565 related articles for article (PubMed ID: 16545566)
1. Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy.
Goto K; Nishino I; Hayashi YK
Neuromuscul Disord; 2006 Apr; 16(4):256-61. PubMed ID: 16545566
[TBL] [Abstract][Full Text] [Related]
2. [Gene diagnosis of facioscapulohumeral muscular dystrophy].
Zhang JL; Shen DG; Zhou PK; Liu JW; Jia N; Liu H; Wang HB; Yang SX; Frants RR
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Jun; 20(3):232-4. PubMed ID: 12778451
[TBL] [Abstract][Full Text] [Related]
3. Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues.
Tsien F; Sun B; Hopkins NE; Vedanarayanan V; Figlewicz D; Winokur S; Ehrlich M
Mol Genet Metab; 2001 Nov; 74(3):322-31. PubMed ID: 11708861
[TBL] [Abstract][Full Text] [Related]
4. Facioscapulohumeral muscular dystrophy molecular testing using a non radioactive protocol.
Kekou K; Fryssira H; Sophocleous C; Mavrou A; Manta P; Metaxotou C
Mol Cell Probes; 2005 Dec; 19(6):422-4. PubMed ID: 16144755
[TBL] [Abstract][Full Text] [Related]
5. A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD).
van der Maarel SM; Deidda G; Lemmers RJ; Bakker E; van der Wielen MJ; Sandkuijl L; Hewitt JE; Padberg GW; Frants RR
J Med Genet; 1999 Nov; 36(11):823-8. PubMed ID: 10544225
[TBL] [Abstract][Full Text] [Related]
6. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.
Deak KL; Lemmers RJ; Stajich JM; Klooster R; Tawil R; Frants RR; Speer MC; van der Maarel SM; Gilbert JR
Neurology; 2007 Feb; 68(8):578-82. PubMed ID: 17229919
[TBL] [Abstract][Full Text] [Related]
7. Recurrent somatic mosaicism for D4Z4 contractions in a family with facioscapulohumeral muscular dystrophy.
Buzhov BT; Lemmers RJ; Tournev I; van der Wielen MJ; Ishpekova B; Petkov R; Petrova J; Frants RR; Padberg GW; van der Maarel SM
Neuromuscul Disord; 2005 Jul; 15(7):471-5. PubMed ID: 15935668
[TBL] [Abstract][Full Text] [Related]
8. Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q.
Jiang G; Yang F; van Overveld PG; Vedanarayanan V; van der Maarel S; Ehrlich M
Hum Mol Genet; 2003 Nov; 12(22):2909-21. PubMed ID: 14506132
[TBL] [Abstract][Full Text] [Related]
9. 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; 68(8):569-77. PubMed ID: 17151338
[TBL] [Abstract][Full Text] [Related]
10. Facioscapulohumeral muscular dystrophy. Phenotype-genotype correlation in patients with borderline D4Z4 repeat numbers.
Butz M; Koch MC; Müller-Felber W; Lemmers RJ; van der Maarel SM; Schreiber H
J Neurol; 2003 Aug; 250(8):932-7. PubMed ID: 12928911
[TBL] [Abstract][Full Text] [Related]
11. Clinical and genetic analysis of Korean patients with facioscapulohumeral muscular dystrophy.
Ki CS; Lee ST; Kim KS; Kim JW; Hong YH; Sung JJ; Park KS; Lee KW
J Korean Med Sci; 2008 Dec; 23(6):959-63. PubMed ID: 19119436
[TBL] [Abstract][Full Text] [Related]
12. Typical facioscapulohumeral dystrophy phenotype in patients without FSHD 4q35 deletion.
Krasnianski M; Neudecker S; Eger K; Jakubiczka S; Zierz S
J Neurol; 2003 Sep; 250(9):1084-7. PubMed ID: 14504970
[TBL] [Abstract][Full Text] [Related]
13. Molecular diagnosis of facioscapulohumeral muscular dystrophy.
Upadhyaya M; Cooper DN
Expert Rev Mol Diagn; 2002 Mar; 2(2):160-71. PubMed ID: 11962336
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 14568813
[TBL] [Abstract][Full Text] [Related]
15. Diagnostic challenges in facioscapulohumeral muscular dystrophy.
Sacconi S; Salviati L; Bourget I; Figarella D; Péréon Y; Lemmers R; van der Maarel S; Desnuelle C
Neurology; 2006 Oct; 67(8):1464-6. PubMed ID: 17060574
[TBL] [Abstract][Full Text] [Related]
16. Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy.
van Overveld PG; Enthoven L; Ricci E; Rossi M; Felicetti L; Jeanpierre M; Winokur ST; Frants RR; Padberg GW; van der Maarel SM
Ann Neurol; 2005 Oct; 58(4):569-76. PubMed ID: 16178028
[TBL] [Abstract][Full Text] [Related]
17. Molecular combing reveals allelic combinations in facioscapulohumeral dystrophy.
Nguyen K; Walrafen P; Bernard R; Attarian S; Chaix C; Vovan C; Renard E; Dufrane N; Pouget J; Vannier A; Bensimon A; Lévy N
Ann Neurol; 2011 Oct; 70(4):627-33. PubMed ID: 22028222
[TBL] [Abstract][Full Text] [Related]
18. [Genetic analysis of facioscapulohumeral muscular dystrophy (FSHD)].
Goto K; Song MD; Lee JH; Arahata K
Rinsho Shinkeigaku; 1995 Dec; 35(12):1416-8. PubMed ID: 8752415
[TBL] [Abstract][Full Text] [Related]
19. Polymorphism of the D4Z4 locus associated with facioscapulohumeral muscular dystrophy 1A in Shanghai population.
Zhang YZ; Sun SC; Wu HC; Fan QS; Song YJ; Yu W; Jeanpierre M; Urtizberea JA
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):380-2. PubMed ID: 16086272
[TBL] [Abstract][Full Text] [Related]
20. Atypical facet of Möbius syndrome: association with facioscapulohumeral muscular dystrophy.
Kolski HK; Leonard NJ; Lemmers RJ; Bamforth JS
Muscle Nerve; 2008 Apr; 37(4):526-9. PubMed ID: 18059038
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
