Zobrazeno 1 - 10
of 239
pro vyhledávání: '"Laurence E. Becker"'
Autor:
Jonathan L. Finlay, Peter C. Burger, Ian F. Pollack, Floyd H. Gilles, Allen J. Yates, Jeffrey C. Allen, Richard L. Davis, Laurence E. Becker, Eric Bouffet, James M. Boyett
Publikováno v:
Journal of Neurosurgery: Pediatrics. 17:453-459
OBJECT The impact of central pathology review on outcome has been described in pediatric patients with high-grade glioma (HGG). The objective of this report was to analyze the impact of the central pathology review on outcome in the subgroup of patie
Autor:
Sylvain Baruchel, Mark W. Kieran, Giannoula Klement, Robert S. Kerbel, Laurence E. Becker, Christof Senger, Benjamin Gesundheit
Publikováno v:
Medical and Pediatric Oncology. 41:516-526
Background The clinical manifestations of childhood pilocytic astrocytoma (PA) and anaplastic astrocytoma (AA) markedly differ, especially in the time to progression and prognosis. Because of the aggressive course and poor survival rate of AA, one wo
Autor:
John W. Haycock, Oleh Hornykiewicz, Lee Ang, Laurence E. Becker, Stephen J. Kish, Yoshiaki Furukawa
Publikováno v:
Journal of Neurochemistry. 87:574-585
Because age-related changes in brain dopaminergic innervation are assumed to influence human disorders involving dopamine (DA), we measured the levels of several presynpatic DAergic markers [DA, homovanillic acid, tyrosine hydroxylase (TH), aromatic
Autor:
Peter C. Burger, Ian F. Pollack, Gregor Dueckers, Laurence E. Becker, Maryam Fouladi, Allen J. Yates, Daniel Hunt, Floyd H. Gilles, Jonathan L. Finlay, James M. Boyett, Richard L. Davis
Publikováno v:
Cancer. 98:1243-1252
BACKGROUND The objectives of the current study were to determine the outcome of children who were treated with chemotherapy and radiotherapy on the Children's Cancer Group (CCG) high-grade glioma protocol (CCG-945) who were diagnosed with low-grade g
Autor:
Michael S. Salman, J. Raymond Buncic, Elise Heon, Laurence E. Becker, Carol A. Westall, Susan Blaser
Publikováno v:
Scopus-Elsevier
Pontocerebellar hypoplasia type 1 is a rare disease characterized by pontocerebellar hypoplasia and anterior horn cell degeneration. The oldest reported child died at the age of 26 months. Two siblings were diagnosed with pontocerebellar hypoplasia t
Autor:
Mark T Mackay, James T. Rutka, Laurence E. Becker, Bruria Ben-Zeev, Hiroshi Otsubo, N. A. Chuang, O. C. Snead, S. H. Chuang, Shelly K. Weiss
Publikováno v:
Neurology. 60:580-587
Background: Balloon cells are a key feature of tuberous sclerosis (TS) but are also seen in focal cortical dysplasia (FCD). The authors compare the clinical and MRI characteristics in children with medically refractory localization-related epilepsy w
Publikováno v:
Journal of Neurochemistry. 65:636-642
Although much evidence has implicated polyamines in brain development and function, little information is available on these substances in human brain. We examined the influence of regional distribution and aging on putrescine, spermidine, and spermi
Publikováno v:
Acta Neuropathologica. 104:418-424
Cerebral cortical lesions of tuberous sclerosis (TSC) and focal cortical dysplasia (FCD) show disturbances in laminar architecture and cellular differentiation. We immunohistochemically studied the expression of doublecortin, a fetal neuronal protein
Autor:
Laurence E. Becker, Peter C. Burger, Naji Aldosari, Sandra H. Bigner, Roger E. McLendon, James L. Kepner, Henry S. Friedman
Publikováno v:
Archives of Pathology & Laboratory Medicine. 126:540-544
Context.—Brain tumors are the most common solid tumor in childhood, and medulloblastoma is the most common malignant brain tumor in this age group. Cytogenetic abnormalities that have been described in childhood medulloblastoma include loss of 17p,