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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Agricultural Economics 1 (1987), S. 273-290 
    ISSN: 0169-5150
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Economics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Alimentary pharmacology & therapeutics 3 (1989), S. 0 
    ISSN: 1365-2036
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: A large number of clinical studies have been performed to establish the safety and efficacy of H2-receptor antagonist therapy. Few if any of these studies have attempted to address the rationale for the dosage and/or dosage regimens being studied. This study is the first large-scale clinical trial, the purpose of which is to validate the chosen regimen and to address the issue of an optimal therapy for a specific patient population. A regimen of a single nightly dosage is generally acknowledged to offer the potential for improved patient compliance. Furthermore, recent research had suggested that suppression of nocturnal acid secretion is all that is required to heal duodenal ulcers. Hence such a regimen offered the potential for an effective lowered dosage of cimetidine with minimal interference with gastric physiology, increased safety and substantial efficacy. This multicentre, double-blind, placebo-controlled trial therefore evaluated a 4-week course of single night-time dosage of cimetidine. After 4 weeks of treatment the cumulative, endoscopically proven, ulcer healing rate with an 800 mg regimen was 73%, which was statistically higher and significantly superior to the 41% healing seen with placebo (P 〈 0.001). The 400 mg nocte dosage regimen of cimetidine normally used as maintenance therapy was significantly inferior to the 800 mg nocte regimen (P = 0.01), and increasing the dosage to 1600 mg nocte for 4 weeks failed to provide a significant improvement in healing over the 800 mg nocte regimen. This 800 mg nocte regimen provided rapid pain relief, with 75 YO of the patients being free of night-time pain and 65% free of day-time pain, by the end of the first week. The 400 mg ‘maintenance dosage’ was unable to provide this degree of rapid, complete and early relief to patients with a duodenal ulcer. Furthermore, increasing the dosage to 1600 mg nocte failed to increase the level of early pain relief significantly, perhaps because the extensive response of duodenal ulcer patients to the 800 mg nocte regimen leaves little room for improvement. Based both on the early symptom relief and the ulcer healing rate during 4 weeks of treatment, it is concluded that an 800 mg night-time dosage of cimetidine may be an optimal regimen for many duodenal ulcer patients, particularly those who in the physician's opinion will benefit from a once-daily regimen.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    World Development 14 (1986), S. 1253-1267 
    ISSN: 0305-750X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Geography , Political Science , Sociology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    World Development 15 (1987), S. 1179-1187 
    ISSN: 0305-750X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Geography , Political Science , Sociology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Selecta mathematica 3 (1997), S. 303-314 
    ISSN: 1420-9020
    Keywords: Key words. $ ({\frak g}, K) $-modules, Cohen-Macaulay categories, Grothendieck duality.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Abstract. Let $ ({\frak g}, K) $ be a Harish-Chandra pair. In this paper we prove that if P and P' are two projective $ ({\frak g}, K) $ -modules, then Hom(P, P') is a Cohen-Macaulay module over the algebra $ {\cal Z}({\frak g}, K) $ of K-invariant elements in the center of $ U({\frak g}) $ . This fact implies that the category of $ ({\frak g}, K) $ -modules is locally equivalent to the category of modules over a Cohen-Macaulay algebra, where by a Cohen-Macaulay algebra we mean an associative algebra that is a free finitely generated module over a polynomial subalgebra of its center.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Selecta mathematica 5 (1999), S. 1-28 
    ISSN: 1420-9020
    Keywords: Key words. Representation theory, automorphic forms.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Abstract. Let G be the group of points of a split reductive algebraic group G over a local field k and let X = G / U where U is the group of k-points of a maximal unipotent subgroup of G. In this paper we construct a certain canonical G-invariant space ${\cal S}(X)$ (called the Schwartz space of X) of functions on X, which is an extension of the space of smooth compactly supported functions on X. We show that the space of all elements of $ {\cal S}(X)^I $ , which are invariant under the Iwahori subgroup I of G, coincides with the space generated by the elements of the so called periodic Lusztig basis, introduced recently by G. Lusztig (cf. [10] and [11]). We also give an interpretation of this space in terms of a certain equivariant K-group (this was also done by G. Lusztig — cf. [12]). Finally we present a global analogue of $ {\cal S}(X) $ , which allows us to give a somewhat non-traditional treatment of the theory of the principal Eisenstein series.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Transformation groups 2 (1997), S. 31-56 
    ISSN: 1531-586X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Abstract This paper is devoted to a systematic study of quantum completely integrable systems (i.e., complete systems of commuting differential operators) from the point of view of algebraic geometry. We investigate the eigenvalue problem for such systems and the correspondingD-module when the eigenvalues are in generic position. In particular, we show that the differential Galois group of this eigenvalue problem is reductive at generic eigenvalues. This implies that a system is algebraically integrable (i.e., its eigenvalue problem is explicitly solvable in quadratures) if and only if the differential Galois group is commutative for generic eigenvalues. We apply this criterion of algebraic integrability to two examples: finite-zone potentials and the elliptic Calogero-Moser system. In the second example, we obtain a proof of the Chalyh-Veselov conjecture that the Calogero-Moser system with integer parameter is algebraically integrable, using the results of Felder and Varchenko.
    Type of Medium: Electronic Resource
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  • 8
    Publication Date: 2014-09-10
    Description: Adolescent idiopathic scoliosis (AIS) causes spinal deformity in 3% of children. Despite a strong genetic basis, few genes have been associated with AIS and the pathogenesis remains poorly understood. In a genome-wide rare variant burden analysis using exome sequence data, we identified fibrillin-1 ( FBN1 ) as the most significantly associated gene with AIS. Based on these results, FBN1 and a related gene, fibrillin-2 ( FBN2 ), were sequenced in a total of 852 AIS cases and 669 controls. In individuals of European ancestry, rare variants in FBN1 and FBN2 were enriched in severely affected AIS cases (7.6%) compared with in-house controls (2.4%) (OR = 3.5, P = 5.46 x 10 –4 ) and Exome Sequencing Project controls (2.3%) (OR = 3.5, P = 1.48 x 10 –6 ). Scoliosis severity in AIS cases was associated with FBN1 and FBN2 rare variants ( P = 0.0012) and replicated in an independent Han Chinese cohort ( P = 0.0376), suggesting that rare variants may be useful as predictors of curve progression. Clinical evaluations revealed that the majority of AIS cases with rare FBN1 variants do not meet diagnostic criteria for Marfan syndrome, though variants are associated with tall stature ( P = 0.0035) and upregulation of the transforming growth factor beta pathway. Overall, these results expand our definition of fibrillin-related disorders to include AIS and open up new strategies for diagnosing and treating severe AIS.
    Print ISSN: 0964-6906
    Electronic ISSN: 1460-2083
    Topics: Biology , Medicine
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  • 9
    Publication Date: 2014-10-14
    Keywords: Secondary prevention, Other hypertension, Exercise/exercise testing/rehabilitation
    Electronic ISSN: 1524-4539
    Topics: Medicine
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  • 10
    Publication Date: 2015-06-17
    Description: Background— ACTA2 mutations are the major cause of familial thoracic aortic aneurysms and dissections. We sought to characterize these aortic diseases in a large case series of individuals with ACTA2 mutations. Methods and Results— Aortic disease, management, and outcome associated with the first aortic event (aortic dissection or aneurysm repair) were abstracted from the medical records of 277 individuals with 41 various ACTA2 mutations. Aortic events occurred in 48% of these individuals, with the vast majority presenting with thoracic aortic dissections (88%) associated with 25% mortality. Type A dissections were more common than type B dissections (54% versus 21%), but the median age of onset of type B dissections was significantly younger than type A dissections (27 years versus 36 years). Only 12% of aortic events were repair of ascending aortic aneurysms, which variably involved the aortic root, ascending aorta, and aortic arch. Overall, cumulative risk of an aortic event at age 85 years was 0.76 (95% confidence interval, 0.64–0.86). After adjustment for intrafamilial correlation, sex and race, mutations disrupting p.R179 and p.R258 were associated with significantly increased risk for aortic events, whereas p.R185Q and p.R118Q mutations showed significantly lower risk of aortic events compared with other mutations. Conclusions— ACTA2 mutations are associated with high risk of presentation with an acute aortic dissection. The lifetime risk for an aortic event is only 76%, suggesting that additional environmental or genetic factors play a role in expression of aortic disease in individuals with ACTA2 mutations.
    Keywords: Clinical genetics, CV surgery: aortic and vascular disease
    Print ISSN: 1942-325X
    Electronic ISSN: 1942-3268
    Topics: Medicine
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