SPAETERGEBNISSE BEI OBEREN SPRUNGGELENKSARTHRODESEN NACH CHARNLEY. = RESULTATS TARDIFS APRES ARTHRODESES TIBIOTARSIENNES DE CHARNLEYRIMOLDI M.1977; AKTUELLE TRAUMATOL.; DTSCH.; DA. 1977; VOL. 7; NO 5; PP. 315-324; ABS. ANGL.; BIBL. 15 REF.Article

DOSAGGIO NEI LEUCOCITI DI ALCUNI ENZIMI IMPLICATI NELLE NEUROPATIE DA ERRORI METABOLICI CONGENITI = IDENTIFICATION DE QUELQUES ENZYMES LEUCOCYTAIRES RESPONSABLES DE NEUROPATHIES PAR TROUBLES METABOLIQUES CONGENITAUXDONATO SD; RIMOLDI M; TETTAMANTI G et al.1971; RIV. PATOL. NERV. MENTALE; ITAL.; DA. 1971; VOL. 92; NO 2; PP. 126-138; ABS. ANGL.; BIBL. 16 REF.Serial Issue

EVIDENCE FOR AUTOSOMAL RECESSIVE INHERITANCE IN SYSTEMIC CARNITINE DEFICIENCYDI DONATO S; RIMOLDI M; CORNELIO F et al.1982; ANN. NEUROL.; ISSN 0364-5134; USA; DA. 1982; VOL. 11; NO 2; PP. 190-192; BIBL. 9 REF.Article

MUSCLE CARNITINE PALMITYLTRANSFERASE DEFICIENCY: A CASE WITH ENZYME DEFICIENCY IN CULTURED FIBROBLASTSDIDONATO S; CORNELIO F; PACINI L et al.1978; ANN. NEUROL.; USA; DA. 1978; VOL. 4; NO 5; PP. 465-467; BIBL. 15 REF.Article

DIAGNOSTICA ENZIMATICA DELLE GLICOLIPIDOSI = DIAGNOSTIC ENZYMATIQUE DES GLYCOLIPIDOSESZAMBOTTI V; DI DONATO S; RIMOLDI M et al.1972; QUAD. SCLAVO DIAGNOST. CLIN. LAB.; ITAL.; DA. 1972; VOL. 8; NO 1; PP. 183-198; ABS. ANGL.; BIBL. 13REF.Serial Issue

FATAL ATAXIC ENCEPHALOPATHY AND CARNITINE ACETYLTRANSFERASE DEFICIENCY: A FUNCTIONAL DEFECT OF PYRUVATE OXIDATION.DIDONATO S; RIMOLDI M; MOISE A et al.1979; NEUROLOGY; USA; DA. 1979; VOL. 29; NO 12; PP. 1578-1583; BIBL. 20 REF.Article

HEPATIC KETOGENESIS AND MUSCLE CARNITINE DEFICIENCYDI DONATO S; CORNELIO F; STORCHI G et al.1979; NEUROLOGY; USA; DA. 1979; VOL. 29; NO 6; PP. 780-785; BIBL. 20 REF.Article

CYTOCHROME-C-OXIDASE DEFICIENCY IN MUSCLES OF A FLOPPY INFANT WITHOUT MITOCHONDRIAL MYOPATHYRIMOLDI M; BOTTACCHI E; ROSSI L et al.1982; J. NEUROL.; ISSN 506702; DEU; DA. 1982; VOL. 227; NO 4; PP. 201-207; ABS. GER; BIBL. 19 REF.Article

HETEROGENEITY OF CARNITINE-PALMITOYLTRANSFERASE DEFICIENCYDI DONATO S; CASTIGLIONE A; RIMOLDI M et al.1981; J. NEUROL. SCI.; ISSN 0022-510X; NLD; DA. 1981; VOL. 50; NO 2; PP. 207-215; BIBL. 2 P.Article

KETOGENIC RESPONSE TO FASTING IN HUMAN CARNITINE DEFICIENCIESDI DONATO S; PELUCHETTI D; RIMOLDI M et al.1980; CLIN. CHIM. ACTA; NLD; DA. 1980; VOL. 100; NO 3; PP. 209-214; BIBL. 16 REF.Article

ACID MALTASE DEFICIENCY IN ADULTS. CLINICAL, MORPHOLOGICAL AND BIOCHEMICAL STUDY OF THREE PATIENTSBERTAGNOLIO B; DI DONATO S; PELUCHETTI D et al.1978; EUROP. NEUROL.; CHE; DA. 1978; VOL. 17; NO 4; PP. 193-204; BIBL. 21 REF.Article

A new stable-isotope dilution method for measurement of orotic acid utilizing solvent-extracted urineRIMOLDI, M; BERGOMI, P; ROMEO, A et al.Journal of inherited metabolic disease. 1994, Vol 17, Num 2, pp 243-244, issn 0141-8955Article

Lytic rabbit IgG for tissue culture tryptomastigotes of Trypanosoma cruzi alters the extent and form of complement depositionRIMOLDI, M. T; TARTANIAN, A; JOINER, K. A et al.Experimental parasitology. 1989, Vol 68, Num 2, pp 160-167, issn 0014-4894Article

The parafascicular thalamic nucleus modulates messenger RNA encoding glutamate decarboxylase 67 in rat striatumGIORGI, S; RIMOLDI, M; ROSSI, A et al.Neuroscience. 1997, Vol 80, Num 3, pp 793-801, issn 0306-4522Article

Parafascicular thalamic nucleus deafferentation reduces c-fos expression induced by dopamine D-1 receptor stimulation in rat striatumGIORGI, S; RIMOLDI, M; CONSOLO, S et al.Neuroscience. 2001, Vol 103, Num 3, pp 653-661, issn 0306-4522Article

Debrancher deficiency neuromuscular disorder with pseudohypertrophy in two brothersMARBINI, A; GEMIGNANI, F; SACCARDI, F et al.Journal of neurology. 1989, Vol 236, Num 7, pp 418-420, issn 0340-5354Article

Experience on therapy of adrenoleukodystrophy and adrenomyeloneuropathyUZIEL, G; BERTINI, E; BARDELLI, P et al.Developmental neuroscience. 1991, Vol 13, Num 4-5, pp 274-279, issn 0378-5866Article

Riboflavin-responsive glutaric aciduria type II presenting as a leukodystrophyUZIEL, G; GARAVAGLIA, B; CICERI, E et al.Pediatric neurology. 1995, Vol 13, Num 4, pp 333-335, issn 0887-8994Article

Heteregeneous findings in four cases of cerebellar ataxia associated with hypogonadism (Holmes' type ataxia)DE MICHELE, G; FILLA, A; STRIANO, S et al.Clinical neurology and neurosurgery. 1993, Vol 95, Num 1, pp 23-28, issn 0303-8467Article

The neuromuscular pathology of experimental Chagas' diseaseMOLINA, H. A; CARDONI, R. L; RIMOLDI, M. T et al.Journal of the neurological sciences. 1987, Vol 81, Num 2-3, pp 287-300, issn 0022-510XArticle

4-Hydroxybutyric aciduria : clinical finginds and vigabatrin therapyUZIEL, G; BARDELLI, P; PANTALEONI, C et al.Journal of inherited metabolic disease. 1993, Vol 16, Num 3, pp 520-522, issn 0141-8955Article

Propionylcarnitine excretion in propionic and methylmalonic acidurias: a cause of carnitine deficiencyDI DONATO, S; RIMOLDI, M; GARAVAGLIA, B et al.Clinica chimica acta. 1984, Vol 139, Num 1, pp 13-21, issn 0009-8981Article

Antibody-dependent cytotoxicity of human and mouse mononuclear cells against Trypanosoma cruzi epimastigotesCARDONI, R. L; RIMOLDI, M. T; DE BRACCO, M. M. E et al.Cellular immunology (Print). 1984, Vol 86, Num 2, pp 518-524, issn 0008-8749Article

Normalization of short-chain acylcoenzyme A dehydrogenase after riboflavin treatment in a girl with multiple acylcoenzyme A dehydrogenase-deficient myopathyDIDONATO, S; GELLERA, C; PELUCHETTI, D et al.Annals of neurology. 1989, Vol 25, Num 5, pp 479-484, issn 0364-5134Article

Increased striatal expression of glutamate decarboxylase 67 after priming of 6-hydroxydopamine-lesioned ratsCONSOLO, S; MORELLI, M; RIMOLDI, M et al.Neuroscience. 1999, Vol 89, Num 4, pp 1183-1187, issn 0306-4522Article