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4. Emery-Dreifuss syndrome: genetic and clinical varieties. Rudenskaya GE; Ginter EK; Petrin AN; Djomina NA Am J Med Genet; 1994 Apr; 50(3):228-33. PubMed ID: 8042665 [TBL] [Abstract][Full Text] [Related]
5. Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study. Flanigan KM; Kerr L; Bromberg MB; Leonard C; Tsuruda J; Zhang P; Gonzalez-Gomez I; Cohn R; Campbell KP; Leppert M Ann Neurol; 2000 Feb; 47(2):152-61. PubMed ID: 10665485 [TBL] [Abstract][Full Text] [Related]
6. Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28. Yates JR; Warner JP; Smith JA; Deymeer F; Azulay JP; Hausmanowa-Petrusewicz I; Zaremba J; Borkowska J; Affara NA; Ferguson-Smith MA J Med Genet; 1993 Feb; 30(2):108-11. PubMed ID: 8445613 [TBL] [Abstract][Full Text] [Related]
7. Genotype-phenotype analysis in X-linked Emery-Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotype. Yates JR; Bagshaw J; Aksmanovic VM; Coomber E; McMahon R; Whittaker JL; Morrison PJ; Kendrick-Jones J; Ellis JA Neuromuscul Disord; 1999 May; 9(3):159-65. PubMed ID: 10382909 [TBL] [Abstract][Full Text] [Related]
8. Emery-dreifuss humeroperoneal muscular dystrophy: an x-linked myopathy with unusual contractures and bradycardia. Hopkins LC; Jackson JA; Elsas LJ Ann Neurol; 1981 Sep; 10(3):230-7. PubMed ID: 7294729 [TBL] [Abstract][Full Text] [Related]
9. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene. Bonne G; Mercuri E; Muchir A; Urtizberea A; Bécane HM; Recan D; Merlini L; Wehnert M; Boor R; Reuner U; Vorgerd M; Wicklein EM; Eymard B; Duboc D; Penisson-Besnier I; Cuisset JM; Ferrer X; Desguerre I; Lacombe D; Bushby K; Pollitt C; Toniolo D; Fardeau M; Schwartz K; Muntoni F Ann Neurol; 2000 Aug; 48(2):170-80. PubMed ID: 10939567 [TBL] [Abstract][Full Text] [Related]
10. Emery-Dreifuss muscular dystrophy: report of five cases in a family and review of the literature. Merlini L; Granata C; Dominici P; Bonfiglioli S Muscle Nerve; 1986; 9(6):481-5. PubMed ID: 3736581 [TBL] [Abstract][Full Text] [Related]
11. Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysis. Wulff K; Ebener U; Wehnert CS; Ward PA; Reuner U; Hiebsch W; Herrmann FH; Wehnert M Dis Markers; 1997 Apr; 13(2):77-86. PubMed ID: 9160182 [TBL] [Abstract][Full Text] [Related]
12. [Pseudohypertrophic forms of progressive muscular dystrophy with the onset at puberty and a malignant course of the myodystrophic process]. Badalian LO; Arkhipov BA; Temin PA; Zavadenko NN; Voloshina TG Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(3):61-4. PubMed ID: 3381616 [TBL] [Abstract][Full Text] [Related]
13. [Emery-Dreifuss muscular dystrophy--reported a family with 5 cases]. Luo D Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1991 Dec; 24(6):330-1, 382. PubMed ID: 1800056 [TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 8619529 [TBL] [Abstract][Full Text] [Related]
16. Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene: from congenital onset with severe phenotype to milder classic Emery-Dreifuss variant. Mercuri E; Poppe M; Quinlivan R; Messina S; Kinali M; Demay L; Bourke J; Richard P; Sewry C; Pike M; Bonne G; Muntoni F; Bushby K Arch Neurol; 2004 May; 61(5):690-4. PubMed ID: 15148145 [TBL] [Abstract][Full Text] [Related]
17. Becker muscular dystrophy recombinant DNA studies in identical twins. Ionasescu V; Ionasescu R; Searby C; Burns T Muscle Nerve; 1988 Apr; 11(4):287-90. PubMed ID: 3398874 [TBL] [Abstract][Full Text] [Related]