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Blood|January 15, 1995
One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of JewsO Shpilberg, H Peretz, A Zivelin, et al.Cancer Research|October 2, 2024
Impact of Structural Racism and Social Determinants of Health on Disparities in Breast Cancer MortalityMary Falcone, Bodour Salhia, Chanita Hughes Halbert, et al.Archives of Pathology & Laboratory Medicine|February 1, 1988
Pseudomonas cepacia-associated pneumonia in cystic fibrosis. Relation of clinical features to histopathologic patterns of pneumoniaJ F Tomashefski, M J Thomassen, M C Bruce, et al.Zeitschrift Fur Gastroenterologie|June 14, 2003
Increasing sensitivity of morphological diagnosis in hepatocellular carcinoma (HCC) by combination of cytological and fine-needle histological examination after ultrasound guided fine needle biopsyM Caselitz, N Masche, J S Bleck, et al.Chest|December 1, 1978
Pulmonary function and morbidity in 40 adult patients with cystic fibrosisR J Fink, C F Doershuk, A S Tucker, et al.The Journal of Pediatrics|February 1, 1984
Dosing implications of rapid elimination of trimethoprim-sulfamethoxazole in patients with cystic fibrosisM D Reed, R C Stern, J S Bertino, et al.Pediatric Research|September 1, 1981
Are measurements of urine enzymes useful during aminoglycoside therapy?M D Reed, M W Vermeulen, R C Stern, et al.Annals of Internal Medicine|August 1, 1977
Cystic fibrosis diagnosed after age 13. Twenty-five teenage and adult patients including three asymptomatic menR C Stern, T F Boat, C F Doershuk, et al.Cancer Genetics and Cytogenetics|April 1, 1996
Structural aberrations of chromosome 6 in three uterine smooth muscle tumorsY Hennig, U Deichert, C Stern, et al.Gastroenterology|May 1, 1976
Symptomatic hepatic disease in cystic fibrosis: incidence, course, and outcome of portal systemic huntingR C Stern, D P Stevens, T F Boat, et al.Pageof 56