SANTORO, MICHELE
SANTORO, MICHELE
Istituto di Fisiologia Clinica - IFC
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
Epidemiology of aplasia cutis congenita: A population-based study in Europe
2023 Coi, A; Barisic, I; Garne, E; Pierini, A; Addor, Mc; Aizpurua Atxega, A; Ballardini, E; Braz, P; Broughan, Jm; Caverocarbonell, C; de Walle, Hek; Draper, Es; Gatt, M; Hausler, M; Kinsnerovaskainen, A; Kurinczuk, Jj; Lelong, N; Luyt, K; Mezzasalma, L; Mullaney, C; Nelen, V; Odak, L; O'Mahony, Mt; Perthus, I; Randrianaivo, H; Rankin, J; Rissmann, A; Rouget, F; Schaub, B; Tucker, D; Wellesley, D; Wisniewska, K; Yevtushok, L; Santoro, M
European study showed that children with congenital anomalies often underwent multiple surgical procedures at different ages across Europe
2023 Garne, Ester; Loane, Maria; Tan, Joachim; Ballardini, Elisa; Brigden, Joanna; Caverocarbonell, Clara; Coi, Alessio; Damkjaer, Mads; Garciavillodre, Laura; Gissler, Mika; Given, Joanne; Heino, Anna; Jordan, Sue; Limb, Elizabeth; Neville, Amanda; Rissmann, Anke; Santoro, Michele; Scanlon, Ieuan; Kjaer Urhoj, Stine; Wellesley, Diana; Morris, Joan
Malattie rare
2023 Gorini, F; Coi, A; Santoro, M; Baldacci, S; Mezzasalma, L; Pieroni, F; Marrucci, S; Berni, C; Scaletti, C; Pierini, A
Profile of Drug Utilization in Patients with Rare Diseases in Tuscany, Italy: A Population-Based Study
2023 Gorini, F; Santoro, M; Pierini, A; Mezzasalma, L; Baldacci, S; Coi, A
Risk factors for mortality in infancy and childhood in children with major congenital anomalies: A European population-based cohort study
2023 Tan, Joachim; V Glinianaia, Svetlana; Rankin, Judith; Pierini, Anna; Santoro, Michele; Coi, Alessio; Garne, Ester; Loane, Maria; E Given, Joanne; Brigden, Joanna; Ballardini, Elisa; Cavero-Carbonell, Clara; K de Walle, Hermien E; García-Villodre, Laura; Gatt, Miriam; Gissler, Mika; Heino, Anna; Jordan, Sue; Khoshnood, Babak; Klungsoyr, Kari; Lelong, Nathalie; L Lutke, Renée; J Neville, Amanda; Tucker, David; K Urhoj, Stine; Wellesley, Diana; K Morris, Joan
SENTIERI - Epidemiological Study of Residents in National Priority Contaminated Sites. Sixth Report
2023 Zona, Amerigo; Fazzo, Lucia; Benedetti, Marta; Bruno, Caterina; Vecchi, Simona; Pasetto, Roberto; Minichilli, Fabrizio; De Santis, Marco; Maria Nannavecchia, Anna; Di Fonzo, Davide; Contiero, Paolo; Ricci, Paolo; Bisceglia, Lucia; Manno, Valerio; Minelli, Giada; Santoro, Michele; Gorini, Francesca; Ancona, Carla; Scondotto, Salvatore; Elena Soggiu, Maria; Scaini, Federica; Beccaloni, Eleonora; Marsili, Daniela; Francesco Villa, Marco; Maifredi, Giovanni; Magoni, Michele; Iavarone, Ivano
Survival, hospitalisation and surgery in children born with Pierre Robin sequence: a European population-based cohort study
2023 Santoro, Michele; Garne, Ester; Coi, Alessio; Tan, Joachim; Loane, Maria; Ballardini, Elisa; Caverocarbonell, Clara; Ek de Walle, Hermien; Gatt, Miriam; Gissler, Mika; Jordan, Sue; Klungsøyr, Kari; Lelong, Natalie; Kjaer Urhoj, Stine; G Wellesley, Diana; K Morris, Joan
Gastrostomy and congenital anomalies: a European population-based study
2022 Garne, E; Tan, J; Loane, M; Baldacci, S; Ballardini, E; Brigden, J; Caverocarbonell, C; Garcíavillodre, L; Gissler, M; Given, J; Heino, A; Jordan, S; Limb, E; Neville, Aj; Rissmann, A; Santoro, M; Scanlon, L; Urhoj, Sk; Wellesley, Dg; Morris, J
Healthcare Burden of Rare Diseases: A Population-Based Study in Tuscany (Italy)
2022 Baldacci, Silvia; Santoro, Michele; Pierini, Anna; Mezzasalma, Lorena; Gorini, Francesca; Coi, Alessio
Hospital length of stay among children with and without congenital anomalies across 11 European regions--A population-based data linkage study
2022 Kjaer Urhoj, Stine; Tan, Joachim; K Morris, Joan; Given, Joanne; Astolfi, Gianni; Baldacci, Silvia; Barisic, Ingeborg; Brigden, Joanna; Caverocarbonell, Clara; Evans, Hannah; Gissler, Mika; Heino, Anna; Jordan, Sue; Lutke, Renee; Odak, Ljubica; Puccini, Aurora; Santoro, Michele; Scanlon, Ieuan; K de Walle, Hermien E; Wellesley, Diana; Zurriaga, Oscar; Loane, Maria; Garne, Ester
La Percezione del Rischio
2022 Bianchi, F; Bustaffa, E; Coi, A; Cori, L; Curzio, O; Gorini, F; Minichilli, F; Santoro, M
Orphan Drug Use in Patients With Rare Diseases: A Population-Based Cohort Study
2022 Gorini, F; Santoro, M; Pierini, A; Mezzasalma, L; Baldacci, S; Bargagli, E; Boncristiano, A; Brunetto, Mr; Cameli, P; Cappelli, F; Castaman, G; Coco, B; Donati, Ma; Guerrini, R; Linari, S; Murro, V; Olivotto, I; Parronchi, P; Pochiero, F; Rossi, O; Scappini, B; Sodi, A; Vannucchi, Ma; Coi, A
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| Epidemiology of aplasia cutis congenita: A population-based study in Europe | 1-gen-2023 | Coi, A; Barisic, I; Garne, E; Pierini, A; Addor, Mc; Aizpurua Atxega, A; Ballardini, E; Braz, P; Broughan, Jm; Caverocarbonell, C; de Walle, Hek; Draper, Es; Gatt, M; Hausler, M; Kinsnerovaskainen, A; Kurinczuk, Jj; Lelong, N; Luyt, K; Mezzasalma, L; Mullaney, C; Nelen, V; Odak, L; O'Mahony, Mt; Perthus, I; Randrianaivo, H; Rankin, J; Rissmann, A; Rouget, F; Schaub, B; Tucker, D; Wellesley, D; Wisniewska, K; Yevtushok, L; Santoro, M | |
| European study showed that children with congenital anomalies often underwent multiple surgical procedures at different ages across Europe | 1-gen-2023 | Garne, Ester; Loane, Maria; Tan, Joachim; Ballardini, Elisa; Brigden, Joanna; Caverocarbonell, Clara; Coi, Alessio; Damkjaer, Mads; Garciavillodre, Laura; Gissler, Mika; Given, Joanne; Heino, Anna; Jordan, Sue; Limb, Elizabeth; Neville, Amanda; Rissmann, Anke; Santoro, Michele; Scanlon, Ieuan; Kjaer Urhoj, Stine; Wellesley, Diana; Morris, Joan | |
| Malattie rare | 1-gen-2023 | Gorini, F; Coi, A; Santoro, M; Baldacci, S; Mezzasalma, L; Pieroni, F; Marrucci, S; Berni, C; Scaletti, C; Pierini, A | |
| Profile of Drug Utilization in Patients with Rare Diseases in Tuscany, Italy: A Population-Based Study | 1-gen-2023 | Gorini, F; Santoro, M; Pierini, A; Mezzasalma, L; Baldacci, S; Coi, A | |
| Risk factors for mortality in infancy and childhood in children with major congenital anomalies: A European population-based cohort study | 1-gen-2023 | Tan, Joachim; V Glinianaia, Svetlana; Rankin, Judith; Pierini, Anna; Santoro, Michele; Coi, Alessio; Garne, Ester; Loane, Maria; E Given, Joanne; Brigden, Joanna; Ballardini, Elisa; Cavero-Carbonell, Clara; K de Walle, Hermien E; García-Villodre, Laura; Gatt, Miriam; Gissler, Mika; Heino, Anna; Jordan, Sue; Khoshnood, Babak; Klungsoyr, Kari; Lelong, Nathalie; L Lutke, Renée; J Neville, Amanda; Tucker, David; K Urhoj, Stine; Wellesley, Diana; K Morris, Joan | |
| SENTIERI - Epidemiological Study of Residents in National Priority Contaminated Sites. Sixth Report | 1-gen-2023 | Zona, Amerigo; Fazzo, Lucia; Benedetti, Marta; Bruno, Caterina; Vecchi, Simona; Pasetto, Roberto; Minichilli, Fabrizio; De Santis, Marco; Maria Nannavecchia, Anna; Di Fonzo, Davide; Contiero, Paolo; Ricci, Paolo; Bisceglia, Lucia; Manno, Valerio; Minelli, Giada; Santoro, Michele; Gorini, Francesca; Ancona, Carla; Scondotto, Salvatore; Elena Soggiu, Maria; Scaini, Federica; Beccaloni, Eleonora; Marsili, Daniela; Francesco Villa, Marco; Maifredi, Giovanni; Magoni, Michele; Iavarone, Ivano | |
| Survival, hospitalisation and surgery in children born with Pierre Robin sequence: a European population-based cohort study | 1-gen-2023 | Santoro, Michele; Garne, Ester; Coi, Alessio; Tan, Joachim; Loane, Maria; Ballardini, Elisa; Caverocarbonell, Clara; Ek de Walle, Hermien; Gatt, Miriam; Gissler, Mika; Jordan, Sue; Klungsøyr, Kari; Lelong, Natalie; Kjaer Urhoj, Stine; G Wellesley, Diana; K Morris, Joan | |
| Gastrostomy and congenital anomalies: a European population-based study | 1-gen-2022 | Garne, E; Tan, J; Loane, M; Baldacci, S; Ballardini, E; Brigden, J; Caverocarbonell, C; Garcíavillodre, L; Gissler, M; Given, J; Heino, A; Jordan, S; Limb, E; Neville, Aj; Rissmann, A; Santoro, M; Scanlon, L; Urhoj, Sk; Wellesley, Dg; Morris, J | |
| Healthcare Burden of Rare Diseases: A Population-Based Study in Tuscany (Italy) | 1-gen-2022 | Baldacci, Silvia; Santoro, Michele; Pierini, Anna; Mezzasalma, Lorena; Gorini, Francesca; Coi, Alessio | |
| Hospital length of stay among children with and without congenital anomalies across 11 European regions--A population-based data linkage study | 1-gen-2022 | Kjaer Urhoj, Stine; Tan, Joachim; K Morris, Joan; Given, Joanne; Astolfi, Gianni; Baldacci, Silvia; Barisic, Ingeborg; Brigden, Joanna; Caverocarbonell, Clara; Evans, Hannah; Gissler, Mika; Heino, Anna; Jordan, Sue; Lutke, Renee; Odak, Ljubica; Puccini, Aurora; Santoro, Michele; Scanlon, Ieuan; K de Walle, Hermien E; Wellesley, Diana; Zurriaga, Oscar; Loane, Maria; Garne, Ester | |
| La Percezione del Rischio | 1-gen-2022 | Bianchi, F; Bustaffa, E; Coi, A; Cori, L; Curzio, O; Gorini, F; Minichilli, F; Santoro, M | |
| Orphan Drug Use in Patients With Rare Diseases: A Population-Based Cohort Study | 1-gen-2022 | Gorini, F; Santoro, M; Pierini, A; Mezzasalma, L; Baldacci, S; Bargagli, E; Boncristiano, A; Brunetto, Mr; Cameli, P; Cappelli, F; Castaman, G; Coco, B; Donati, Ma; Guerrini, R; Linari, S; Murro, V; Olivotto, I; Parronchi, P; Pochiero, F; Rossi, O; Scappini, B; Sodi, A; Vannucchi, Ma; Coi, A |