Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies

Por Uwineza, Annette, Hitayezu, Janvier, Jamar, Mauricette, Caberg, Jean-Hubert, Murorunkwere, Seraphine, Janvier, Ndinkabandi, Bours, Vincent, Mutesa, Leon
Publicado no J Trop Pediatr (2016)

Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies

Por Uwineza, Annette, Caberg, Jean-Hubert, Hitayezu, Janvier, Hellin, Anne Cecile, Jamar, Mauricette, Dideberg, Vinciane, Rusingiza, Emmanuel K, Bours, Vincent, Mutesa, Leon
Publicado em 2014

Pattern of congenital heart diseases in Rwandan children with genetic defects

Por Teteli, Raissa, Uwineza, Annette, Butera, Yvan, Hitayezu, Janvier, Murorunkwere, Seraphine, Umurerwa, Lamberte, Ndinkabandi, Janvier, Hellin, Anne-Cécile, Jamar, Mauricette, Caberg, Jean-Hubert, Muganga, Narcisse, Mucumbitsi, Joseph, Rusingiza, Emmanuel Kamanzi, Mutesa, Leon
Publicado no Pan Afr Med J (2014)

High Prevalence of Cysticercosis in People with Epilepsy in Southern Rwanda

Por Rottbeck, Ruth, Nshimiyimana, Jules Fidèle, Tugirimana, Pierrot, Düll, Uta E., Sattler, Janko, Hategekimana, Jean-Claudien, Hitayezu, Janvier, Bruckmaier, Irmengard, Borchert, Matthias, Gahutu, Jean Bosco, Dieckmann, Sebastian, Harms, Gundel, Mockenhaupt, Frank P., Ignatius, Ralf
Publicado em 2013