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Items: 1 to 20 of 98

1.

Anaesthesia and orphan disease: management of cardiac and perioperative risks in a patient with Emery-Dreifuss muscular dystrophy.

Funnell A, Morgan J, McFadzean W.

Eur J Anaesthesiol. 2012 Dec;29(12):596-8. doi: 10.1097/EJA.0b013e3283585457. No abstract available.

PMID:
23010897
2.

Genetic pattern of 3 cases of Emery-Dreifuss muscular dystrophy in a family.

Yazdanpanah P, Javan A, Nadimi B, Shirazi HR.

East Mediterr Health J. 2007 Jan-Feb;13(1):201-5. Review. No abstract available.

PMID:
17546924
3.

[Case with Emery-Dreifuss muscular dystrophy diagnosed forty-two years after onset and implanted with a cardiac resynchronization therapy defibrillator].

Sakiyama Y, Watanabe E, Otsuka M, Hirahara T, Momomura S, Hayashi Y.

Rinsho Shinkeigaku. 2014;54(6):489-94. Japanese.

PMID:
24990833
4.

Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations.

Sanna T, Dello Russo A, Toniolo D, Vytopil M, Pelargonio G, De Martino G, Ricci E, Silvestri G, Giglio V, Messano L, Zachara E, Bellocci F.

Eur Heart J. 2003 Dec;24(24):2227-36.

5.

Cardioembolic stroke prompting diagnosis of LMNA-associated Emery-Dreifuss muscular dystrophy.

Redondo-Vergé L, Yaou RB, Fernández-Recio M, Dinca L, Richard P, Bonne G.

Muscle Nerve. 2011 Oct;44(4):587-9. doi: 10.1002/mus.22179.

PMID:
21922471
6.
7.

Lamin A/C assembly defects in Emery-Dreifuss muscular dystrophy can be regulated by culture medium composition.

Holt I, Nguyen TM, Wehnert M, Morris GE.

Neuromuscul Disord. 2006 Jun;16(6):368-73.

PMID:
16697197
8.

Emery-Dreifuss muscular dystrophy: a novel mutation in the LMNA gene.

Lassuthová P, Baránková L, Kraus J, Maríková T, Seeman P.

Pediatr Neurol. 2009 Aug;41(2):127-30. doi: 10.1016/j.pediatrneurol.2009.03.009.

PMID:
19589462
9.

[The first Japanese case of autosomal dominant Emery-Dreifuss muscular dystrophy with a novel mutation in the lamin A/C gene].

Onishi Y, Higuchi J, Ogawa T, Namekawa A, Hayashi H, Odakura H, Goto K, Hayashi YK.

Rinsho Shinkeigaku. 2002 Feb;42(2):140-4. Japanese.

PMID:
12424964
10.

[Cardiologic findings in Hauptmann-Thannhauser muscular dystrophy (autosomal dominant Emery-Dreifuss muscular dystrophy)].

Cuneo A, Holdt LM, Klingel K, Kandolf R, Tebbe U.

Dtsch Med Wochenschr. 2007 Sep;132(39):2006-9. German.

PMID:
17882738
11.

Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy.

Cenni V, Sabatelli P, Mattioli E, Marmiroli S, Capanni C, Ognibene A, Squarzoni S, Maraldi NM, Bonne G, Columbaro M, Merlini L, Lattanzi G.

J Med Genet. 2005 Mar;42(3):214-20.

12.

Emery-Dreifuss muscular dystrophy.

De Smet L.

Genet Couns. 2004;15(1):91-4.

PMID:
15083706
13.

Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophy.

Walter MC, Witt TN, Weigel BS, Reilich P, Richard P, Pongratz D, Bonne G, Wehnert MS, Lochmüller H.

Neuromuscul Disord. 2005 Jan;15(1):40-4.

PMID:
15639119
14.

Anaesthetic management of a patient with Emery-Dreifuss muscular dystrophy.

Shende D, Agarwal R.

Anaesth Intensive Care. 2002 Jun;30(3):372-5.

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18.

Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.

Mercuri E, Counsell S, Allsop J, Jungbluth H, Kinali M, Bonne G, Schwartz K, Bydder G, Dubowitz V, Muntoni F.

Neuropediatrics. 2002 Feb;33(1):10-4.

PMID:
11930270
19.

Cardiomyopathy and atrioventricular block in Emery-Dreifuss muscular dystrophy--a case report.

Kanada M, Demirtaş M, Güzel R, San M, Tuncer I.

Angiology. 2002 Jan-Feb;53(1):109-12.

PMID:
11863303
20.

Elective caesarean section for a woman with Emery-Dreifuss muscular dystrophy.

Kim OM, Elliott D.

Anaesth Intensive Care. 2010 Jul;38(4):744-7.

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