Development of a research platform for children with arthrogryposis multiplex congenita: study protocol for a pilot registry

por Dahan-Oliel, Noémi, Bedard, Tanya, Darsaklis, Vasiliki Betty, Hall, Judith Goslin, van Bosse, Harold J P, Hamdy, Reggie C
Publicado 2018

A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita

por Latypova, Xenia, Creadore, Stefan Giovanni, Dahan-Oliel, Noémi, Gustafson, Anxhela Gjyshi, Wei-Hung Hwang, Steven, Bedard, Tanya, Shazand, Kamran, van Bosse, Harold J. P., Giampietro, Philip F., Dieterich, Klaus
Publicado 2021

Validation of case definition algorithms for the ascertainment of congenital anomalies

por Nava de Escalante, Yonabeth, Abayomi, Aanu, Langlois, Sylvie, Ye, Xibiao, Erickson, Anders, Ngo, Henry, Armour, Rosemary, Okamoto, Reiko, Arbour, Laura, Bedard, Tanya, Der, Kenny, Van Allen, Margot, Skarsgard, Erik, Lavoie, Martin, Henry, Bonnie
Publicado 2022

Epidemiology, aetiology, interventions and genomics in children with arthrogryposis multiplex congenita: protocol for a multisite registry

por Dahan-Oliel, Noémi, van Bosse, Harold, Darsaklis, Vasiliki Betty, Rauch, Frank, Bedard, Tanya, Bardai, Ghalib, James, Michelle, Raney, Ellen, Freese, Krister, Hyer, Lauren, Altiok, Haluk, Pellett, Jonathan, Giampietro, Philip, Hall, Judith, Hamdy, Reggie Charles
Publicado 2022

International multidisciplinary collaboration toward an annotated definition of arthrogryposis multiplex congenita

por Dahan‐Oliel, Noémi, Cachecho, Sarah, Barnes, Douglas, Bedard, Tanya, Davison, Ann M., Dieterich, Klaus, Donohoe, Maureen, Fąfara, Alicja, Hamdy, Reggie, Hjartarson, Helgi T., S. Hoffman, Naimisha, Kimber, Eva, Komolkin, Igor, Lester, Ruth, Pontén, Eva, van Bosse, Harold J. P., Hall, Judith G.
Publicado 2019