Search results for "Oct"

showing 10 items of 3052 documents

Taenia asiatica: the Most Neglected Human Taenia and the Possibility of Cysticercosis

2013

Not only Taenia solium and Taenia saginata, but also Taenia asiatica infects humans. The last species is not included in the evaluation of the specificity of the immunodiagnostic techniques for taeniasis/cysticercosis. There is currently no specific immunodiagnostic method for T. asiatica available. Therefore, due to the fact that molecular techniques (the only tool to distinguish the 3 Taenia species) are normally not employed in routine diagnostic methods, the 2 questions concerning T. asiatica (its definite geographic distribution and its ability to cause human cysticercosis), remain open, turning T. asiatica into the most neglected agent of human taeniasis-cysticercosis.

Diagnostic methodshuman taeniasisArticles from Symposium on Asian Taenia (October 2011 Osong Korea)Taenia soliumTaenia soliummedicineHelminthsTaeniasisAnimalsHumansTaeniasisTaenia asiaticabiologyTaeniaClinical Laboratory TechniquescysticercosisNeglected DiseasesCysticercosisTaenia saginatabiology.organism_classificationmedicine.diseaseVirologyTaenia asiaticamedicine.drug_formulation_ingredientInfectious DiseasesParasitologyTaeniaParasitologyThe Korean Journal of Parasitology
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Subcutaneous octreotide versus oral loperamide in the treatment of diarrhea following chemotherapy

1993

Forty patients with chemotherapy-related diarrhea were randomized to receive (i) octreotide 0.5 mg three times per day s.c. or (ii) loperamide 4 mg three times per day p.o. until complete remission of diarrhea was achieved. In the octreotide group 80% of patients showed complete resolution of loose bowel movements within 4 days of therapy, while in the loperamide group this goal was obtained in only 30% of cases (p < 0.001). If after 4 days no benefit was seen, patients were considered to have failed antidiarrheal therapy. Failure was recorded in only one case (5%) treated with s.c. octreotide and in five patients (25%) who received loperamide. The mean duration of antidiarrheal therapy nec…

DiarrheaMaleLoperamidemedicine.medical_specialtyAbdominal painCancer Researchmedicine.medical_treatmentInjections SubcutaneousOctreotideAdministration OralOctreotideGastroenterologyLoperamidelaw.inventionRandomized controlled triallawChemotherapy-related diarrheaInternal medicineNeoplasmsAntineoplastic Combined Chemotherapy ProtocolsMedicineHumansPharmacology (medical)PharmacologyChemotherapybusiness.industryMiddle AgedClinical trialDiarrheaEndocrinologyOncologyChemotherapy-related diarrhea; Loperamide; Octreotide; Cancer Research; Oncology; PharmacologyDefecationFemalemedicine.symptombusinessmedicine.drug
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An unusual case of chronic diarrhea: a case report

2022

Gastroenteropancreatic-neuroendocrine neoplasms or tumors (GEP-NEN or NETs) are rare tumors arising from the diffuse neuroendocrine system. This clinical case highlights the complexity of the diagnostic process and the difficulties in interpreting the examinations for this type of tumor, showing how the negativity of firstlevel examinations did not prevent from performing further investigations, in the presence of a suggestive clinical presentation. The search of similar cases in the published literature suggests that this represents an unusual presentation of a NET.

DiarrheaSettore MED/09 - Medicina InternaPositron-Emission TomographyPositron Emission Tomography Computed TomographyEmergency MedicineInternal MedicineHumansOctreotide68Gallium-DOTATOC PET/CT Chromogranin A Diarrhea Gastroenteropancreatic-neuroendocrine tumor
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CCDC 142834: Experimental Crystal Structure Determination

2001

Related Article: R.Broussier, E.Bentabet, M.Laly, P.Richard, L.G.Kuz'mina, P.Serp, N.Wheatley, P.Kalck, B.Gautheron|2000|J.Organomet.Chem.|613|77|doi:10.1016/S0022-328X(00)00501-5

Dichloro-(22'33'44'55'-octamethyl-1-diphenylphosphino-1'-(diphenylphosphine sulfide)ferrocene-PS)-palladium(ii) dichloromethane solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Selective, homogeneous hydrogenation of cycloheptatriene to cycloheptene catalyzed by (η4-cycloocta-1,5-diene)(η6-cyclohepta-1,3,5-triene)ruthenium(0)

1980

Abstract In the presence of small amounts of [Ru(η 4 -COD)](η 6 -C 8 H 10 )] (1), cycloheptatriene is hydrogenated to cycloheptene, under one atmosphere of hydrogen at room temperature in homogeneous phase. The formation of a small amount of cyclooctene and the existence of an induction period, which do not occur when [Ru(η 4 -COD)(η 6 -C 7 H 8 )] (2) is used as the catalyst, suggest that 2 is the real catalyst. The selectivity of this hydrogenation is 100% in n-hexane as solvent, 99.5% in THF, and low in ethanol. Conversion is quantitative in THF and ethanol, but not more than 65% in n-hexane. In the presence of 1 or 2, cycloheptene is rapidly hydrogenated to cycloheptane in THF and ethano…

DieneInduction periodOrganic Chemistrychemistry.chemical_elementCycloheptatrienePhotochemistryBiochemistryMedicinal chemistryCatalysisRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryCycloocteneMaterials ChemistryCycloheptenePhysical and Theoretical ChemistryCycloheptaneJournal of Organometallic Chemistry
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Selective homogeneous hydrogenation of cycloocta-1,5, and cycloocta-1,3-diene to cyclooctene in the presence of (η4-cycloocta-1,5-diene)(η6-cycloocta…

1983

Cyclooctadiene isomers (1,3- and 1,5-COD) are selectively, homogenously hydrogenated to cyclooctene (C8H14) in tetrahydrofuran (THF) solution, under mild conditions of temperature (20 °C) and hydrogen pressure (1 atm), in the presence of catalytic amounts of (cycloocta-1,5-diene)(cycloocta-1,3,5,-triene)ruthenium(0), [Ru(η4-COD)(η6-C8H10)] (1). The rate of hydrogenation is higher when 1,3-COD is the substrate. Evidence for the isomerization 1,5-COD → 1,3-COD is reported. Similar studies carried out in several alcoholic solutions, although showing a decreased selectivity in the hydrogenation, confirm the isomerization 1,5-COD → 1,3-COD, and allow a discrimination between the isomerization an…

DieneNorbornadienechemistry.chemical_elementNoyori asymmetric hydrogenationPhotochemistryMedicinal chemistryCatalysisRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryCycloocteneMaterials ChemistryPhysical and Theoretical ChemistryIsomerizationCyclooctadieneInorganica Chimica Acta
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CCDC 894411: Experimental Crystal Structure Determination

2013

Related Article: S.Fustero, P.Bello, J.Miro, M.Sanchez-Rosello, M.A.Maestro, J.Gonzalez, C.del Pozo|2013|Chem.Commun.|49|1336|doi:10.1039/c2cc37796a

Diethyl 10-methoxy-1-(4-methoxyphenyl)-26-bis(trifluoromethyl)-233a3b45611b-octahydro-1H-dipyrrolo[12-a:3'2'-c]quinoline-26-dicarboxylateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Achieving branched polyethylene waxes by aryliminocycloocta[b]pyridylnickel precatalysts: Synthesis, characterization, and ethylene polymerization

2017

Cycloocta[b]pyridin-10-one was prepared to form the corresponding imino derivatives, which then reacted with (DME)NiBr2 to form 10-aryliminocycloocta[b]pyridylnickel bromides (Ni1–Ni5). The new compounds were characterized by means of FT-IR spectroscopy as well as elemental analysis and the organic ligands were also analyzed by the NMR measurements. Furthermore, the molecular structure of a representative complex Ni3 was determined by the single crystal X-ray diffraction, indicating the distorted tetrahedral geometry around the nickel atom. Upon the activation with either methylaluminoxane (MAO) or diethylaluminium chloride (Et2AlCl), the title nickel complexes exhibited high activity in et…

Diethylaluminium chloridePolymers and Plastics010405 organic chemistryChemistryOrganic ChemistryDispersityMethylaluminoxaneCationic polymerizationnickel complexPolyethylene010402 general chemistryBranching (polymer chemistry)01 natural sciences0104 chemical scienceschemistry.chemical_compoundPolymerization10-aryliminocycloocta[b]pyridinePolymer chemistryMaterials ChemistryCoordination polymerizationcationic polymerizationpolyethyl-eneJournal of Polymer Science Part A-Polymer Chemistry
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New conditions for the generation of dianions of carboxylic acids

1998

Abstract Lithium carboxylic acid enediolates are generated efficiently using lithium amides prepared from thienyllithium or butyllithium and either diethylamine, piperazine, N,N′-dibenzylethylenediamine, N-benzylpiperazine or 1,3,3-trimethyl-6-azabicyclo[3.2.1]octane, even in catalytic amounts.

Diethylaminechemistry.chemical_classificationCarboxylic acidOrganic Chemistrychemistry.chemical_elementBiochemistryCatalysischemistry.chemical_compoundPiperazinechemistryDrug DiscoveryButyllithiumOrganic chemistryLithiumOctaneTetrahedron Letters
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Compressibility Systematics of Calcite-Type Borates: An Experimental and Theoretical Structural Study on ABO(3) (A = Al, Sc, Fe, and In)

2014

The structural properties of calcite-type orthoborates ABO(3) (A = Al, Fe, Sc, and In) have been investigated at high pressures up to 32 GPa. They were studied experimentally using synchrotron powder X-ray diffraction and theoretically by means of ab initio total-energy calculations. We found that the calcite-type structure remains stable up to the highest pressure explored in the four studied compounds. Experimental and calculated static geometries (unit-cell parameters and internal coordinates), bulk moduli, and their pressure derivatives are in good agreement. The compressibility along the c axis is roughly three times that along the a axis. Our data clearly indicate that the compressibi…

DiffractionAb initioThermodynamicschemistry.chemical_elementCrystal structureHigh-pressure behaviorchemistry.chemical_compoundstructure carbonatesCationshigh pressure behavior; augmented-wave method; structure carbonatesPhysical and Theoretical ChemistryBoronCalciteCrystal-structuresMetal refinementOxidesFeBO3Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyGeneral Energyhigh pressure behaviorchemistryOctahedronAugmented-wave methodFISICA APLICADATransitionCompressibilityaugmented-wave methodCarbonateStructure carbonates
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