CONTRIBUTION A L'ETUDE GEOLOGIQUE DE LA REGION DE LOURDES ET DU CHAINON PIBESTE-ESTIBETE (HAUTES-PYRENEES).VILLANOVA M.1962; THESE.DOCT.TROIS.CYCLE.TOULOUSE.; 1962, P. 1 A 173Miscellaneous

CONTRIBUTION A L'ETUDE GEOLOGIQUE DE LA REGION DE LOURDES ET DU CHAINON PIBESTE-ESTIBETE (HAUTES-PYRENEES).VILLANOVA M.1962; TOULOUSE-THESE. DOCT. TROIS. CYCLE.; 1962, P. 1 A 173Thesis

LA DYNAMIQUE DES FOSSES A TURBIDITES ET DE LEUR CONTENU SEDIMENTAIRE DANS LE SYSTEME PYRENEENFEUILLEE P; VILLANOVA M; WINNOCK E et al.1973; BULL. SOC. GEOL. FR.; FR. ; 1973, VOL. 15, NUM. 0001, P. 61 A 76Serial Issue

EVOLUTION DU DOMAINE MARIN PYRENEEN DU SENONIEN SUPERIEUR A L'EOCENE INFERIEUR.HENRY J; LANUSSE R; VILLANOVA M et al.1971; PUBL. INST. FR. PETROLE, COLLECT. COLLOQ. SEMINAIRES; FRA; 1971, VOL. 22, NUM. PART01Miscellaneous

SERIES STRATIGRAPHIQUES ET PALEOGEOGRAPHIE DU CRETACE SUPERIEUR DANS LA REGION DE LOURDES.CAPDECOMME H; DELOFFRE R; HENRY J et al.1965; BULL. SOC. GEOL. FR; FRA; 1965, VOL. 7, NUM. 0003, P. 392 A 398Miscellaneous

MICROFAUNES, CENOMANIENNES ET SANTONIENNES DANS LE "CALCAIRE DES CANONS" (VALLEE D'ASPE, SAINTE-ENGRACE, BASSES-PYRENEES).CUVILLIER J; HENRY J; RIBIS R et al.1964; BULL. SOC. GEOL. FR; FRA; 1964, VOL. 6, NUM. 0002, P. 273 A 277Miscellaneous

A process environment supporting Web multimedia information systemsVILLANOVA, M; BELKHATIR, N; MARTIN, H et al.International journal of computers & applications. 2002, Vol 24, Num 2, pp 70-76, issn 1206-212XConference Paper

Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa : a clinicopathological reportMALANDRINI, A; PALMERI, S; FABRIZI, G. M et al.Journal of the neurological sciences. 1998, Vol 155, Num 2, pp 218-221, issn 0022-510XArticle

Ultrastructural study of enteric ganglia in three patients with Rett syndromeMALANDRIN, A; HAYEK, G; VILLANOVA, M et al.Brain & development (Tokyo. 1979). 1998, Vol 20, Num 8, pp 586-588, issn 0387-7604Article

Expression of CD59, a regulator of the membrane attack complex of complement, on human skeletal muscle fibersNAVENOT, J.-M; VILLANOVA, M; LUCAS-HERON, B et al.Muscle & nerve. 1997, Vol 20, Num 1, pp 92-96, issn 0148-639XArticle

Focal myositis : A polymerase chain reaction analysis for a viral etiologyTOTI, P; ROMANO, L; VILLANOVA, M et al.Human pathology. 1997, Vol 28, Num 1, pp 111-113, issn 0046-8177Article

Eosinophilia myalgia syndrome: absence of immunoglobulin reactivity suggests a cellular rather than humoral mechanismVILLANOVA, M; DE CLERCK, L. S; CRAS, P et al.Acta neurologica belgica. 1994, Vol 94, Num 3, pp 200-203, issn 0300-9009Conference Paper

Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophyMERCURI, E; BERTINI, E; CINI, C et al.Neurology. 2007, Vol 68, Num 1, pp 51-55, issn 0028-3878, 5 p.Article

The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndromeCARROZZO, R; TESSA, A; FEDERICO, A et al.Neurology. 2001, Vol 56, Num 5, pp 687-690, issn 0028-3878Article

Neurological involvement in Werner's syndrome : Clinical and biopsy study of a familial caseMALANDRINI, A; DOTTI, M. T; VILLANOVA, M et al.European neurology. 2000, Vol 44, Num 3, pp 187-189, issn 0014-3022Article

Detection of β-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren)VILLANOVA, M; CEUTERICK, C; FEDERICO, A et al.Acta neuropathologica. 1999, Vol 98, Num 1, pp 78-84, issn 0001-6322Article

FACL4, a new gene encoding long-chain Acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardationPICCINI, M; VITELLI, F; BRUTTINI, M et al.Genomics (San Diego, Calif.). 1998, Vol 47, Num 3, pp 350-358, issn 0888-7543Article

Neuronal intranuclear inclusion disease : neuropathologic study of a caseMALANDRINI, A; VILLANOVA, M; TRIPODI, S et al.Brain & development (Tokyo. 1979). 1998, Vol 20, Num 5, pp 290-294, issn 0387-7604Article

Merosin positive congenital muscular dystrophy with severe involvement of the central nervous systemDE STEFANO, N; DOTTI, M. T; VILLANOVA, M et al.Brain & development (Tokyo. 1979). 1996, Vol 18, Num 4, pp 323-326, issn 0387-7604Article

Eosinophilia-myalgia syndrome: a clinicopathological study of four patientsVILLANOVA, M; DE CLERCK, L. S; CRAS, P et al.Clinical neuropathology. 1993, Vol 12, Num 4, pp 201-203, issn 0722-5091Conference Paper

Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASILMALANDRINI, A; ALBANI, F; FERRARI, M et al.Neurology. 2002, Vol 59, Num 4, pp 617-620, issn 0028-3878Article

Type I sialidosis : A clinical, biochemical and neuroradiological studyPALMERI, S; VILLANOVA, M; GUAZZI, G et al.European neurology. 2000, Vol 43, Num 2, pp 88-94, issn 0014-3022Article

Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian familyCASALI, C; FABRIZI, G. M; DIGENNARO, M. G. C et al.Neurology. 1999, Vol 52, Num 5, pp 1103-1104, issn 0028-3878Article

Intégration de processus dans les Systèmes d'Informations Multimédias Distribués - une approche pour le contrôle, la coordination et la communication des activités = Process integration in Multimedia distributed Information Systems - An approach of the control, coordination and communication of activitiesVILLANOVA, M; MARTIN, H; BELKHATIR, N et al.Ecrit et multimédia. Journée jeunes chercheurs. 1999, pp 45-46Conference Paper

Giant axonal neuropathy with subclinical involvement of the central nervous system : Case reportMALANDRINI, A; DOTTI, M. T; BATTISTI, C et al.Journal of the neurological sciences. 1998, Vol 158, Num 2, pp 232-235, issn 0022-510XArticle