A. Marocchi

发表

Development and evaluation of immunochromatographic rapid tests for screening of cannabinoids, cocaine, and opiates in urine.

R. de la Torre, M. Moeller, R. Wennig, 1998, Journal of analytical toxicology.

Serum concentrations of 2,3,7,8-tetrachlorodibenzo-p-dioxin and test results from selected residents of Seveso, Italy.

P. Brambilla, L. Needham, D. Patterson, 1991, Journal of toxicology and environmental health.

Accuracy of cholesterol measurements in Italian clinical laboratories. Joint project GISSI prevention--Italian Society of Clinical Biochemistry. SIBioC GISSI Prevenzione Group.

P. Brambilla, F. Ceriotti, P. Luraschi, 1997, European journal of clinical chemistry and clinical biochemistry : journal of the Forum of European Clinical Chemistry Societies.

Use of radioguided surgery with [111In]-pentetreotide in the management of an ACTH-secreting bronchial carcinoid causing ectopic Cushing’s syndrome

M. Bramerio, P. Dalino, A. Vanzulli, 2005, Journal of endocrinological investigation.

Frequency of butyrylcholinesterase gene mutations in individuals with abnormal inhibition numbers: an Italian-population study.

M. Panteghini, A. Mosca, S. Penco, 2003, Pharmacogenetics.

Dioxin Exposure and health effects on people at Seveso, Italy

P. Brambilla, L. Needham, D. Patterson, 1992 .

A new method for D-glucaric acid excretion measurement that is suitable for automated instruments.

P. Brambilla, L. Colombo, A. Marocchi, 1988, Clinical chemistry.

Clinical laboratory manifestations of exposure to dioxin in children. A six-year study of the effects of an environmental disaster near Seveso, Italy.

N. Mantel, P. Brambilla, D. Young, 1986, JAMA.

Does Down's syndrome support the homocysteine theory of atherogenesis? Experience in elderly subjects with trisomy 21.

E. Porcellini, F. Licastro, D. Lio, 2006, Archives of gerontology and geriatrics.

Stratified analysis of multivariate clinical data: application of a Mantel-Haenszel approach.

N. Mantel, P. Brambilla, A. Marocchi, 1983, Statistics in medicine.

Colony-stimulating activity from the new metastatic TS/A cell line and its high- and low-metastatic clonal derivatives.

P. Lollini, P. Brambilla, P. Nanni, 1985, British Journal of Cancer.

Blood trace metals in a sporadic amyotrophic lateral sclerosis geographical cluster

C. Del Bo’, E. Gianazza, S. Penco, 2017, BioMetals.

Mitochondrial DNA copy number and D-loop region methylation in carriers of amyotrophic lateral sclerosis gene mutations.

F. Coppedè, L. Migliore, C. Lunetta, 2018, Epigenomics.

Increase in DNA methylation in patients with amyotrophic lateral sclerosis carriers of not fully penetrant SOD1 mutations

F. Coppedè, L. Migliore, S. Penco, 2018, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression

M. Corbo, F. Avemaria, S. Penco, 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

De Novo MGC4607 Gene Heterozygous Missense Variants in a Child with Multiple Cerebral Cavernous Malformations

V. Capra, F. Avemaria, S. Penco, 2012, Journal of Molecular Neuroscience.

Phenotypic Heterogeneity in a SOD1 G93D Italian ALS Family: An Example of Human Model to Study a Complex Disease

M. Corbo, F. Avemaria, S. Penco, 2011, Journal of Molecular Neuroscience.

Serum metal evaluation in a small cohort of Amyotrophic Lateral Sclerosis patients reveals high levels of thiophylic species

E. Gianazza, S. Penco, C. Lunetta, 2016 .

N-terminal pro-B-type natriuretic peptide and echocardiographic abnormalities in severely obese patients: correlation with visceral fat.

B. Ambrosi, M. Corsi, A. Malavazos, 2006, Clinical chemistry.

Unexpectedly dangerous escargot stew: oleandrin poisoning through the alimentary chain.

F. Guidugli, A. Marocchi, F. Zoppi, 2006, Journal of analytical toxicology.

SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study.

C. Carcassi, M. Giagheddu, G. Siciliano, 2005, Journal of neurology.

Total serum tryptase: a predictive marker for KIT mutation in acute myeloid leukemia.

F. Ferrara, G. Pizzolo, G. Nadali, 2009, Leukemia research.

Pru p 3-Sensitised Italian Peach-Allergic Patients Are Less Likely to Develop Severe Symptoms When Also Presenting IgE Antibodies to Pru p 1 and Pru p 4

M. Nichelatti, E. Pastorello, V. Pravettoni, 2011, International Archives of Allergy and Immunology.

A Novel MGC4607/CCM2 Gene Mutation Associated with Cerebral Spinal and Cutaneous Cavernous Angiomas

L. Tassi, S. Benedetti, O. Mecarelli, 2015, Journal of Molecular Neuroscience.

Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation.

L. Tassi, P. Brunori, R. Rocchi, 2007, Archives of neurology.

NOTCH3 gene mutations in subjects clinically suspected of CADASIL

R. Sterzi, E. Scarpini, G. Mandrile, 2011, Journal of the Neurological Sciences.

Automation of the Pre-Analytical Phase: A Performance Evaluation of Alternative Scenarios

T. Tolio, A. Marocchi, C. De Capitani, 2002 .

Altered vessel signalling molecules in subjects with Downs syndrome.

E. Porcellini, F. Licastro, M. Trabucchi, 2006, International journal of immunopathology and pharmacology.

Molecular analysis of PDGFRA and PDGFRB genes by rapid single-strand conformation polymorphism (SSCP) in patients with core-binding factor leukaemias with KIT or FLT3 mutation.

F. Ferrara, A. Cuneo, G. Pizzolo, 2008, Anticancer research.

Erratum to: Is the SHRPS Strain a Suitable Model of Spontaneous CADASIL?

E. Tremoli, M. Abbate, S. Penco, 2012, Journal of Molecular Neuroscience.

Molecular screening test in familial forms of cerebral cavernous malformation: the impact of the Multiplex Ligation-dependent Probe Amplification approach.

L. Tassi, S. Penco, E. Bianchi, 2009, Journal of neurosurgery.

Colony-stimulating factor produced by murine adrenocortical tumor cells.

A. Pessina, P. Brambilla, M. Neri, 1986, Journal of the National Cancer Institute.

Measurement of ionized magnesium with AVL 988/4 electrolyte analyzer: preliminary analytical and clinical results.

F. Pazzucconi, E. Guagnellini, A. Marocchi, 1996, Scandinavian journal of clinical and laboratory investigation. Supplementum.

Paraoxonase 1 L55M, Q192R and paraoxonase 2 S311C alleles in atherothrombosis

R. De Maria, O. Parodi, J. Campolo, 2012, Molecular and Cellular Biochemistry.

Combined evaluation of genotype and phenotype of thiopurine S-methyltransferase (TPMT) in the clinical management of patients in chronic therapy with azathioprine

C. Perno, F. Mattioli, F. Scaglione, 2019, Drug metabolism and personalized therapy.

The role of chromogranin A in the management of patients with phaeochromocytoma

M. Boniardi, P. Dalino, M. Gambacorta, 2006, Clinical endocrinology.

Familial cerebral cavernous malformation: report of a further Italian family

L. Pantoni, D. Inzitari, A. Poggesi, 2009, Neurological Sciences.

Glutamate-cysteine ligase polymorphism, hypertension, and male sex are associated with cardiovascular events. Biochemical and genetic characterization of Italian subpopulation.

L. Colombo, O. Parodi, J. Campolo, 2007, American heart journal.

Increased urinary D-glucaric acid excretion by children living in an area polluted with tetrachlorodibenzoparadioxin (TCDD).

P. Brambilla, P. Brambilla, G. Idéo, 1982, Clinica chimica acta; international journal of clinical chemistry.

Myocardial necrosis in ICU patients with acute non-cardiac disease: a prospective study

L. Prencipe, S. Arlati, A. Marocchi, 2000, Intensive Care Medicine.

A novel type of familial transthyretin amyloidosis, ATTR Asn124Ser, with co-localization of κ light chains

Masaaki Nakamura, Y. Ando, G. Colussi, 2007, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Genetic Variations Within KRIT1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a Large Italian Family Harbouring a Krit1/CCM1 Mutation

P. Brunori, S. Buscone, S. Battistini, 2010, Journal of Molecular Neuroscience.

De Novo MGC4607 Gene Heterozygous Missense Variants in a Child with Multiple Cerebral Cavernous Malformations

V. Capra, F. Avemaria, S. Penco, 2012, Journal of Molecular Neuroscience.

Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis

F. Coppedè, L. Migliore, K. Lunnon, 2020, Clinical epigenetics.

Experience with External Quality Assessment of Drugs of Abuse Testing in the Lombardy Region in Italy

M. Amigoni, A. Marocchi, M. Cassani, 2002, Clinical chemistry and laboratory medicine.

Results of a pilot study of endoscopic screening of first degree relatives of colorectal cancer patients in Italy.

P. Brambilla, L. Merlino, S. Ghezzi, 1997, Journal of epidemiology and community health.

SOD1 mutations in amyotrophic lateral sclerosis

C. Carcassi, M. Giagheddu, G. Siciliano, 2005, Journal of Neurology.

Assessment of the Role of Genetic Polymorphism in Venous Thrombosis Through Artificial Neural Networks

M Buscema, M. Buscema, M. Intraligi, 2005, Annals of human genetics.

Erratum to: Is the SHRPS Strain a Suitable Model of Spontaneous CADASIL?

E. Tremoli, M. Abbate, S. Penco, 2012, Journal of Molecular Neuroscience.

Mutational Screening of NOTCH3 Gene Reveals Two Novel Mutations: Complexity of CADASIL Diagnosis

S. Penco, G. Gesu, A. Burlina, 2014, Journal of Molecular Neuroscience.

Paraoxonase 1 L55M, Q192R and paraoxonase 2 S311C alleles in atherothrombosis

O. Parodi, J. Campolo, S. Penco, 2013, Molecular and Cellular Biochemistry.

Serum Proteome in a Sporadic Amyotrophic Lateral Sclerosis Geographical Cluster

C. Banfi, E. Gianazza, S. Penco, 2017, Proteomics. Clinical applications.

A Novel MGC4607/CCM2 Gene Mutation Associated with Cerebral Spinal and Cutaneous Cavernous Angiomas

L. Tassi, S. Benedetti, O. Mecarelli, 2015, Journal of Molecular Neuroscience.

New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background

Paolo Massimo Buscema, Enzo Grossi, Alessandro Marocchi, 2008, BMC Bioinformatics.

Homocysteine, vitamin B12, serum and erythrocyte folate in peritoneal dialysis patients.

C. Patrosso, E. Taioli, S. Finazzi, 2001, Clinical nephrology.

A Two-Center Evaluation of the Blood Gas Immediate Response Mobile Analyzer (IRMA)

F. Ceriotti, P. Bonini, A. Marocchi, 2002, Clinical chemistry and laboratory medicine.

Human data derived from the seveso accident - Relevance for human risk assessment

P. Brambilla, S. Signorini, P. Mocarelli, 1992 .

Genetic variability of the fructosamine 3-kinase gene in diabetic patients

A. Mosca, R. Paleari, A. Lapolla, 2011, Clinical chemistry and laboratory medicine.

MODULAR ANALYTICS: A New Approach to Automation in the Clinical Laboratory

Hiroshi Mitsumaki, Franz Keller, Gary L. Horowitz, 2005, Journal of automated methods & management in chemistry.

Renal cell carcinoma and normal kidney protein expression

D. Hochstrasser, M. Wilkins, S. Frutiger, 1997, Electrophoresis.

Anti-dsDNA autoantibodies in serum of Down's syndrome patients.

F. Licastro, M. Corsi, A. Marocchi, 2004, Clinica chimica acta; international journal of clinical chemistry.