5th IFIP Congress

por Freiman, C V, Griffith, J E, Rosenfeld, J L
Publicado 1972

5th IFIP Congress

por Freiman, C V, Griffith, J E, Rosenfeld, J L
Publicado 1972

Financial Incentive Does Not Affect P300 in the Complex Trial Protocol (CTP) Version of the Concealed Information Test (CIT) in Malingering Detection. II. Uninstructed Subjects

por Rosenfeld, J. Peter, Davydova, Elena, Labkovsky, Elena, Ward, Anne
Publicado 2019

Letter: Blood levels of 5-fluorouracil during intravenous infusion.

por Kawai, M., Rosenfeld, J., McCulloch, P., Hillcoat, B. L.
Publicado 1976

Clinical response and plasma levels of 5-fluorouracil in patients with colonic cancer treated by drug infusion.

por Hillcoat, B. L., McCulloch, P. B., Figueredo, A. T., Ehsan, M. H., Rosenfeld, J. M.
Publicado 1978

Epidemiological Trends of Spine Trauma: An Australian Level 1 Trauma Centre Study

por Tee, J. W., Chan, C. H. P., Fitzgerald, M. C. B., Liew, S. M., Rosenfeld, J. V.
Publicado 2013

Inception of an Australian Spine Trauma Registry: The Minimum Dataset

por Tee, J. W., Chan, C. H. P., Gruen, R. L., Fitzgerald, M. C. B., Liew, S. M., Cameron, P. A., Rosenfeld, J. V.
Publicado 2012

Early Predictors of Health-Related Quality of Life Outcomes in Polytrauma Patients with Spine Injuries: A Level 1 Trauma Center Study

por Tee, J. W., Chan, C. H. P., Gruen, R. L., Fitzgerald, M. C. B., Liew, S. M., Cameron, P. A., Rosenfeld, J. V.
Publicado 2013

De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations

por Probst, F. J., James, R. A., Burrage, L. C., Rosenfeld, J. A., Bohan, T. P., Melver, C. H. Ward, Magoulas, P., Austin, E., Franklin, A. I. A., Azamian, M., Xia, F., Patel, A., Bi, W., Bacino, C., Belmont, J.W., Ware, S. M., Shaw, C., Cheung, S.W., Lalani, S. R.
Publicado 2015

Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes

por Loviglio, M N, Leleu, M, Männik, K, Passeggeri, M, Giannuzzi, G, van der Werf, I, Waszak, S M, Zazhytska, M, Roberts-Caldeira, I, Gheldof, N, Migliavacca, E, Alfaiz, A A, Hippolyte, L, Maillard, A M, Van Dijck, A, Kooy, R F, Sanlaville, D, Rosenfeld, J A, Shaffer, L G, Andrieux, J, Marshall, C, Scherer, S W, Shen, Y, Gusella, J F, Thorsteinsdottir, U, Thorleifsson, G, Dermitzakis, E T, Deplancke, B, Beckmann, J S, Rougemont, J, Jacquemont, S, Reymond, A
Publicado 2017

De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

por Palmer, E E, Stuhlmann, T, Weinert, S, Haan, E, Van Esch, H, Holvoet, M, Boyle, J, Leffler, M, Raynaud, M, Moraine, C, van Bokhoven, H, Kleefstra, T, Kahrizi, K, Najmabadi, H, Ropers, H-H, Delgado, M R, Sirsi, D, Golla, S, Sommer, A, Pietryga, M P, Chung, W K, Wynn, J, Rohena, L, Bernardo, E, Hamlin, D, Faux, B M, Grange, D K, Manwaring, L, Tolmie, J, Joss, S, Cobben, J M, Duijkers, F A M, Goehringer, J M, Challman, T D, Hennig, F, Fischer, U, Grimme, A, Suckow, V, Musante, L, Nicholl, J, Shaw, M, Lodh, S P, Niu, Z, Rosenfeld, J A, Stankiewicz, P, Jentsch, T J, Gecz, J, Field, M, Kalscheuer, V M
Publicado 2018