Merlini L - Search Results

1

Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery-Dreifuss muscular dystrophy patients and carriers.

Sabatelli P, Squarzoni S, Petrini S, Capanni C, Ognibene A, Cartegni L, Cobianchi F, Merlini L, Toniolo D, Maraldi NM. Sabatelli P, et al. Among authors: merlini l. Neuromuscul Disord. 1998 Apr;8(2):67-71. doi: 10.1016/s0960-8966(97)00147-8. Neuromuscul Disord. 1998. PMID: 9608558

2

X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample.

Mora M, Cartegni L, Di Blasi C, Barresi R, Bione S, Raffaele di Barletta M, Morandi L, Merlini L, Nigro V, Politano L, Donati MA, Cornelio F, Cobianchi F, Toniolo D. Mora M, et al. Among authors: merlini l. Ann Neurol. 1997 Aug;42(2):249-53. doi: 10.1002/ana.410420218. Ann Neurol. 1997. PMID: 9266737

3

Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy.

Cartegni L, di Barletta MR, Barresi R, Squarzoni S, Sabatelli P, Maraldi N, Mora M, Di Blasi C, Cornelio F, Merlini L, Villa A, Cobianchi F, Toniolo D. Cartegni L, et al. Among authors: merlini l. Hum Mol Genet. 1997 Dec;6(13):2257-64. doi: 10.1093/hmg/6.13.2257. Hum Mol Genet. 1997. PMID: 9361031

4

Immunocytochemical detection of emerin within the nuclear matrix.

Squarzoni S, Sabatelli P, Ognibene A, Toniolo D, Cartegni L, Cobianchi F, Petrini S, Merlini L, Maraldi NM. Squarzoni S, et al. Among authors: merlini l. Neuromuscul Disord. 1998 Jun;8(5):338-44. doi: 10.1016/s0960-8966(98)00031-5. Neuromuscul Disord. 1998. PMID: 9673989

5

Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy.

Ognibene A, Sabatelli P, Petrini S, Squarzoni S, Riccio M, Santi S, Villanova M, Palmeri S, Merlini L, Maraldi NM. Ognibene A, et al. Among authors: merlini l. Muscle Nerve. 1999 Jul;22(7):864-9. doi: 10.1002/(sici)1097-4598(199907)22:7<864::aid-mus8>3.0.co;2-g. Muscle Nerve. 1999. PMID: 10398203

6

Decreased expression of laminin beta 1 in chromosome 21-linked Bethlem myopathy.

Merlini L, Villanova M, Sabatelli P, Malandrini A, Maraldi NM. Merlini L, et al. Neuromuscul Disord. 1999 Jul;9(5):326-9. doi: 10.1016/s0960-8966(99)00022-x. Neuromuscul Disord. 1999. PMID: 10407855

7

Emerin presence in platelets.

Squarzoni S, Sabatelli P, Capanni C, Petrini S, Ognibene A, Toniolo D, Cobianchi F, Zauli G, Bassini A, Baracca A, Guarnieri C, Merlini L, Maraldi NM. Squarzoni S, et al. Among authors: merlini l. Acta Neuropathol. 2000 Sep;100(3):291-8. doi: 10.1007/s004019900169. Acta Neuropathol. 2000. PMID: 10965799

8

Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndrome.

Villanova M, Mercuri E, Bertini E, Sabatelli P, Morandi L, Mora M, Sewry C, Brockington M, Brown SC, Ferreiro A, Maraldi NM, Toda T, Guicheney P, Merlini L, Muntoni F. Villanova M, et al. Among authors: merlini l. Neuromuscul Disord. 2000 Dec;10(8):541-7. doi: 10.1016/s0960-8966(00)00139-5. Neuromuscul Disord. 2000. PMID: 11053679

9

Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy.

Sabatelli P, Lattanzi G, Ognibene A, Columbaro M, Capanni C, Merlini L, Maraldi NM, Squarzoni S. Sabatelli P, et al. Among authors: merlini l. Muscle Nerve. 2001 Jun;24(6):826-9. doi: 10.1002/mus.1076. Muscle Nerve. 2001. PMID: 11360268

10

Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy.

Cenni V, Sabatelli P, Mattioli E, Marmiroli S, Capanni C, Ognibene A, Squarzoni S, Maraldi NM, Bonne G, Columbaro M, Merlini L, Lattanzi G. Cenni V, et al. Among authors: merlini l. J Med Genet. 2005 Mar;42(3):214-20. doi: 10.1136/jmg.2004.026112. J Med Genet. 2005. PMID: 15744034 Free PMC article.

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