Medicina D - Search Results

1

Mineralization of alpha-1-antitrypsin inclusion bodies in Mmalton alpha-1-antitrypsin deficiency.

Callea F, Giovannoni I, Francalanci P, Boldrini R, Faa G, Medicina D, Nobili V, Desmet VJ, Ishak K, Seyama K, Bellacchio E. Callea F, et al. Among authors: medicina d. Orphanet J Rare Dis. 2018 May 16;13(1):79. doi: 10.1186/s13023-018-0821-7. Orphanet J Rare Dis. 2018. PMID: 29769092 Free PMC article.

2

Z and Mmalton-1-antitrypsin deficiency-associated hepatocellular carcinoma: a genetic study.

Francalanci P, Santorelli FM, Saccani S, Bonetti MF, Medicina D, Coni P, Faa G, Callea F. Francalanci P, et al. Among authors: medicina d. Liver Int. 2009 Nov;29(10):1593-6. doi: 10.1111/j.1478-3231.2009.02091.x. Epub 2009 Sep 10. Liver Int. 2009. PMID: 19744266

3

Genetic and immunological characterization of fibrinogen inclusion bodies in patients with hepatic fibrinogen storage and liver disease.

Medicina D, Fabbretti G, Brennan SO, George PM, Kudryk B, Callea F. Medicina D, et al. Ann N Y Acad Sci. 2001;936:522-5. doi: 10.1111/j.1749-6632.2001.tb03538.x. Ann N Y Acad Sci. 2001. PMID: 11460509

4

Intestinal Wegener's granulomatosis in a patient with severe alpha-1-antitrypsin deficiency resulting from a unique combination of two deficiency alleles (PiZ and PiMProcida).

Lonardo A, Medicina D, Leonelli M, Bagni A, Callea F. Lonardo A, et al. Among authors: medicina d. Eur J Gastroenterol Hepatol. 2002 Dec;14(12):1389-92. doi: 10.1097/00042737-200212000-00017. Eur J Gastroenterol Hepatol. 2002. PMID: 12468963

5

Identification and characterisation of eight novel SERPINA1 Null mutations.

Ferrarotti I, Carroll TP, Ottaviani S, Fra AM, O'Brien G, Molloy K, Corda L, Medicina D, Curran DR, McElvaney NG, Luisetti M. Ferrarotti I, et al. Among authors: medicina d. Orphanet J Rare Dis. 2014 Nov 26;9:172. doi: 10.1186/s13023-014-0172-y. Orphanet J Rare Dis. 2014. PMID: 25425243 Free PMC article.

6

Inborn errors of metabolism and hepatocellular carcinoma (HCC).

Callea F, Medicina D, Fabbretti G, Bercich L, Bonetti MF. Callea F, et al. Among authors: medicina d. Adv Clin Path. 2000 Oct;4(4):211-3. Adv Clin Path. 2000. PMID: 11436160 No abstract available.

7

Fibrinogen brescia: hepatic endoplasmic reticulum storage and hypofibrinogenemia because of a gamma284 Gly-->Arg mutation.

Brennan SO, Wyatt J, Medicina D, Callea F, George PM. Brennan SO, et al. Among authors: medicina d. Am J Pathol. 2000 Jul;157(1):189-96. doi: 10.1016/s0002-9440(10)64530-0. Am J Pathol. 2000. PMID: 10880389 Free PMC article.

8

Molecular characterization of the new defective P(brescia) alpha1-antitrypsin allele.

Medicina D, Montani N, Fra AM, Tiberio L, Corda L, Miranda E, Pezzini A, Bonetti F, Ingrassia R, Scabini R, Facchetti F, Schiaffonati L. Medicina D, et al. Hum Mutat. 2009 Aug;30(8):E771-81. doi: 10.1002/humu.21043. Hum Mutat. 2009. PMID: 19437508

9

Diagnostic flow chart for targeted detection of alpha1-antitrypsin deficiency.

Corda L, Bertella E, Pini L, Pezzini A, Medicina D, Boni E, Guerini M, Trivella S, Grassi V, Tantucci C. Corda L, et al. Among authors: medicina d. Respir Med. 2006 Mar;100(3):463-70. doi: 10.1016/j.rmed.2005.06.009. Epub 2005 Jul 25. Respir Med. 2006. PMID: 16043335 Free article.

10

From immunohistochemistry to in situ hybridization.

Callea F, Sergi C, Medicina D, Pizzorni S, Brisigotti M, Fabbretti G, Bonino F. Callea F, et al. Among authors: medicina d. Liver. 1992 Aug;12(4 Pt 2):290-5. doi: 10.1111/j.1600-0676.1992.tb01063.x. Liver. 1992. PMID: 1447961 Review.

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