Floyd H. Gilles, MD, University of Chicago

Affiliations: 
Neuropathology Childrens Hospital Los Angeles, Los Angeles, CA, United States 
Area:
Pathology of brain tumors. Fetal and Pediatric Neuropathology
Website:
http://www.chla.org/site/apps/kb/cs/contactdisplay.asp?c=ipINKTOAJsG&b=3832751&sid=7pLHJZMxHcKSIWOrEkG&r=1
Google:
"Floyd Gilles"
Bio:

http://www.chla.org/site/apps/nlnet/content2.aspx?c=ipINKTOAJsG&b=3793521&ct=7129815

https://my.usc.edu/wp/faculty/ViewDetail.do?uscpvid=scgz3sx6

Mean distance: 16.69 (cluster 24)
 
SNBCP
Cross-listing: Neuropathology Tree

BETA: Related publications

Publications

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Gilles FH, Leviton A. (2020) Neonatal white matter damage and the fetal inflammatory response. Seminars in Fetal & Neonatal Medicine. 101111
Gilles F, Gressens P, Dammann O, et al. (2017) Hypoxia-ischemia is not an antecedent of most preterm brain damage: the illusion of validity. Developmental Medicine and Child Neurology
Bouffet E, Allen JC, Boyett JM, et al. (2015) The influence of central review on outcome in malignant gliomas of the spinal cord: the CCG-945 experience. Journal of Neurosurgery. Pediatrics. 1-7
Blüml S, Margol AS, Sposto R, et al. (2015) Molecular subgroups of medulloblastoma identification using noninvasive magnetic resonance spectroscopy. Neuro-Oncology
Shiroishi MS, Panigrahy A, Moore KR, et al. (2015) Combined MRI and MRS improves pre-therapeutic diagnoses of pediatric brain tumors over MRI alone. Neuroradiology. 57: 951-6
Margol AS, Robison NJ, Gnanachandran J, et al. (2015) Tumor-associated macrophages in SHH subgroup of medulloblastomas. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 21: 1457-65
Xu J, Margol AS, Shukla A, et al. (2015) Disseminated medulloblastoma in a child with germline BRCA2 6174delT mutation and without Fanconi anemia Frontiers in Oncology. 5
Erdreich-Epstein A, Robison N, Ren X, et al. (2014) PID1 (NYGGF4), a new growth-inhibitory gene in embryonal brain tumors and gliomas. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 20: 827-36
Shaaban S, Ramos-Platt L, Gilles FH, et al. (2013) RYR1 mutations as a cause of ophthalmoplegia, facial weakness, and malignant hyperthermia. Jama Ophthalmology. 131: 1532-40
Paquette LB, Wisnowski JL, Ceschin R, et al. (2013) Abnormal cerebral microstructure in premature neonates with congenital heart disease. Ajnr. American Journal of Neuroradiology. 34: 2026-33
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