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Jackson, Christopher; Bauer, M F; Schaller, André; Kotzaeridou, U; Ferrarini, A; Hahn, Dagmar Karen; Chehade, H; Barbey, F; Tran, C; Gallati, S; Haeberli, Annemarie; Eggimann, S; Bonafé, L; Nuoffer, Jean-Marc (2016). A novel mutation in BCS1L associated with deafness, tubulopathy, growth retardation and microcephaly. European journal of pediatrics, 175(4), pp. 517-525. Springer 10.1007/s00431-015-2661-y
Ferrarini, A; Osterheld, MC; Vial, Y; de Viragh, PA; Cotting, J; Martinet, D; Beckmann, JS; Fellmann, F (2010). Familial occurrence of an association of multiple intestinal atresia and choanal atresia: a new syndrome? American journal of medical genetics. Part B - Neuropsychiatric genetics, 149A(12), pp. 2661-2665. Hoboken, N.J.: Wiley-Liss 10.1002/ajmg.a.33132
Simonetti, GD; Santoro, L; Ferrarini, A; Crosazzo-Franscini, L; Fossali, E; Bianchetti, MG; CHILD, Project (2007). Systemic hypertension and proteinuria in childhood chronic renal parenchymal disease: role of antihypertensive drug management. Pediatric drugs, 9(6), pp. 413-8. Heidelberg: Springer
