Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Sarah, Milla"'
Publikováno v:
Journal of the American College of Radiology. 20:503-509
Autor:
Ramy Abramsky, Rebeka Acosta, Laura Acosta Izquierdo, Bushra Albeshri, Mountasser Almouqdad, Yasmeen Asfour, Suzan Asfour, Topun Austin, Ashley Bach, Jim Barkovich, Richard Beare, Nadya Ben Fadel, Angelika Berger, Borja Blanco, Martijn Boomsma, Samudragupta Bora, Vivian Boswinkel, Theresa Chin, Liam Collins-Jones, Robert Cooper, Gautam Dagur, Jorge Davila, Linda de Vries, Laxmikant Shesrao, null Deshmukh, Gregor Dovjak, Andrea Edwards, Mohamed El-Dib, Hoda Elshibiny, Dafna Eshel, Ron Eshel, Donna Ferriero, Dawn Gano, Olivia Girvan, Hannah Glass, Katharina Goeral, Agneta Golan, Michelle Gurvitz, Terrie Inder, Dima Jamjoom, Nadja Kadom, Gregor Kasprian, Thanaa Khalil, Katrin Klebermass-Schrehof, Jake Kleinmahon, Martine Krüse-Ruijter, Hannah Lambing, Sarah Lee, Alexander Leemans, Lara Leijser, Brigitte Lemyre, Yi Li, Camille Maltais-Bilodeau, Kyla Marks, Charles McCulloch, Sarah Milla, Elka Miller, Aradhana Mishra, Nicholas Mitsakakis, Khorshid Mohammad, Susanne Mulder-de Tollenaer, Chelsea Munster, Jacqueline Nijboer, Jacqueline Nijboer-Oosterveld, Ingrid Nijholt, Rosa Novoa, Cynthia Ortinau, Emma Porter, Daniela Prayer, Deepti Reddy, Stephanie Redpath, Elizabeth Rogers, Victor Schmidbauer, James Scott, Elizabeth Sewell, Eilon Shany, Ilan Shelef, Elizabeth Singh, Cornelis Slump, Tina Steele, Eniko Szakmar, Chantal Tax, Kirsten Thiim, Julie Uchitel, Jochen van Osch, Gerda van Wezel-Meijler, Anouk Verschuur, Mei-Nga Wu-Smit, Edward Yang, Hussein Zein
Publikováno v:
Journal of Neonatal-Perinatal Medicine. 15:389-409
Publikováno v:
Pediatrics and Neonatology, Vol 57, Iss 5, Pp 440-443 (2016)
Tuberous sclerosis (TS) is an autosomal dominant condition associated with mutations in the TSC1 and/or TSC2 genes. Clinical manifestations are multisystemic, and they often include lesions in the brain, skin, heart, kidneys, and bones. TSC2 gene mut
Externí odkaz:
https://doaj.org/article/6ac1afb6d9d04543882a5b05544cd5e9
Autor:
Marina L Reppucci, Connor Prendergast, Shannon N Acker, Sarah Milla, Jeffrey J Tutman, Amanda Rutherford, Jonathan Orsborn, Jose Luis Diaz-Miron
Publikováno v:
Journal of the American College of Surgeons. 236:S80-S80
Autor:
Marina L Reppucci, Connor Prendergast, Shannon N Acker, Sarah Milla, Jeffrey Tutman, Amanda Rutherford, Jonathan Orsborn, Jose Luis Diaz-Miron
Publikováno v:
Journal of the American College of Surgeons. 236:S81-S81
Autor:
Mark E. Bittman, Susan Sharp, Curtis P. Langlotz, Matthew P. Lungren, Shailee V. Lala, David Eng, Alexander J. Towbin, Nishith Khandwala, Michael L. Francavilla, Brian M. Everist, Kirsten Ecklund, David B. Larson, Sarah Milla, Safwan Halabi, Ross W. Filice, Jayne Seekins, Sanjay P. Prabhu, Rebecca Dennis, Jin Long, Naomi Strubel, Arash R. Zandieh, Christopher G. Anton, Nancy R. Fefferman, Summer L. Kaplan, Cicero T. Silva, Brian J. Dillon
Publikováno v:
Radiology. 301(3)
Background Previous studies suggest that use of artificial intelligence (AI) algorithms as diagnostic aids may improve the quality of skeletal age assessment, though these studies lack evidence from clinical practice. Purpose To compare the accuracy
Publikováno v:
Journal of the American College of Radiology
Autor:
Daniel J. Podberesky, Peter D. Pizzutillo, Sarah Milla, Brian D. Coley, John Ragheb, Charles N. Paidas, Matthew D. Garber, Dorothy I. Bulas, Richard B. Gunderman, Boaz Karmazyn, John S. Myseros, Jeffrey S. Prince, Marc S. Keller, Abhaya V. Kulkarni, James S. Meyer
Publikováno v:
Journal of the American College of Radiology. 14:S338-S349
The appropriate imaging for pediatric patients being evaluated for suspected physical abuse depends on the age of the child, the presence of neurologic signs and symptoms, evidence of thoracic or abdominopelvic injuries, and whether the injuries are
Publikováno v:
Journal of Pediatric and Adolescent Gynecology. 33:234-235
Autor:
Jose-Alberto Palma, Yvonne W. Lui, Lucy Norcliffe-Kaufmann, Sarah Milla, James S. Babb, Horacio Kaufmann, Benjamin Cohen, Eugene Won
Publikováno v:
Clin Auton Res
PURPOSE: Familial dysautonomia (FD) is a rare autosomal recessive disease that affects development of sensory and autonomic neurons, including those in the cranial nerves. We aimed to determine whether conventional brain magnetic resonance imaging (M