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Articles Written by: DAVIS C. L.
Background Recurrent sinopulmonary and cutaneous viral infections with elevated serum levels of IgE are features of some variants of combined immunodeficiency. The genetic causes of these variants are unknown.
Methods We collected longitudinal ...
From ZHANG, Q., DAVIS, J. C., LAMBORN, I. T., FREEMAN, A. F., JING, H., FAVREAU, A. J., MATTHEWS, H. F., DAVIS, J., TURNER, M. L., UZEL, G., HOLLAND, S. M., SU, H. C.,
New England Journal of Medicine -- Recent Issues,
18 Nov 2009
Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings.
To the Editor: The outcomes for living kidney donors, shown in the study by Ibrahim et al. (Jan. 29 issue),1 are ...
From DAVIS, C. L., COOPER, M., FREEMAN, W. L., ROSS, L. F., THISTLETHWAITE, J. R., DOLS, L. F.C., WEIMAR, W., IJZERMANS, J. N.M., IBRAHIM, H. N., MATAS, A. J.,
New England Journal of Medicine -- Recent Issues,
27 May 2009
Background Although virus-induced wheezing is common in preschool-age children, optimal management remains elusive. We examined the efficacy and safety of preemptive treatment with high-dose fluticasone in reducing the severity of recurrent ...
From DUCHARME, F. M., LEMIRE, C., NOYA, F. J.D., DAVIS, G. M., ALOS, N., LEBLOND, H., SAVDIE, C., COLLET, J.-P., KHOMENKO, L., RIVARD, G., PLATT, R. W.,
New England Journal of Medicine -- Recent Issues,
21 Jan 2009
Background Rare mutations affecting the FOXP2 transcription factor cause a monogenic speech and language disorder. We hypothesized that neural pathways downstream of FOXP2 influence more common phenotypes, such as specific language impairment.
Methods ...
From VERNES, S. C., NEWBURY, D. F., ABRAHAMS, B. S., WINCHESTER, L., NICOD, J., GROSZER, M., ALARCON, M., OLIVER, P. L., DAVIES, K. E., GESCHWIND, D. H., MONACO, A. P., FISHER, S. E.,
New England Journal of Medicine -- Recent Issues,
26 Nov 2008
Background Rare mutations affecting the FOXP2 transcription factor cause a monogenic speech and language disorder. We hypothesized that neural pathways downstream of FOXP2 influence more common phenotypes, such as specific language impairment.
Methods ...
From VERNES, S. C., NEWBURY, D. F., ABRAHAMS, B. S., WINCHESTER, L., NICOD, J., GROSZER, M., ALARCON, M., OLIVER, P. L., DAVIES, K. E., GESCHWIND, D. H., MONACO, A. P., FISHER, S. E.,
New England Journal of Medicine -- Recent Issues,
5 Nov 2008
Background The efficacy and safety of testosterone treatment for hypoactive sexual desire disorder in postmenopausal women not receiving estrogen therapy are unknown.
Methods We conducted a double-blind, placebo-controlled, 52-week trial in which 814 ...
From DAVIS, S. R., MOREAU, M., KROLL, R., BOUCHARD, C., PANAY, N., GASS, M., BRAUNSTEIN, G. D., HIRSCHBERG, A. L., RODENBERG, C., PACK, S., KOCH, H., MOUFAREGE, A., STUDD, J., THE APHRODITE STUDY TEAM,
New England Journal of Medicine -- Recent Issues,
5 Nov 2008
Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings.
To the Editor: In the trial reported by Morley et al. (Feb. 14 issue),1 a significant reduction in the use of ...
From NANAN, R. K.H., LIU, A. J.W., POULTON, A., ZANARDO, V., TREVISANUTO, D., CHIARELLI, S., HUGHES-DAVIES, T., MORLEY, C. J., DAVIS, P. G., DOYLE, L. W.,
New England Journal of Medicine -- Recent Issues,
4 Jun 2008
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To the Editor: Tuberous sclerosis is an autosomal dominant disorder characterized by hamartomatous growths in many organs and caused by inherited mutations of the TSC1 or TSC2 gene. Acquired (somatic) mutations of either gene occur within ...
From DAVIES, D. M., JOHNSON, S. R., TATTERSFIELD, A. E., KINGSWOOD, J. C., COX, J. A., MCCARTNEY, D. L., DOYLE, T., ELMSLIE, F., SAGGAR, A., DE VRIES, P. J., SAMPSON, J. R.,
New England Journal of Medicine -- Recent Issues,
9 Jan 2008
Background Rheumatoid arthritis has a complex mode of inheritance. Although HLA-DRB1 and PTPN22 are well-established susceptibility loci, other genes that confer a modest level of risk have been identified recently. We carried out a genomewide ...
From PLENGE, R. M., SEIELSTAD, M., PADYUKOV, L., LEE, A. T., REMMERS, E. F., DING, B., LIEW, A., KHALILI, H., CHANDRASEKARAN, A., DAVIES, L. R.L., LI, W., TAN, A. K.S., BONNARD, C., ONG, R. T.H., THALAMUTHU, A., PETTERSSON, S., LIU, C., TIAN, C., CHEN, W. V.,
New England Journal of Medicine -- Recent Issues,
19 Sep 2007
Background Rheumatoid arthritis has a complex mode of inheritance. Although HLA-DRB1 and PTPN22 are well-established susceptibility loci, other genes that confer a modest level of risk have been identified recently. We carried out a genomewide ...
From PLENGE, R. M., SEIELSTAD, M., PADYUKOV, L., LEE, A. T., REMMERS, E. F., DING, B., LIEW, A., KHALILI, H., CHANDRASEKARAN, A., DAVIES, L. R.L., LI, W., TAN, A. K.S., BONNARD, C., ONG, R. T.H., THALAMUTHU, A., PETTERSSON, S., LIU, C., TIAN, C., CHEN, W. V.,
New England Journal of Medicine -- Recent Issues,
5 Sep 2007
