Literature DB >> 10636647

Macular dystrophy of malattia leventinese. A 25 year follow up.

J C Zech, S Zaouche, F Mourier, H Placuchu, J D Grange, C Trepsat.   

Abstract

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Year:  1999        PMID： 10636647      PMCID： PMC1722836          DOI： 10.1136/bjo.83.10.1194b

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN： 0007-1161            Impact factor:   4.638


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  4 in total

1.  The second Japanese family with Malattia Leventinese/Doyne honeycomb retinal dystrophy.

Authors:  Nobuko Enomoto; Takaaki Hayashi; Tomokazu Matsuura; Koji Tanaka; Remi Takeuchi; Goji Tomita; Ryusaburo Mori
Journal:  Doc Ophthalmol       Date:  2021-11-25       Impact factor: 2.379

2.  Indocyanine green angiography features of Malattia leventinese.

Authors:  E H Souied; N Leveziel; G Querques; J Darmon; G Coscas; G Soubrane
Journal:  Br J Ophthalmol       Date:  2006-03       Impact factor: 4.638

3.  A novel haplotype with the R345W mutation in the EFEMP1 gene associated with autosomal dominant drusen in a Japanese family.

Authors:  Tomokazu Takeuchi; Takaaki Hayashi; Matthew Bedell; Kang Zhang; Hisashi Yamada; Hiroshi Tsuneoka
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-10-22       Impact factor: 4.799

4.  First reported case of Doyne honeycomb retinal dystrophy (Malattia Leventinese/autosomal dominant drusen) in Scandinavia.

Authors:  Inger Norlyk Sheyanth; Ihab Bishara Lolas; Henrik Okkels; Ligor Pradeep Kiruparajan; Søren Kromann Abildgaard; Michael Bjørn Petersen
Journal:  Mol Genet Genomic Med       Date:  2021-03-10       Impact factor: 2.183
  4 in total

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