COI, ALESSIO
COI, ALESSIO
Istituto di Fisiologia Clinica - IFC
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
Antiasthmatic prescriptions in children with and without congenital anomalies: a population-based study
2023 Divin, Natalie; Emma Given, Joanne; Tan, Joachim; Astolfi, Gianni; Ballardini, Elisa; Barrachinabonet, Laia; Caverocarbonell, Clara; Coi, Alessio; Garne, Ester; Gissler, Mika; Heino, Anna; Jordan, Susan; Pierini, Anna; Scanlon, Ieuan; Kjær Urhøj, Stine; K Morris, Joan; Loane, Maria
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 Maria Loane ; Joanne E Given ; Joachim Tan ; Ingeborg Barii ; Laia BarrachinaBonet ; Clara CaveroCarbonell ; Alessio Coi ; James Densem ; Ester Garne ; Mika Gissler ; Anna Heino ; Sue Jordan ; Renee Lutke ; Amanda J Neville ; Ljubica Odak ; Aurora Puccini ; Michele Santoro ; Ieuan Scanlon ; Stine K Urhoj ; Hermien E K de Walle ; Diana Wellesley ; Joan K Morris
Epidemiology of aplasia cutis congenita: A population-based study in Europe
2023 Coi A.; Barisic I.; Garne E.; Pierini A.; Addor M.C.; Aizpurua Atxega A.; Ballardini E.; Braz P.; Broughan J.M.; CaveroCarbonell C.; de Walle H.E.K.; Draper E.S.; Gatt M.; Hausler M.; KinsnerOvaskainen A.; Kurinczuk J.J.; Lelong N.; Luyt K.; Mezzasalma L.; Mullaney C.; Nelen V.; Odak L.; O'Mahony M.T.; 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
Hospital Length of Stay and Surgery among European Children with Rare Structural Congenital Anomalies--A Population-Based Data Linkage Study
2023 Garne, E; Tan, J; Damkjaer, M; Ballardini, E; Caverocarbonell, C; Coi, A; Garciavillodre, L; Gissler, M; Given, J; Heino, A; Jordan, S; Limb, E; Loane, M; Neville, Aj; Pierini, A; Rissmann, A; Tucker, D; Urhoj, Sk; Morris, J
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
Survival, hospitalisation and surgery in children born with Pierre Robin sequence: a European population-based cohort study
2023 Michele Santoro ; Ester Garne ; Alessio Coi ; Joachim Tan ; Maria Loane ; Elisa Ballardini ; Clara CaveroCarbonell ; Hermien Ek de Walle ; Miriam Gatt ; Mika Gissler ; Sue Jordan ; Kari Klungsøyr ; Natalie Lelong ; Stine Kjaer Urhoj ; Diana G Wellesley ; Joan K Morris
Clinical Patterns, Survival, Comorbidities, and Treatment Regimens in 149 Patients With Pemphigus in Tuscany (Italy): A 12-Year Hospital-Based Study
2022 Quintarelli L.; Coi A.; Maglie R.; Corra A.; Mariotti E.B.; Aimo C.; Ruffo di Calabria V.; Verdelli A.; Bianchi B.; Del Bianco E.; Antiga E.; Caproni M.
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
La Percezione del Rischio
2022 Bianchi F.; Bustaffa E.; Coi A.; Cori L.; Curzio O.; Gorini F.; Minichilli F.; Santoro M.
Neutrophil Gelatinase-Associated Lipocalin as Potential Predictive Biomarker of Melanoma and Non-Melanoma Skin Cancers in Psoriatic Patients: A Pilot Study
2022 Verdelli, A; Caproni, M; Coi, A; Corra, A; Degl'Innocenti, D; Vasarri, M; Quintarelli, L; Volpi, V; Cipollini, Em; Barletta, E
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
Prescription of cardiovascular medication in children with congenital heart defects across six European Regions from 2000 to 2014: data from the EUROlinkCAT population-based cohort study
2022 Damkjaer, M; Urhoj, Sk; Tan, J; Briggs, G; Loane, M; Given, Je; Barrachinabonet, L; Caverocarbonell, C; Coi, A; Neville, Aj; Heino, A; Kiurukuhlefelt, S; Jordan, S; Scanlon, I; Pierini, A; Puccini, A; Garne, E; Morris, Jk
Preterm birth and prescriptions for cardiovascular, antiseizure, antibiotics and antiasthmatic medication in children up to 10 years of age: a population-based data linkage cohort study across six European regions.
2022 Damkjaer M; Loane M; Urhøj SK; Ballardini E; CaveroCarbonell C; Coi A; GarcíaVillodre L; Given JE; Gissler M; Heino A; Jordan S; Neville A; Pierini A; Tan J; Scanlon I; Garne E; Morris JK.
Survival of children with rare structural congenital anomalies: a multi-registry cohort study
2022 Alessio Coi; Michele Santoro; Anna Pierini; Judith Rankin; Svetlana V. Glinianaia; Joachim Tan; AbigailKate Reid; Ester Garne; Maria Loane; Joanne Given; Elisa Ballardini; Clara CaveroCarbonell; Hermien E. K. de Walle; Miriam Gatt; Laura GarcíaVillodre; Mika Gissler; Sue Jordan; Sonja KiuruKuhlefelt; Stine Kjaer Urhoj; Kari Klungsøyr; Nathalie Lelong; L. Renée Lutke; Amanda J. Neville; Makan Rahshenas; Ieuan Scanlon; Diana Wellesley;Joan K. Morris
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| Antiasthmatic prescriptions in children with and without congenital anomalies: a population-based study | 1-gen-2023 | Divin, Natalie; Emma Given, Joanne; Tan, Joachim; Astolfi, Gianni; Ballardini, Elisa; Barrachinabonet, Laia; Caverocarbonell, Clara; Coi, Alessio; Garne, Ester; Gissler, Mika; Heino, Anna; Jordan, Susan; Pierini, Anna; Scanlon, Ieuan; Kjær Urhøj, Stine; K Morris, Joan; Loane, Maria | |
| 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 | Maria Loane ; Joanne E Given ; Joachim Tan ; Ingeborg Barii ; Laia BarrachinaBonet ; Clara CaveroCarbonell ; Alessio Coi ; James Densem ; Ester Garne ; Mika Gissler ; Anna Heino ; Sue Jordan ; Renee Lutke ; Amanda J Neville ; Ljubica Odak ; Aurora Puccini ; Michele Santoro ; Ieuan Scanlon ; Stine K Urhoj ; Hermien E K de Walle ; Diana Wellesley ; Joan K Morris | |
| Epidemiology of aplasia cutis congenita: A population-based study in Europe | 1-gen-2023 | Coi A.; Barisic I.; Garne E.; Pierini A.; Addor M.C.; Aizpurua Atxega A.; Ballardini E.; Braz P.; Broughan J.M.; CaveroCarbonell C.; de Walle H.E.K.; Draper E.S.; Gatt M.; Hausler M.; KinsnerOvaskainen A.; Kurinczuk J.J.; Lelong N.; Luyt K.; Mezzasalma L.; Mullaney C.; Nelen V.; Odak L.; O'Mahony M.T.; 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 | |
| Hospital Length of Stay and Surgery among European Children with Rare Structural Congenital Anomalies--A Population-Based Data Linkage Study | 1-gen-2023 | Garne, E; Tan, J; Damkjaer, M; Ballardini, E; Caverocarbonell, C; Coi, A; Garciavillodre, L; Gissler, M; Given, J; Heino, A; Jordan, S; Limb, E; Loane, M; Neville, Aj; Pierini, A; Rissmann, A; Tucker, D; Urhoj, Sk; Morris, J | |
| 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 | |
| Survival, hospitalisation and surgery in children born with Pierre Robin sequence: a European population-based cohort study | 1-gen-2023 | Michele Santoro ; Ester Garne ; Alessio Coi ; Joachim Tan ; Maria Loane ; Elisa Ballardini ; Clara CaveroCarbonell ; Hermien Ek de Walle ; Miriam Gatt ; Mika Gissler ; Sue Jordan ; Kari Klungsøyr ; Natalie Lelong ; Stine Kjaer Urhoj ; Diana G Wellesley ; Joan K Morris | |
| Clinical Patterns, Survival, Comorbidities, and Treatment Regimens in 149 Patients With Pemphigus in Tuscany (Italy): A 12-Year Hospital-Based Study | 1-gen-2022 | Quintarelli L.; Coi A.; Maglie R.; Corra A.; Mariotti E.B.; Aimo C.; Ruffo di Calabria V.; Verdelli A.; Bianchi B.; Del Bianco E.; Antiga E.; Caproni M. | |
| 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 | |
| La Percezione del Rischio | 1-gen-2022 | Bianchi F.; Bustaffa E.; Coi A.; Cori L.; Curzio O.; Gorini F.; Minichilli F.; Santoro M. | |
| Neutrophil Gelatinase-Associated Lipocalin as Potential Predictive Biomarker of Melanoma and Non-Melanoma Skin Cancers in Psoriatic Patients: A Pilot Study | 1-gen-2022 | Verdelli, A; Caproni, M; Coi, A; Corra, A; Degl'Innocenti, D; Vasarri, M; Quintarelli, L; Volpi, V; Cipollini, Em; Barletta, E | |
| 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 | |
| Prescription of cardiovascular medication in children with congenital heart defects across six European Regions from 2000 to 2014: data from the EUROlinkCAT population-based cohort study | 1-gen-2022 | Damkjaer, M; Urhoj, Sk; Tan, J; Briggs, G; Loane, M; Given, Je; Barrachinabonet, L; Caverocarbonell, C; Coi, A; Neville, Aj; Heino, A; Kiurukuhlefelt, S; Jordan, S; Scanlon, I; Pierini, A; Puccini, A; Garne, E; Morris, Jk | |
| Preterm birth and prescriptions for cardiovascular, antiseizure, antibiotics and antiasthmatic medication in children up to 10 years of age: a population-based data linkage cohort study across six European regions. | 1-gen-2022 | Damkjaer M; Loane M; Urhøj SK; Ballardini E; CaveroCarbonell C; Coi A; GarcíaVillodre L; Given JE; Gissler M; Heino A; Jordan S; Neville A; Pierini A; Tan J; Scanlon I; Garne E; Morris JK. | |
| Survival of children with rare structural congenital anomalies: a multi-registry cohort study | 1-gen-2022 | Alessio Coi; Michele Santoro; Anna Pierini; Judith Rankin; Svetlana V. Glinianaia; Joachim Tan; AbigailKate Reid; Ester Garne; Maria Loane; Joanne Given; Elisa Ballardini; Clara CaveroCarbonell; Hermien E. K. de Walle; Miriam Gatt; Laura GarcíaVillodre; Mika Gissler; Sue Jordan; Sonja KiuruKuhlefelt; Stine Kjaer Urhoj; Kari Klungsøyr; Nathalie Lelong; L. Renée Lutke; Amanda J. Neville; Makan Rahshenas; Ieuan Scanlon; Diana Wellesley;Joan K. Morris |