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

MATERNAL PHENYLKETONURIA. RESULTS OF DIETARY THERAPYLENKE RR; LEVY HL.1982; AM. J. OBSTET. GYNECOL.; ISSN 0002-9378; USA; DA. 1982; VOL. 142; NO 5; PP. 548-553; BIBL. 34 REF.Article

STARCH GEL ELECTROPHORESIS FOR GALACTOSE-1-PHOSPHATE URIDYLYL-TRANSFERASE APPLIED TO DRIED FILTER PAPER BLOOD SPECIMENS.HAMMERSEN G; LEVY HL.1977; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1977; VOL. 77; NO 3; PP. 295-299; BIBL. 17 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

A NEW METHOD OF SCREENING FOR INHERITED DISORDERS OF GALACTOSE METABOLISMPAIGEN K; PACHOLEC F; LEVY HL et al.1982; J. LAB. CLIN. MED.; ISSN 0022-2143; USA; DA. 1982; VOL. 99; NO 6; PP. 895-907; BIBL. 44 REF.Article

AN EVALUATION OF ROUTINE FOLLOW-UP BLOOD SCREENING OF INFANTS FOR PHENYLKETONURIASEPE SJ; LEVY HL; MOUNT FW et al.1979; NEW ENGL. J. MED.; USA; DA. 1979; VOL. 300; NO 11; PP. 606-609; BIBL. 10 REF.Article

GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE IN FIBROBLASTS: ISOZYMES IN NORMAL AND VARIANT STATES. = GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE DANS LES FIBROBLASTES: ISOZYMES CHEZ LES INDIVIDUS NORMAUX ET CHEZ LES VARIANTSHAMMERSEN G; MANDELL R; LEVY HL et al.1975; ANN. HUM. GENET.; G.B.; DA. 1975; VOL. 39; NO 2; PP. 147-150; BIBL. 9 REF.Article

MASSACHUSETTS METABOLIC DISORDERS SCREENING PROGRAM. I. TECHNICS AND RESULTS OF URINE SCREENING = LE PROGRAMME DE DEPISTAGE DES TROUBLES METABOLIQUES DANS LE MASSACHUSETTS. I. TECHNIQUES ET RESULTATS DU DEPISTAGE URINAIRELEVY HL; MADIGAN PM; SHIH VE et al.1972; PEDIATRICS; U.S.A.; DA. 1972; VOL. 49; NO 6; PP. 825-836; BIBL. 37REF.Serial Issue

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

NONENZYMATICALLY GALACTOSYLATED SERUM ALBUMIN IN A GALACTOSEMIC INFANTURBANOWSKI JC; COHENFORD MA; LEVY HL et al.1982; N. ENGL. J. MED.; ISSN 0028-4793; USA; DA. 1982; VOL. 306; NO 2; PP. 84-86; BIBL. 20 REF.Article

A STUDY OF CARDIOVASCULAR RISK IN HETEROZYGOTES FOR HEMOCYSTINURIAMUDD SH; HAVLIK R; LEVY HL et al.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 6; PP. 883-893; BIBL. 21 REF.Article

THIAMINE-RESPONSIVE INTERMITTENT BRANCHED-CHAIN KETOACIDURIAPUESCHEL SM; BRESNAN MJ; SHIH VE et al.1979; J. PEDIATR.; USA; DA. 1979; VOL. 94; NO 4; PP. 628-631; BIBL. 10 REF.Article

SCREENING FOR CONGENITAL HYPOTHYROIDISM: RESULTS IN THE NEWBORN POPULATION OF NEW ENGLANDMITCHELL ML; LARSEN PR; LEVY HL et al.1978; J.A.M.A.; USA; DA. 1978; VOL. 239; NO 22; PP. 2348-2351; BIBL. 12 REF.Article