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Items: 9

1.

Studies of intestinal transport defect in Hartnup disease.

Shih VE, Bixby EM, Alpers DH, Bartoscas CS, Thier SO.

Gastroenterology. 1971 Oct;61(4):445-53. No abstract available.

PMID:
5157127
2.

Mental deficiency and a new aminoaciduria.

Ampola MG, Efron ML, Bixby EM, Meshorer E.

Am J Dis Child. 1969 Jan;117(1):66-70. No abstract available.

PMID:
4973015
3.

Hydroxyprolinemia. 3. The origin of free hydroxyproline in hydroxyprolinemia. Collagen turnover. Evidence for biosynthetic pathway in man.

Efron ML, Bixby EM, Hockaday TD, Smith LH Jr, Meshorer E.

Biochim Biophys Acta. 1968 Sep 3;165(2):238-50. No abstract available.

PMID:
5683524
4.

Beta mercaptolactate-cysteine disulfide: analog of cystine in the urine of a mentally retarded patient.

Crawhall JC, Parker R, Sneddon W, Young EP, Ampola MG, Efron ML, Bixby EM.

Science. 1968 Apr 26;160(3826):419-20.

PMID:
5644041
5.

[The polymorphic forms of alpha 1-acid glycoprotein of mentally retarded patients].

Debray-Sachs M, Schmid K, Bixby EM.

Ann Biol Clin (Paris). 1966 Jan-Feb;24(1):203-12. French. No abstract available.

PMID:
5906418
6.

HYDROXYPROLINEMIA. II. A RARE METABOLIC DISEASE DUE TO A DEFICIENCY OF THE ENZYME "HYDROXYPROLINE OXIDASE".

EFRON ML, BIXBY EM, PRYLES CV.

N Engl J Med. 1965 Jun 24;272:1299-309. No abstract available.

PMID:
14299138
7.

Evaluation of the Bacillus subtilis inhibition-assay technic as a screening procedure for the detection of phenylketonuria.

BIXBY EM, PALLATAO LG, PRYLES CV.

N Engl J Med. 1963 Mar 21;268:648-51. No abstract available.

PMID:
13971272
8.

Urinary excretion of 17-ketosteroids in various conditions of oligophrenia correlated with some autopsy observations.

BENDA CE, BIXBY EM.

J Clin Endocrinol Metab. 1947 Jul;7(7):503-18. No abstract available.

PMID:
20260949
9.

Serum amylase in mongolism.

BIXBY EM.

Am J Ment Defic. 1947 Jan;51(3):372-7. No abstract available.

PMID:
20248904

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