Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("PANDOLFO, M")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 83

  • Page / 4
Export

Selection :

  • and

LA DISTENSIONE VESCICALE SECONDO HELMSTEIN NEL TRATTAMENTO DELLE EMORRAGIE POSTATTINICHE. = LA DISTENSION VESICALE SELON LA TECHNIQUE DE HELMSTEIN DANS LE TRAITEMENT DES HEMORRAGIES APRES IRRADIATIONMARTINIELLO R; PANDOLFO M.1976; UROLOGIA; ITAL.; DA. 1976; VOL. 43; NO 6; PP. 591-594; ABS. ANGL.; BIBL. 1/2 P.Article

Molecular pathogenesis of Friedreich ataxiaPANDOLFO, M.Archives of neurology (Chicago). 1999, Vol 56, Num 10, pp 1201-1208, issn 0003-9942Article

A rapid method to isolate (GT)n repeats from yeast artificial chromosomesPANDOLFO, M.Nucleic acids research. 1992, Vol 20, Num 5, issn 0305-1048, p. 1154Article

Le rôle de l'Inspection de la pharmacie en matière de conception de locaux professionnels: officines, hôpitaux, industries, laboratoires d'analyses de biologie médicalePANDOLFO, M.1987, 33 p.Thesis

A Pvu II RFLP in the human ADH3 genePANDOLFO, M; SMITH, M.Nucleic acids research. 1988, Vol 16, Num 24, issn 0305-1048, 11857 [1 p.]Article

Le rôle de l'Inspection de la pharmacie en matière de conception de locaux professionnels: officines, hôpitaux, industries, laboratoires d'analyses de biologie médicalePANDOLFO, M.1987, 33 p.Thesis

Acute behavioural change in a young woman evolving towards cerebellar syndromeNAEIJE, G; DE HEMPTINNE, Q; DEPONDT, C et al.Clinical neurology and neurosurgery (Dutch-Flemish ed.). 2010, Vol 112, Num 6, pp 509-511, issn 0303-8467, 3 p.Article

Spinocerebellar ataxia types 1, 2, 3, and 6 : Disease severity and nonataxia symptomsSCHMITZ-HÜBSCH, T; COUDERT, M; RIBAI, P et al.Neurology. 2008, Vol 71, Num 13, pp 982-989, issn 0028-3878, 8 p.Article

Acute sodium overload produces renal tubulointerstitial inflammation in normal ratsROSON, M. I; CAVALLERO, S; PENNA, S. Della et al.Kidney international. 2006, Vol 70, Num 8, pp 1439-1446, issn 0085-2538, 8 p.Article

Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in Italian Lesch-Nyhan patients: Identification of nine novel mutationsBERTELLI, M; RANDI, D; MICHELI, V et al.Journal of inherited metabolic disease. 2004, Vol 27, Num 6, pp 767-773, issn 0141-8955, 7 p.Article

Friedreich's ataxia : Point mutations and clinical presentation of compound heterozygotesCOSSEE, M; DÜRR, A; MÜLLER, U et al.Annals of neurology. 1999, Vol 45, Num 2, pp 200-206, issn 0364-5134Article

Unusual EEG pattern linked to chromosome 3p in a family with idiopathic generalized epilepsyZARA, F; LABUDA, M; GAROFALO, P. G et al.Neurology. 1998, Vol 51, Num 2, pp 493-498, issn 0028-3878Article

Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia familiesMOSELEY, M. L; BENZOW, K. A; RANUM, L. P. W et al.Neurology. 1998, Vol 51, Num 6, pp 1666-1671, issn 0028-3878Article

Familial essential tremor in 4 kindreds : Prospects for genetic mappingJANKOVIC, J; BEACH, J; PANDOLFO, M et al.Archives of neurology (Chicago). 1997, Vol 54, Num 3, pp 289-294, issn 0003-9942Article

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranesCAMPUZANO, V; MONTERMINI, L; AUTHIER, F. J et al.Human molecular genetics (Print). 1997, Vol 6, Num 11, pp 1771-1780, issn 0964-6906Article

Regional localization by in situ hybridization of a human chromosome 9 marker tightly linked to the Friedreich's ataxia locusRAIMONDI, E; ANTONELLI, A; DRIESEL, A. J et al.Human genetics. 1990, Vol 85, Num 1, pp 125-126, issn 0340-6717, 2 p.Article

Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3HEDERA, P; BLAIR, M. A; ABOU-KHALIL, B et al.Neurology. 2007, Vol 68, Num 24, pp 2107-2112, issn 0028-3878, 6 p.Article

Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesiaBRUNO, M. K; LEE, H.-Y; GWINN-HARDY, K et al.Neurology. 2007, Vol 68, Num 21, pp 1782-1789, issn 0028-3878, 8 p.Article

Phenotypic variability in Friedreich ataxia : Role of the associated GAA triplet repeat expansionMONTERMINI, L; RICHTER, A; LEMIEUX, B et al.Annals of neurology. 1997, Vol 41, Num 5, pp 675-682, issn 0364-5134Article

The Friedreich ataxia GAA triplet repeat : premutation and normal allelesMONTERMINI, L; ANDERMANN, E; TURANO, M et al.Human molecular genetics (Print). 1997, Vol 6, Num 8, pp 1261-1266, issn 0964-6906Article

Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedrich's ataxia locus on chromosome 9qPALAU, F; DE MICHELE, G; FILLA, A et al.Annals of neurology. 1995, Vol 37, Num 3, pp 359-362, issn 0364-5134Article

Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1FIGUERA, L. E; PANDOLFO, M; DUNNE, P. W et al.Nature genetics. 1995, Vol 10, Num 2, pp 202-207, issn 1061-4036Article

The Friedreich ataxia critical region spans a 150-kb interval on chromosome 9q13MONTERMINI, L; RODIUS, F; WENHERT, M et al.American journal of human genetics. 1995, Vol 57, Num 5, pp 1061-1067, issn 0002-9297Article

Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian populationPIANESE, L; COCOZZA, S; VARRONE, S et al.Journal of medical genetics. 1994, Vol 31, Num 2, pp 133-135, issn 0022-2593Conference Paper

Evidence of a genetic marker associated with early onset in Friedrich's ataxiaCOCOZZA, S; ANTONELLI, A; PORCELLINI, A et al.Journal of neurology. 1993, Vol 240, Num 4, pp 254-256, issn 0340-5354Article

  • Page / 4