NILPOTENT RINGS.

Por KRUSE R L., PRICE D T.
Publicado em C1969

The natural history of the use of healthcare information by women with breast cancer: a conceptual model.

Por Longo, D. R., Patrick, T. B., Kruse, R. L.
Publicado em 2001

Biological safety cabinetry.

Por Kruse, R H, Puckett, W H, Richardson, J H
Publicado em 1991

A prospective investigation of the impact of smoking bans on tobacco cessation and relapse

Por Longo, D., Johnson, J., Kruse, R., Brownson, R., Hewett, J.
Publicado em 2001

Implementing smoking bans in American hospitals: results of a national survey

Por Longo, D., Feldman, M., Kruse, R., Brownson, R., Petroski, G., Hewett, J.
Publicado em 1998

THE EFFECT OF INTERNET SUPPORT GROUPS ON CAREGIVER SOCIAL SUPPORT AND SELF-EFFICACY: A META ANALYSIS

Por Oliver, D.P., Patil, S., Benson, J.J., Gage, A., Washington, K., Kruse, R., Demiris, G.
Publicado no Innov Aging (2017)

Re-alignment and intramedullary rodding of the humerus and forearm in children with osteogenesis imperfecta: revision rate and effect on fracture rate

Por Franzone, J. M., Bober, M. B., Rogers, K. J., McGreal, C. M., Kruse, R. W.
Publicado no J Child Orthop (2017)

A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome

Por Mangold, E, Pagenstecher, C, Leister, M, Mathiak, M, Rutten, A, Friedl, W, Propping, P, Ruzicka, T, Kruse, R
Publicado em 2004

A comparative study of vascular injection fluids in fresh‐frozen and embalmed human cadaver forearms

Por Doomernik, D. E., Kruse, R. R., Reijnen, M. M. P. J., Kozicz, T. L., Kooloos, J. G. M.
Publicado no J Anat (2016)

Prenatal phthalate exposure and reduced masculine play in boys

Por Swan, S. H., Liu, F., Hines, M., Kruse, R. L., Wang, C., Redmon, J. B., Sparks, A., Weiss, B.
Publicado em 2009

Microsatellite instability—a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with col...

Por Lamberti, C, Kruse, R, Ruelfs, C, Caspari, R, Wang, Y, Jungck, M, Mathiak, M, Malayeri, H, Friedl, W, Sauerbruch, T, Propping, P
Publicado em 1999

A gene for universal congenital alopecia maps to chromosome 8p21-22.

Por Nöthen, M M, Cichon, S, Vogt, I R, Hemmer, S, Kruse, R, Knapp, M, Höller, T, Faiyaz ul Haque, M, Haque, S, Propping, P, Ahmad, M, Rietschel, M
Publicado em 1998

Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria.

Por Kruse, R, Rütten, A, Lamberti, C, Hosseiny-Malayeri, H R, Wang, Y, Ruelfs, C, Jungck, M, Mathiak, M, Ruzicka, T, Hartschuh, W, Bisceglia, M, Friedl, W, Propping, P
Publicado em 1998

Intradiscal Pressure Changes during Manual Cervical Distraction: A Cadaveric Study

Por Gudavalli, M. R., Potluri, T., Carandang, G., Havey, R. M., Voronov, L. I., Cox, J. M., Rowell, R. M., Kruse, R. A., Joachim, G. C., Patwardhan, A. G., Henderson, C. N. R., Goertz, C.
Publicado em 2013

A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.

Por Betz, R C, Lee, Y A, Bygum, A, Brandrup, F, Bernal, A I, Toribio, J, Alvarez, J I, Kukuk, G M, Ibsen, H H, Rasmussen, H B, Wienker, T F, Reis, A, Propping, P, Kruse, R, Cichon, S, Nöthen, M M
Publicado em 2000