Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 27

1.

Novel mutations and genotype-phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD).

Kondo-Iida E, Kobayashi K, Watanabe M, Sasaki J, Kumagai T, Koide H, Saito K, Osawa M, Nakamura Y, Toda T.

Hum Mol Genet. 1999 Nov;8(12):2303-9.

PMID:
10545611
2.
3.

[Fukuyama-type congenital muscular dystrophy].

Toda T.

Rinsho Shinkeigaku. 2000 Dec;40(12):1297-9. Review. Japanese.

PMID:
11464484
4.

The Fukuyama congenital muscular dystrophy story.

Toda T, Kobayashi K, Kondo-Iida E, Sasaki J, Nakamura Y.

Neuromuscul Disord. 2000 Mar;10(3):153-9. Review.

PMID:
10734260
5.

[Fukuyama congenital muscular dystrophy and related alpha-dystroglycanopathies].

Murakami T, Nishino I.

Brain Nerve. 2008 Oct;60(10):1159-64. Review. Japanese.

PMID:
18975603
6.
7.

[Molecular genetics and merosin abnormality in Fukuyama-type congenital muscular dystrophy (FCMD)].

Toda T, Kobayashi K.

Nihon Rinsho. 1997 Dec;55(12):3169-75. Review. Japanese.

PMID:
9436430
8.

Functions of fukutin, a gene responsible for Fukuyama type congenital muscular dystrophy, in neuromuscular system and other somatic organs.

Yamamoto T, Shibata N, Saito Y, Osawa M, Kobayashi M.

Cent Nerv Syst Agents Med Chem. 2010 Jun 1;10(2):169-79. Review.

PMID:
20518731
9.

Fukuyama-type congenital muscular dystrophy (FCMD) and alpha-dystroglycanopathy.

Toda T, Kobayashi K, Takeda S, Sasaki J, Kurahashi H, Kano H, Tachikawa M, Wang F, Nagai Y, Taniguchi K, Taniguchi M, Sunada Y, Terashima T, Endo T, Matsumura K.

Congenit Anom (Kyoto). 2003 Jun;43(2):97-104. Review.

PMID:
12893968
10.

[Recent advances in Fukuyama type congenital muscular dystrophy].

Saito K.

No To Hattatsu. 1995 Nov;27(6):447-54. Review. Japanese.

PMID:
8534509
11.

Prenatal diagnosis of Fukuyama congenital muscular dystrophy.

Saito K.

Prenat Diagn. 2006 May;26(5):415-7. Review.

PMID:
16570239
12.

Expression and localization of fukutin, POMGnT1, and POMT1 in the central nervous system: consideration for functions of fukutin.

Yamamoto T, Kato Y, Kawaguchi M, Shibata N, Kobayashi M.

Med Electron Microsc. 2004 Dec;37(4):200-7. Review.

PMID:
15614444
13.

Glycosylation defects: a new mechanism for muscular dystrophy?

Grewal PK, Hewitt JE.

Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R259-64. Epub 2003 Aug 12. Review.

PMID:
12925572
14.

Broader clinical spectrum of Fukuyama-type congenital muscular dystrophy manifested by haplotype analysis.

Yoshioka M, Toda T, Kuroki S, Hamano K.

J Child Neurol. 1999 Nov;14(11):711-5. Review.

PMID:
10593547
15.

The 10 autosomal recessive limb-girdle muscular dystrophies.

Zatz M, de Paula F, Starling A, Vainzof M.

Neuromuscul Disord. 2003 Sep;13(7-8):532-44. Review.

PMID:
12921790
16.

[Recent advances in congenital muscular dystrophy research].

Nonaka I.

No To Hattatsu. 2005 Mar;37(2):115-21. Review. Japanese.

PMID:
15773323
17.

Congenital muscular dystrophies: 1997 update.

Voit T.

Brain Dev. 1998 Mar;20(2):65-74. Review.

PMID:
9545174
18.

[Congenital muscular dystrophy and alpha-dystroglycanopathy].

Saito F, Matsumura K, Hagiwara H, Shimizu T.

Rinsho Shinkeigaku. 2008 Aug;48(8):543-9. Review. Japanese.

PMID:
18939472
19.

Fukutin and alpha-dystroglycanopathies.

Toda T, Chiyonobu T, Xiong H, Tachikawa M, Kobayashi K, Manya H, Takeda S, Taniguchi M, Kurahashi H, Endo T.

Acta Myol. 2005 Oct;24(2):60-3. Review.

PMID:
16550916
20.

[Current status and future prospects of research on Fukuyama muscular dystrophy].

Toda T.

Nihon Rinsho. 2015 Aug;73(8):1425-36. Review. Japanese.

PMID:
26281700

Supplemental Content

Support Center