Mantovani V - Search Results

1

Mutations of the CFTR gene in pancreatic disease.

Pezzilli R, Morselli-Labate AM, Mantovani V, Romboli E, Selva P, Migliori M, Corinaldesi R, Gullo L. Pezzilli R, et al. Among authors: mantovani v. Pancreas. 2003 Nov;27(4):332-6. doi: 10.1097/00006676-200311000-00011. Pancreas. 2003. PMID: 14576497

2

Mutations of the CFTR gene in idiopathic pancreatic hyperenzymemia.

Gullo L, Mantovani V, Manca M, Migliori M, Bastagli L, Pezzilli R. Gullo L, et al. Among authors: mantovani v. Pancreas. 2005 Nov;31(4):350-2. doi: 10.1097/01.mpa.0000181485.04528.24. Pancreas. 2005. PMID: 16258369

3

SPINK1 and PRSS1 mutations in benign pancreatic hyperenzymemia.

Gullo L, Laghi L, Migliori M, Lucrezio L, Bianchi P, Randolph AE, Mantovani V, Bastagli L, Pezzilli R, Malesci A. Gullo L, et al. Among authors: mantovani v. Pancreas. 2008 Jul;37(1):31-5. doi: 10.1097/MPA.0b013e31816172b7. Pancreas. 2008. PMID: 18580441

4

Simple method for haplotyping the poly(TG) repeat in individuals carrying the IVS8 5T allele in the CFTR gene.

Mantovani V, Garagnani P, Selva P, Rossi C, Ferrari S, Cenci M, Calza N, Cerreta V, Luiselli D, Romeo G. Mantovani V, et al. Clin Chem. 2007 Mar;53(3):531-3. doi: 10.1373/clinchem.2006.074807. Epub 2007 Jan 18. Clin Chem. 2007. PMID: 17234733

5

Molecular analysis of HLA genes for the selection of unrelated bone marrow donor.

Mantovani V, Martinelli G, Bragliani M, Buzzi M, Selva P, Collina E, Farabegoli P, Rosti GA, Bandini G, Tura S, et al. Mantovani V, et al. Bone Marrow Transplant. 1995 Sep;16(3):329-35. Bone Marrow Transplant. 1995. PMID: 8535303

6

A patient with pancreas divisum, recurrent acute pancreatitis, and homozygosity for the cystic fibrosis transmembrane regulator-associated protein 5T allele.

Montagnani M, Cazzato S, Mutignani M, Cevenini M, Guidetti E, Zvi IB, Aldini R, Saraceni G, Cavoli C, Garagnani P, Ferrari S, Mantovani V. Montagnani M, et al. Among authors: mantovani v. Clin Gastroenterol Hepatol. 2013 May;11(5):579-81. doi: 10.1016/j.cgh.2013.02.012. Epub 2013 Feb 13. Clin Gastroenterol Hepatol. 2013. PMID: 23416327

7

Identification of eight novel glucokinase mutations in Italian children with maturity-onset diabetes of the young.

Mantovani V, Salardi S, Cerreta V, Bastia D, Cenci M, Ragni L, Zucchini S, Parente R, Cicognani A. Mantovani V, et al. Hum Mutat. 2003 Oct;22(4):338. doi: 10.1002/humu.9179. Hum Mutat. 2003. PMID: 12955723

8

HLA-DP polymorphism in northern Italian celiac patients.

Mantovani V, Corazza GR, Frisoni M, Zaniboni MG, Bragliani M, Valentini RA, Barboni P, Lambertini A, Gasbarrini G. Mantovani V, et al. Tissue Antigens. 1992 Oct;40(4):182-6. doi: 10.1111/j.1399-0039.1992.tb02043.x. Tissue Antigens. 1992. PMID: 1361687

9

Molecular analysis of HLA-DQ A alleles in coeliac disease lack of a unique disease-associated sequence.

Mantovani V, Corazza GR, Angelini G, Delfino L, Frisoni M, Mirri P, Valentini RA, Barboni P, Gasbarrini G, Ferrara GB. Mantovani V, et al. Clin Exp Immunol. 1991 Jan;83(1):74-8. doi: 10.1111/j.1365-2249.1991.tb05591.x. Clin Exp Immunol. 1991. PMID: 1671007 Free PMC article.

10

CYP21 analysis and phenotype/genotype relationship in the screened population of the Italian Emilia-Romagna region.

Balsamo A, Cacciari E, Baldazzi L, Tartaglia L, Cassio A, Mantovani V, Piazzi S, Cicognani A, Pirazzoli P, Mainetti B, Zappulla F. Balsamo A, et al. Among authors: mantovani v. Clin Endocrinol (Oxf). 2000 Jul;53(1):117-25. doi: 10.1046/j.1365-2265.2000.01048.x. Clin Endocrinol (Oxf). 2000. PMID: 10931088

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