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Spontaneous expulsion of intracorneal ring segment in pellucid marginal degeneration: A case report.
Moskwa, R; Rolland le Moal, P; Sot, M; Francois, J; Vermion, J-C; Bloch, F; Chaussard, D; Semler Collery, A; Perone, J-M.
Affiliation
  • Moskwa R; Ophthalmology Department, Metz-Thionville Regional Hospital Center, Mercy Hospital, 1, allée du Chateau, CS 45001 Metz Cedex 03, France.
  • Rolland le Moal P; Ophthalmology Department, Metz-Thionville Regional Hospital Center, Mercy Hospital, 1, allée du Chateau, CS 45001 Metz Cedex 03, France.
  • Sot M; Ophthalmology Department, Metz-Thionville Regional Hospital Center, Mercy Hospital, 1, allée du Chateau, CS 45001 Metz Cedex 03, France.
  • Francois J; Ophthalmology Department, Metz-Thionville Regional Hospital Center, Mercy Hospital, 1, allée du Chateau, CS 45001 Metz Cedex 03, France.
  • Vermion JC; Ophthalmology Department, Metz-Thionville Regional Hospital Center, Mercy Hospital, 1, allée du Chateau, CS 45001 Metz Cedex 03, France.
  • Bloch F; Ophthalmology Department, Metz-Thionville Regional Hospital Center, Mercy Hospital, 1, allée du Chateau, CS 45001 Metz Cedex 03, France.
  • Chaussard D; Ophthalmology Department, Metz-Thionville Regional Hospital Center, Mercy Hospital, 1, allée du Chateau, CS 45001 Metz Cedex 03, France.
  • Semler Collery A; Ophthalmology Department, Metz-Thionville Regional Hospital Center, Mercy Hospital, 1, allée du Chateau, CS 45001 Metz Cedex 03, France.
  • Perone JM; Ophthalmology Department, Metz-Thionville Regional Hospital Center, Mercy Hospital, 1, allée du Chateau, CS 45001 Metz Cedex 03, France. Electronic address: Jm.perone@chr-metz-thionville.fr.
J Fr Ophtalmol ; 44(1): e47-e49, 2021 Jan.
Article in En | MEDLINE | ID: mdl-33480847
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Corneal Dystrophies, Hereditary / Corneal Diseases Type of study: Diagnostic_studies Limits: Humans Language: En Journal: J Fr Ophtalmol Year: 2021 Document type: Article
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Corneal Dystrophies, Hereditary / Corneal Diseases Type of study: Diagnostic_studies Limits: Humans Language: En Journal: J Fr Ophtalmol Year: 2021 Document type: Article