167 related articles for article (PubMed ID: 1519650)
1. Glaucoma-lens ectopia-microspherophakia-stiffness-shortness (GEMSS) syndrome: a dominant disease with manifestations of Weill-Marchesani syndromes.
Verloes A; Hermia JP; Galand A; Koulischer L; Dodinval P
Am J Med Genet; 1992 Sep; 44(1):48-51. PubMed ID: 1519650
[TBL] [Abstract][Full Text] [Related]
2. Uncontrolled glaucoma secondary to an arteriovenous malformation in a Weill-Marchesani patient.
Derose CJ; Jeffrey A
Optometry; 2001 Oct; 72(10):641-8. PubMed ID: 11712631
[TBL] [Abstract][Full Text] [Related]
3. Histopathological study of microspherophakia in the Weill-Marchesani syndrome.
Nagata M; Takagi S; Yamasaki A; Tsunematsu S; Kumagami T; Itamochi C; Tamai A
Jpn J Ophthalmol; 1995; 39(1):89-95. PubMed ID: 7643490
[TBL] [Abstract][Full Text] [Related]
4. Weill-Marchesani syndrome in three generations.
Evereklioglu C; Hepsen IF; Er H
Eye (Lond); 1999 Dec; 13 ( Pt 6)():773-7. PubMed ID: 10707143
[TBL] [Abstract][Full Text] [Related]
5. [Secondary glaucoma in the Weill-Marchesani syndrome].
Bosun I
Oftalmologia; 1993; 37(4):335-8. PubMed ID: 8286319
[TBL] [Abstract][Full Text] [Related]
6. Weill Marchesani syndrome with chronic angle closure glaucoma in Ethiopia: a case report.
Tenkir A; Bekele S; Solomon B
Ethiop Med J; 2009 Jan; 47(1):81-3. PubMed ID: 19743786
[TBL] [Abstract][Full Text] [Related]
7. Weill-Marchesani syndrome.
Kulkarni ML; Venkataramana V; Sureshkumar C; Satishchandra
Indian Pediatr; 1995 Aug; 32(8):923-6. PubMed ID: 8635842
[No Abstract] [Full Text] [Related]
8. Weill-Marchesani syndrome and secondary glaucoma associated with ectopia lentis.
Chu BS
Clin Exp Optom; 2006 Mar; 89(2):95-9. PubMed ID: 16494613
[TBL] [Abstract][Full Text] [Related]
9. Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2.
Faivre L; Mégarbané A; Alswaid A; Zylberberg L; Aldohayan N; Campos-Xavier B; Bacq D; Legeai-Mallet L; Bonaventure J; Munnich A; Cormier-Daire V
Hum Genet; 2002 Apr; 110(4):366-70. PubMed ID: 11941487
[TBL] [Abstract][Full Text] [Related]
10. Weill-Marchesani syndrome in mother and son.
Young ID; Fielder AR; Casey TA
Clin Genet; 1986 Dec; 30(6):475-80. PubMed ID: 3493095
[TBL] [Abstract][Full Text] [Related]
11. Sclerosis of the skin in the GEMSS syndrome. An overproduction of normal collagen.
Kunz M; Paulus W; Sollberg S; Weilbach F; Voeske W; Ludwig G; Bröcker EB; Hamm H
Arch Dermatol; 1995 Oct; 131(10):1170-4. PubMed ID: 7574834
[TBL] [Abstract][Full Text] [Related]
12. [Lens coloboma and lens dislocation in Stickler (Marshall) syndrome].
Schlote T; Völker M; Knorr M; Thiel HJ
Klin Monbl Augenheilkd; 1997 Apr; 210(4):227-8. PubMed ID: 9235398
[TBL] [Abstract][Full Text] [Related]
13. Long-term complications of iris-claw phakic intraocular lens implantation in Weill-Marchesani syndrome.
Burakgazi AZ; Ozbek Z; Rapuano CJ; Rhee DJ
Cornea; 2006 Apr; 25(3):361-3. PubMed ID: 16633042
[TBL] [Abstract][Full Text] [Related]
14. [Glaucoma attacks in Weill-Marchesani syndrome].
Czechowicz-Janicka K; Staszkiewicz J
Klin Oczna; 1992; 94(2-3):76-7. PubMed ID: 1640689
[TBL] [Abstract][Full Text] [Related]
15. [Weill-Marchesani syndrome].
Herrera J; Morales M
Rev Chil Pediatr; 1986; 57(6):571-2. PubMed ID: 3499643
[No Abstract] [Full Text] [Related]
16. [Weill Marchesani syndrome. Report of a case].
el Kettani A; Hamdani M; Rais L; el Belhadji M; Rachid R; Laouissi N; Zaghloul K; Amraoui A
J Fr Ophtalmol; 2001 Nov; 24(9):944-8. PubMed ID: 11912838
[TBL] [Abstract][Full Text] [Related]
17. Treatment of the Weill-Marchesani syndrome.
Ritch R; Wand M
Ann Ophthalmol; 1981 Jun; 13(6):665-7. PubMed ID: 6455083
[No Abstract] [Full Text] [Related]
18. Weill-Marchesani syndrome with advanced glaucoma and corneal endothelial dysfunction: a case report and literature review.
Guo H; Wu X; Cai K; Qiao Z
BMC Ophthalmol; 2015 Jan; 15():3. PubMed ID: 25571963
[TBL] [Abstract][Full Text] [Related]
19. Weill-Marchesani syndrome--possible linkage of the autosomal dominant form to 15q21.1.
Wirtz MK; Samples JR; Kramer PL; Rust K; Yount J; Acott TS; Koler RD; Cisler J; Jahed A; Gorlin RJ; Godfrey M
Am J Med Genet; 1996 Oct; 65(1):68-75. PubMed ID: 8914744
[TBL] [Abstract][Full Text] [Related]
20. Clinical homogeneity and genetic heterogeneity in Weill-Marchesani syndrome.
Faivre L; Dollfus H; Lyonnet S; Alembik Y; Mégarbané A; Samples J; Gorlin RJ; Alswaid A; Feingold J; Le Merrer M; Munnich A; Cormier-Daire V
Am J Med Genet A; 2003 Dec; 123A(2):204-7. PubMed ID: 14598350
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]