Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Kimberley Fisher"'
Autor:
Robin B. Dail, Kayla C. Everhart, Victor Iskersky, Weili Chang, Kimberley Fisher, Karen Warren, Heidi J. Steflik, James W. Hardin
Publikováno v:
Tropical Medicine and Infectious Disease, Vol 9, Iss 4, p 70 (2024)
Background: The birthrate of Black preterm (BPT) infants is 65% higher than White preterm (WPT) infants with a BPT mortality that is 2.3 times higher. The incidence of culture-positive late-onset sepsis is as high as 41% in very-preterm infants. The
Externí odkaz:
https://doaj.org/article/5d13a9d6c10b40d8972963db23994b43
Autor:
Deesha D. Mago-Shah, Kamlesh Athavale, Kimberley Fisher, Elizabeth Heyward, David Tanaka, C. Michael Cotten
Publikováno v:
Journal of Perinatology. 43:629-634
Autor:
Makenzie Beaman, Kimberley Fisher, Marie McDonald, Queenie K. G. Tan, David Jackson, Benjamin T. Cocanougher, Andrew P. Landstrom, Charlotte A. Hobbs, Michael Cotten, Jennifer L. Cohen
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 11; Pages: 1924
Rapid genome sequencing in critically ill infants is increasingly identified as a crucial test for providing targeted and informed patient care. We report the outcomes of a pilot study wherein eight critically ill neonates received rapid whole genome
Autor:
Naimisha Movva, Mina Suh, Heidi Reichert, Bradley Hintze, Mark P Sendak, Zachary Wolf, Shannon Carr, Tom Kaminski, Meghan White, Kimberley Fisher, Charles T Wood, Jon P Fryzek, Christopher B Nelson, William F Malcolm
Publikováno v:
The Journal of infectious diseases. 226(Suppl 2)
Background Surveillance in 2020–2021 showed that seasonal respiratory illnesses were below levels seen during prior seasons, with the exception of interseasonal respiratory syncytial virus (RSV). Methods Electronic health record data of infants age
Autor:
Geoffrey Hall, Trevor Burt, Kimberley Fisher, Rick Pittman, John Sleasman, Rebecca Buckley, Michael Cotten, Talal Mousallem
Publikováno v:
Journal of Allergy and Clinical Immunology. 151:AB212
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
Autor:
C. Michael Cotten, Kimberley Fisher, Kathryn Gustafson, William F Malcolm, Lynn Cheatham, Joanne Kurtzberg
Publikováno v:
Transplantation and Cellular Therapy. 28:S230
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
Publikováno v:
Archives of Natural History. 41:223-229
An unpublished collection of watercolours entitled “The Fruits of the Lima market. by Mrs. D. E. Smith, between the years 1850 & ”53” can be credited to Dorothea Eliza Smith (1804–1864), wife of the Scottish physician Archibald Smith (1797–
Publikováno v:
Journal of Obstetric, Gynecologic & Neonatal Nursing. 42:121-131
Objective To describe parents' care experiences during hospitalization of their children to identify strategies that could improve the provision of patient and family‐centered care (PFCC). Design A two‐phase mixed‐method descriptive design was