Laganà C - Search Results

1

Absence of deletion and duplication of MLL2 and KDM6A genes in a large cohort of patients with Kabuki syndrome.

Priolo M, Micale L, Augello B, Fusco C, Zucchetti F, Prontera P, Paduano V, Biamino E, Selicorni A, Mammì C, Laganà C, Zelante L, Merla G. Priolo M, et al. Among authors: lagana c. Mol Genet Metab. 2012 Nov;107(3):627-9. doi: 10.1016/j.ymgme.2012.06.019. Epub 2012 Jul 6. Mol Genet Metab. 2012. PMID: 22840376

2

MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment.

Priolo M, Sparago A, Mammì C, Cerrato F, Laganà C, Riccio A. Priolo M, et al. Among authors: lagana c. Eur J Hum Genet. 2008 May;16(5):565-71. doi: 10.1038/sj.ejhg.5202001. Epub 2008 Jan 23. Eur J Hum Genet. 2008. PMID: 18212817

3

NFIX mutations affecting the DNA-binding domain cause a peculiar overgrowth syndrome (Malan syndrome): a new patients series.

Gurrieri F, Cavaliere ML, Wischmeijer A, Mammì C, Neri G, Pisanti MA, Rodella G, Laganà C, Priolo M. Gurrieri F, et al. Among authors: lagana c. Eur J Med Genet. 2015 Sep;58(9):488-91. doi: 10.1016/j.ejmg.2015.06.009. Epub 2015 Jul 17. Eur J Med Genet. 2015. PMID: 26193383

4

Ectodermal dysplasias: a new clinical-genetic classification.

Priolo M, Laganà C. Priolo M, et al. Among authors: lagana c. J Med Genet. 2001 Sep;38(9):579-85. doi: 10.1136/jmg.38.9.579. J Med Genet. 2001. PMID: 11546825 Free PMC article.

5

Malpuech syndrome: broadening the clinical spectrum and molecular analysis by array-CGH.

Priolo M, Ciccone R, Bova I, Campolo G, Laganà C, Zuffardi O. Priolo M, et al. Among authors: lagana c. Eur J Med Genet. 2007 Mar-Apr;50(2):139-43. doi: 10.1016/j.ejmg.2006.10.004. Epub 2006 Oct 28. Eur J Med Genet. 2007. PMID: 17140870

6

A peculiar mutation in the DNA-binding/dimerization domain of NFIX causes Sotos-like overgrowth syndrome: a new case.

Priolo M, Grosso E, Mammì C, Labate C, Naretto VG, Vacalebre C, Caridi P, Laganà C. Priolo M, et al. Among authors: lagana c. Gene. 2012 Dec 10;511(1):103-5. doi: 10.1016/j.gene.2012.08.040. Epub 2012 Sep 13. Gene. 2012. PMID: 22982744 Review.

7

Genetic risk of prediabetes and diabetes development in chronic myeloid leukemia patients treated with nilotinib.

Martino B, Mammì C, Labate C, Rodi S, Ielo D, Priolo M, Postorino M, Tripepi G, Ronco F, Laganà C, Musolino C, Greco M, La Nasa G, Caocci G. Martino B, et al. Among authors: lagana c. Exp Hematol. 2017 Nov;55:71-75. doi: 10.1016/j.exphem.2017.07.007. Epub 2017 Jul 28. Exp Hematol. 2017. PMID: 28757432 Free article.

8

Pulmonary agenesis/hypoplasia, microphthalmia, and diaphragmatic defects: report of an additional case.

Priolo M, Casile G, Laganà C. Priolo M, et al. Among authors: lagana c. Clin Dysmorphol. 2004 Jan;13(1):45-6. doi: 10.1097/00019605-200401000-00013. Clin Dysmorphol. 2004. PMID: 15127767

9

The incidence of JAK2 V617F mutation in bcr/abl-negative chronic myeloproliferative disorders: assessment by two different detection methods.

Lucia E, Martino B, Mammi C, Vigna E, Mazzone C, Gentile M, Qualtieri G, Bisconte MG, Naccarato M, Gentile C, Laganà C, Romeo F, Neri A, Nobile F, Morabito F. Lucia E, et al. Among authors: lagana c. Leuk Lymphoma. 2008 Oct;49(10):1907-15. doi: 10.1080/10428190802290652. Leuk Lymphoma. 2008. PMID: 18720212

10

Utility of the clinical practice of administering thrombophilic screening and antithrombotic prophylaxis with low-molecular-weight heparin to healthy donors treated with G-CSF for mobilization of peripheral blood stem cells.

Martino M, Luise F, Oriana V, Console G, Moscato T, Mammì C, Messina G, Massara E, Irrera G, Piromalli A, Lombardo VT, Laganà C, Iacopino P. Martino M, et al. Among authors: lagana c. Tumori. 2007 Mar-Apr;93(2):155-9. doi: 10.1177/030089160709300208. Tumori. 2007. PMID: 17557562 Clinical Trial.

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