Results 51 to 60 of about 578 (106)

MÚLTIPLOS COLOBOMAS DE ÍRIS EM UM CÃO NA AUSÊNCIA DE CATARATA-RELATO DE CASO [PDF]

, 2011
Os colobomas são defeitos congênitos causados por um defeito durante a embriogênise. Podem acometer qualquer estrutura ocular (íris, coroide, nervo óptico, pupila, pálpebras); as etiologias são bastante variadas, sendo a maioria de aparecimento isolado e
ALVARES, Alessandra Aparecida Alça, RUSSO, Cláudia, SALEM, Najla Feres Mohamed   +2 more
core  

Mirizzi syndrome: a surgical challenge. [PDF]

Arq Bras Cir Dig, 2014
Lacerda Pde S, Ruiz MR, Melo A, Guimarães LS, Silva-Junior RA, Nakajima GS.   +5 more
europepmc   +1 more source

Effect of cochlear implant in children suffering genetic hypoacusis caused by Waardenburg Syndrome and 35delG mutation [PDF]

, 2016
Introduction: Sensorineural hypoacusia is the most common form of hearing impairment, it is estimated that over 80% of all congenital hearing losses are from genetic origin, being distinguished in syndromic and non-syndromic; 35delG mutation is the most ...
Alejandro Torres Fortuny, Antonio Paz Cordovés, Emilio Luis Morales Jiménez, Estela Morales Peralta, Gerda Alianna González Sánchez, Sandra Elena Quintana Mirabal, Yesy Martín García   +6 more
core   +1 more source

Epigenetic regulation in neural crest development. [PDF]

Dev Biol, 2014
Hu N, Strobl-Mazzulla PH, Bronner ME.
europepmc   +1 more source

Sulfasalazine-induced DRESS syndrome (Drug Rash with Eosinophilia and Systemic Symptoms). [PDF]

Sao Paulo Med J, 2008
Aquino RT, Vergueiro CS, Magliari ME, de Freitas TH.   +3 more
europepmc   +1 more source

[Not Available]. [PDF]

Aten Primaria, 2016
Cortés Rico O, Pallás Alonso CR, Sánchez Ruiz-Cabello FJ, Revuelta JC, Esparza Olcina J, Sánchez-Ventura JG, Aguado JG, Rubio AM, Mengual Gil JM, Moína MM.   +9 more
europepmc   +1 more source

Molecular mechanism of melanin transfer from donor melanocytes to recipient keratinocytes [PDF]

, 2015
Tese de mestrado, Biologia (Biologia Molecular e Genética), Universidade de Lisboa, Faculdade de Ciências, 2015The skin is the largest organ of the human body. From ancient times, the color of skin has been an intriguing feature. Moreover, a large number
Festas, Tiago André Carrilho
core  

[Childhood and adolescence program]. [PDF]

Aten Primaria, 2014
Colomer Revuelta J, Cortes Rico O, Esparza Olcina MJ, Galbe Sánchez-Ventura J, García Aguado J, Martínez Rubio A, Mengual Gil JM, Moína MM, Pallás Alonso CR, Sánchez Ruiz-Cabello FJ, Soriano Faura FJ, Grupo de la Infancia y Adolescencia del PAPPS.   +11 more
europepmc   +1 more source

ALTERAÇÕES DENTÁRIAS NA SÍNDROME DE WAARDENBURG [PDF]

, 2014
EM, FREITAS, H, MARTELLI JÚNIOR, LMR, PARANAÍBA, RD, COLETTA, SN, AQUINO   +4 more
core   +5 more sources

A cohort study of neurodevelopmental disorders and/or congenital anomalies using high resolution chromosomal microarrays in southern Brazil highlighting the significance of ASD. [PDF]

Sci Rep
Chaves TF, Ocampos M, Barbato IT, de Camargo Pinto LL, de Luca GR, Barbato Filho JH, Bernardi P, Costa Netto Muniz Y, Francesca Maris A.   +8 more
europepmc   +1 more source