Zobrazeno 1 - 9
of 9
pro vyhledávání: '"John C Wellons III"'
Autor:
Matthew E. Pontell, MD, Aaron Yengo-Kahn, MD, Emily Taylor, WHNP-BC, J Michael Newton, MD, PhD, Kelly A. Bennett, MD, MS, FRCS(C), John C. Wellons, III, MD, MSPH, Stephane A. Braun, MD, FRCS(C)
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 10, Iss 4S, Pp 13-14 (2022)
Externí odkaz:
https://doaj.org/article/e49efbb09507452592602e7efad73449
Autor:
Matthew E. Pontell, MD, Aaron Yengo-Kahn, MD, Emily Taylor, WHNP-BC, Morgan Kane, OTR/L, J. Michael Newton, MD, PhD, Kelly A. Bennett, MD, MS, John C. Wellons, III, MD, MSPH, Stephane A. Braun, MD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 10, Iss 6S, Pp 82-82 (2022)
Externí odkaz:
https://doaj.org/article/8ba3c5fb7c2f42f186940d78c361d5ae
Autor:
Andrew T. Hale, Lisa Bastarache, Diego M. Morales, John C. Wellons, III, David D. Limbrick, Jr., Eric R. Gamazon
Publikováno v:
Cell Reports, Vol 35, Iss 5, Pp 109085- (2021)
Summary: We conducted PrediXcan analysis of hydrocephalus risk in ten neurological tissues and whole blood. Decreased expression of MAEL in the brain was significantly associated (Bonferroni-adjusted p < 0.05) with hydrocephalus. PrediXcan analysis o
Externí odkaz:
https://doaj.org/article/f80596f420154b849b59ff8b720c8e14
Autor:
Joseph H. Miller, Michael J. Montalbano, Joel Raborn, Amber Gordon, Elias Rizk, R. Shane Tubbs, Hyunmi Kim, John C. Wellons, III
Publikováno v:
Translational Research in Anatomy, Vol 5, Iss , Pp 1-4 (2016)
Introduction: Hamartomas involving the floor of the fourth ventricle and cerebellum are rare, but can be associated with medically recalcitrant hemifacial spasm. These lesions present early in the neonatal or infantile period and respond well to surg
Externí odkaz:
https://doaj.org/article/1dd4c5efef08435b95021fa340cbccf7
Autor:
Sarah M. Tittman, Ashley M. Nassiri, Nauman F. Manzoor, Robert J. Yawn, Bret C. Mobley, John C. Wellons, III, Alejandro Rivas
Publikováno v:
Otolaryngology Case Reports, Vol 12, Iss , Pp - (2019)
Juvenile xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis, most often presenting with skin lesions of the head, neck, and upper trunk. Intracranial presentations have been previously described, however, due to its rarity, treatment algori
Externí odkaz:
https://doaj.org/article/13135c0d59da49a9b3458509e32e9027
Autor:
Philipp R Aldana, Ricardo A Hanel, Joseph Piatt, Sabrina H Han, Manisha M Bansal, Corinna Schultz, Cynthia Gauger, John M Pederson, John C Wellons III, Monica L Hulbert, Lori C Jordan, Adnan Qureshi, Kelsey Garrity, Adam P Robert, Asmaa Hatem, Jennifer Stein, Emily Beydler, P. David Adelson, Stephanie Greene, Paul Grabb, James Johnston, Shih‐Shan Lang, Jeffrey Leonard, Suresh N Magge, Alex Scott, Sanjay Shah, Edward R Smith, Jodi Smith, Jennifer Strahle, Sudhakar Vadivelu, Jennifer Webb, David Wrubel
Publikováno v:
Pediatric Blood & Cancer. 70
Autor:
Deborah X. Xie, Matthew M. Dedmon, MD, PhD, Brendan P. O'Connell, MD, Le Lucy He, MD, John C. Wellons, III, MD, MSPH, Alejandro Rivas, MD
Publikováno v:
Otolaryngology Case Reports, Vol 3, Iss C, Pp 7-9 (2017)
Vascular malformations of the central nervous system such as cavernous malformations and arteriovenous malformations are rare lesions with controversial management recommendations in the pediatric population. We report a case of a 3-year-old male who
Externí odkaz:
https://doaj.org/article/47156e2a72924ebe85384b68fb156cee
Publikováno v:
Pediatric neurosurgery. 39(2)
We report two cases of children with occult spinal dysraphism who were also found to have many associated brain anomalies seen in the Chiari II malformation. No previous report has commented on the possible association between the Chiari II malformat
Publikováno v:
Pediatric neurosurgery. 38(1)