Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mark S. O'Brien"'
Autor:
Michael Gelsomino, Ambre’ L. Pownall, Eylem Ocal, Mark S O'Brien, Blake C. Phillips, Gregory W. Albert, Horace J. Spencer
Publikováno v:
Journal of Neurosurgery: Pediatrics. 14:167-172
Object Many patients with myelomeningocele (MMC) develop hydrocephalus, and most will undergo CSF diversion. The goal of this retrospective study was to determine whether there was a change in the shunt rate over the 7 consecutive years of the study.
Autor:
Blake C, Phillips, Michael, Gelsomino, Ambre' L, Pownall, Eylem, Ocal, Horace J, Spencer, Mark S, O'Brien, Gregory W, Albert
Publikováno v:
Journal of neurosurgery. Pediatrics. 14(2)
Many patients with myelomeningocele (MMC) develop hydrocephalus, and most will undergo CSF diversion. The goal of this retrospective study was to determine whether there was a change in the shunt rate over the 7 consecutive years of the study. The au
Autor:
Beth C. Vogel, Ian R. Crocker, Thad T. Ghim, Nicolas Krawiecki, Patricia C. Davis, Mark S. O'Brien, Lillian R. Meacham, Joseph Petronio
Publikováno v:
Medical and Pediatric Oncology. 29:86-91
Endocrine dysfunction can be challenging to diagnose in children treated for brain tumors. Treatments are available for hormonal replacement and when necessary, hormonal suppression. Without these endocrine treatment regimens, life can be unnecessari
Autor:
Mark E. Harris, Mark S. O’Brien
Publikováno v:
Neurosurgery Clinics of North America. 4:625-632
The majority of infants presenting with progressive hydrocephalus are now treated surgically with ventricular shunting. It is difficult to predict the eventual developmental outcome of most treated patients. This article reviews the results of surgic
Publikováno v:
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus. 13(1)
Papilledema is considered one of the cardinal ophthalmologic signs of shunt failure. However, the prevalence of papilledema in children with shunt malfunction has not been systematically investigated. The purpose of this study is to determine the sen
Autor:
Ali F. Krisht, Mark S. O'Brien
Publikováno v:
Neurosurgery. 30:798-800
Arachnoid cysts are neurosurgical entities that have long been considered to be congenital in origin. Many examples in the literature suggest that there is a subgroup of arachnoid cysts that are required. The authors present the clinical history of a
Publikováno v:
Annals of Neurology. 7:340-343
Familial congenital spinal arachnoid cysts causing progressive paraplegia are reported in two adolescent siblings as part of a hereditary syndrome. The other features of this unusual dominantly inherited disorder include double rows of eyelashes, par
Publikováno v:
Pediatric Neurosurgery. 11:242-249
A case of Arnold-Chiari malformation (Chiari type II) is reported to describe the usefulness of metrizamide cisternography in the diagnosis and management of this condition.
Publikováno v:
Neurosurgery. 23:465-482
In this report we have discussed the complications of surgery for subdural hematoma. The complications are varied and many depend primarily on the type of treatment required by the patient. We have considered the problems associated with: percutaneou
Publikováno v:
Child's Nervous System. 4:244-248
A newborn baby girl with intracranial extracerebral glioneural (brain) heterotopia in the right frontoparietal area is described. The heterotopic brain was predominantly composed of neuronal and glial elements, with partial cerebellar differentiation