PIERINI, ANNA

PIERINI, ANNA  

Istituto di Fisiologia Clinica - IFC  

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Children with Hirschsprung's disease have high morbidity in the first 5 years of life 1-gen-2024 Damkjaer, M.; Tan, J.; Morris, J. K.; Loane, M.; Given, J.; Cavero-Carbonell, C.; Gissler, M.; Neville, A. J.; Pierini, A.; Rissmann, A.; Tucker, D.; Garne, E.
Gastroschisis prevalence patterns in 27 surveillance programs from 24 countries, International Clearinghouse for Birth Defects Surveillance and Research, 1980–2017 1-gen-2024 Feldkamp, M. L.; Canfield, M. A.; Krikov, S.; Prieto-Merino, D.; Sipek, A.; Lelong, N.; Amar, E.; Rissmann, A.; Csaky-Szunyogh, M.; Tagliabue, G.; Pierini, A.; Gatt, M.; Bergman, J. E. H.; Szabova, E.; Bermejo-Sanchez, E.; Tucker, D.; Dastgiri, S.; Bidondo, M. P.; Canessa, A.; Zarante, I.; Hurtado-Villa, P.; Martinez, L.; Mutchinick, O. M.; Camelo, J. L.; Benavides-Lara, A.; Thomas, M. A.; Liu, S.; Nembhard, W. N.; Gray, E. B.; Nance, A. E.; Mastroiacovo, P.; Botto, L. D.
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
A multi-program analysis of cleft lip with cleft palate prevalence and mortality using data from 22 International Clearinghouse for Birth Defects Surveillance and Research programs, 1974-2014 1-gen-2023 Mc Goldrick, N; Revie, G; Groisman, B; Hurtado-Villa, P; Sipek, A; Khoshnood, B; Rissmann, A; Dastgiri, S; Landau, D; Tagliabue, G; Pierini, A; Gatt, M; Mutchinick, O. M.; Martínez, L; de Walle, H. E. K.; Szabova, E; Lopez Camelo, J; Bermejo-Sánchez, E; Källén, K; Morgan, M; Wertelecki, W; Nance, A; Stallings, E. B.; Nembhard, Wn; Mossey, P
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
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
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
Ethics and legal requirements for data linkage in 14 European countries for children with congenital anomalies 1-gen-2023 Claridge, Hugh; Tan, Joachim; Loane, Maria; Garne, Ester; Barisic, Ingeborg; Caverocarbonell, Clara; Dias, Carlos; Gatt, Miriam; Jordan, Susan; Khoshnood, Babak; Kiurukuhlefelt, Sonja; Klungsoyr, Kari; Mokoroa Carollo, Olatz; Nelen, Vera; J Neville, Amanda; Pierini, Anna; Randrianaivo, Hanitra; Rissmann, Anke; Tucker, David; de Walle, Hermien; Wertelecki, Wladimir; K 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
Maternal Age and the Prevalence of Congenital Heart Defects in Europe, 1995 to 2015; a register-based study 1-gen-2023 Mamasoula, Chrysovalanto; Bigirumurame, Theophile; Chadwick, Thomas; Addor, Marie-Claude; Cavero-Carbonell, Clara; Dias, Carlos M.; Echevarría-González-de-Garibay, Luis-Javier; Gatt, Miriam; Khoshnood, Babak; Klungsoyr, Kari; Randall, Kay; Stoianova, Sylvia; Haeusler, Martin; Nelen, Vera; Neville, Amanda J.; Perthus, Isabelle; Pierini, Anna; Bertaut-Nativel, Bénédicte; Rissmann, Anke; Rouget, Florence; Schaub, Bruno; Tucker, David; Wellesley, Diana; Zymak-Zakutnia, Natalya; Barisic, Ingeborg; de Walle, Hermien E. K.; Lanzoni, Monica; Sayers, Gerardine; Mullaney, Carmel; Pennington, Lindsay; Rankin, Judith
Prescriptions for insulin and insulin analogues in children with and without major congenital anomalies: a data linkage cohort study across six European regions 1-gen-2023 Given, Joanne; K Morris, Joan; Garne, Ester; Ballardini, Elisa; Barrachinabonet, Laia; Caverocarbonell, Clara; Gissler, Mika; Gorini, Francesca; Heino, Anna; Jordan, Sue; J Neville, Amanda; Pierini, Anna; Scanlon, Ieuan; Tan, Joachim; K Urhoj, Stine; Loane, Maria
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
Surveillance of multiple congenital anomalies; searching for new associations 1-gen-2023 K Morris, Joan; H Bergman, Jorieke E; Barisic, Ingeborg; Wellesley, Diana; Tucker, David; Limb, Elizabeth; Addor, Marieclaude; Caverocarbonell, Clara; Matias Dias, Carlos; S Draper, Elisabeth; Javier EchevarríaGonzálezdeGaribay, Luis; Gatt, Miriam; Klungsøyr, Kari; Lelong, Nathalie; Luyt, Karen; Maternakiryluk, Anna; Nelen, Vera; Neville, Amanda; Perthus, Isabelle; Pierini, Anna; Randrianaivoranjatoelina, Hanitra; Rankin, Judith; Rissmann, Anke; Rouget, Florence; Sayers, Geraldine; Wertelecki, Wladimir; Kinsnerovaskainen, Agnieszka; Garne, Ester
Ten-year survival of children with trisomy 13 or trisomy 18: a multi-registry European cohort study 1-gen-2023 Glinianaia Svetlana, V; Rankin, Judith; Tan, Joachim; Loane, Maria; Garne, Ester; Caverocarbonell, Clara; de Walle Hermien, E K; Gatt, Miriam; Gissler, Mika; Klungsoyr, Kari; Lelong, Natalie; Neville, Amanda; Pierini, Anna; Tucker David, F; Urhoj Stine, Kjaer; Wellesley Diana, Gay; Morris Joan, K
The burden of disease for children born alive with Turner syndrome--A European cohort study 1-gen-2023 Rud Andersen, Ann-Louise; Kjaer Urhoj, Stine; Tan, Joachim; Cavero-Carbonell, Clara; Gatt, Miriam; Gissler, Mika; Klungsoyr, Kari; Khoshnood, Babak; Morris, Joan; Neville, Amanda J.; Pierini, Anna; Scanlon, Ieuan; de Walle, Hermien E. K.; Wellesley, Diana; Garne, Ester; Loane, Maria