Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 95

1.

Scapuloperoneal syndromes. Absence of linkage to the 4q35 FSHD locus.

Tawil R, Myers GJ, Weiffenbach B, Griggs RC.

Arch Neurol. 1995 Nov;52(11):1069-72.

PMID:
7487558
2.

FSH dystrophy 4q35 deletion in patients presenting with facial-sparing scapular myopathy.

Felice KJ, North WA, Moore SA, Mathews KD.

Neurology. 2000 May 23;54(10):1927-31.

PMID:
10822431
3.

Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy.

Wilhelmsen KC, Blake DM, Lynch T, Mabutas J, De Vera M, Neystat M, Bernstein M, Hirano M, Gilliam TC, Murphy PL, Sola MD, Bonilla E, Schotland DL, Hays AP, Rowland LP.

Ann Neurol. 1996 Apr;39(4):507-20. Review.

PMID:
8619529
4.

Application of chromosome 4q35-qter marker (pFR-1) for DNA rearrangement of facioscapulohumeral muscular dystrophy patients in Taiwan.

Hsu YD, Kao MC, Shyu WC, Lin JC, Huang NE, Sun HF, Yang KD, Tsao WL.

J Neurol Sci. 1997 Jul;149(1):73-9.

PMID:
9168169
5.
6.

Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31.

Isozumi K, DeLong R, Kaplan J, Deng HX, Iqbal Z, Hung WY, Wilhelmsen KC, Hentati A, Pericak-Vance MA, Siddique T.

Hum Mol Genet. 1996 Sep;5(9):1377-82.

PMID:
8872481
7.

Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35.

Weiffenbach B, Bagley R, Falls K, Hyser C, Storvick D, Jacobsen SJ, Schultz P, Mendell J, Willems van Dijk K, Milner EC, et al.

Am J Hum Genet. 1992 Aug;51(2):416-23.

8.

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD).

Gilbert JR, Stajich JM, Speer MC, Vance JM, Stewart CS, Yamaoka LH, Samson F, Fardeau M, Potter TG, Roses AD, et al.

Am J Hum Genet. 1992 Aug;51(2):424-7.

9.

DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: clinical correlations.

Goto K, Lee JH, Matsuda C, Hirabayashi K, Kojo T, Nakamura A, Mitsunaga Y, Furukawa T, Sahashi K, Arahata K.

Neuromuscul Disord. 1995 May;5(3):201-8.

PMID:
7633185
10.

Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35.

Mathews KD, Mills KA, Bosch EP, Ionasescu VV, Wiles KR, Buetow KH, Murray JC.

Am J Hum Genet. 1992 Aug;51(2):428-31.

11.

FSHD-like patients without 4q35 deletion.

Yamanaka G, Goto K, Ishihara T, Oya Y, Miyajima T, Hoshika A, Nishino I, Hayashi YK.

J Neurol Sci. 2004 Apr 15;219(1-2):89-93.

PMID:
15050443
12.

Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.

Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R.

Neurology. 2007 Feb 20;68(8):569-77. Epub 2006 Dec 6.

PMID:
17151338
13.

Molecular genetics of facioscapulohumeral muscular dystrophy.

Wijmenga C, Frants RR, Hewitt JE, van Deutekom JC, van Geel M, Wright TJ, Padberg GW, Hofker MH, van Ommen GJ.

Neuromuscul Disord. 1993 Sep-Nov;3(5-6):487-91. Review.

PMID:
8186699
14.

[A family with facioscapulohumeral muscular dystrophy and hereditary long QT syndrome].

Kimura T, Moriwaki T, Sawada J, Naka T, Hazama T, Nakata T.

Rinsho Shinkeigaku. 1997 Aug;37(8):690-2. Japanese.

PMID:
9404145
15.

Facioscapulohumeral muscular dystrophy.

Tawil R, Van Der Maarel SM.

Muscle Nerve. 2006 Jul;34(1):1-15. Review.

PMID:
16508966
16.

[Facioscapulohumeral muscular dystrophy. The spectrum of clinical manifestations and molecular genetic changes].

Krasnianski M, Neudecker S, Eger K, Schulte-Mattler W, Zierz S.

Nervenarzt. 2003 Feb;74(2):151-8. German.

PMID:
12596016
17.

No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markers.

Passos-Bueno MR, Wijmenga C, Takata RE, Marie SK, Vainzof M, Pavanello RC, Hewitt JE, Bakker E, Carvalho A, Akiyama J, et al.

Hum Mol Genet. 1993 May;2(5):557-62.

PMID:
8518794
18.

Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD).

Gilbert JR, Stajich JM, Wall S, Carter SC, Qiu H, Vance JM, Stewart CS, Speer MC, Pufky J, Yamaoka LH, et al.

Am J Hum Genet. 1993 Aug;53(2):401-8.

19.

Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD)

Lunt PW, Jardine PE, Koch MC, Maynard J, Osborn M, Williams M, Harper PS, Upadhyaya M.

Hum Mol Genet. 1995 May;4(5):951-8. Erratum in: Hum Mol Genet 1995 Jul;4(7):1243-4.

PMID:
7633457
20.

Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletion.

Krasnianski M, Eger K, Neudecker S, Jakubiczka S, Zierz S.

Arch Neurol. 2003 Oct;60(10):1421-5.

PMID:
14568813

Supplemental Content

Support Center