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Human Genetics|January 1, 1996
Pseudohypoparathyroidism type Ia: two new heterozygous frameshift mutations in exons 5 and 10 of the Gs alpha geneH Shapira, M Mouallem, M S Shapiro, et al.
Southern Medical Journal|October 1, 1988
Complex interaction of rifampin and warfarinS Almog, U Martinowitz, H Halkin, et al.
Postgraduate Medical Journal|July 1, 1984
Development of Hodgkin's disease in the course of liver cirrhosis and impaired monocyte functionM Dan, A Hassner, M Jedwab, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1982
Deficient activity of receptor-cyclase coupling protein is transformed lymphoblasts of patients with pseudohypoparathyroidism, type IZ Farfel, M E Abood, A S Brickman, et al.
The Journal of Rheumatology|May 1, 1996
Bilateral patellar metastases as the clinical presentation of bronchogenic adenocarcinomaR Pauzner, V Istomin, G Segal-Lieberman, et al.
International Journal of Dermatology|March 1, 1984
Allopurinol-induced toxic epidermal necrolysisM Dan, M Jedwab, M Peled, et al.
Clinical Pharmacology and Therapeutics|May 1, 1975
Controlled trial of propranolol in intermittent claudicationN Reichert, S Shibolet, R Adar, et al.
American Heart Journal|January 1, 1987
Review of echocardiographically diagnosed right heart entrapment of pulmonary emboli-in-transit with emphasis on managementZ Farfel, M Shechter, Z Vered, et al.
American Journal of Medical Genetics|July 1, 1992
Albright hereditary osteodystrophy with hypothyroidism, normocalcemia, and normal Gs protein activity: a family presenting with congenital osteoma cutisS Izraeli, A Metzker, G Horev, et al.
Clinical Cardiology|February 1, 1991
Cardiac conduction defects associated with hyponatremiaM Mouallem, E Friedman, Y Shemesh, et al.
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