AAAAAA
Results:
1-18
|
Results: 18
Authors:
Miller, CH
Dilley, A
Richardson, L
Hooper, WC
Evatt, BL
Citation: Ch. Miller et al., Population differences in von Willebrand factor levels affect the diagnosis of von Willebrand disease in African-American women, AM J HEMAT, 67(2), 2001, pp. 125-129
Authors:
Benson, JM
Ellingsen, D
El-Jamil, M
Jenkins, M
Miller, CH
Dilley, A
Evatt, BL
Hooper, WC
Citation: Jm. Benson et al., Factor V leiden and factor V R2 allele: High-throughput analysis and association with venous thromboembolism, THROMB HAEM, 86(5), 2001, pp. 1188-1192
Authors:
Dilley, A
Greening, J
Lynn, B
Leary, R
Morris, V
Citation: A. Dilley et al., The use of cross-correlation analysis between high-frequency ultrasound images to measure longitudinal median nerve movement, ULTRASOUN M, 27(9), 2001, pp. 1211-1218
Authors:
Hicks, J
Dilley, A
Patel, D
Barrish, J
Zhu, SH
Brandt, M
Citation: J. Hicks et al., Lipoblastoma and lipoblastomatosis in infancy and childhood: Histopathologic, ultrastructural, and cytogenetic features, ULTRA PATH, 25(4), 2001, pp. 321-333
Authors:
Dilley, A
Hooper, WC
El-Jamil, M
Renshaw, M
Wenger, NK
Evatt, BL
Citation: A. Dilley et al., Mutations in the genes regulating methylene tetrahydrofolate reductase (MTHFR C -> T677) and cystathione beta-synthase (CBS G -> A919, CBS T -> c833)are not associated with myocardial infarction in African Americans, THROMB RES, 103(2), 2001, pp. 109-115
Authors:
Hooper, WC
El-Jamil, M
Dilley, A
Philipp, C
Ellingsen, D
Phillips, D
Evatt, BL
Citation: Wc. Hooper et al., The relationship between the tissue plasminogen activator Alu I/D polymorphism and venous thromboembolism during pregnancy, THROMB RES, 102(1), 2001, pp. 33-37
Authors:
Eldridge, J
Dilley, A
Austin, H
EL-Jamil, M
Wolstein, L
Doris, J
Hooper, WC
Meehan, PL
Evatt, B
Citation: J. Eldridge et al., The role of protein C, protein S, and resistance to activated protein C inLegg-Perthes disease, PEDIATRICS, 107(6), 2001, pp. 1329-1334
Authors:
Dilley, A
Drews, C
Miller, C
Lally, C
Austin, H
Ramaswamy, D
Lurye, D
Evatt, B
Citation: A. Dilley et al., von Willebrand disease and other inherited bleeding disorders in women with diagnosed menorrhagia, OBSTET GYN, 97(4), 2001, pp. 630-636
Authors:
Dilley, A
Wesson, D
Munden, M
Hicks, J
Brandt, M
Minifee, P
Nuchtern, J
Citation: A. Dilley et al., The impact of ultrasound examinations on the management of children with suspected appendicitis: A 3-year analysis, J PED SURG, 36(2), 2001, pp. 303-307
Authors:
Zachariou, Z
Dilley, A
Lloyd, DA
Citation: Z. Zachariou et al., The impact of ultrasound examinations on the management of children with suspected appendicitis: A 3-year analysis - Discussion, J PED SURG, 36(2), 2001, pp. 307-308
Authors:
Austin, H
Hooper, WC
Lally, C
Dilley, A
Ellingsen, D
Wideman, C
Wenger, NK
Rawlins, P
Silva, V
Evatt, B
Citation: H. Austin et al., Venous thrombosis in relation to fibrinogen and factor VII genes among African-Americans, J CLIN EPID, 53(10), 2000, pp. 997-1001
Authors:
Hooper, WC
Lally, C
Austin, H
Renshaw, M
Dilley, A
Wenger, NK
Phillips, DJ
Whitsett, C
Rawlins, P
Evatt, BL
Citation: Wc. Hooper et al., The role of the t-PA I/D and PAI-1 4G/5G polymorphisms in African-Americanadults with a diagnosis of myocardial infarction or venous thromboembolism, THROMB RES, 99(3), 2000, pp. 223-230
Authors:
Dilley, A
Austin, H
El-Jamil, M
Hooper, WC
Barnhart, E
Evatt, BL
Sullivan, PS
Ellingsen, D
Patterson-Barnett, A
Eller, D
Randall, H
Philipp, C
Citation: A. Dilley et al., Genetic factors associated with thrombosis in pregnancy in a United Statespopulation, AM J OBST G, 183(5), 2000, pp. 1271-1277
Authors:
Dilley, A
Crudder, S
Citation: A. Dilley et S. Crudder, von Willebrand disease in women: The need for recognition and understanding, J WOMEN H G, 8(4), 1999, pp. 443-445
Authors:
Dilley, A
Adams, S
Citation: A. Dilley et S. Adams, Untitled, J PED SURG, 34(7), 1999, pp. 1183-1183
Authors:
Hooper, WC
Lally, C
Austin, H
Benson, J
Dilley, A
Wenger, NK
Whitsett, C
Rawlins, P
Evatt, BL
Citation: Wc. Hooper et al., The relationship between polymorphisms in the endothelial cell nitric oxide synthase gene and the platelet GPIIIa gene with myocardial infarction andvenous thromboembolism in African Americans, CHEST, 116(4), 1999, pp. 880-886
Authors:
Philipp, CS
Dilley, A
Saidi, P
Evatt, B
Austin, H
Zawadsky, J
Harwood, D
Ellingsen, D
Barnhart, E
Phillips, DJ
Hooper, WC
Citation: Cs. Philipp et al., Deletion polymorphism in the angiotensin-converting enzyme gene as a thrombophilic risk factor after hip arthroplasty, THROMB HAEM, 80(6), 1998, pp. 869-873
Authors:
Dilley, A
Austin, H
Hooper, WC
El-Jamil, M
Whitsett, C
Wenger, NK
Benson, J
Evatt, B
Citation: A. Dilley et al., Prevalence of the prothrombin 20210 G-to-A variant in blacks: Infants, patients with venous thrombosis, patients with myocardial infarction, and control subjects, J LA CL MED, 132(6), 1998, pp. 452-455
Risultati:
1-18
|