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Biochemical evaluation of patients with cancer-associated hypercalcemia: evidence for humoral and nonhumoral groups A. F. Stewart and Others Abstract
A new genetic basis for hemoglobin-H disease
Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndrome
Phenylketonuria: epitome of human biochemical genetics (second of two parts)
Increased production of prostaglandin D2 in patients with systemic mastocytosis
Functional importance of the coronary collaterals
Malpractice liability and immunity of full-time salaried physicians
Aspirin and dipyridamole ineffective in treatment of necrobiosis lipoidica
Weekly clinicopathological exercises. Case 49-1980
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The multiple causes of hypercalcemia in malignant disease L. M. Sherwood
Systemic carnitine deficiency
Shedding from normal and cancer-cell surfaces
Anaphylaxis from tolmetin S. Ahmad
Treatment of hemophilia with prothrombin-complex concentrates
Glycosylated hemoglobin (HbA1) in a case of insulinoma
Military medicine
Reliability of data from death certificates
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