Hereditary fructose intolerance. An inborn defect of hepatic fructose-1-phosphate splitting aldolase.
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Adipose Tissue↗
Biomedical subjects
A PRADER
Publications and source records attributed to A PRADER.
Catch-up growth following illness or starvation. An example of developmental canalization in man.
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Growth↗
DISACCHARIDASE ACTIVITIES IN HUMAN INTESTINAL MUCOSA.
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Colonic Neoplasms↗
Human intestinal disaccharidases and hereditary disaccharide intolerance. The hydrolysis of sucrose, isomaltose, palatinose (isomaltulose), and a 1,6-alpha-oligosaccharide (isomalto-oligosaccharide) preparation.
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Disaccharidases↗
[THE OCULO-CEREBRO-RENAL SYNDROME (LOWE). CLINICAL, METABOLIC AND ELECTROENCEPHALOGRAPHIC FINDINGS IN 3 CASES].
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Ammonia↗
[ADDISON'S DISEASE WITH CEREBRAL SCLEROSIS IN CHILDHOOD. A HEREDITARY SYNDROME TRANSMITTED THROUGH CHROMOSOME X?].
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17-Ketosteroids↗
[The treatment of growth disorders with anabolic steroids and growth hormone].
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Dwarfism↗
[Gluco-amino-phosphate-diabetes (De Toni-Debre-Fanconi syndrome) and disorder of cystine metabolism].
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Cystine↗
[The clinical aspects of common chromosomal abnormalities].
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Chromosome Aberrations↗
[On the genetics of the congenital adrenogenital syndrome (virilizing adrenal hyperplasia)].
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Adrenal Hyperplasia, Congenital↗
[On the genitics of congenital lipoid hyperplasia of the adrenals].
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Adrenal Glands↗
[Diarrhea due to hereditary deficiency of intestinal saccharase activity (saccharose intolerance)].
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Child↗
The influence of anabolic steroids on growth.
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Biological Phenomena↗
[Study of 8 cases of isolated precocious sexual pilosity or "premature pubarche"].
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Child↗
[The "Tarzan type": short spine, degenerative intervertebral disk changes and narrow pelvis].
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Humans↗
[Saccharose intolerance. Diarrhea due to herediatary lack of intestinal saccharase activity].
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Child↗
[Primary tubulopathies. IV. Mechanism of tubular acidosis].
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Acidosis↗
[Primary tubulopathies. I. A case of idiopathic renal tubular acidosis (Albright's syndrome)].
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Acidosis, Renal Tubular↗