Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Diana Curtis"'
Autor:
Rebecca K. Sripada, Cassaundra L. Peterson, John J. Dziak, Inbal Nahum-Shani, Erika M. Roberge, Amber A. Martinson, Katherine Porter, Peter Grau, Diana Curtis, Sydney McElroy, Sarah Bryant, Isabel Gracy, Cosette Pryor, Heather M. Walters, Karen Austin, Carolina Ehlinger, Nina Sayer, Shannon Wiltsey-Stirman, Kathleen Chard
Publikováno v:
Trials, Vol 24, Iss 1, Pp 1-18 (2023)
Abstract Background Approximately ten percent of US military veterans suffer from posttraumatic stress disorder (PTSD). Cognitive processing therapy (CPT) is a highly effective, evidence-based, first-line treatment for PTSD that has been widely adopt
Externí odkaz:
https://doaj.org/article/639c6d7ccb4344dd92e5637e6baa8a6b
Autor:
Edward L Alexander, Assar A Rather, Radu A Nedelcoviciu, Michael Amygdalos, Deborah Eberly, Marilyn Mitchell, Diana Curtis, Glen Tinkoff
Publikováno v:
Journal of the American College of Surgeons. 235:S91-S92
Publikováno v:
Clinical Genetics. 33:270-276
This project studied the effect of reinforcement of genetic counselling in the home, on consultand recall of information discussed in the clinic. Acceptable recall was observed in 84% of 227 patients scored for recall of rate of recurrence, understan
Publikováno v:
Clinical Genetics. 25:68-72
A family is reported in which various skeletal abnormalities have been segregating over three generations. The Great-grandfather (11) of the consultand had features consistent with Grebe chondrodysplasia. The other members of the family have brachyda
Autor:
Diana Curtis
Publikováno v:
Studies in American Fiction. 34:69-85
Samuel Clemens, better known as Mark Twain, was born on November 30, 1835 in Florida, Missouri, less than six weeks after Samuel Colt obtained the English patent for his first revolver. In time, Twain's innovative use of language would drastically re
Autor:
Diana Curtis
Publikováno v:
The Explicator. 63:112-114
Autor:
Patrick Willems, Jan Hendrickx, Vibeke Winter, Alberto Ponzone, Katrine Schneiderman, Marion Mack, Teresa Parrella, Yuan Tsang Chen, Niels Gregersen, Stephen G. Kahler, Jia Huan Ding, Brage S. Andresen, Peter Bross, Wen Zhang, Riccardo Ponzone, Charles R. Roe, Thomas Deufel, Steen Kølvraa, Lars Bolund, Diana Curtis
Publikováno v:
Gregersen, N, Winter, V, Curtis, D, Deufel, T, Mack, M, Hendrickx, J, Willems, P J, Ponzone, A, Parrella, T, Ponzone, R, Ding, J H, Zhang, W, Chen, Y T, Kahler, S, Roe, C R, Kølvraa, S, Schneiderman, K, Andresen, B S, Bross, P & Bolund, L 1993, ' Medium-chain Acyl-CoA dehydrogenase (MCAD) Deficiency : The prevalent mutation G985 (K304E) is subject to a strong founder effect from northwestern Europe ', Human Heredity, vol. 43, no. 6, pp. 342-350 . https://doi.org/10.1159/000154157
Human heredity
Human heredity
Medium-chain acyl CoA dehydrogenase (MCAD) deficiency is a potentially fatal inherited defect of fatty acid P-oxidation. Approximately 90% of the disease-causing alleles in diagnosed patients are due to a single base mutation, an A (adenine) to G (gu
Autor:
J. Ott, P.W. Kleyn, K. Asplund, Alberto Ponzone, Vibeke Winter, K. Das, E. Lieberman, Diana Curtis, Susan E. Hodge, Marion Mack, C. Triantaphyllidis, Niels Gregersen, G. Hallmans, Ivan Balazsc, Veronica J. Vieland, Brage S. Andresen, Patrick Willems, Stephen G. Kahler, A. Petalopoulos, S. Linn, Yuan Tsang Chen, V.A. Stepanov, S.C. Schoenbaum, Liu Mingjun, S.J. O’Brien, Jia-Huan Ding, N.P. Anagnou, N.K. Moschonas, W. Modi, T.C. Gilliam, L. Beckman, Riccardo Ponzone, L.M. Brzustowicz, Lars Bolund, J. Papamatheakis, S.V. Lemza, T.L. Munsat, Jan Hendrickx, C. Sikström, Elias O. da-Suva, David A. Greenberg, G. Beckman, M. Fousteri, H. Seuanez, L.H. Castüla, Wen Zhang, Katrine Schneiderman, Charles R. Roe, C. Mérette, G.K. Penchaszadeh, Peter Bross, A. Kouvatsi, Xin Zhenghan, Steen Kølvraa, T. Lehner, Teresa Parrella, Thomas Deufel
Publikováno v:
Human Heredity. 43:I-VI
Genetic counselling for myotonic dystrophy: A comparison of lens examination and DNA linkage studies
Publikováno v:
Eye. 5:93-98
Genetic counselling in presymptomatic individuals with a family history of myotonic dystrophy (DM) is problematic. A genetic test to identify the presymptomatic carrier of the gene for DM would therefore be advantageous. We report studies comparing o
Autor:
Alexandra I. F. Blakemore, Diana Curtis, Niels Rüdiger, Peter Bross, Daniel P. Kelly, Vibeke Winter, Peter Engel, Lars Bolund, Niels Gregersen, Brage S. Andresen, Arnold W. Strauss, Sandro Ghisla, Ernst Christensen, Steen Kølvraa, Stefan Engst
Publikováno v:
Gregersen, N, Andresen, B S, Bross, P, Winter, V, Rüdiger, N, Engst, S, Ghisla, S, Christensen, E, Kelly, D, Strauss, A W, Kølvraa, S, Bolund, L, Blakemore, A, Curtis, D & Engel, P 1991, ' Characterization of a disease-causing Lys329 to Glu mutation in 16 patients with medium-chain Acyl-CoA dehydrogenase deficiency ', Journal of Inherited Metabolic Disease, vol. 14, no. 3, pp. 314-316 . https://doi.org/10.1007/BF01811691
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency (McKusick 20145) is the most common inherited defect of the beta-oxidation of fatty acid (Roe and Coates, 1989). It causes life-threatening attacks of hypoglycaemia and lethargy, and has led to su