Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Natalia Ximena Minguez"'
Autor:
Carina Rinaudo, Pablo Chiaradia, Natalia Ximena Minguez, Federico Andrés Cremona, Francisco Lucero Saá
Publikováno v:
Ocular Immunology and Inflammation. 28:703-707
Ectodermal dysplasia (ED) is a group of several genetic conditions with absence or dysgenesis of at least two ectodermal derivatives: teeth, skin and its appendages including hair, nails, eccrine and sebaceous glands. The most important clinical find
Autor:
Francisco Lucero Saá, Federico Andrés Cremona, Pablo Chiaradia, María Laura Igarzabal, Natalia Ximena Minguez
Publikováno v:
Case Reports in Ophthalmology
Case Reports in Ophthalmology, Vol 8, Iss 2, Pp 446-451 (2017)
Case Reports in Ophthalmology, Vol 8, Iss 2, Pp 446-451 (2017)
Familial amyloidosis of the Finnish type or Meretoja syndrome is a rare autosomic dominant inherited systemic condition. It was first described by Meretoja in Finland in 1969. It is a disease produced by a single mutation in the gene coding for gelso
Autor:
Jeremias Gaston Galletti, Fernando Fuentes Bonthoux, Pablo Raul Ruisenor Vazquez, Jonatan David Galletti, Marianella Delrivo, Tomás Pförtner, Natalia Ximena Minguez
Publikováno v:
Journal of refractive surgery (Thorofare, N.J. : 1995). 31(2)
PURPOSE: To evaluate intereye corneal asymmetry in Pentacam (Oculus Optikgeräte GmbH, Wetzlar, Germany) indices as a diagnostic method between normal patients and patients with keratoconus. METHODS: A retrospective, observational case series of 177
Autor:
Jeremias Gaston Galletti, Jonatan David Galletti, Ruiseñor Vázquez Pr, Tomás Pförtner, Marianella Delrivo, Natalia Ximena Minguez, Fuentes Bonthoux F
Publikováno v:
American Journal of Ophthalmology. 159:209-210