• Users Online: 28610
  • Home
  • Print this page
  • Email this page

    Article Cited by others

BRIEF REPORT

Unusual dendritic keratitis

Gokhale Nikhil S, Dherai Alpa J, Desai Haresh, Ashavaid T F

Year : 2007| Volume: 55| Issue : 1 | Page no: 57-59

   This article has been cited by
 
1 A child with dendritiform eye lesions and developmental delay
Vasiliki Gliagias, Ksenia Denisova, Joann J. Kang
American Journal of Ophthalmology Case Reports. 2022; 28: 101701
[Pubmed]  [Google Scholar] [DOI]
2 Tyrosinemia type II: Mutation update, 11 novel mutations and description of 5 independent subjects with a novel founder mutation
L. Peña-Quintana, G. Scherer, M.L. Curbelo-Estévez, F. Jiménez-Acosta, B. Hartmann, F. La Roche, S. Meavilla-Olivas, C. Pérez-Cerdá, N. García-Segarra, Y. Giguère, P. Huppke, G.A. Mitchell, E. Mönch, D. Trump, C. Vianey-Saban, E.R. Trimble, I. Vitoria-Miñana, D. Reyes-Suárez, T. Ramírez-Lorenzo, A. Tugores
Clinical Genetics. 2017; 92(3): 306
[Pubmed]  [Google Scholar] [DOI]
3 In Vivo Confocal Microscopic Features of Corneal Pseudodendritic Lesions in Tyrosinemia Type II
Sibel Kocabeyoglu,Mehmet C. Mocan,Murat Irkec
Cornea. 2014; 33(10): 1106
[Pubmed]  [Google Scholar] [DOI]
4 Confocal Microscopy of Corneal Crystals in a Patient With Hereditary Tyrosinemia Type I, Treated With NTBC
Pieter-Paul Schauwvlieghe,Jaak Jaeken,Philippe Kestelyn,Ilse Claerhout
Cornea. 2013; 32(1): 91
[Pubmed]  [Google Scholar] [DOI]
5 Richner–Hanhart Syndrome Detected by Expanded Newborn Screening
Thomas Meissner,Regina Christine Betz,Sandra M. Pasternack,Sibylle Eigelshoven,Thomas Ruzicka,Roland Kruse,Gitta Laitenberger,Ertan Mayatepek
Pediatric Dermatology. 2008; 25(3): 378
[Pubmed]  [Google Scholar] [DOI]
6 Richner-Hanhart Syndrome Detected by Expanded Newborn Screening.
Meissner, T. and Betz, R.C. and Pasternack, S.M.M.D. and Eigelshoven, S. and Ruzicka, T. and Kruse, R. and Laitenberger, G. and Mayatepek, E.
Pediatric Dermatology. 2008; 25(3): 378-380
[Pubmed]  [Google Scholar]

 

Read this article