Mitochondrial involvement in Parkinson's disease : the controversy continuesDIMAURO, S.Neurology. 1993, Vol 43, Num 11, pp 2170-2172, issn 0028-3878Article

LATE-ONSET ACID MALTASE DEFICIENCY. DETECTION OF PATIENTS AND HETEROZYGOTES BY URINARY ENZYME ASSAY.MEHLER M; DIMAURO S.1976; ARCH. NEUROL.; U.S.A.; DA. 1976; VOL. 33; NO 10; PP. 692-695; BIBL. 17 REF.Article

DISORDERS OF GLYCOGEN AND LIPID METABOLISM.DIMAURO S; EASTWOOD AB.1977; ADV. NEUROL.; NETHERL.; DA. 1977; VOL. 17; PP. 123-142; BIBL. 4 P. 1/2Article

RESIDUAL ACID MALTASE ACTIVITY IN LATE-ONSET ACID MALTASE DEFICIENCY.MEHLER M; DIMAURO S.1977; NEUROLOGY; U.S.A.; DA. 1977; VOL. 27; NO 2; PP. 178-184; BIBL. 34 REF.Article

TISSUE CARNITINE IN REYE SYNDROMEWILLNER JH; CHUTORIAN AM; DIMAURO S et al.1978; ANN. NEUROL.; USA; DA. 1978; VOL. 4; NO 5; PP. 468-469; BIBL. 18 REF.Article

INDAGINE CONOSCITIVA SU ALCUNI ASPETTI DELL' APICOLTURA SICILIANA = ENQUETE SUR QUELQUES ASPECTS DE L'APICULTURE SICILIENNELONGO S; DIMAURO S; COCO A et al.1980; TEC. AGRIC.; ITA; DA. 1980; VOL. 32; NO 1-2; PP. 49-62; BIBL. 4 REF.Article

MUCOLIPIDOSIS II (I-CELL DISEASE): STUDIES OF MUSCLE BIOPSY AND MUSCLE CULTURESSHANSKE S; MIRANDA AF; PENN AS et al.1981; PEDIATR. RES.; ISSN 0031-3998; USA; DA. 1981; VOL. 15; NO 10; PP. 1334-1339; BIBL. 32 REF.Article

GLYCOGEN DEBRANCHER DEFICIENCY IS REPRODUCED IN MUSCLE CULTUREMIRANDA AF; DIMAURO S; ANTLER A et al.1981; ANN. NEUROL.; ISSN 0364-5134; USA; DA. 1981; VOL. 9; NO 3; PP. 283-288; BIBL. 26 REF.Article

THE ADULT FORM OF ACID MALTASE (ALPHA -1,4-GLUCOSIDASE) DEFICIENCY.KARPATI G; CARPENTER S; EISEN A et al.1977; ANN. NEUROL.; U.S.A.; DA. 1977; VOL. 1; NO 3; PP. 276-280; BIBL. 27 REF.Article

Mitochondrial encephalomyopathiesDIMAURO, S; MORAES, C. T.Archives of neurology (Chicago). 1993, Vol 50, Num 11, pp 1197-1208, issn 0003-9942Article

ENCEPHALOPATHY AND FATAL MYOPATHY IN TWO SIBLINGSPARKER D; ROOT AW; SCHIMMEL S et al.1982; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1982; VOL. 136; NO 7; PP. 598-601; BIBL. 16 REF.Article

CARBOHYDRATE METABOLISM IN HYPOTHYROID MYOPATHY.MCDANIEL HG; PITTMAN CS; OH SJ et al.1977; METABOLISM; U.S.A.; DA. 1977; VOL. 26; NO 8; PP. 867-873; BIBL. 30 REF.Article

Mitochondrial defects of brain and muscleDE VIVO, D. C; DIMAURO, S.Biology of the neonate. 1990, Vol 58, pp 54-69, issn 0006-3126, SUP1Article

CARNITINE DEFICIENCY PRESENTING AS FAMILIAL CARDIOMYOPATHY: A TREATABLE DEFECT IN CARNITINE TRANSPORTWABER LJ; VALLE D; NEILL C et al.1982; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1982; VOL. 101; NO 5; PP. 700-705; BIBL. 16 REF.Article

HEREDITARY CARNITINE DEFICIENCY OF MUSCLE = DEFICIENCE MUSCULAIRE HEREDITAIRE DE CARNITINEVANDYKE DH; GRIGGS RC; MARKESBERY W et al.1975; NEUROLOGY; U.S.A.; DA. 1975; VOL. 25; NO 2; PP. 154-159; BIBL. 26REF.Article

A DISORDER OF MUSCLE LIPID METABOLISM AND MYOGLOBINURIA. ABSENCE OF CARNITINE PALMITYL TRANSFERASE = UNE PERTURBATION DU METABOLISME LIPIDIQUE MUSCULAIRE AVEC MYOGLOBINURIE. ABSENCE DE CARNITINE PALMITYL TRANSFERASEBANK WJ; DIMAURO S; BONILLA E et al.1975; NEW ENGL. J. MED.; U.S.A.; DA. 1975; VOL. 292; NO 9; PP. 443-449; BIBL. 41REF.Article

PHOSPHORYLASE ISOENZYMES IN NORMAL AND MYOPHOSPHORYLASE-DEFICIENT HUMAN HEARTMIRANDA AF; NETTE EG; HARTLAGE PL et al.1979; NEUROLOGY; USA; DA. 1979; VOL. 29; NO 11; PP. 1538-1541; BIBL. 8 REF.Article

STUDIES OF FRAGMENTED SARCOPLASMIC RETICULUM FROM HUMAN SKELETAL MUSCLE.SCARPA A; DIMAURO S; BONILLA E et al.1978; ANN. NEUROL.; U.S.A.; DA. 1978; VOL. 3; NO 3; PP. 194-201; BIBL. 42 REF.Article

ADULT-ONSET ACID MALTASE DEFICIENCY. MORPHOLOGIC AND BIOCHEMICAL ABNORMALITIES REPRODUCTED IN CULTURED MUSCLEASKANAS V; ENGEL WK; DIMAURO S et al.1976; NEW ENGL. J. MED.; U.S.A.; DA. 1976; VOL. 294; NO 11; PP. 573-578; BIBL. 37 REF.Article

CARNITINE PALMITYL TRANSFERASE DEFICIENCY: MYOGLOBINURIA AND RESPIRATORY FAILUREBERTORINI T; YU YAN YEH; TREVISAN C et al.1980; NEUROLOGY; USA; DA. 1980; VOL. 30; NO 3; PP. 263-271; BIBL. 50 REF.Article

NEUROMUSCULAR DISORDER ASSOCIATED WITH A DEFECT IN MITOCHONDRIAL ENERGY SUPPLY.SCHOTLAND DL; DIMAURO S; BONILLA E et al.1976; ARCH. NEUROL.; U.S.A.; DA. 1976; VOL. 33; NO 7; PP. 475-479; BIBL. 17 REF.Article

CORTICOSTEROID-RESPONSIVE SKELETAL MUSCLE DISEASE ASSOCIATED WITH PARTIAL CARNITINE DEFICIENCY. STUDIES OF LIVER AND METABOLIC ALTERATIONS.WHITAKER JN; DIMAURO S; SOLOMON SS et al.1977; AMER. J. MED.; U.S.A.; DA. 1977; VOL. 63; NO 5; PP. 805-815; BIBL. 1 P. 1/2Article

LUFT'S DISEASE. FURTHER BIOCHEMICAL AND ULTRASTRUCTURAL STUDIES OF SKELETAL MUSCLE IN THE SECOND CASEDIMAURO S; BONILLA E; LEE CP et al.1976; J. NEUROL. SCI.; NETHERL.; DA. 1976; VOL. 27; NO 2; PP. 217-232; BIBL. 1 P. 1/2Article

MUSCLE PHOSPHOFRUCTOKINASE DEFICIENCY: ABNORMAL POLYSACCHARIDE IN A CASE OF LATE-ONSET MYOPATHYHAYS AP; HALLETT M; DELFS J et al.1981; NEUROLOGY; ISSN 0028-3878; USA; DA. 1981; VOL. 31; NO 9; PP. 1077-1086; BIBL. 47 REF.Article

DEBRANCHER DEFICIENCY: NEUROMUSCULAR DISORDER IN 5 ADULTSDIMAURO S; HARTWIG GB; HAYS A et al.1979; ANN. NEUROL.; USA; DA. 1979; VOL. 5; NO 5; PP. 422-436; BIBL. 62 REF.Article