Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Michelle A. Springer"'
Publikováno v:
Oncology (Williston Park, N.Y.). 31(1)
Autor:
Peter R. Baker, Anne Chun Hui Tsai, Karen Swisshelm, Jennifer March, Gary Bellus, Michelle A. Springer, Kathleen Brown
Publikováno v:
Journal of Craniofacial Surgery. 21:1369-1375
Supernumerary, derivative, and ring X chromosomes are relatively common in Turner syndrome females but have been reported rarely in males. To date, less than 10 cases have been published, of which only 2 have been partially characterized in defining
Autor:
Maimoona A. Zariwala, Richard J. Wenstrup, Girish V. Putcha, Kasinathan Muralidharan, Ishrag Khababa, Soma Das, Bai-Lin Wu, Stacey Withrow, Nancy Carson, Fred Schaefer, Jessica K. Booker, Karen E. Weck, Rong Mao, Michelle A. Springer, Iris M. Otani, Melissa A Dempsey, Margaret A. Kenna, Marcy L. Hoffmann, John H. Greinwald, Bassem A. Bejjani, Linda Jo Bone Jeng, John C. Carey, Stacey L. Bleoo, Elaine B. Spector, Iris Schrijver, Margaret Lilley, Heidi L. Rehm, William K. Seltzer, Julie M. Gastier-Foster
Publikováno v:
Genetics in Medicine. 9:413-426
Purpose: The aim of the study was to determine the actual GJB2 and GJB6 mutation frequencies in North America after several years of generalized testing for autosomal recessive nonsyndromic sensorineural hearing loss to help guide diagnostic testing
Autor:
Timothy M. Hoffman, John R. Hayes, Peter C. Dyke, Andrew R. Yates, Clifford L. Cua, Timothy F. Feltes, Michelle A. Springer, Roozbeh Taeed
Publikováno v:
Pediatric Critical Care Medicine. 8:254-257
The purpose of this study was to assess the association of calcium replacement therapy with morbidity and mortality in infants after cardiac surgery involving cardiopulmonary bypass.Retrospective chart review.The cardiac intensive care unit at a tert
Autor:
Loris McGavran, Brenda Lunt, Cara Wells, Jean Jirikowic, Michelle A. Springer, Karen Swisshelm, Matthew R.G. Taylor
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 12(1)
Purpose: Array comparative genomic hybridization is now a widely used clinical tool for the evaluation of intellectual disability. The current 10% yield of positive findings is based largely on pediatric data. Adults with unexplained intellectual dis
Autor:
Bryce A. Kerlin, Carol A. Blanchong, Michelle A. Springer, Kay L. Monda, Stephanie L. Savelli, Jennifer D. Thornton
Publikováno v:
Journal of pediatric and adolescent gynecology. 19(4)
Venous thromboembolic events (VTE) are not common in children; however over the past ten years the incidence has increased. Reasons for the increase are two-fold. Physicians have an increased awareness of clotting events in children and imaging modal
Autor:
Michelle M. Springer
Publikováno v:
Government Publications Review. 16:80-82