick, Michael J. Miller
Publikováno v:
Tissue Engineering; 2005, Vol. 11 Issue 1/2, p214-225, 12p