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Genética

 

A triagem auditiva neonatal na Rede Municipal do Rio de Janeiro, Brasil

Body Composition of Individuals with Mucopolysaccharidosis

Clinical Characteristics of Alopecia Areata in Down Syndrome

Displasia Ectodermica FOO

Enzyme replacement therapy for Mucopolysaccharidosis Type I among patients followed within the MPS Brazil Network

Familial Study of Paracentric Inversion in Chromosome 3p

High prevalence of methicillin resistance and PVL genes among Staphylococcus aureus isolates from the nares and skin lesions of pediatric patients with atopic dermatitis

HLA antigens in individuals with down syndrome and alopecia areata

IGF-IandIGFBindingProtein-3GenerationTestsandResponse toGrowthHormoneinChildrenwithSilver-RussellSyndrome

Insuline Resistance in adolescents with down syndrome

Mental retardation in Duchenne muscular dystrophy

Moderately progressive Ullrich congenital muscular dystrophy

Mutation analysis of the PAH gene in phenylketonuria patients from Rio de Janeiro, Southeast BrazilMutation analysis of the PAH gene in phenylketonuria patients from Rio de Janeiro, Southeast Brazil

Plexiform neurofibroma in the ear canal of a patient with Type I Neurofibromatosis

Prevalence of communication, swallowing and orofacial myofunctional disorders in children and adolescents at the time of admission at a cancer hospital

Profile of pacients assessed for cochlear implants

Psychomotor Development in Pre-School with Visual Deficiency

Sistema Publico de Saúde no Brasil 2010

 

 

UFRJ Departamento de Pediatria da Faculdade de Medicina da UFRJ
Desenvolvido por: TIC/UFRJ