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Titlebook: Barriers and Fluids of the Eye and Brain; Malcolm B. Segal Textbook 1992Latest edition Macmillan Publishers Limited 1992 pathophysiology.p

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Paolo Mori,Gabriele Lenzini,Steven Furnellorphological and physiological techniques of histological and ultrastructural analysis (Price ., 1976; James ., 1980; Diggs ., 1986) correlated with autoradiography (Strecker ., 1973, 1974), radioactive transfer measurements (James ., 1970, 1972) and cisternography, we have documented certain associ
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https://doi.org/10.1007/978-3-319-93354-2en shown that metaphit (1-1-(3-isothiocyanatophenyl-cyclohexylpiperidine), a derivative of PCP, in . studies irreversibly binds to the PCP site of PCP/NMDA (N-methyl-.-aspartate) receptor, presumably by an acylation process (Rafferty ., 1985). Recently, in . studies, metaphit has been found to induc
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https://doi.org/10.1007/978-3-030-49443-8ut not clonic seizures. However, at a dose of 10 mg/kg it acted as a convulsant agent (Hayes and Balster, 1985). PCP-like drugs, when evaluated with respect to potential anti/pro-convulsant actions, demonstrated only anticonvulsant properties. Modulation of the N-methyl-.-aspartate (NMDA) receptor s
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Yasser Rahrovani,Alain Pinsonneaults, 1983; Palfrey and Rao, 1983; Tas ., 1987). Scant attention, however, has been paid to the mammalian choroid plexus (CP) in regard to the function, or even the existence, of cation-Cl cotransport. Pharmacologic investigations of the CP-CSF system of intact animals have furnished evidence for catio
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Benjamin Müller,Sebastian Olbrichle outwardly after birth by doming of the skull. It progresses rapidly, with onset of symptoms appearing after weaning and death at 6–7 weeks of age. The purpose of this study was to determine the effects of hydrocephalus on cortical thickness and the developing microvasculature and cell density (ne
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Information Systems Security and Privacyating hydrophilic substrates from blood to brain extracellular and cerebrospinal fluids is markedly retarded, and it has been accepted that any molecule, above a limiting size, circulating in the blood may gain access to the brain interstitial space only if there is a specific transport system for t
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,Blood—Brain Barrier Permeability to Peptides and Proteins,ating hydrophilic substrates from blood to brain extracellular and cerebrospinal fluids is markedly retarded, and it has been accepted that any molecule, above a limiting size, circulating in the blood may gain access to the brain interstitial space only if there is a specific transport system for t
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