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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1950 1
1954 1
1959 2
1960 1
1961 1
1966 2
1968 1
1972 1
1985 1
1989 1
1991 2
1992 1
1993 2
1994 1
1995 6
1996 5
1997 2
1998 3
1999 2
2000 1
2004 2
2005 4
2023 0

Text availability

Article attribute

Article type

Publication date

PubMed (OMIM) for id: 358391

42 results

Results by year

Filters applied: . Clear all
Page 1
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes.
Piluso G, Politano L, Aurino S, Fanin M, Ricci E, Ventriglia VM, Belsito A, Totaro A, Saccone V, Topaloglu H, Nascimbeni AC, Fulizio L, Broccolini A, Canki-Klain N, Comi LI, Nigro G, Angelini C, Nigro V. Piluso G, et al. J Med Genet. 2005 Sep;42(9):686-93. doi: 10.1136/jmg.2004.028738. J Med Genet. 2005. PMID: 16141003 Free PMC article.
Calpains and disease.
Zatz M, Starling A. Zatz M, et al. N Engl J Med. 2005 Jun 9;352(23):2413-23. doi: 10.1056/NEJMra043361. N Engl J Med. 2005. PMID: 15944426 Review. No abstract available.
Molecular diagnosis in LGMD2A: mutation analysis or protein testing?
Fanin M, Fulizio L, Nascimbeni AC, Spinazzi M, Piluso G, Ventriglia VM, Ruzza G, Siciliano G, Trevisan CP, Politano L, Nigro V, Angelini C. Fanin M, et al. Hum Mutat. 2004 Jul;24(1):52-62. doi: 10.1002/humu.20058. Hum Mutat. 2004. PMID: 15221789
Formal genetics of muscular dystrophy.
MORTON NE, CHUNG CS. MORTON NE, et al. Am J Hum Genet. 1959 Dec;11(4):360-79. Am J Hum Genet. 1959. PMID: 14424475 Free PMC article. No abstract available.
42 results