Mora M - Search Results

1

LAMA2 gene analysis in congenital muscular dystrophy: new mutations, prenatal diagnosis, and founder effect.

Di Blasi C, Piga D, Brioschi P, Moroni I, Pini A, Ruggieri A, Zanotti S, Uziel G, Jarre L, Della Giustina E, Scuderi C, Jonsrud C, Mantegazza R, Morandi L, Mora M. Di Blasi C, et al. Among authors: mora m. Arch Neurol. 2005 Oct;62(10):1582-6. doi: 10.1001/archneur.62.10.1582. Arch Neurol. 2005. PMID: 16216942

2

Decorin and biglycan expression is differentially altered in several muscular dystrophies.

Zanotti S, Negri T, Cappelletti C, Bernasconi P, Canioni E, Di Blasi C, Pegoraro E, Angelini C, Ciscato P, Prelle A, Mantegazza R, Morandi L, Mora M. Zanotti S, et al. Among authors: mora m. Brain. 2005 Nov;128(Pt 11):2546-55. doi: 10.1093/brain/awh635. Epub 2005 Sep 23. Brain. 2005. PMID: 16183658

3

Severe congenital muscular dystrophy in a LAMA2-mutated case.

Di Blasi C, van Alfen N, Colleoni F, ter Laak H, Mora M. Di Blasi C, et al. Among authors: mora m. Pediatr Neurol. 2007 Sep;37(3):212-4. doi: 10.1016/j.pediatrneurol.2007.05.008. Pediatr Neurol. 2007. PMID: 17765811

4

Fukutin gene mutations in an Italian patient with early onset muscular dystrophy but no central nervous system involvement.

Saredi S, Ruggieri A, Mottarelli E, Ardissone A, Zanotti S, Farina L, Morandi L, Mora M, Moroni I. Saredi S, et al. Among authors: mora m. Muscle Nerve. 2009 Jun;39(6):845-8. doi: 10.1002/mus.21271. Muscle Nerve. 2009. PMID: 19396839

5

Prevalence of congenital muscular dystrophy in Italy: a population study.

Graziano A, Bianco F, D'Amico A, Moroni I, Messina S, Bruno C, Pegoraro E, Mora M, Astrea G, Magri F, Comi GP, Berardinelli A, Moggio M, Morandi L, Pini A, Petillo R, Tasca G, Monforte M, Minetti C, Mongini T, Ricci E, Gorni K, Battini R, Villanova M, Politano L, Gualandi F, Ferlini A, Muntoni F, Santorelli FM, Bertini E, Pane M, Mercuri E. Graziano A, et al. Among authors: mora m. Neurology. 2015 Mar 3;84(9):904-11. doi: 10.1212/WNL.0000000000001303. Epub 2015 Feb 4. Neurology. 2015. PMID: 25653289 Free PMC article.

6

Clinical heterogeneity of adhalin deficiency.

Morandi L, Barresi R, Di Blasi C, Jung D, Sunada Y, Confalonieri V, Dworzak F, Mantegazza R, Antozzi C, Jarre L, Pini A, Gobbi G, Bianchi C, Cornelio F, Campbell KP, Mora M. Morandi L, et al. Among authors: mora m. Ann Neurol. 1996 Feb;39(2):196-202. doi: 10.1002/ana.410390209. Ann Neurol. 1996. PMID: 8967751

7

Clinical correlations in 16 patients with total or partial laminin alpha2 deficiency characterized using antibodies against 2 fragments of the protein.

Morandi L, Di Blasi C, Farina L, Sorokin L, Uziel G, Azan G, Pini A, Toscano A, Lanfossi M, Galbiati S, Cornelio F, Mora M. Morandi L, et al. Among authors: mora m. Arch Neurol. 1999 Feb;56(2):209-15. doi: 10.1001/archneur.56.2.209. Arch Neurol. 1999. PMID: 10025426

8

Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping.

Di Blasi C, He Y, Morandi L, Cornelio F, Guicheney P, Mora M. Di Blasi C, et al. Among authors: mora m. Brain. 2001 Apr;124(Pt 4):698-704. doi: 10.1093/brain/124.4.698. Brain. 2001. PMID: 11287370

9

Abnormal lysosomal and ubiquitin-proteasome pathways in 19p13.3 distal myopathy.

Di Blasi C, Moghadaszadeh B, Ciano C, Negri T, Giavazzi A, Cornelio F, Morandi L, Mora M. Di Blasi C, et al. Among authors: mora m. Ann Neurol. 2004 Jul;56(1):133-8. doi: 10.1002/ana.20158. Ann Neurol. 2004. PMID: 15236412

10

Proteoglycans are differentially altered in muscular dystrophies.

Zanotti S, Mora M. Zanotti S, et al. Among authors: mora m. ScientificWorldJournal. 2006 Apr 4;6:446-8. doi: 10.1100/tsw.2006.88. ScientificWorldJournal. 2006. PMID: 16604255 Free PMC article. Review. No abstract available.

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