Pedemonte M - Search Results

1

Long term follow-up of scoliosis progression in type II SMA patients.

Coratti G, Pera MC, D'Amico A, Bruno C, Bovis F, Gullì C, Brolatti N, Pedemonte M, Apicella M, Antonaci L, Ricci M, Capasso A, Cicala G, Cutrona C, de Sanctis R, Carnicella S, Forcina N, Catteruccia M, Damasio MB, Labianca L, Leone A, Bertini E, Pane M, Mercuri E. Coratti G, et al. Among authors: pedemonte m. Neuromuscul Disord. 2022 Dec;32(11-12):879-885. doi: 10.1016/j.nmd.2022.11.004. Epub 2022 Nov 17. Neuromuscul Disord. 2022. PMID: 36456406

2

Early decrease of IIx myosin heavy chain transcripts in Duchenne muscular dystrophy.

Pedemonte M, Sandri C, Schiaffino S, Minetti C. Pedemonte M, et al. Biochem Biophys Res Commun. 1999 Feb 16;255(2):466-9. doi: 10.1006/bbrc.1999.0213. Biochem Biophys Res Commun. 1999. PMID: 10049732

3

GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features.

Biancheri R, Zara F, Striano P, Pedemonte M, Cassandrini D, Stringara S, Manganelli F, Santoro L, Schenone A, Bellone E, Minetti C. Biancheri R, et al. Among authors: pedemonte m. J Neurol. 2006 Sep;253(9):1234-5. doi: 10.1007/s00415-006-0149-4. Epub 2006 Apr 10. J Neurol. 2006. PMID: 16607474 No abstract available.

4

Ubiquitin expression in acute steroid myopathy with loss of myosin thick filaments.

Minetti C, Hirano M, Morreale G, Pedemonte M, Cordone G, Hays AP, Bonilla E. Minetti C, et al. Among authors: pedemonte m. Muscle Nerve. 1996 Jan;19(1):94-6. doi: 10.1002/(SICI)1097-4598(199601)19:1<94::AID-MUS14>3.0.CO;2-3. Muscle Nerve. 1996. PMID: 8538677 No abstract available.

5

Hepatic amyloidosis in intravenous drug abusers and AIDS patients.

Osick LA, Lee TP, Pedemonte MB, Jacob L, Chauhan P, Navarro C, Comer GM. Osick LA, et al. Among authors: pedemonte mb. J Hepatol. 1993 Aug;19(1):79-84. doi: 10.1016/s0168-8278(05)80179-5. J Hepatol. 1993. PMID: 8301046

6

Transgenic overexpression of caveolin-3 in skeletal muscle fibers induces a Duchenne-like muscular dystrophy phenotype.

Galbiati F, Volonte D, Chu JB, Li M, Fine SW, Fu M, Bermudez J, Pedemonte M, Weidenheim KM, Pestell RG, Minetti C, Lisanti MP. Galbiati F, et al. Among authors: pedemonte m. Proc Natl Acad Sci U S A. 2000 Aug 15;97(17):9689-94. doi: 10.1073/pnas.160249097. Proc Natl Acad Sci U S A. 2000. PMID: 10931944 Free PMC article.

7

Clinical and molecular findings in patients with giant axonal neuropathy (GAN).

Bruno C, Bertini E, Federico A, Tonoli E, Lispi ML, Cassandrini D, Pedemonte M, Santorelli FM, Filocamo M, Dotti MT, Schenone A, Malandrini A, Minetti C. Bruno C, et al. Among authors: pedemonte m. Neurology. 2004 Jan 13;62(1):13-6. doi: 10.1212/01.wnl.0000101676.41505.a7. Neurology. 2004. PMID: 14718689

8

Multiplex real-time PCR for detection of deletions and duplications in dystrophin gene.

Traverso M, Malnati M, Minetti C, Regis S, Tedeschi S, Pedemonte M, Bruno C, Biassoni R, Zara F. Traverso M, et al. Among authors: pedemonte m. Biochem Biophys Res Commun. 2006 Jan 6;339(1):145-50. doi: 10.1016/j.bbrc.2005.11.006. Epub 2005 Nov 9. Biochem Biophys Res Commun. 2006. PMID: 16297882

9

Expanding the clinical spectrum of POMT1 phenotype.

D'Amico A, Tessa A, Bruno C, Petrini S, Biancheri R, Pane M, Pedemonte M, Ricci E, Falace A, Rossi A, Mercuri E, Santorelli FM, Bertini E. D'Amico A, et al. Among authors: pedemonte m. Neurology. 2006 May 23;66(10):1564-7; discussion 1461. doi: 10.1212/01.wnl.0000216145.66476.36. Neurology. 2006. PMID: 16717220

10

POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum.

Biancheri R, Bertini E, Falace A, Pedemonte M, Rossi A, D'Amico A, Scapolan S, Bergamino L, Petrini S, Cassandrini D, Broda P, Manfredi M, Zara F, Santorelli FM, Minetti C, Bruno C. Biancheri R, et al. Among authors: pedemonte m. Arch Neurol. 2006 Oct;63(10):1491-5. doi: 10.1001/archneur.63.10.1491. Arch Neurol. 2006. PMID: 17030669

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