Mora M - Search Results

1

Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients.

Farina L, Morandi L, Milanesi I, Ciceri E, Mora M, Moroni I, Pantaleoni C, Savoiardo M. Farina L, et al. Among authors: mora m. Neuroradiology. 1998 Dec;40(12):807-11. doi: 10.1007/s002340050689. Neuroradiology. 1998. PMID: 9877136

2

Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalities.

Mora M, Moroni I, Uziel G, di Blasi C, Barresi R, Farina L, Morandi L. Mora M, et al. Neuromuscul Disord. 1996 Oct;6(5):377-81. doi: 10.1016/0960-8966(96)00359-8. Neuromuscul Disord. 1996. PMID: 8938702

3

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

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

A novel homozygous ISPD gene mutation causing phenotype variability in a consanguineous family.

Baranello G, Saredi S, Sansanelli S, Savadori P, Canioni E, Chiapparini L, Balestri P, Malandrini A, Arnoldi MT, Pantaleoni C, Morandi L, Mora M. Baranello G, et al. Among authors: mora m. Neuromuscul Disord. 2015 Jan;25(1):55-9. doi: 10.1016/j.nmd.2014.08.007. Epub 2014 Sep 10. Neuromuscul Disord. 2015. PMID: 25444434

6

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.

7

Exome sequencing detects compound heterozygous nonsense LAMA2 mutations in two siblings with atypical phenotype and nearly normal brain MRI.

Saredi S, Gibertini S, Matalonga L, Farina L, Ardissone A, Moroni I, Mora M. Saredi S, et al. Among authors: mora m. Neuromuscul Disord. 2019 May;29(5):376-380. doi: 10.1016/j.nmd.2019.04.001. Epub 2019 Apr 10. Neuromuscul Disord. 2019. PMID: 31040037

8

Dystrophin analysis in Duchenne and Becker muscular dystrophy carriers: correlation with intracellular calcium and albumin.

Morandi L, Mora M, Gussoni E, Tedeschi S, Cornelio F. Morandi L, et al. Among authors: mora m. Ann Neurol. 1990 Nov;28(5):674-9. doi: 10.1002/ana.410280512. Ann Neurol. 1990. PMID: 1979724

9

Dystrophin-associated protein abnormalities in dystrophin-deficient muscle fibers from symptomatic and asymptomatic Duchenne/Becker muscular dystrophy carriers.

Di Blasi C, Morandi L, Barresi R, Blasevich F, Cornelio F, Mora M. Di Blasi C, et al. Among authors: mora m. Acta Neuropathol. 1996 Oct;92(4):369-77. doi: 10.1007/s004010050532. Acta Neuropathol. 1996. PMID: 8891069

10

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

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