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Preface
What is Aniridia: Epidemiology, clinical features and genetic implications
Optical Coherence Tomography imaging in patients with PAX6 mutations
Aniridic Glaucoma: Diagnosis and Treatment
Management of Glaucoma in Congenital Aniridia
Clinical and surgical management of cataract in congenital aniridia
The ocular surface in aniridia
Aniridic Keratopathy: Conservative approaches
Lamellar and penetrating keratoplasty in congenital aniridia
Boston KPRo Type I as a viable alternative to visual rehabilitation in aniridia patients: advances and limitations
Cell therapy for regeneration of the corneal epithelium aniridic patients
Strategies for success in limbal allograft transplantation for aniridia
The paediatric patient: identifying congenital aniridia as soon as possible
Early diagnosis: the key roles of neonatologists, paediatricians and paediatric ophthalmologists
Aniridia guides and aniridia-syndrome (Pax6-Syndrome)
Assessing the visual function in congenital aniridia and following the child during daily life
Children with aniridia and healthcare systems: from needs assessment to a comprehensive programme of care and assistance
European/international guidelines on Aniridia: the patients? point of view
What to do when diagnosed with Aniridia: the role of patients ́associations
Conclusions and future perspectives
Index.

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