Serino ML - Search Results

1

F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes.

Branchini A, Morfini M, Lunghi B, Belvini D, Radossi P, Bury L, Serino ML, Giordano P, Cultrera D, Molinari AC, Napolitano M, Bigagli E, Castaman G, Pinotti M, Bernardi F; GePKHIS Study Group of AICE. Branchini A, et al. Among authors: serino ml. J Thromb Haemost. 2022 Jan;20(1):69-81. doi: 10.1111/jth.15552. Epub 2021 Oct 24. J Thromb Haemost. 2022. PMID: 34626083 Free PMC article.

2

A photometric method for the dosage of factor XIII applied to the study of chronic hepatopathies.

Ballerini G, Gemmati D, Moratelli S, Morelli P, Serino ML. Ballerini G, et al. Among authors: serino ml. Thromb Res. 1995 Jun 1;78(5):451-6. doi: 10.1016/0049-3848(95)99611-b. Thromb Res. 1995. PMID: 7660361

3

Anticardiolipin antibody-related thrombocytopenia: persistent remission after splenectomy.

Ballerini G, Gemmati D, Moratelli S, Morelli P, Serino ML. Ballerini G, et al. Among authors: serino ml. Haematologica. 1995 May-Jun;80(3):248-51. Haematologica. 1995. PMID: 7672720

4

A novel mutation (Leu817Pro) causing type 2A von Willebrand disease.

Gemmati D, Serino ML, Moratelli S, Ballerini G, Furbetta M, Lunghi B, Marchetti G, Bernardi F. Gemmati D, et al. Among authors: serino ml. Br J Haematol. 1996 Jan;92(1):241-3. doi: 10.1046/j.1365-2141.1996.00301.x. Br J Haematol. 1996. PMID: 8562403

5

Resistance to activated protein C and low levels of protein S activity in nine thrombophilic families: a correct diagnosis.

Gemmati D, Serino ML, Verzola I, Mari R, Moratelli S, Ballerini G. Gemmati D, et al. Among authors: serino ml. Blood Coagul Fibrinolysis. 1997 Mar;8(2):118-23. doi: 10.1097/00001721-199703000-00006. Blood Coagul Fibrinolysis. 1997. PMID: 9518043

6

Coexistence of antithrombin deficiency, factor V Leiden and hyperhomocysteinemia in a thrombotic family.

Gemmati D, Serino ML, Moratelli S, Mari R, Ballerini G, Scapoli GL. Gemmati D, et al. Among authors: serino ml. Blood Coagul Fibrinolysis. 1998 Mar;9(2):173-6. doi: 10.1097/00001721-199803000-00008. Blood Coagul Fibrinolysis. 1998. PMID: 9622215

7

A modified functional global test to measure protein C, protein S activities and the activated protein C-resistance phenotype.

Gemmati D, Serino ML, Scapoli GL. Gemmati D, et al. Among authors: serino ml. Thromb Res. 1998 Nov 1;92(3):141-8. doi: 10.1016/s0049-3848(98)00120-0. Thromb Res. 1998. PMID: 9806366

8

Thrombotic risk in thalassemic patients.

Moratelli S, De Sanctis V, Gemmati D, Serino ML, Mari R, Gamberini MR, Scapoli GL. Moratelli S, et al. Among authors: serino ml. J Pediatr Endocrinol Metab. 1998;11 Suppl 3:915-21. J Pediatr Endocrinol Metab. 1998. PMID: 10091165

9

Low folate levels and thermolabile methylenetetrahydrofolate reductase as primary determinant of mild hyperhomocystinemia in normal and thromboembolic subjects.

Gemmati D, Previati M, Serino ML, Moratelli S, Guerra S, Capitani S, Forini E, Ballerini G, Scapoli GL. Gemmati D, et al. Among authors: serino ml. Arterioscler Thromb Vasc Biol. 1999 Jul;19(7):1761-7. doi: 10.1161/01.atv.19.7.1761. Arterioscler Thromb Vasc Biol. 1999. PMID: 10397696

10

A common mutation in the gene for coagulation factor XIII-A (VAL34Leu): a risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases.

Gemmati D, Serino ML, Ongaro A, Tognazzo S, Moratelli S, Resca R, Moretti M, Scapoli GL. Gemmati D, et al. Among authors: serino ml. Am J Hematol. 2001 Jul;67(3):183-8. doi: 10.1002/ajh.1104. Am J Hematol. 2001. PMID: 11391716 Free article.

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