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Year | Number of Results |
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2003 | 2 |
2005 | 3 |
2007 | 1 |
2008 | 1 |
2024 | 0 |
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Page 1
Biochemical and ultrastructural evidence of endoplasmic reticulum stress in LGMD2I.
Virchows Arch. 2007 Dec;451(6):1047-55. doi: 10.1007/s00428-007-0515-3. Epub 2007 Oct 20.
Virchows Arch. 2007.
PMID: 17952692
LGMD2E patients risk developing dilated cardiomyopathy.
Fanin M, Melacini P, Boito C, Pegoraro E, Angelini C.
Fanin M, et al. Among authors: boito c.
Neuromuscul Disord. 2003 May;13(4):303-9. doi: 10.1016/s0960-8966(02)00280-8.
Neuromuscul Disord. 2003.
PMID: 12868499
Item in Clipboard
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian study.
Messina S, Mora M, Pegoraro E, Pini A, Mongini T, D'Amico A, Pane M, Aiello C, Bruno C, Biancheri R, Berardinelli A, Boito C, Farina L, Morandi L, Moroni I, Pezzani R, Pichiecchio A, Ricci E, Ruggieri A, Saredi S, Scuderi C, Tessa A, Toscano A, Tortorella G, Trevisan CP, Uggetti C, Santorelli FM, Bertini E, Mercuri E.
Messina S, et al. Among authors: boito c.
Neuromuscul Disord. 2008 Jul;18(7):565-71. doi: 10.1016/j.nmd.2008.04.004. Epub 2008 Jun 2.
Neuromuscul Disord. 2008.
PMID: 18513969
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Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy.
Brockington M, Torelli S, Prandini P, Boito C, Dolatshad NF, Longman C, Brown SC, Muntoni F.
Brockington M, et al. Among authors: boito c.
Hum Mol Genet. 2005 Mar 1;14(5):657-65. doi: 10.1093/hmg/ddi062. Epub 2005 Jan 20.
Hum Mol Genet. 2005.
PMID: 15661757
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Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I.
Boito CA, Melacini P, Vianello A, Prandini P, Gavassini BF, Bagattin A, Siciliano G, Angelini C, Pegoraro E.
Boito CA, et al.
Arch Neurol. 2005 Dec;62(12):1894-9. doi: 10.1001/archneur.62.12.1894.
Arch Neurol. 2005.
PMID: 16344347
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Novel sarcoglycan gene mutations in a large cohort of Italian patients.
Boito C, Fanin M, Siciliano G, Angelini C, Pegoraro E.
Boito C, et al.
J Med Genet. 2003 May;40(5):e67. doi: 10.1136/jmg.40.5.e67.
J Med Genet. 2003.
PMID: 12746421
Free PMC article.
No abstract available.
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A novel out-of-frame mutation in the neurofilament light chain gene (NEFL) does not result in Charcot-Marie-Tooth disease type 2E.
Andrigo C, Boito C, Prandini P, Mostacciuolo ML, Siciliano G, Angelini C, Pegoraro E.
Andrigo C, et al. Among authors: boito c.
Neurogenetics. 2005 Feb;6(1):49-50. doi: 10.1007/s10048-004-0202-3. Epub 2005 Jan 15.
Neurogenetics. 2005.
PMID: 15654615
No abstract available.
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