Genetic counselors and legal recognition: A made‐for‐Canada approach

por Lambert, Deborah M., Patrinos, Dimitri, Knoppers, Bartha Maria, Zawati, Ma’n H.
Publicado 2021

A retrospective review of the contribution of rare diseases to paediatric mortality in Ireland

por Gunne, Emer, McGarvey, Cliona, Hamilton, Karina, Treacy, Eileen, Lambert, Deborah M., Lynch, Sally Ann
Publicado 2020

Polymorphisms of the Flavin containing monooxygenase 3 (FMO3) gene do not predispose to essential hypertension in Caucasians

por Dolan, Ciara, Shields, Denis C, Stanton, Alice, O'Brien, Eoin, Lambert, Deborah M, O'Brien, John K, Treacy, Eileen P
Publicado 2005

Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database

por Nguengang Wakap, Stéphanie, Lambert, Deborah M., Olry, Annie, Rodwell, Charlotte, Gueydan, Charlotte, Lanneau, Valérie, Murphy, Daniel, Le Cam, Yann, Rath, Ana
Publicado 2019

The role of primary care in management of rare diseases in Ireland

por Byrne, Niall, Turner, Jacqueline, Marron, Rita, Lambert, Deborah M., Murphy, Daniel N., O’Sullivan, Grace, Mason, Maureen, Broderick, Frank, Burke, Mary C., Casey, Sheila, Doyle, Marguerite, Gibney, David, Mason, Fergus, Molony, David, Ormond, Deirdre, O’ Sé, Colm, O’Shea, Conor, Treacy, Eileen P.
Publicado 2020