L'OMOCISTINURIA. SINTESI CLINICA E DESCRIZIONE DI UN CASO = L'HOMOCYSTINURIE. REVUE CLINIQUE ET DESCRIPTION D'UN CASZAMMARCHI E; BORGHERESI S.1976; MINERVA PEDIATR.; ITAL.; DA. 1976; VOL. 28; NO 12; PP. 730-742; ABS. ANGL.; BIBL. 2 P.Article

LA DIFFERENZIAZIONE DELLE IPERFENILALANINEMIE MEDIANTE DIETA DA CARICO. = LA DIFFERENCIATION DES HYPERPHENYLALANINEMIES AU MOYEN DU REGIME DE CHARGEZAMMARCHI E; BARDINI MR; DE NIGRIS L et al.1978; MINERVA PEDIATR.; ITA; DA. 1978; VOL. 30; NO 9; PP. 713-726; ABS. ANGL.; BIBL. 13 REF.Article

LA TIROSINEMIA DEL NEONATO. II. CORRELAZIONE FRA I LIVELLI EMATICI DI BILIRUBINA E DI TIROSINA IN UN GRUPPO DI SOGGETTI IMMATURI. = LA TYROSINEMIE DU NOUVEAU-NE. II. CORRELATIONS ENTRE LES TAUX SANGUINS DE BILIRUBINE ET DE TYROSINE DANS UN GROUPE DE PREMATURESZAMMARCHI E; MAFFEI C; DABIZZI S et al.1978; MINERVA PEDIATR.; ITAL.; DA. 1978; VOL. 30; NO 8; PP. 615-618; ABS. ANGL.; BIBL. 26 REF.Article

CISTINOSI. DESCRIZIONE DI UN CASO CON IPERALDOSTERONISMO = CYSTINOSE. DESCRIPTION D'UN CAS AVEC HYPERALDOSTERONISMECALANDI C; ADAMI LAMI CONTI C; EMANUELE G et al.1978; MINERVA PEDIATR.; ITA; DA. 1978; VOL. 30; NO 20; PP. 1611-1620; ABS. ENG; BIBL. 58 REF.Article

LA TIROSINEMIA DEL NEONATO. IV. COMPORTAMENTO DELLA FENILALANINA IN RELAZIONE AL PESO ALLA NASCITA, ALLA TIROSINEMIA ED ALL'APPORTO PROTEICO. = LA TYROSINEMIE DU NOUVEAU-NE. IV. COMPORTEMENT DE LA PHENYLALAMINE EN RAPPORT AVEC LE POIDS A LA NAISSANCE, LA TYROSINEMIE ET L'APPORT PROTEIQUEZAMMARCHI E; BOUGLEUX T; BIADAIOLI R et al.1978; MINERVA PEDIATR.; ITA; DA. 1978; VOL. 30; NO 9; PP. 681-685; ABS. ANGL.; BIBL. 15 REF.Article

LA TIROSINEMIA DEL NEONATO. I. RISULTATI DELLE RICERCHE SU 172 IMMATURI SUDDIVISI PER GRUPPI DI PESO, ETA GESTAZIONALE ED INDICE DI IMMATURITA. = LA TYROSINEMIE DU NOUVEAU-NE. I. RESULTATS DES RECHERCHES SUR 172 PREMATURES, DIVISES EN GROUPES D'APRES LES POIDS, AGES GESTATIONNELS ET INDICES DE PREMATURITE.ZAMMARCHI E; MAFFEI C; BOUGLEUX T et al.1978; MINERVA PEDIATR.; ITA; DA. 1978; VOL. 30; NO 7; PP. 545-554; ABS. ANGL.; BIBL. 1 P.Article

Biochemical evaluation of a patient with a familial form of leucine-sensitive hypoglycemia and concomitant hyperammonemiaZAMMARCHI, E; FILIPPI, L; NOVEMBRE, E et al.Metabolism, clinical and experimental. 1996, Vol 45, Num 8, pp 957-960, issn 0026-0495Article

Self-mutilation in a patient with mucolipidosis IIIZAMMARCHI, E; SAVELLI, A; DONATI, M. A et al.Pediatric neurology. 1994, Vol 11, Num 1, pp 68-70, issn 0887-8994Article

Cryptogenic hepatitis masking the diagnosis of ornithine transcarbamylase deficiencyZAMMARCHI, E; DONATI, M. A; FILIPPI, L et al.Journal of pediatric gastroenterology and nutrition. 1996, Vol 22, Num 4, pp 380-383, issn 0277-2116Conference Paper

Neonatal onset of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with favorable outcomeZAMMARCHI, E; CIANI, F; PASQUINI, E et al.The Journal of pediatrics. 1997, Vol 131, Num 3, pp 440-443, issn 0022-3476Article

Different neurologic outcomes in two patients with neonatal hyperinsulinemic hypoglycemiaZAMMARCHI, E; FILIPPI, L; FONDA, C et al.Child's nervous system (Print). 1996, Vol 12, Num 7, pp 413-416, issn 0256-7040Article

Fructose-1, 6-diphosphatase deficiency misdiagnosed as reye syndromeZAMMARCHI, E; DONATI, M. A; CIANI, F et al.Clinical pediatrics. 1995, Vol 34, Num 10, pp 561-564, issn 0009-9228Article

The preventive effects and duration of action of two doses of inhaled furosemide on exercise-induced asthma in childrenNOVEMBRE, E; FRONGIA, G; LOMBARDI, E et al.Journal of allergy and clinical immunology. 1995, Vol 96, Num 6, pp 906-909, issn 0091-6749, 1Article

Familial infantile myasthenia: a neuromuscular cause of respiratory failureZAMMARCHI, E; DONATI, M. A; MASI, S et al.Child's nervous system (Print). 1994, Vol 10, Num 5, pp 347-349, issn 0256-7040Article

Failure of early dextromethorphan and sodium benzoate therapy in an infant with konketotic hyperglycinemiaZAMMARCHI, E; DONATI, M. A; CIANI, F et al.Neuropediatrics. 1994, Vol 25, Num 5, pp 274-276, issn 0174-304XArticle

Successful prenatal molecular diagnosis of carbamyl-phosphate synthetase I deficiency in two at-risk pregnanciesFUNGHINI, S; MORRONE, A; PASQUINI, E et al.Journal of inherited metabolic disease. 2005, Vol 28, Num 5, pp 801-802, issn 0141-8955, 2 p.Article

Unusual presentation of the immotile cilia syndrome in two childrenZAMMARCHI, E; CALZOLARI, C; PIGNOTTI, M. S et al.Acta paediatrica (Oslo). 1993, Vol 82, Num 3, pp 312-313, issn 0803-5253Article

Hepatitis C virus antibodies in a long-term follow-up of beta-thalassaemic children with acute and chronic non-A non-B hepatitisRESTI, M; AZZARI, C; ROSSI, M. E et al.European journal of pediatrics. 1992, Vol 151, Num 8, pp 573-576, issn 0340-6199Conference Paper

Free tryptophan decrease in jaundiced newborn infants during phototherapyZAMMARCHI, E; LA ROSA, S; PIERRO, U et al.Biology of the neonate. 1989, Vol 55, Num 4, pp 224-227, issn 0006-3126, 4 p.Article

Hypocitrullinemia in expanded newborn screening by LC―MS/MS is not a reliable marker for ornithine transcarbamylase deficiencyCAVICCHI, C; MALVAGIA, S; LA MARCA, G et al.Journal of pharmaceutical and biomedical analysis. 2009, Vol 49, Num 5, pp 1292-1295, issn 0731-7085, 4 p.Article

Mother-to-infant transmission of hepatitis C virusRESTI, M; AZZARI, C; LEGA, L et al.Acta paediatrica (Oslo). 1995, Vol 84, Num 3, pp 251-255, issn 0803-5253Article

Lethal late onset cblB methylmalonic aciduriaCIANI, F; DONATI, M. A; TULLI, G et al.Critical care medicine. 2000, Vol 28, Num 6, pp 2119-2121, issn 0090-3493Article

Early-infantile galactosialidosis : Clinical, biochemical, and molecular observations in a new patientZAMMARCHI, E; DONATI, M. A; MORRONE, A et al.American journal of medical genetics. 1996, Vol 64, Num 3, pp 453-458, issn 0148-7299Article

Prenatal diagnosis by minisatellite analysis in Italian families with phenylketonuriaROMANO, V; DIANZANI, I; PONZONE, A et al.Prenatal diagnosis. 1994, Vol 14, Num 10, pp 959-962, issn 0197-3851Article

An X:autosome translocation stabilizes truncated dystrophin : implications for lack of truncated dystrophins in Duchenne muscular dystrophyFIDZIANSKA, A; MORRONE, A; PEGORARO, E et al.Neuropediatrics. 1995, Vol 26, Num 3, pp 163-167, issn 0174-304XArticle