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Items: 40

1.

Road traffic injuries in Mozambique.

Romão F, Nizamo H, Mapasse D, Rafico MM, José J, Mataruca S, Efron ML, Omondi LO, Leifert T, Bicho JM.

Inj Control Saf Promot. 2003 Mar-Jun;10(1-2):63-7.

PMID:
12772487
2.

Galactosemia screening of newborns in Massachusetts.

Shih VE, Levy HI, Karolkewicz V, Houghton S, Efron ML, Isselbacher KJ, Beutler E, MacCready RA.

N Engl J Med. 1971 Apr 8;284(14):753-7. No abstract available.

PMID:
4926707
3.

Pyridoxine-unresponsive homocystinuria.

Shih VE, Efron ML.

N Engl J Med. 1970 Nov 26;283(22):1206-8. No abstract available.

PMID:
5472941
4.

Lowe's syndrome: a search or the carrier state.

Holmes LB, McGowan BL, Efron ML.

Pediatrics. 1969 Sep;44(3):358-64. No abstract available.

PMID:
5809892
5.

Effect of elevated plasma phenylalanine levels on other amino acids in phenylketonuric and normal subjects.

Efron ML, Kang ES, Visakorpi J, Fellers FX.

J Pediatr. 1969 Mar;74(3):399-405. No abstract available.

PMID:
5764775
6.
7.

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
8.

D-methioninuria due to DL-methionine ingestion. An artefact detected by a mass screening program for errors of amino acid metabolism.

Efron ML, McPherson TC, Shih VE, Welsh CF, MacCready RA.

Am J Dis Child. 1969 Jan;117(1):104-7. No abstract available.

PMID:
4235732
10.

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
11.

Hartnup disorder in a New England family.

Pomeroy J, Efron ML, Dayman J, Hoefnagel D.

N Engl J Med. 1968 May 30;278(22):1214-6. No abstract available.

PMID:
5647741
12.

Concerning amino acids in human saliva.

Dryefus PM, Levy HL, Efron ML.

Experientia. 1968 May 15;24(5):447-8. No abstract available.

PMID:
5674976
13.

Excretion of delta-aminolevulinic acid in the absence of demonstrable erythropoiesis.

Shahidi NT, Efron ML.

Proc Soc Exp Biol Med. 1968 May;128(1):314-7. No abstract available.

PMID:
5656709
14.

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
16.

The aminoacidurias.

Efron ML, Ampola MG.

Pediatr Clin North Am. 1967 Nov;14(4):881-903. Review. No abstract available.

PMID:
4875467
17.

Citrullinemia with defective urea production.

Morrow G 3rd, Barness LA, Efron ML.

Pediatrics. 1967 Oct;40(4):565-74. No abstract available.

PMID:
6051056
18.

Isovaleric acidemia. Clinical features of a new genetic defect of leucine metabolism.

Budd MA, Tanaka K, Holmes LB, Efron ML, Crawford JD, Isselbacher KJ.

N Engl J Med. 1967 Aug 17;277(7):321-7. No abstract available.

PMID:
4378266
19.

Rapid short-column chromatography of amino acids. A method for blood and urine specimens in the diagnosis and treatment of metabolic disease.

Shih VE, Efron ML, Mechanic GL.

Anal Biochem. 1967 Aug;20(2):299-311. No abstract available.

PMID:
6048171
20.

Diet therapy for inborn errors of amino acid metabolism.

Efron ML.

J Am Diet Assoc. 1967 Jul;51(1):40-5. No abstract available.

PMID:
6027632
21.
22.

Argininosuccinic aciduria. Report of two new cases and demonstration of intermittent elevation of blood ammonia.

Moser HW, Efron ML, Brown H, Diamond R, Neumann CG.

Am J Med. 1967 Jan;42(1):9-26. No abstract available.

PMID:
6016480
23.

Isovaleric acidemia.

Efron ML.

Am J Dis Child. 1967 Jan;113(1):74-6. No abstract available.

PMID:
6015910
24.

Treatment of hydroxyprolinemia and hyperprolinemia.

Efron ML.

Am J Dis Child. 1967 Jan;113(1):166-9. No abstract available.

PMID:
6015897
25.

Isovaleric acidemia: a new genetic defect of leucine metabolism.

Tanaka K, Budd MA, Efron ML, Isselbacher KJ.

Proc Natl Acad Sci U S A. 1966 Jul;56(1):236-42. No abstract available.

26.

Argininosuccinic acid in monilethrix.

Efron ML, Hoefnagel D.

Lancet. 1966 Feb 5;1(7432):321-2. No abstract available.

PMID:
4158907
27.

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
29.

AMINOACIDURIA.

EFRON ML.

N Engl J Med. 1965 May 27;272:1107-13 CONCL. Review. No abstract available.

PMID:
14281555
30.

AMINOACIDURIA.

EFRON ML.

N Engl J Med. 1965 May 20;272:1058-67 CONTD. Review. No abstract available.

PMID:
14281543
31.

PHENYLKETONURIC FAMILIES.

EFRON ML, MACCREADY RA.

JAMA. 1965 Feb 1;191:391-2. No abstract available.

PMID:
14232443
32.

A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.

EFRON ML, YOUNG D, MOSER HW, MACCREADY RA.

N Engl J Med. 1964 Jun 25;270:1378-83. No abstract available.

PMID:
14152868
33.

RENAL TUBULAR TRANSPORT OF PROLINE, HYDROXYPROLINE, AND GLYCINE IN HEALTH AND IN FAMILIAL HYPERPROLINEMIA.

SCRIVER CR, EFRON ML, SCHAFER IA.

J Clin Invest. 1964 Mar;43:374-85. No abstract available.

34.

THE METABOLIC DEFECT OF PRIMARY HYPEROXALURIA.

SMITH LH Jr, HOCKADAY TD, EFRON ML, CLAYTON JE.

Trans Assoc Am Physicians. 1964;77:317-25. No abstract available.

PMID:
14275433
35.

CONTRIBUTIONS OF A CLINICAL GENETICS LABORATORY TO THE DIAGNOSIS AND TREATMENT OF DISEASE IN CHILDHOOD.

GERALD PS, EFRON ML.

Postgrad Med. 1963 Sep;34:216-21. No abstract available.

PMID:
14045779
36.

Atypical variants of the 'ataxia telangiectasia' syndrome. Report of two cases, including one with apparent dominant inheritance.

PAINE RS, EFRON ML.

Dev Med Child Neurol. 1963 Feb;5:14-23. No abstract available.

PMID:
13941122
37.

Familial hyperprolinemia, cerebral dysfunction and renal anomalies occurring in a family with hereditary nephropathy and deafness.

Schafer IA, Scriver CR, Efron ML.

N Engl J Med. 1962 Jul 12;267:51-60. No abstract available.

PMID:
14497974
38.

New renal tubular amino-acid transport system and a new hereditary disorder of amino-acid metabolism.

SCRIVER CR, SCHAFER IA, EFRON ML.

Nature. 1961 Nov 18;192:672-3. No abstract available.

PMID:
13910063
39.

Chemical studies of several varieties of Hb M.

GERALD PS, EFRON ML.

Proc Natl Acad Sci U S A. 1961 Nov 15;47:1758-67. No abstract available.

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