SANTORO, MICHELE
SANTORO, MICHELE
Istituto di Fisiologia Clinica - IFC
Analysis of Prevalence and Mortality Among Neonates and Children With Intestinal Atresia: A Multinational Study, 1974–2015
2026 Carreno, A.; Aguilera, M. P.; Ibanez, L.; Sarmiento, K.; Gili, J. A.; Siffel, C.; Nembhard, W. N.; Bergman, J. E. H.; Bermejo-Sanchez, E.; Tagliabue, G.; Dastgiri, S.; Feldkamp, M. L.; Pocius, S.; Gatt, M.; Martinez, L.; Canessa, M. A.; Groisman, B.; Kallen, K.; Landau, D.; Lelong, N.; Morgan, M.; Arteaga-Vazquez, J.; Santoro, M.; Rissmann, A.; Sipek, A.; Szabova, E.; Wertelecki, W.; Canfield, M. A.; Mastroiacovo, P.; Zarante, I.
Antiseizure Prescription for Children With Severe Congenital Heart Defects and Children With Gastrointestinal Anomalies
2026 Damkjaer, Mads; Morris, Joan K.; Ballardini, Elisa; Barrachina-Bonet, Laia; Cavero-Carbonell, Clara; Coi, Alessio; Gissler, Mika; Given, Joanne; Heino, Anna; Jordan, Sue; Neville, Amanda; Santoro, Michele; Tan, Joachim; Tucker, David; Wellesley, Diana; Kjaer Urhoj, Stine; Garne, Ester; Loane, Maria
Epidemiology of idiopathic pulmonaryfibrosis: a population registry-based study
2026 Gorini, Francesca; Santoro, Michele; Pierini, Anna; Cameli, Paolo; Chimera, Davide; Lavorini, Federico; Pistelli, Francesco; Rosi, Elisabetta; Tavanti, Laura; Tomassetti, Sara; Carrozzi, Laura; Bargagli, Elena; Coi, Alessio
Heterogeneity of the prevalence of congenital hip dislocation in Europe
2026 Garne, E.; Rissmann, A.; Dias, C. M.; Buzzoni, C.; Lynch, C.; Dumoulin, C.; Cavero-Carbonell, C.; Tucker, D.; Broekstra, D.; Ballardini, E.; Hond, E. D.; Rouget, F.; Rodriguez-Rasero, F.; Cousin, I.; Monier, I.; Morris, J.; Sichitiu, J.; Klungsoyr, K.; Odak, L.; Ceresola, M.; O'Mahony, M.; Santoro, M.; Zymak-Zakutnia, N.; Wood, R.; Pertile, R.; Stevens, S.
Mortality amongst European children with congenital anomalies: Associations with socio-economic status in the EUROLINKCAT cohort
2026 Jordan, S.; Tucker, D.; Scanlon, I.; Thayer, D. S.; Ballardini, E.; Cavero-Carbonell, C.; Damkjaer, M.; Gatt, M.; Gissler, M.; Ostapchuk, L.; Santoro, M.; Stevens, S.; Wellesley, D.; Wertelecki, W.; Given, J.; Loane, M.; Evans, H. T.
Sirenomelia: A Review of European Prevalence Data and Epidemiological Analysis of 17 Cases Registered in Wales
2026 Emmerson, C.; Olson, M.; Williams, C.; Maddison, R.; Tucker, D.; Davies, L.; Perraud, A.; Bailey, L.; Humphreys, C.; Hughes, R.; Sichitiu, J.; Amores, M. O.; Barisic, I.; Santoro, M.; Carbonell, C. C.; Draper, E. S.; Haeusler, M.; Monier, I.; Latos-Bielenska, A.; Dias, C. M.; Hond, E. D.; Ballardini, E.; O'Mahony, M.; Perthus, I.; Rankin, J.; Rissmann, A.; Rouget, F.; Stevens, S.; Bergman, J. E. H.; Wellesley, D.; Wertelecki, W.
Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the EUROCAT Network
2025 Bergman, J. E. H.; Perraud, A.; Garne, E.; Barisic, I.; Tucker, D.; Ballardini, E.; Bruneau, L.; Cavero-Carbonell, C.; Cousin, I.; Gatt, M.; Kovacheva, K.; Latos-Bielenska, A.; O'Mahony, M.; Monier, I.; Perthus, I.; Pertile, R.; Rissmann, A.; Rouget, F.; Santoro, M.; Sichitiu, J.; Verellen-Dumoulin, C.; Wertelecki, W.; Wellesley, D.; Morris, J. K.
Health outcomes and drug utilisation in children with Noonan syndrome: a European cohort study
2025 Santoro, M.; Barisic, I.; Coi, A.; Tan, J.; Garne, E.; Loane, M.; Odak, L.; Abate, M. V.; Ballardini, E.; Cavero-Carbonell, C.; Gatt, M.; Gissler, M.; Klungsoyr, K.; Lelong, N.; Tucker, D.; Wellesley, D.; Morris, J. K.
Morbidity in children with major kidney anomalies: a European population-based study
2025 Garne, E.; Damkjaer, M.; Rissmann, A.; Cavero-Carbonell, C.; Gissler, M.; Neville, A.; Santoro, M.; Tan, J.; Tucker, D.; Loane, M.; Morris, J.
Prenatal detection rate of congenital anomalies over a period of 30 years: A population-based registry study
2025 Santoro, M.; Coi, A.; Masini, G.; Pasquini, L.
The Healthcare Needs of Children With Down Syndrome in the First Year of Life: An Analysis of the EUROlinkCAT Data Linkage Study
2025 Seaton, S. E.; Rankin, J.; Cavero-Carbonell, C.; Garne, E.; Gissler, M.; Loane, M.; Neville, A. J.; Santoro, M.; Tan, J.; Tucker, D.; Morris, J. K.
The Role of Microbiota in the Pathogenesis of Bullous Pemphigoid and Pemphigus Vulgaris: Evidence, Controversies, and Perspectives
2025 Gorini, Francesca; Coi, Alessio; Santoro, Michele; Tonacci, Alessandro; Sansone, Francesco; Biancamaria Mariotti, Elena; Donati, Marta; Verdelli, Alice; Rita Nasca, Maria; Amerio, Paolo; Antiga, Emiliano; Barletta, Emanuela; Caproni, Marzia
Higher risk of cerebral palsy, seizures/epilepsy, visual- and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study
2024 Urhoj, S. K.; Morris, J.; Loane, M.; Ballardini, E.; Barrachina-Bonet, L.; Cavero-Carbonell, C.; Coi, A.; Gissler, M.; Given, J.; Heino, A.; Jordan, S.; Neville, A.; Santoro, M.; Tan, J.; Tucker, D.; Wellesley, D.; Garne, E.; Damkjaer, M.
Hypothyroidism in Patients with Down Syndrome: Prevalence and Association with Congenital Heart Defects
2024 Gorini, F.; Coi, A.; Pierini, A.; Assanta, N.; Bottoni, A.; Santoro, M.
Medication use during pregnancy and the risk of gastroschisis: a systematic review and meta-analysis of observational studies
2024 Baldacci, Silvia; Santoro, Michele; Mezzasalma, Lorena; Pierini, Anna; Coi, Alessio
Orofacial Clefts and Maternal Risk Factors: A Population-Based Case–Control Study
2024 Santoro, Michele; Mezzasalma, Lorena; Coi, Alessio; Pierini, Anna
The Association of Prenatal Diagnoses with Mortality and Long‑TermMorbidity in Children with Specific Isolated Congenital Anomalies:A European Register‑Based Cohort Study
2024 Heino, A; Morris, Jk; Garne, E; Baldacci, S; Barisic, I; Cavero-Carbonell, C; García-Villodre, L; Given, J; Jordan, S; Loane, M; Lutke, Lr; Neville, Aj; Santoro, M; Scanlon, I; Tan, J; de Walle, Hek; Kiuru-Kuhlefelt, S; Gissler, M
Accuracy of congenital anomaly coding in live birth children recorded in European health care databases, a EUROlinkCAT study
2023 K Bakker, Marian; Loane, Maria; Garne, Ester; Ballardini, Elisa; Caverocarbonell, Clara; García, Laura; Gissler, Mika; Given, Joanne; Heino, Anna; Jamrydziurla, Anna; Jordan, Sue; Kjaer Urhoj, Stine; Latosbieleska, Anna; Limb, Elisabeth; Lutke, Renee; J Neville, Amanda; Pierini, Anna; Santoro, Michele; Scanlon, Ieuan; Tan, Joachim; Wellesley, Diana; K de Walle, Hermien E; K Morris, Joan
Causes of death in children with congenital anomalies up to age 10 in eight European countries
2023 Rissmann, Anke; Tan, Joachim; Glinianaia Svetlana, V; Rankin, Judith; Pierini, Anna; Santoro, Michele; Coi, Alessio; Garne, Ester; Loane, Maria; Given, Joanne; Reid, Abigail; Aizpurua, Amaia; Akhmedzhanova, Diana; Ballardini, Elisa; Barisic, Ingeborg; Caverocarbonell, Clara; de Walle Hermien, E K; Gatt, Miriam; Gissler, Mika; Heino, Anna; Jordan, Sue; Urhoj Stine, Kjaer; Klungsoyr, Kari; Lutke, Renee; Mokoroa, Olatz; Neville Amanda, Julie; Thayer Daniel, S; Wellesley Diana, G; Yevtushok, Lyubov; Zurriaga, Oscar; Morris, Joan
Creating a population-based cohort of children born with and without congenital anomalies using birth data matched to hospital discharge databases in 11 European regions: Assessment of linkage success and data quality
2023 Loane, Maria; E Given, Joanne; Tan, Joachim; Barii, Ingeborg; Barrachinabonet, Laia; Caverocarbonell, Clara; Coi, Alessio; Densem, James; Garne, Ester; Gissler, Mika; Heino, Anna; Jordan, Sue; Lutke, Renee; J Neville, Amanda; Odak, Ljubica; Puccini, Aurora; Santoro, Michele; Scanlon, Ieuan; K Urhoj, Stine; K de Walle, Hermien E; Wellesley, Diana; K Morris, Joan
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Analysis of Prevalence and Mortality Among Neonates and Children With Intestinal Atresia: A Multinational Study, 1974–2015 | 1-gen-2026 | Carreno, A.; Aguilera, M. P.; Ibanez, L.; Sarmiento, K.; Gili, J. A.; Siffel, C.; Nembhard, W. N.; Bergman, J. E. H.; Bermejo-Sanchez, E.; Tagliabue, G.; Dastgiri, S.; Feldkamp, M. L.; Pocius, S.; Gatt, M.; Martinez, L.; Canessa, M. A.; Groisman, B.; Kallen, K.; Landau, D.; Lelong, N.; Morgan, M.; Arteaga-Vazquez, J.; Santoro, M.; Rissmann, A.; Sipek, A.; Szabova, E.; Wertelecki, W.; Canfield, M. A.; Mastroiacovo, P.; Zarante, I. | |
| Antiseizure Prescription for Children With Severe Congenital Heart Defects and Children With Gastrointestinal Anomalies | 1-gen-2026 | Damkjaer, Mads; Morris, Joan K.; Ballardini, Elisa; Barrachina-Bonet, Laia; Cavero-Carbonell, Clara; Coi, Alessio; Gissler, Mika; Given, Joanne; Heino, Anna; Jordan, Sue; Neville, Amanda; Santoro, Michele; Tan, Joachim; Tucker, David; Wellesley, Diana; Kjaer Urhoj, Stine; Garne, Ester; Loane, Maria | |
| Epidemiology of idiopathic pulmonaryfibrosis: a population registry-based study | 1-gen-2026 | Gorini, Francesca; Santoro, Michele; Pierini, Anna; Cameli, Paolo; Chimera, Davide; Lavorini, Federico; Pistelli, Francesco; Rosi, Elisabetta; Tavanti, Laura; Tomassetti, Sara; Carrozzi, Laura; Bargagli, Elena; Coi, Alessio | |
| Heterogeneity of the prevalence of congenital hip dislocation in Europe | 1-gen-2026 | Garne, E.; Rissmann, A.; Dias, C. M.; Buzzoni, C.; Lynch, C.; Dumoulin, C.; Cavero-Carbonell, C.; Tucker, D.; Broekstra, D.; Ballardini, E.; Hond, E. D.; Rouget, F.; Rodriguez-Rasero, F.; Cousin, I.; Monier, I.; Morris, J.; Sichitiu, J.; Klungsoyr, K.; Odak, L.; Ceresola, M.; O'Mahony, M.; Santoro, M.; Zymak-Zakutnia, N.; Wood, R.; Pertile, R.; Stevens, S. | |
| Mortality amongst European children with congenital anomalies: Associations with socio-economic status in the EUROLINKCAT cohort | 1-gen-2026 | Jordan, S.; Tucker, D.; Scanlon, I.; Thayer, D. S.; Ballardini, E.; Cavero-Carbonell, C.; Damkjaer, M.; Gatt, M.; Gissler, M.; Ostapchuk, L.; Santoro, M.; Stevens, S.; Wellesley, D.; Wertelecki, W.; Given, J.; Loane, M.; Evans, H. T. | |
| Sirenomelia: A Review of European Prevalence Data and Epidemiological Analysis of 17 Cases Registered in Wales | 1-gen-2026 | Emmerson, C.; Olson, M.; Williams, C.; Maddison, R.; Tucker, D.; Davies, L.; Perraud, A.; Bailey, L.; Humphreys, C.; Hughes, R.; Sichitiu, J.; Amores, M. O.; Barisic, I.; Santoro, M.; Carbonell, C. C.; Draper, E. S.; Haeusler, M.; Monier, I.; Latos-Bielenska, A.; Dias, C. M.; Hond, E. D.; Ballardini, E.; O'Mahony, M.; Perthus, I.; Rankin, J.; Rissmann, A.; Rouget, F.; Stevens, S.; Bergman, J. E. H.; Wellesley, D.; Wertelecki, W. | |
| Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the EUROCAT Network | 1-gen-2025 | Bergman, J. E. H.; Perraud, A.; Garne, E.; Barisic, I.; Tucker, D.; Ballardini, E.; Bruneau, L.; Cavero-Carbonell, C.; Cousin, I.; Gatt, M.; Kovacheva, K.; Latos-Bielenska, A.; O'Mahony, M.; Monier, I.; Perthus, I.; Pertile, R.; Rissmann, A.; Rouget, F.; Santoro, M.; Sichitiu, J.; Verellen-Dumoulin, C.; Wertelecki, W.; Wellesley, D.; Morris, J. K. | |
| Health outcomes and drug utilisation in children with Noonan syndrome: a European cohort study | 1-gen-2025 | Santoro, M.; Barisic, I.; Coi, A.; Tan, J.; Garne, E.; Loane, M.; Odak, L.; Abate, M. V.; Ballardini, E.; Cavero-Carbonell, C.; Gatt, M.; Gissler, M.; Klungsoyr, K.; Lelong, N.; Tucker, D.; Wellesley, D.; Morris, J. K. | |
| Morbidity in children with major kidney anomalies: a European population-based study | 1-gen-2025 | Garne, E.; Damkjaer, M.; Rissmann, A.; Cavero-Carbonell, C.; Gissler, M.; Neville, A.; Santoro, M.; Tan, J.; Tucker, D.; Loane, M.; Morris, J. | |
| Prenatal detection rate of congenital anomalies over a period of 30 years: A population-based registry study | 1-gen-2025 | Santoro, M.; Coi, A.; Masini, G.; Pasquini, L. | |
| The Healthcare Needs of Children With Down Syndrome in the First Year of Life: An Analysis of the EUROlinkCAT Data Linkage Study | 1-gen-2025 | Seaton, S. E.; Rankin, J.; Cavero-Carbonell, C.; Garne, E.; Gissler, M.; Loane, M.; Neville, A. J.; Santoro, M.; Tan, J.; Tucker, D.; Morris, J. K. | |
| The Role of Microbiota in the Pathogenesis of Bullous Pemphigoid and Pemphigus Vulgaris: Evidence, Controversies, and Perspectives | 1-gen-2025 | Gorini, Francesca; Coi, Alessio; Santoro, Michele; Tonacci, Alessandro; Sansone, Francesco; Biancamaria Mariotti, Elena; Donati, Marta; Verdelli, Alice; Rita Nasca, Maria; Amerio, Paolo; Antiga, Emiliano; Barletta, Emanuela; Caproni, Marzia | |
| Higher risk of cerebral palsy, seizures/epilepsy, visual- and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study | 1-gen-2024 | Urhoj, S. K.; Morris, J.; Loane, M.; Ballardini, E.; Barrachina-Bonet, L.; Cavero-Carbonell, C.; Coi, A.; Gissler, M.; Given, J.; Heino, A.; Jordan, S.; Neville, A.; Santoro, M.; Tan, J.; Tucker, D.; Wellesley, D.; Garne, E.; Damkjaer, M. | |
| Hypothyroidism in Patients with Down Syndrome: Prevalence and Association with Congenital Heart Defects | 1-gen-2024 | Gorini, F.; Coi, A.; Pierini, A.; Assanta, N.; Bottoni, A.; Santoro, M. | |
| Medication use during pregnancy and the risk of gastroschisis: a systematic review and meta-analysis of observational studies | 1-gen-2024 | Baldacci, Silvia; Santoro, Michele; Mezzasalma, Lorena; Pierini, Anna; Coi, Alessio | |
| Orofacial Clefts and Maternal Risk Factors: A Population-Based Case–Control Study | 1-gen-2024 | Santoro, Michele; Mezzasalma, Lorena; Coi, Alessio; Pierini, Anna | |
| The Association of Prenatal Diagnoses with Mortality and Long‑TermMorbidity in Children with Specific Isolated Congenital Anomalies:A European Register‑Based Cohort Study | 1-gen-2024 | Heino, A; Morris, Jk; Garne, E; Baldacci, S; Barisic, I; Cavero-Carbonell, C; García-Villodre, L; Given, J; Jordan, S; Loane, M; Lutke, Lr; Neville, Aj; Santoro, M; Scanlon, I; Tan, J; de Walle, Hek; Kiuru-Kuhlefelt, S; Gissler, M | |
| Accuracy of congenital anomaly coding in live birth children recorded in European health care databases, a EUROlinkCAT study | 1-gen-2023 | K Bakker, Marian; Loane, Maria; Garne, Ester; Ballardini, Elisa; Caverocarbonell, Clara; García, Laura; Gissler, Mika; Given, Joanne; Heino, Anna; Jamrydziurla, Anna; Jordan, Sue; Kjaer Urhoj, Stine; Latosbieleska, Anna; Limb, Elisabeth; Lutke, Renee; J Neville, Amanda; Pierini, Anna; Santoro, Michele; Scanlon, Ieuan; Tan, Joachim; Wellesley, Diana; K de Walle, Hermien E; K Morris, Joan | |
| Causes of death in children with congenital anomalies up to age 10 in eight European countries | 1-gen-2023 | Rissmann, Anke; Tan, Joachim; Glinianaia Svetlana, V; Rankin, Judith; Pierini, Anna; Santoro, Michele; Coi, Alessio; Garne, Ester; Loane, Maria; Given, Joanne; Reid, Abigail; Aizpurua, Amaia; Akhmedzhanova, Diana; Ballardini, Elisa; Barisic, Ingeborg; Caverocarbonell, Clara; de Walle Hermien, E K; Gatt, Miriam; Gissler, Mika; Heino, Anna; Jordan, Sue; Urhoj Stine, Kjaer; Klungsoyr, Kari; Lutke, Renee; Mokoroa, Olatz; Neville Amanda, Julie; Thayer Daniel, S; Wellesley Diana, G; Yevtushok, Lyubov; Zurriaga, Oscar; Morris, Joan | |
| Creating a population-based cohort of children born with and without congenital anomalies using birth data matched to hospital discharge databases in 11 European regions: Assessment of linkage success and data quality | 1-gen-2023 | Loane, Maria; E Given, Joanne; Tan, Joachim; Barii, Ingeborg; Barrachinabonet, Laia; Caverocarbonell, Clara; Coi, Alessio; Densem, James; Garne, Ester; Gissler, Mika; Heino, Anna; Jordan, Sue; Lutke, Renee; J Neville, Amanda; Odak, Ljubica; Puccini, Aurora; Santoro, Michele; Scanlon, Ieuan; K Urhoj, Stine; K de Walle, Hermien E; Wellesley, Diana; K Morris, Joan |