PubMed (OMIM) for id: 358391

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

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.

2

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.

3

The frequency of limb girdle muscular dystrophy 2A in northeastern Italy.

Fanin M, Nascimbeni AC, Fulizio L, Angelini C. Fanin M, et al. Neuromuscul Disord. 2005 Mar;15(3):218-24. doi: 10.1016/j.nmd.2004.11.003. Epub 2005 Jan 28. Neuromuscul Disord. 2005. PMID: 15725583

4

Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures.

Mercuri E, Bushby K, Ricci E, Birchall D, Pane M, Kinali M, Allsop J, Nigro V, Sáenz A, Nascimbeni A, Fulizio L, Angelini C, Muntoni F. Mercuri E, et al. Neuromuscul Disord. 2005 Feb;15(2):164-71. doi: 10.1016/j.nmd.2004.10.008. Epub 2004 Nov 26. Neuromuscul Disord. 2005. PMID: 15694138

5

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

6

[Simple recessive form of progressive muscular dystrophy with a genealogical chart from Emmental, Switzerland].

PFANDLER U. PFANDLER U. Dtsch Med Wochenschr. 1950 Sep 15;75(37):1221-5. doi: 10.1055/s-0028-1117646. Dtsch Med Wochenschr. 1950. PMID: 14773342 Undetermined Language. No abstract available.

7

The mutational load due to detrimental genes in man.

MORTON NE. MORTON NE. Am J Hum Genet. 1960 Sep;12(3):348-64. Am J Hum Genet. 1960. PMID: 14424476 Free PMC article. No abstract available.

8

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.

9

Discrimination of genetic entities in muscular dystrophy.

CHUNG CS, MORTON NE. CHUNG CS, et al. Am J Hum Genet. 1959 Dec;11(4):339-59. Am J Hum Genet. 1959. PMID: 13810212 Free PMC article. No abstract available.

10

Progressive muscular dystrophy: autosomal recessive type.

JACKSON CE, CAREY JH. JACKSON CE, et al. Pediatrics. 1961 Jul;28:77-84. Pediatrics. 1961. PMID: 13718465 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

42 results

Results by year