Zobrazeno 1 - 10
of 334
pro vyhledávání: '"Laurence E. Becker"'
Autor:
Takashima, Sachio
Publikováno v:
Neuropathology. Dec2002, Vol. 22 Issue 4, p367-368. 2p.
Autor:
Sachio Takashima
Publikováno v:
Neuropathology. 22:367-368
Autor:
Harvey B. Sarnat
Publikováno v:
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 23:236-237
Akademický článek
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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