NEONATAL SCREENING FOR INBORN ERRORS OF AMINO ACID METABOLISM = RECHERCHE NEONATALE DES ERREURS HEREDITAIRES DU METABOLISME DES ACIDES AMINESLEVY HL.1974; CLIN. ENDOCRINOL. METABOL.; G.B.; DA. 1974; VOL. 3; NO 1; PP. 153-166; BIBL. 1P.Article

HISTIDINAEMIA. I: RECONCILING RETROSPECTIVE AND PROSPECTIVE FINDINGSSCRIVER CR; LEVY HL.1983; JOURNAL OF INHERITED METABOLIC DISEASE; ISSN 0141-8955; GBR; DA. 1983; VOL. 6; NO 2; PP. 51-53; BIBL. 15 REF.Article

MATERNAL PHENYLKETONURIA AND HYPERPHENYLALARINEMIA. AN INTERNATIONAL SURVEY OF THE OUTCOME OF UNTREATED AND TREATED PREGNANCYLENKE RR; LEVY HL.1980; N. ENGL. J. MED.; ISSN 0028-4793; USA; DA. 1980; VOL. 303; NO 21; PP. 1202-1208; BIBL. 36 REF.Article

COMPARISON OF TREATED AND UNTREATED PREGNANCIES IN A MOTHER WITH PHENYLKETONURIALEVY HL; KAPLAN GN; ERICKSON AM et al.1982; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1982; VOL. 100; NO 6; PP. 876-880; BIBL. 16 REF.Article

DIET TERMINATION IN CHILDREN WITH PHENYLKETONURIA: A REVIEW OF PSYCHOLOGICAL ASSESSMENTS USED TO DETERMINE OUTCOMEWAISBREN SE; SCHNELL RR; LEVY HL et al.1980; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1980; VOL. 3; NO 4; PP. 148-153; BIBL. 2 P.Article

MASSACHUSETTS METABOLIC DISORDERS SCREENING PROGRAM. II: METHYLMALONIC ACIDURIACOULOMBE JT; SHIH VE; LEVY HL et al.1981; PEDIATRICS (EVANSTON); ISSN 0031-4005; USA; DA. 1981; VOL. 67; NO 1; PP. 26-31; BIBL. 20 REF.Article

ASYMPTOMATIE TYPE II HYPERPROLINAEMIA ASSOCIATED WITH HYPERGLYCINAEMIA IN THREE SIBS. = HYPERPROLINEMIE DE TYPE II ASYMPTOMATIQUE ASSOCIEE A UNE HYPERGLYCINEMIE CHEZ TROIS GERMAINSPAVONE L; MOLLICA F; LEVY HL et al.1975; ARCH. DIS. CHILDH.; G.B.; DA. 1975; VOL. 50; NO 8; PP. 637-641; BIBL. 24 REF.Article

ROUTINE NEWBORN SCREENING FOR HISTIDINEMIA. CLINICAL AND BIOCHEMICAL RESULTS = RECHERCHE DE ROUTINE DE L'HISTIDINEMIE CHEZ LE NOUVEAU-NE. RESULTATS CLINIQUES ET BIOCHIMIQUELEVY HL; SHIH VE; MADIGAN PM et al.1974; NEW ENGL. J. MED.; U.S.A.; DA. 1974; VOL. 291; NO 23; PP. 1214-1219; BIBL. 1P.Article

PERICARDIAL FLUID ANALYSIS IN SCLERODERMA (SYSTEMIC SCLEROSIS).GLADMAN DD; GORDON DA; UROWITZ MB et al.1976; AMER. J. MED.; U.S.A.; DA. 1976; VOL. 60; NO 7; PP. 1064-1068; BIBL. 34 REF.Article

EVIDENCE FOR LIVER DISEASE PRECEDING AMINO ACID ABNORMALITIES IN HEREDITARY TYROSINEMIAKOSTETTER MK; LEVY HL; WINTER HS et al.1983; NEW ENGLAND JOURNAL OF MEDICINE; ISSN 0028-4793; USA; DA. 1983; VOL. 308; NO 21; PP. 1265-1267; BIBL. 26 REF.Article

HISTIDINAEMIA. II: IMPACT; A RETROSPECTIVE STUDYROSENMANN A; SCRIVER CR; CLOW CL et al.1983; JOURNAL OF INHERITED METABOLIC DISEASE; ISSN 0141-8955; GBR; DA. 1983; VOL. 6; NO 2; PP. 54-57; BIBL. 2 P.Article

SEPSIS DUE TO ESCHERICHIA COLI IN NEONATES WITH GALACTOSEMIA.LEVY HL; SEPE SJ; SHIH VE et al.1977; NEW ENGL. J. MED.; U.S.A.; DA. 1977; VOL. 297; NO 15; PP. 823-825; BIBL. 20 REF.Article

HYPERAMMONEMIA DUE TO A DEFFECT IN HEPATIC ORNITHINE TRANSCARBAMYLASE = HYPERAMMONIEMIE PAR DEFAUT D'ORNITHINE TRANSCARBAMYLASE HEPATIQUESUNSHINE P; LINDENBAUM JE; LEVY HL et al.1972; PEDIATRICS; U.S.A.; DA. 1972; VOL. 50; NO 1; PP. 100-111; BIBL. 37 REF.Serial Issue

HISTIDINAEMIA. III: IMPACT; A PROSPECTIVE STUDYCOULOMBE JT; KAMMERER BL; LEVY HL et al.1983; JOURNAL OF INHERITED METABOLIC DISEASE; ISSN 0141-8955; GBR; DA. 1983; VOL. 6; NO 2; PP. 58-61; BIBL. 10 REF.Article

CYSTATHIONINURIA AND HOMOCYSTINURIA = CYSTATHIONINURIE ET HOMOCYSTINURIELEVY HL; MUDD SH; UHLENDORF BW et al.1975; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1975; VOL. 58; NO 1; PP. 51-59; BIBL. 42REF.Article

SPEECH AND LANGUAGE DEFICITS IN EARLY-TREATED CHILDREN WITH GALACTOSEMIAWAISBREN SE; NORMAN TR; SCHNELL RR et al.1983; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1983; VOL. 102; NO 1; PP. 75-77; BIBL. 9 REF.Article

CARDIOVASCULAR RISK IN HETEROZYGOTES FOR HOMOCYSTINURIAMUDD SH; HAVLIK R; LEVY HL et al.1982; AMERICAN JOURNAL OF HUMAN GENETICS; ISSN 0002-9297; USA; DA. 1982; VOL. 34; NO 6; PP. 1018-1021; BIBL. 10 REF.Article

MEASUREMENT OF METHYLMALONIC ACID IN URINE FILTER PAPER SPECIMENS BY GAS CHROMATOGRAPHYMATIES M; SHIH VE; EVANS J et al.1981; CLIN. CHIM. ACTA; ISSN 0009-8981; NLD; DA. 1981; VOL. 114; NO 2-3; PP. 303-308; BIBL. 12 REF.Article

COMPARISON OF GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE IN FETAL AND ADULT TISSUES = COMPARAISON DE LA GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE DANS LES TISSUS DES FOETUS ET ADULTESHAMMERSEN G; LEVY HL; FRIGOLETTO F et al.1975; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1975; VOL. 60; NO 3; PP. 281-284; BIBL. 17REF.Article

ARGINASE DEFICIENCY IN MACACA FASCICULARIS. I. ARGINASE ACTIVITY AND ARGININE CONCENTRATION IN ERYTHROCYTES AND IN LIVER = LE DEFICIT EN ARGINASE CHEZ LE M.F. I. L'ACTIVITE DE L'ARGINASE ET LE TAUX D'ARGENINE DANS LES ERYTHROCYTES ET LE FOIESHIH VE; JONES TC; LEVY HL et al.1972; PEDIATR. RES.; SWITZ.; DA. 1972; VOL. 6; NO 6; PP. 548-551; BIBL. 19REF.Serial Issue