Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Richard G. Curless"'
Publikováno v:
Pediatric Neurology. 26:374-378
Five children with brainstem tumors and two control patients had magnetic resonance spectroscopy studies of the brainstem. Two of the malignant tumor patients had magnetic resonance spectroscopy studies before and after radiation therapy. The third w
Autor:
M. Chaneles, T. Dubrovsky, M. J. D. Post, Carol K. Petito, N. Altman, Charles D. Wood, D. Start, Richard G. Curless, G. Scott
Publikováno v:
Neurology. 51:560-565
Objective: To identify cerebral aneurysmal arteriopathy in children with longstanding AIDS.Background: Five cases are described from the authors' experience, and eight additional cases are reviewed from the literature. Details are presented in regard
Autor:
Steven Falcone, Richard G. Curless, Carol K. Petito, R. Michael Siatkowski, Elena Pegoraro, Richard J. Kanoff
Publikováno v:
Pediatric Neurology. 18:76-80
Walker-Warburg syndrome is an autosomal-recessive genetic disorder characterized by congenital muscular dystrophy in association with complex developmental abnormalities of the central nervous system and the eyes. Two patients with Walker-Warburg syn
Autor:
Makram R. Ebeid, Eric P. Hoffman, J. L. Baquero, W. G. Feero, Richard G. Curless, Jianzhou Wang, R. A. Ayala
Publikováno v:
Annals of Neurology. 37:408-411
A patient is presented with hyperkalemic periodic paralysis (HyperPP) and a cardiac dysrhythmia. An amino acid substitution (Val783Ile) in the adult skeletal muscle sodium channel gene was detected. Although lack of available family members precluded
Publikováno v:
Pediatric Neurology. 26:219-221
Hematogenous brain metastases are uncommon in childhood. Three patients and a literature review that includes centers reporting up to 36 years of experience are presented in this study. The total of 2,040 patients includes our three examples of one n
Publikováno v:
Cancer Genetics and Cytogenetics. 44:263-269
Bone marrow monosomy 7 is the most frequent karyotypic abnormality found in patients with chronic myeloproliferative disorders. To a review of 46 previously reported pediatric patients we add three additional cases. Clinical presentation is usually d
Publikováno v:
Pediatric Neurology. 18:269-271
Three of ten children with optic gliomas satisfy the 1987 National Institutes of Health consensus criteria for neurofibromatosis type 1 (NF-1). The diagnosis in these cases is based on the presence of café-au-lait skin lesions in addition to the opt
Autor:
Richard G. Curless, Debra A. Katz, William J. Weiner, Jeffrey Gelblum, Richard A. Perryman, Peter L. Ferrer
Publikováno v:
The Journal of Pediatrics. 124:737-739
Choreoathetosis developed in three patients after cardiopulmonary bypass with hypothermia. None had significant hypotension or hypoxemia; all had hypocapnia and respiratory alkalosis during the rewarming period. We postulate that hypocapnia-induced c
Autor:
Glenn Morrison, Jonathan R. Jagid, Jocelyn H. Bruce, Alireza Minagar, Richard G. Curless, John Ragheb, Steven Falcone, Rita L. Romaguera
Publikováno v:
Clinical neurology and neurosurgery. 103(1)
Objective and importance: Adrenocortical carcinoma (ACC) is rare in the pediatric population, and brain metastasis seldom occurs. Clinical presentation: The authors report a case of metastatic ACC to the brain in a 9-year-old patient who had an adren
Publikováno v:
Pediatric Neurology. 8:151-153
An 18-year-old Hispanic female developed symptoms of a Histoplasma capsulatum infection at 912 years of age. Initial problems of ataxia and hydrocephalus were followed by seizures and a cranial nerve palsy which developed over several years. T 1 -wei