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Amino acid metabolism by the kidney.
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[Electrophoretic and electrophoretic-chromatographic picture in diseases of defective renal transport of amino acids with particular reference to personal cases].
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[Prevention of cysteine calculosis by the continuous administration of alpha-mercaptopropionylglycine].
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Dibasic amino acid transport: lessons from human disease.
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Screening for aminoacid disorders in mental retardation.
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[Correlations between biochemical data and clinical course of newborn infants].
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[Certain aspects of the biochemistry of urine in families with handicapped children].
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[Keratosis follicularis spinulosa decalvans and amino-aciduria (author's transl)].
A new case of keratosis follicularis spinulosa decalvans (Siemens, 1925) in a 12 1/2 year old boy is related. This X-dominant inherited disturbance of follicular keratinization is associated with an amino-aciduria in the propositus and his mother, especially an increase of aspartic acid in urin and blood. The scarring infundibular plugs are constituted by nucleated keratin, which brightened up in polarized light and seems to be of internal trichilemmal origin.
[Artificial and secondary hyperaminoaciduria (author's transl)].
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Calcium deficient puberty rickets with acidosis responding to large dose of oral calcium.
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[Detection of hereditary metabolic diseases at the pediatric clinic].
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[Maple syrup urine disease: report of a mild variant case and results of dietary treatment].
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Renal handling of amino acids: recent results of tubular microperfusion.
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Ultrastructure and function of the ellipsoids of the spleen. Their relationship with fat metabolism and red blood cells.
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[Hyperaminoacidemia and hyperaminoaciduria of benign nature and their diagnostic values].
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[Parathormone and the kidneys].
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[Renal tubule transport defect of amino acids].
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