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Items: 1 to 20 of 99

1.

Canine X-linked muscular dystrophy in Japan (CXMDJ).

Shimatsu Y, Katagiri K, Furuta T, Nakura M, Tanioka Y, Yuasa K, Tomohiro M, Kornegay JN, Nonaka I, Takeda S.

Exp Anim. 2003 Apr;52(2):93-7.

2.

Major clinical and histopathological characteristics of canine X-linked muscular dystrophy in Japan, CXMDJ.

Shimatsu Y, Yoshimura M, Yuasa K, Urasawa N, Tomohiro M, Nakura M, Tanigawa M, Nakamura A, Takeda S.

Acta Myol. 2005 Oct;24(2):145-54.

PMID:
16550932
3.

Cardiac involvement in Beagle-based canine X-linked muscular dystrophy in Japan (CXMDJ): electrocardiographic, echocardiographic, and morphologic studies.

Yugeta N, Urasawa N, Fujii Y, Yoshimura M, Yuasa K, Wada MR, Nakura M, Shimatsu Y, Tomohiro M, Takahashi A, Machida N, Wakao Y, Nakamura A, Takeda S.

BMC Cardiovasc Disord. 2006 Dec 4;6:47.

4.

Canine muscular dystrophy: confirmation of X-linked inheritance.

Cooper BJ, Valentine BA, Wilson S, Patterson DF, Concannon PW.

J Hered. 1988 Nov-Dec;79(6):405-8.

PMID:
3209849
5.

Canine X-linked muscular dystrophy. An animal model of Duchenne muscular dystrophy: clinical studies.

Valentine BA, Cooper BJ, de Lahunta A, O'Quinn R, Blue JT.

J Neurol Sci. 1988 Dec;88(1-3):69-81.

PMID:
3225630
7.

Mutation segregation and rapid carrier detection of X-linked muscular dystrophy in dogs.

Bartlett RJ, Winand NJ, Secore SL, Singer JT, Fletcher S, Wilton S, Bogan DJ, Metcalf-Bogan JR, Bartlett WT, Howell JM, Cooper BJ, Kornegay JN.

Am J Vet Res. 1996 May;57(5):650-4.

PMID:
8723876
8.

Familial occurrence of mitral valve prolapse in X-linked muscular dystrophy.

Biddison JH, Dembo DH, Spalt H, Hayes MG, LeDoux CW.

Circulation. 1979 Jun;59(6):1299-304.

PMID:
436221
9.

Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ).

Fukushima K, Nakamura A, Ueda H, Yuasa K, Yoshida K, Takeda S, Ikeda S.

BMC Musculoskelet Disord. 2007 Jun 28;8:54.

10.
11.

X-linked Duchenne muscular dystrophy in an unusual family with manifesting carriers.

Kaladhar Reddy B, Anandavalli TE, Reddi OS.

Hum Genet. 1984;67(4):460-2.

PMID:
6490012
12.

Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.

Lindlöf M, Kääriäinen H, Davies KE, de la Chapelle A.

J Med Genet. 1986 Dec;23(6):560-72. Erratum in: J Med Genet 1987 Mar;24(3):171.

13.

Manifesting carrier of x-linked Duchenne muscular dystrophy.

Meola G, Scarpini E, Silani V, Scarlato G.

J Neurol Sci. 1981 Mar;49(3):455-63.

PMID:
7217994
14.

[Molecular biology in diagnosis and detection of deletion in Duchenne muscular dystrophy].

Graninger W, Wintersberger W, Meron G, Smolen J, Toifl K, Vormittag W.

Wien Klin Wochenschr. 1991;103(7):207-9. German.

PMID:
2063586
15.

Canine X-linked muscular dystrophy as an animal model of Duchenne muscular dystrophy: a review.

Valentine BA, Winand NJ, Pradhan D, Moise NS, de Lahunta A, Kornegay JN, Cooper BJ.

Am J Med Genet. 1992 Feb 1;42(3):352-6. Review.

PMID:
1536178
16.

[Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy].

Guízar Vázquez J, Navarrete Cadena C, Rico R, Mora G, Zavala C.

Bol Med Hosp Infant Mex. 1981 Jan-Feb;38(1):23-33. Spanish.

PMID:
7284070
17.

Canine X-linked muscular dystrophy studied with in vivo phosphorus magnetic resonance spectroscopy.

McCully K, Giger U, Argov Z, Valentine B, Cooper B, Chance B, Bank W.

Muscle Nerve. 1991 Nov;14(11):1091-8.

PMID:
1745283
18.

X-linked muscular dystrophy.

Furukawa T, Peter JB.

Ann Neurol. 1977 Nov;2(5):414-6.

PMID:
569459
19.

The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs.

Cooper BJ, Winand NJ, Stedman H, Valentine BA, Hoffman EP, Kunkel LM, Scott MO, Fischbeck KH, Kornegay JN, Avery RJ, et al.

Nature. 1988 Jul 14;334(6178):154-6.

PMID:
3290691
20.

Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome.

Thomas NS, Williams H, Elsas LJ, Hopkins LC, Sarfarazi M, Harper PS.

J Med Genet. 1986 Dec;23(6):596-8.

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