Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Annie I. Drapeau"'
Autor:
Kathleen M. Schieffer, Alexander Z. Feldman, Esko A. Kautto, Sean McGrath, Anthony R. Miller, Maria Elena Hernandez-Gonzalez, Stephanie LaHaye, Katherine E. Miller, Daniel C. Koboldt, Patrick Brennan, Benjamin Kelly, Amy Wetzel, Vibhuti Agarwal, Margaret Shatara, Suzanne Conley, Diana P. Rodriguez, Rolla Abu-Arja, Ala Shaikhkhalil, Matija Snuderl, Brent A. Orr, Jonathan L. Finlay, Diana S. Osorio, Annie I. Drapeau, Jeffrey R. Leonard, Christopher R. Pierson, Peter White, Vincent Magrini, Elaine R. Mardis, Richard K. Wilson, Catherine E. Cottrell, Daniel R. Boué
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-11 (2021)
Abstract Retinoblastoma is a childhood cancer of the retina involving germline or somatic alterations of the RB Transcriptional Corepressor 1 gene, RB1. Rare cases of sellar-suprasellar region retinoblastoma without evidence of ocular or pineal tumor
Externí odkaz:
https://doaj.org/article/85b8e7d1df914feb8bd8c86c7a9bff75
Autor:
Gabriella, Pendola, George W, Koutsouras, Joseph, Piatt, Bruce A, Kaufman, Carolina, Sandoval-Garcia, Annie I, Drapeau
Publikováno v:
Journal of Neurosurgery: Pediatrics. 31:186-191
OBJECTIVE Quality improvement (QI) is a methodology used to implement sustainable, meaningful change to improve patient outcomes. Given the complex pathologies observed in pediatric neurosurgery, QI projects could potentially improve patient care. Ov
Autor:
Annie I. Drapeau, Christian Mpody, Michael A. Gross, Rafael Lemus, Joseph D. Tobias, Olubukola Nafiu
Publikováno v:
Journal of Neurosurgical Anesthesiology.
Publikováno v:
Journal of Child Neurology. 36:1047-1053
Aims: Examine ophthalmologic outcomes and complications of lumbar drain and cerebrospinal fluid shunts in pediatric fulminant intracranial hypertension. Methods: Patients under 21 years of age with a diagnosis of fulminant intracranial hypertension w
Publikováno v:
Operative Neurosurgery. 20:529-534
Background Minimal invasive suturectomy is one of the many surgical approaches to treat isolated single suture craniosynostosis. This approach can be technically challenging in metopic craniosynostosis given the narrow corridor and steep angle of the
Publikováno v:
The Cleft Palate Craniofacial Journal. :105566562311685
Objective Posterior cranial distraction (PCD) is a surgical technique to address craniosynostosis, especially in syndromic patients. The technique has the ability to significantly expand the cranium, while requiring minimal dural dissection, compared
Autor:
Anne E. Graver, Helen Duenas, Gregory D. Pearson, Varun S. Shah, Annie I. Drapeau, Lance S. Governale, Luke G F Smith, Amanda Onwuka
Publikováno v:
Pediatric Neurosurgery. 56:511-518
Introduction: We sought to compare outcomes and parental satisfaction between 2 approaches for sagittal craniosynostosis: strip craniectomy with spring-mediated skull remodeling (SMSR) and strip craniectomy with postoperative helmet (SCH). Methods: P
Publikováno v:
Pediatric neurology. 133
Markers of quality of care in various surgical specialties have been shown to correlate with hospital volumes. This study investigates the effect of hospital volume and patient-related factors on the outcomes of children undergoing brain tumor resect
Autor:
Alexander Z. Feldman, Jeffrey R. Leonard, Catherine E. Cottrell, Brent A. Orr, Peter White, Ala K. Shaikhkhalil, Amy Wetzel, Rolla Abu-Arja, Vibhuti Agarwal, Jonathan L. Finlay, Diana S Osorio, Richard K. Wilson, Annie I. Drapeau, Christopher R. Pierson, Sean McGrath, Stephanie LaHaye, Daniel C. Koboldt, Katherine E. Miller, Diana P Rodriguez, Matija Snuderl, Patrick J. Brennan, Kathleen M. Schieffer, Esko A. Kautto, Elaine R. Mardis, Maria Elena Hernandez-Gonzalez, Margaret Shatara, Vincent Magrini, Benjamin J. Kelly, Suzanne Conley, Anthony R. Miller, Daniel R. Boue
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-11 (2021)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
Retinoblastoma is a childhood cancer of the retina involving germline or somatic alterations of the RB Transcriptional Corepressor 1 gene, RB1. Rare cases of sellar-suprasellar region retinoblastoma without evidence of ocular or pineal tumors have be