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Triagem de mutações no gene FOXC2 em uma família com a síndrome Linfedema Distiquíase
(Universidade Federal de Minas GeraisBrasilICB - DEPARTAMENTO DE BIOLOGIA GERALPrograma de Pós-Graduação em GenéticaUFMG, 2016-10-31)
The Lymphedema-Distichiasis Syndrome (LDS) is a developmental disorder of the lymphatic system, which causes edema in several regions of the body and distichiasis, that is, the birth of extra rows of eyelashes originated ...
Axenfeld-Rieger syndrome: more than meets the eye
(2022)
Background Axenfeld-Rieger syndrome (ARS) is characterised by typical anterior segment anomalies, with or without systemic features. The discovery of causative genes identified ARS subtypes with distinct phenotypes, but ...
Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucoma
(Assoc Research Vision Ophthalmology IncRockvilleEUA, 2006)
Nphs2 Mutations Account For Only 15% Of Nephrotic Syndrome Cases
(BioMed Central Ltd., 2015)
Transcutaneous Laser Treatment Of Leg Veins
(Springer-Verlag London Ltd, 2014)
Factores asociados a la percepción de dolor pre y postoperatorio en pacientes llevados a Varicectomía de miembros inferiores en una institución en Bogotá
Introduction Chronic venous insufficiency has a high incidence in adults, especially women, pain is a characteristic symptom, even after surgery. It is necessary to identify factors associated with pain in patients with ...