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Orphanet Journal of Rare Diseases
|
March 30, 2022
Survival of children with rare structural congenital anomalies: a multi-registry cohort study
Alessio Coi, Michele Santoro, Anna Pierini, et al.
Paediatric and Perinatal Epidemiology
|
October 11, 2023
Risk factors for mortality in infancy and childhood in children with major congenital anomalies: A European population-based cohort study
Joachim Tan, Svetlana V Glinianaia, Judith Rankin, et al.
International Journal of Environmental Research and Public Health
|
August 8, 2018
Recommendations for Improving the Quality of Rare Disease Registries
Yllka Kodra, Jérôme Weinbach, Manuel Posada-de-la-Paz, et al.
BMJ Paediatrics Open
|
June 23, 2023
Causes of death in children with congenital anomalies up to age 10 in eight European countries
Anke Rissmann, Joachim Tan, Svetlana V Glinianaia, et al.
American Journal of Medical Genetics. Part A
|
July 12, 2019
Epidemiology of achondroplasia: A population-based study in Europe
Alessio Coi, Michele Santoro, Ester Garne, et al.
Neuroepidemiology
|
July 15, 2019
Epidemiology of Dandy-Walker Malformation in Europe: A EUROCAT Population-Based Registry Study
Michele Santoro, Alessio Coi, Ingeborg Barišić, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 27, 2022
Epidemiology of aplasia cutis congenita: A population-based study in Europe
Alessio Coi, Ingeborg Barisic, Ester Garne, et al.
Paediatric and Perinatal Epidemiology
|
June 16, 2021
Epidemiology of Pierre-Robin sequence in Europe: A population-based EUROCAT study
Michele Santoro, Alessio Coi, Ingeborg Barišić, et al.
Paediatric and Perinatal Epidemiology
|
June 8, 2022
Temporal and geographical variations in survival of children born with congenital anomalies in Europe: A multi-registry cohort study
Michele Santoro, Alessio Coi, Anna Pierini, et al.
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of 8
Search research articles
Search
Showing results (71-80 of 79) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 79 results.
Orphanet Journal of Rare Diseases
|
March 30, 2022
Survival of children with rare structural congenital anomalies: a multi-registry cohort study
Alessio Coi, Michele Santoro, Anna Pierini, et al.
Paediatric and Perinatal Epidemiology
|
October 11, 2023
Risk factors for mortality in infancy and childhood in children with major congenital anomalies: A European population-based cohort study
Joachim Tan, Svetlana V Glinianaia, Judith Rankin, et al.
International Journal of Environmental Research and Public Health
|
August 8, 2018
Recommendations for Improving the Quality of Rare Disease Registries
Yllka Kodra, Jérôme Weinbach, Manuel Posada-de-la-Paz, et al.
BMJ Paediatrics Open
|
June 23, 2023
Causes of death in children with congenital anomalies up to age 10 in eight European countries
Anke Rissmann, Joachim Tan, Svetlana V Glinianaia, et al.
American Journal of Medical Genetics. Part A
|
July 12, 2019
Epidemiology of achondroplasia: A population-based study in Europe
Alessio Coi, Michele Santoro, Ester Garne, et al.
Neuroepidemiology
|
July 15, 2019
Epidemiology of Dandy-Walker Malformation in Europe: A EUROCAT Population-Based Registry Study
Michele Santoro, Alessio Coi, Ingeborg Barišić, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 27, 2022
Epidemiology of aplasia cutis congenita: A population-based study in Europe
Alessio Coi, Ingeborg Barisic, Ester Garne, et al.
Paediatric and Perinatal Epidemiology
|
June 16, 2021
Epidemiology of Pierre-Robin sequence in Europe: A population-based EUROCAT study
Michele Santoro, Alessio Coi, Ingeborg Barišić, et al.
Paediatric and Perinatal Epidemiology
|
June 8, 2022
Temporal and geographical variations in survival of children born with congenital anomalies in Europe: A multi-registry cohort study
Michele Santoro, Alessio Coi, Anna Pierini, et al.
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of 8