Fatty acid peroxide formation in tissue homogenates from mice with hereditary myopathy (dystrophia muscularis).
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Animals↗
Biomedical subjects
W H BLAHD
Publications and source records attributed to W H BLAHD.
Metabolic and nutritional studies in mice with a hereditary myopathy (Dystrophia muscularis).
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Animals↗
Concentrations of K and Na in skeletal muscle of mice with a hereditary myopathy (Dystrophia muscularis).
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Animals↗
The differential diagnosis of biliary tract obstruction with radioactive rose bengal.
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Biliary Tract↗
Treatment of hyperthyroidism with individually calculated doses of I131.
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Humans↗
Idiopathic paroxysmal myoglobinuria; detailed study of a case including radioisotope and serum enzyme evaluation.
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Acute Disease↗
Radioisotope studies in neuromuscular disease. II. Studies in muscular dystrophy and myotonia dystrophica with sodium 22 and potassium 42.
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Electrolytes↗
Qualitative study of aminoaciduria in muscular dystrophy and myotonia dystrophica.
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Amino Acid Metabolism, Inborn Errors↗
The turnover rate of serum albumin in the nephrotic syndrome as determined by I 131-labeled albumin.
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Albumins↗
Ascitic fluid and plasma protein exchange in cirrhosis of the liver; studies with radioiodinated human serum albumin and gamma globulin.
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Ascites↗
Isotope studies in neuromuscular disease. I. Radioactive potassium.
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Humans↗
Studies in neuromuscular disease with radioactive potassium.
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Disease↗
Potassium deficiency in man.
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Electrolytes↗
The effect of prolonged administration of epinephrine on adrenal cortical function and epinephrine tolerance in chronic asthmatics.
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Adrenal Cortex↗
A method of human plasmapheresis.
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Humans↗
A case of malignant hypertension secondary to renal ischemia.
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Humans↗
Electrolyte changes produced by ACTH, cortisone, and DOCA in cirrhosis of the liver.
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Adrenal Cortex↗
A case of Hand-Schüller-Christian syndrome treated with cortisone.
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Cortisone↗