Migraine with aura and white matter abnormalities : Notch3 mutationCERONI, M; POLONI, T. E; FERRARI, M et al.Neurology. 2000, Vol 54, Num 9, pp 1869-1871, issn 0028-3878Article

A nonsense mutation (Gln-673-Term) in exon 17 of the human dystrophin gene detected by heteroduplex analysisBARBIERI, A. M; SORIANI, N; TUBIELLO, G. M et al.Human genetics. 1995, Vol 96, Num 3, pp 343-344, issn 0340-6717Article

Identification of sequence elements contributing to the intrinsic curvature of the mouse satellite DNA repeatCARRERA, P; MARTINEZ-BALBAS, M. A; PORTUGAL, J et al.Nucleic acids research. 1991, Vol 19, Num 20, pp 5639-5644, issn 0305-1048Article

Diagnosis of genetic diseases by DNA technologyFERRARI, M; CREMONESI, L; CARRERA, P et al.Pure and applied chemistry. 1991, Vol 63, Num 8, pp 1089-1096, issn 0033-4545Conference Paper

Why do patients engage in medical tourism?RUNNELS, Vivien; CARRERA, P. M.Maturitas (Amsterdam). 2012, Vol 73, Num 4, pp 300-304, issn 0378-5122, 5 p.Article

Tecnologia del DNA ricombinante per lo studio e la diagnosi delle malattie ereditarie = Recombinant DNA technology for the studyand diagnosis of ereditary diseasesFERRARI, M; CARRERA, P.Giornale italiano di chimica clinica. 1991, Vol 16, Num 5, pp 293-304, issn 0392-2227Article

Utilizzo delle tecniche molecolari per lo studio del deficit di 21-idrossilasi = Study of 21 hydroxylase deficiency by molecular techniquesCARRERA, P; FERRARI, M.Giornale italiano di chimica clinica. 1993, Vol 18, Num 3, pp 177-187, issn 0392-2227Article

Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathyBENEDETTI, S; BERTINI, E; QUATTRINI, A et al.Journal of neurology, neurosurgery and psychiatry. 2005, Vol 76, Num 7, pp 1019-1021, issn 0022-3050, 3 p.Article

Genetic heterogeneity in Italian families with familial hemiplegic migraineCARRERA, P; PIATTI, M; STENIRRI, S et al.Neurology. 1999, Vol 53, Num 1, pp 26-33, issn 0028-3878Article

Validation of double gradient denaturing gradient gel electrophoresis through multigenic retrospective analysisCREMONESI, L; CARRERA, P; FUMAGALLI, A et al.Clinical chemistry (Baltimore, Md.). 1999, Vol 45, Num 1, pp 35-40, issn 0009-9147Article

A single mRNA, transcribed from an alternative, erythroid-specific, promoter codes for two non-myristylated forms of NADH-cytochrome b₅ reductasePIETRINI, G; AGGUJARO, D; CARRERA, P et al.The Journal of cell biology. 1992, Vol 117, Num 5, pp 975-986, issn 0021-9525Article

Differential effects of priming at the encoding and judgment stagePHILIPPOT, P; SCHWARZ, N; CARRERA, P et al.European journal of social psychology. 1991, Vol 21, Num 4, pp 293-302, issn 0046-2772Article

Sister chromatid exchanges in first-trimester chorionic villi after in vivo and in vitro exposure to diagnostic ultrasoundCARRERA, P; ORSINI, S; TERZOLI, G et al.Prenatal diagnosis. 1990, Vol 10, Num 3, pp 141-148, issn 0197-3851Article

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

Standard protocols for the analysis of school based data from echo sounder surveysREID, D; SCALABRIN, C; PETITGAS, P et al.Fisheries research. 2000, Vol 47, Num 2-3, pp 125-136, issn 0165-7836Article

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxiaBATTISTINI, S; STENIRRI, S; CARRERA, P et al.Neurology. 1999, Vol 53, Num 1, pp 38-43, issn 0028-3878Article

Ligase chain reaction assay for human mutations : the sickle cell by LCR assayREYES, A. A; CARRERA, P; CARDILLO, E et al.Clinical chemistry (Baltimore, Md.). 1997, Vol 43, Num 1, pp 40-44, issn 0009-9147Conference Paper

Point mutations in Italian patients with classic, non-classic, and cryptic forms of steroid 21-hydroxylase deficiencyCARRERA, P; BORDONE, L; AZZANI, T et al.Human genetics. 1996, Vol 98, Num 6, pp 662-665, issn 0340-6717Article

The Bacillus subtilis neutral protease : a model case for site-directed mutagenesis and protein engineeringGRANDI, G; TOMA, S; MARGARIT, I et al.Chimica oggi. 1990, Vol 8, Num 7-8, pp 9-13, issn 0392-839X, 5 p.Article

Plasmapping: an easy computer tool for display and storage of plasmid mapsMAISANO, F; GRANDI, G; CARRERA, P et al.Chimica oggi. 1987, Num 11, pp 73-74, issn 0392-839XArticle

Twins with severe recurrent chest infectionsMINEN, F; BARBI, E; VENTURA, A et al.Thorax. 2008, Vol 63, Num 12, issn 0040-6376, 1082, 1090 [2 p.]Article

Phenotypic clustering of lamin A/C mutations in neuromuscular patientsBENEDETTI, S; MENDITTO, I; MORANDI, L et al.Neurology. 2007, Vol 69, Num 12, pp 1285-1292, issn 0028-3878, 8 p.Article

Early visual function impairment in CADASILPARISI, V; PIERELLI, F; FATTAPPOSTA, F et al.Neurology. 2003, Vol 60, Num 12, pp 2008-2010, issn 0028-3878, 3 p.Article

Visual electrophysiological responses in subjects with cerebral autosomal arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)PARISI, V; PIERELLI, F; MALANDRINI, A et al.Clinical neurophysiology. 2000, Vol 111, Num 9, pp 1582-1588, issn 1388-2457Article

Rapid detection of 21-hydroxylase deficiency mutations by allele-specific in vitro amplification and capillary zone electrophoresisCARRERA, P; BARBIERI, A. M; FERRARI, M et al.Clinical chemistry (Baltimore, Md.). 1997, Vol 43, Num 11, pp 2121-2127, issn 0009-9147Conference Paper