Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gail M. Schauer"'
Publikováno v:
American Journal of Medical Genetics. 87:45-48
We report on a male fetus with partial trisomy 2p21-2pter and monosomy 15q26-15qter due to t(2,15)(p21;q26). This fetus had a typical trisomy 2p phenotype including minor facial anomalies, musculoskeletal defects and two unusual findings: polydactyly
Publikováno v:
Pediatric Pathology & Laboratory Medicine. 17:951-958
This report describes the clinical and histologic features of a pulmonary tumor in a 14-year-old girl that is most consistent with a rare entity described in the literature as "pulmonary endodermal tumor resembling fetal lung" (PET). This tumor is co
Publikováno v:
The Annals of Thoracic Surgery. 61:229-231
An extremely rare coronary artery anomaly where the left main coronary artery arose anteriorly from the right coronary sinus and coursed in front of the right ventricular outflow tract was present in a patient with tetralogy of Fallot. Preoperative a
Publikováno v:
American journal of physiology. Gastrointestinal and liver physiology. 279(4)
We previously suggested that the profound, sustained vasoconstriction noted in 3-day-old swine intestine after a moderate episode of ischemia-reperfusion (I/R) reflects the unmasking of underlying constrictor tone consequent to a loss of endothelium-
Autor:
Debra L. Kearney, Richard E. Chinnock, Geoffrey L. Rosenthal, Beverly Barton Rogers, Robert J. Gajarski, Kenneth O. Schowengerdt, Jeffrey A. Towbin, Gail M. Schauer, Susan W. Denfield, J K Price, Jiyuan Ni, Neil E. Bowles
Publikováno v:
Circulation. 96(10)
Background Inflammatory diseases of the heart, including myocarditis and cardiac transplant rejection, are important causes of morbidity and mortality in children. Although viral infection may be suspected in either of these clinical conditions, the
Publikováno v:
Journal of pediatric surgery. 30(9)
Congenital diaphragmatic hernia (CDH) continues to be one of the most challenging problems in pediatric surgery. The overall mortality rate remains at 40%, and death is caused by pulmonary hypoplasia and persistent pulmonary hypertension. It has been
Publikováno v:
Journal of surgical oncology. 51(1)
A case of mullerian adenosarcoma of the uterus with sarcomatous overgrowth is described. The patient was also found to have bilateral polycystic ovaries. This 25 year-old white female presented with irregular vaginal bleeding and was diagnosed as hav
Publikováno v:
The Annals of Thoracic Surgery. 67:1151-1152
We describe an aortic valve-sparing operation in a small child with an ascending aortic aneurysm and root dilatation. The operation avoids the need for a prosthetic valve and long-term anticoagulation. Thus, the procedure is an attractive alternative