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Aniridia : recent developments in scientific and clinical research / edited by Mohit Parekh, Barbara Poli, Stefano Ferrari, Corrado Teofili, Diego Ponzin.

Colaborador(es): Tipo de material: TextoTextoEditor: Cham : Springer International Publishing : Springer, 2015Edición: 1st ed. 2015Descripción: viii, 192 páginas : 57 ilustraciones, 54 ilustraciones en colorTipo de contenido:
  • texto
Tipo de medio:
  • computadora
Tipo de portador:
  • recurso en línea
ISBN:
  • 9783319197791
Formatos físicos adicionales: Edición impresa:: Sin títuloClasificación LoC:
  • R-RZ
Recursos en línea:
Contenidos:
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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Springer eBooks

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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