998 resultados para Jackson, Helen Hunt, 1830-1885.


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Vol. 2 has imprint: Wiesbaden, J.F. Bergmann; New York, B. Westermann & Co.; [etc., etc.]; v. 3: Wiesbaden, C.W. Kreidel; New York, L.W. Schmidt; [etc., etc.]

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Editors: 1865-74, H. Hirzel, H. Gretschel; 1875-82, H. Gretschel, G. Wunder; 1883-1901, G. Bornemann (with H. Gretshcel, 1883-92; A. Berberich, Otto Müller, 1892-1901).

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Available on demand as hard copy or computer file from Cornell University Library.

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Available on demand as hard copy or computer file from Cornell University Library.

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Mode of access: Internet.

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Mode of access: Internet.

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Mode of access: Internet.

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Back Row: Don Dufek, Charley Lentz, Don McClelland, Chuck Ortmann, Harry Allis, Dick Farrer

4th Row: Manager Bill Hicky, John Ghindia, Bill Bartlett, Leo Koceski, Bob VanSummern, Dick Kempthorn, Bill Ohlenroth, Al Jackson, Jim Hunt (Trainer)

3rd Row: Bob Erben, Wally Teninga, Jim Atchison, Bob Hollway, Al Wahl, Ozzie Clark, Irv Wisniewski, Don Peterson

2nd Row: Lloyd Heneveld, Dan Dworsky, Ralph Kohl, Dick Rifenburg, Quentin Sickels, Don Hershberger, Ed McNeill

Front Row: Pete Elliott, Gene Derricotte, Athletic Director Fritz Crisler, Dom Tomasi, Coach Bennie Oosterbaan, Alvin Wistert, Stu Wilkins, Joe Soboleski

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AIM To develop a short, enhanced functional ability Quality of Vision (faVIQ) instrument based on previous questionnaires employing comprehensive modern statistical techniques to ensure the use of an appropriate response scale, items and scoring of the visual related difficulties experienced by patients with visual impairment. METHODS Items in current quality-of-life questionnaires for the visually impaired were refined by a multi-professional group and visually impaired focus groups. The resulting 76 items were completed by 293 visually impaired patients with stable vision on two occasions separated by a month. The faVIQ scores of 75 patients with no ocular pathology were compared to 75 age and gender matched patients with visual im pairm ent. RESULTS Rasch analysis reduced the faVIQ items to 27. Correlation to standard visual metrics was moderate (r=0.32-0.46) and to the NEI-VFQ was 0.48. The faVIQ was able to clearly discriminate between age and gender matched populations with no ocular pathology and visual impairment with an index of 0.983 and 95% sensitivity and 95% specificity using a cut off of 29. CONCLUSION The faVIQ allows sensitive assessm ent of quality-of-life in the visually im paired and should support studies which evaluate the effectiveness of low vision rehabilitation services. © Copyright International Journal of Ophthalmology Press.

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Introduction: Patients with rheumatoid arthritis (RA) have increased risk of cardiovascular (CV) events. We sought to test the hypothesis that due to increased inflammation, CV disease and risk factors are associated with increased risk of future RA development. Methods: The population-based Nord-Trøndelag health surveys (HUNT) were conducted among the entire adult population of Nord-Trøndelag, Norway. All inhabitants 20 years or older were invited, and information was collected through comprehensive questionnaires, a clinical examination, and blood samples. In a cohort design, data from HUNT2 (1995-1997, baseline) and HUNT3 (2006-2008, follow-up) were obtained to study participants with RA (n = 786) or osteoarthritis (n = 3,586) at HUNT3 alone, in comparison with individuals without RA or osteoarthritis at both times (n = 33,567). Results: Female gender, age, smoking, body mass index, and history of previous CV disease were associated with self-reported incident RA (previous CV disease: odds ratio 1.52 (95% confidence interval 1.11-2.07). The findings regarding previous CV disease were confirmed in sensitivity analyses excluding participants with psoriasis (odds ratio (OR) 1.70 (1.23-2.36)) or restricting the analysis to cases with a hospital diagnosis of RA (OR 1.90 (1.10-3.27)) or carriers of the shared epitope (OR 1.76 (1.13-2.74)). History of previous CV disease was not associated with increased risk of osteoarthritis (OR 1.04 (0.86-1.27)). Conclusion: A history of previous CV disease was associated with increased risk of incident RA but not osteoarthritis.

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Obesity is heritable and predisposes to many diseases. To understand the genetic basis of obesity better, here we conduct a genome-wide association study and Metabochip meta-analysis of body mass index (BMI), a measure commonly used to define obesity and assess adiposity, in up to 339,224 individuals. This analysis identifies 97 BMI-associated loci (P < 5 × 10−8), 56 of which are novel. Five loci demonstrate clear evidence of several independent association signals, and many loci have significant effects on other metabolic phenotypes. The 97 loci account for ~2.7% of BMI variation, and genome-wide estimates suggest that common variation accounts for >20% of BMI variation. Pathway analyses provide strong support for a role of the central nervous system in obesity susceptibility and implicate new genes and pathways, including those related to synaptic function, glutamate signalling, insulin secretion/action, energy metabolism, lipid biology and adipogenesis.