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SAINT PIERRE D'ALCANTARAANGELINI C.ETUDES FRANCISCAINES. 1973, Vol 23, Num 67-68, pp 381-383Article

PORTRAIT DE SAINT LUCANGELINI C.ET. FRANCISC. 1972, Vol 22, Num 61, PP. 89-93Article

LIPID STORAGE MYOPATHES. A REVIEW OF METABOLIC DEFECT AND OF TREATMENT.ANGELINI C.1976; J. NEUROL.; GERM.; DA. 1976; VOL. 214; NO 1; PP. 1-11; ABS. ALLEM.; BIBL. 16 REF.Article

A REGGE EIKONAL MODEL CALCULATION FOR THE REACTION PP->(DELTA ++(1236)DELTA ++(1236)ANGELINI C; LARICCIA P.1972; LETTERE NUOVO CIMENTO; ITAL.; DA. 1972; VOL. 4; NO 17; PP. 965-968; BIBL. 9 REF.Serial Issue

LE MALATTIE CEREVROVASCOLARI ACUTE GRAVI. = LES MALADIES CEREBROVASCULAIRES AIGUES GRAVESGRITTI G; ANGELINI C.1976; ACTA ANESTHESIOL., SUPPL.; ITAL.; DA. 1976; VOL. 27; PP. 163-186; BIBL. 12 REF.Article

ASSESSMENT OF THE VALUE OF THYMIC SCAN IN MYASTHENIA GRAVISTESTA GF; ANGELINI C.1979; J. NEUROL.; DEU; DA. 1979; VOL. 220; NO 1; PP. 21-29; ABS. GER; BIBL. 28 REF.Article

CARNITINE DEFICIENCY OF SKELETAL MUSCLE. REPORT OF A TREATED CASE.ANGELINI C; LUCKE S; CANTARUTTI F et al.1976; NEUROLOGY; U.S.A.; DA. 1976; VOL. 26; NO 7; PP. 633-637; BIBL. 14 REF.Article

PARALISI SOPRANUCLEARE PROGRESSIVA. CONSIDERAZIONI SU DUE CASI. = PARALYSIE SUPRANUCLEAIRE PROGRESSIVE. A PROPOS DE 2 CASTREVISAN C; TESTA GF; ANGELINI C et al.1975; RIV. PATOL. NERV. MENTALE; ITAL.; DA. 1975 PARU 1976; VOL. 96; NO 3; PP. 159-165; ABS. ANGL.; BIBL. 11 REF.Article

DEFICIT SYSTEMIQUE EN CARNITINE: PLACE DANS LE SYNDROME DE REYECHAPOY P; ANGELINI C; CEDERBAUM S et al.1981; NOUV. PRESSE MED.; ISSN 0301-1518; FRA; DA. 1981; VOL. 10; NO 7; PP. 499-502; ABS. ENG; BIBL. 29 REF.Article

ADULT ACID MALTASE DEFICIENCY. ABNORMALITIES IN FIBROBLASTS CULTURED FROM PATIENTS = DEFICIT EN MALTASE ACIDE CHEZ L'ADULTE. ANOMALIES DES FIBROBLASTES DE MALADES EN CULTUREANGELINI C; ENGEL AG; TITUS JL et al.1972; NEW ENGL. J. MED.; U.S.A.; DA. 1972; VOL. 287; NO 19; PP. 948-951; BIBL. 14REF.Serial Issue

LA SINDROME DA DEFICIENZA DI CARNITINA. = LE SYNDROME DE DEFICIT EN CARNITINEANGELINI C; LUCKE S; CANTARUTTI F et al.1976; ACTA NEUROL.; ITAL.; DA. 1976; VOL. 31; NO 1; PP. 84-89; BIBL. 1 P.Article

FINGERPRINT BODY MYOPATHY. A NEWLY RECOGNIZED CONGENITAL MUSCLE DISEASE = MYOPATHIE EN EMPREINTE DIGITALE. UNE MALADIE CONGENITALE DU MUSCLE CONNUE DEPUIS PEUENGEL AG; ANGELINI C; GOMEZ MR et al.1972; MAYO CLIN. PROC.; U.S.A.; DA. 1972; VOL. 47; NO 6; PP. 377-388; BIBL. 38 REF.Serial Issue

CARNITINE, CARNITINE ACYLTRANSFERASES, AND RAT BRAIN FUNCTIONBRESOLIN N; FREDDO L; VERGANI L et al.1982; EXPERIMENTAL NEUROLOGY; ISSN 0014-4886; USA; DA. 1982; VOL. 78; NO 2; PP. 285-292; BIBL. 15 REF.Article

LE AMIOTROPIE SPINALI PROSSIMALI INFANTILI E GIOVANILI: CONTRIBUTO CLINICO E GENETICO SU VENTI CASI PERSONALI = L'AMYOTROPHIE MEDULLAIRE PROXIMALE INFANTILE ET JUVENILE, CONTRIBUTION CLINIQUE ET GENETIQUE AVEC 20 CAS PERSONNELSTREVISAN C; MOSTACCIVOLO ML; BATTISTELLA PA et al.1978; NEUROPSICHIATR. INFANT.; ITA; DA. 1978; NO 209; PP. 1307-1319; ABS. ENG; BIBL. 12 REF.Article

DUCHENNE MUSCULAR DYSTROPHY. A POPULATION STUDY.DANIELI GA; MOSTACCIUOLO ML; BONFANTE A et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 35; NO 2; PP. 225-231; BIBL. 19 REF.Article

MIODISTROFIA BENIGNA CON IPOGONADISMO IPERGONADOTROPO E CATARATTA CONGENITA. = DYSTROPHIE MUSCULAIRE BENIGNE AVEC HYPOGONADISME HYPERGONADOTROPE ET CATARACTE CONGENITALECONTE G; ANGELINI C; LOCATELLI C et al.1976; MINERVA MED.; ITAL.; DA. 1976; VOL. 67; NO 33; PP. 2104-2112; ABS. ANGL.; BIBL. 15 REF.Article

Defective assembly of sarcoglycan complex in patients with β-sarcoglycan gene mutations. Study of aneural and innervated cultured myotubesFANIN, M; ANGELINI, C.Neuropathology and applied neurobiology (Print). 2002, Vol 28, Num 3, pp 190-199, issn 0305-1846Article

AUTOIMMUNE NEUROMUSCULAR DISEASE INDUCED BY A PREPARATION OF CHOLINE ACETYLTRANSFERASELI PEN CHAO; KAN KSK; ANGELINI C et al.1982; EXP. NEUROL.; ISSN 0014-4886; USA; DA. 1982; VOL. 75; NO 1; PP. 23-35; BIBL. 17 REF.Article

LA SCINTIGRAFIA TIMICA NELLA MIASTENIA GRAVIS: ESPERIENZA SU 52 CASI = LA SCINTIGRAPHIE THYMIQUE DANS LA MYASTHENIE GRAVE. EXPERIENCE DE 52 CASTESTA G; ANGELINI C; TATTO I et al.1978; RIV. PATOL. NERV. MENTALE; ITA; DA. 1978; VOL. 99; NO 4; PP. 244-254; ABS. ENG; BIBL. 11 REF.Article

Pointwise convergence of the wavelet regularized estimatorsANGELINI, C; DE CANDITIIS, D.Communications in statistics. Theory and methods. 2002, Vol 31, Num 9, pp 1561-1578, issn 0361-0926, 18 p.Article

Regeneration in sarcoglycanopathies : expression studies of sarcoglycans and other muscle proteinsFANIN, M; ANGELINI, C.Journal of the neurological sciences. 1999, Vol 165, Num 2, pp 170-177, issn 0022-510XArticle

Long-term cyclosporine treatment in a group of severe myasthenia gravis patientsBONIFATI, D. M; ANGELINI, C.Journal of neurology. 1997, Vol 244, Num 9, pp 542-547, issn 0340-5354Article

Single muscle fibre analyses in 2 brothers with succinate dehydrogenase deficiencyREICHMANN, H; ANGELINI, C.European neurology. 1994, Vol 34, Num 2, pp 95-98, issn 0014-3022Article

OCULO CRANIO-SOMATIC SYNDROME: MITOCHONDRIAL ALTERATIONS AND LACTIC ACIDEMIAANGELINI C; ARMANI M; LUECKE S et al.1979; ACTA NEUROL.; ITA; DA. 1979; VOL. 1; NO 1; PP. 59-63; ABS. ITA; BIBL. 6 REF.Article

MITOCHONDRIA-LIPID-GLYCOGEN (MLG)DISEASE OF MUSCLE. A MORPHOLOGICALLY REGRESSIVE CONGENITAL MYOPATHY = MALADIE DES MITOCHONDRIES, DES LIPIDES ET DU GLYCOGENE MUSCULAIRE. UNE MYOPATHIE CONGENITALE, MORPHOLOGIQUEMENT REGRESSIVEJERUSALEM F; ANGELINI C; ENGEL AG et al.1973; ARCH. NEUROL.; U.S.A.; DA. 1973; VOL. 29; NO 3; PP. 162-169; BIBL. 29REF.Article

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