SCOPUS 정보 검색 플랫폼

Orbit

Volumn 20, Issue 4, 2001, Pages 259-266

Oculopharyngeal muscular dystrophy: What's new?

(4) Codère, François a Brais, Bernard a Rouleau, Guy a Lafontaine, Edwin a

a ROYAL VICTORIA HOSPITAL (Canada)

Author keywords

Autosomal dominant disorders; Eyelid ptosis; Genetic disorders; Heredity; Oculopharyngeal muscular dystrophy

Indexed keywords

CLINICAL FEATURE; CONFERENCE PAPER; DISEASE COURSE; EYE SURGERY; GENE MUTATION; GENEALOGY; GENETIC ANALYSIS; HISTOPATHOLOGY; HISTORY OF MEDICINE; HUMAN; OCULOPHARYNGEAL MUSCULAR DYSTROPHY; PTOSIS; TREATMENT PLANNING;

EID: 0035704155 PISSN: 01676830 EISSN: None Source Type: Journal
DOI: 10.1076/orbi.20.4.259.2617 Document Type: Conference Paper

Times cited : (16)

References (16)

1
- 0344963604
- On isolated bilateral ptosis
- (1890) Arch Ophthalmol , vol.36 , pp. 234-259
- Fuchs, E.¹

2
- 0008077618
- Note sur une forme de ptosis non congénital et héréditaire
- (1892) Progr Mad , vol.20 , pp. 401-403
- Dutil, A.¹

3
- 84939092946
- Progressive vagus-glossopharyngeal paralysis with ptosis: Contribution to the group of family diseases
- (1915) J Nerv Ment Dis , vol.42 , pp. 129-139
- Taylor, E.W.¹

4
- 0008123917
- Hereditary, familial and acquired ptosis of late-onset
- (1948) Can Med Assoc J , vol.59 , pp. 434-438
- Amyot, R.¹

5
- 0000232611
- Oculopharyngeal muscular dystrophy; familial disease of late life characterized by dysphagia and progressive ptosis of the eyelids
- (1962) N Engl Med J , vol.267 , pp. 1267-1272
- Victor, M.¹ Hayes, R.² Adams, R.D.³

6
- 0028915818
- The oculopharyngeal dystrophy locus maps to the region of the cardiac α and β myosin heavy chain genes on chromosome 14q11.2-13
- (1995) Hum Mol Genet , vol.4 , Issue.3 , pp. 429-434
- Brais, B.¹ Xie, Y.G.² Sanson, M.³

7
- 0030730845
- Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy gene
- (1997) Neuromuscul Disord
- Brais, B.¹ Bouchard, J.P.² Gosselin, F.³

8
- 17344371397
- Short GCG expansion in the PABP2 gene causes oculopharyngeal dystrophy
- (1998) Nature Genet , vol.18 , pp. 164-167
- Brais, B.¹ Bouchard, J.P.² Xie, Y.G.³

9
- 0033009388
- Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease
- (1999) Ann Neurol , vol.46 , Issue.1 , pp. 115-118
- Blumen, S.C.¹ Brais, B.² Korczyn, A.D.³

10
- 0033060450
- Oculopharyngeal muscular dystrophy
- (1999) Semin Neurol , vol.19 , Issue.1 , pp. 59-66
- Brais, B.¹ Rouleau, G.A.² Bouchard, J.P.³ Fardeau, M.⁴ Tome, F.M.⁵

11
- 0030775367
- Recent studies on oculopharyngeal muscular dystrophy in Quebec
- (1997) Neuromuscul Disord
- Bouchard, J.P.¹ Brais, B.² Brunet, D.³ Gould, P.V.⁴ Rouleau, G.A.⁵

12
- 0018916724
- Surgery in oculopharyngeal muscular dystrophy
- (1980) Am J Surg , vol.139 , pp. 32-39
- Duranceau, A.C.¹ Forand, M.² Fauteux, J.P.³

13
- 2542509051
- Dysphagia in oculopharyngeal muscular dystrophy: A series of 22 French cases
- (1997) Neuromuscul Disord
- Périé, S.¹ Eymard, B.² Laccourreye, L.³ Chaussade, S.⁴ Fardeau, M.⁵ Lacau St Guily, J.⁶

14
- 0030730848
- Upper esophageal sphincter myotomy in oculopharyngeal muscular dystrophy long-term results
- (1997) Neuromuscul Disord
- Fradet, G.¹ Pouliot, D.² Robichaud, R.³ St-Pierre, S.⁴ Bouchard, J.P.⁵

15
- 0027190009
- Correcton of blepharoptosis in oculopharyngeal muscular dystrophy: Review of 91 cases
- (1993) Can J Ophthalmol , vol.28 , pp. 11-14
- Molgat, Y.M.¹ Rodrigue, D.²

16
- 0030731711
- Surgical correction of blepharoptosis in oculopharyngeal muscular dystrophy
- (1997) Neuromuscul Disord
- Rodrigue, D.¹ Molgat, Y.M.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.