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Author/Creator La Manna, A.

1. 'Frequently recurring' nocturnal polyuria is predictive of response to desmopressin in monosymptomatic nocturnal enuresis in childhood. Issue 2 (April 2019)

Authors:
Marzuillo, P.; Marotta, R.; Guarino, S.; Fedele, M.C.; Palladino, F.; Capalbo, D.; Della Vecchia, N.; Miraglia del Giudice, E.; Polito, C.; La Manna, A.
Journal:
Journal of pediatric urology
Issue:
Volume 15:Issue 2(2019)
Page Start:
166.e1
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Alport syndrome: impact of digenic inheritance in patients management. Issue 1 (22nd February 2017)

Authors:
Fallerini, C.; Baldassarri, M.; Trevisson, E.; Morbidoni, V.; La Manna, A.; Lazzarin, R.; Pasini, A.; Barbano, G.; Pinciaroli, A.R.; Garosi, G.; Frullanti, E.; Pinto, A.M.; Mencarelli, M.A.; Mari, F.; Renieri, A.; Ariani, F.
Journal:
Clinical genetics
Issue:
Volume 92:Issue 1(2017)
Page Start:
34
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases. (17th October 2013)

Authors:
Fallerini, C.; Dosa, L.; Tita, R.; Del Prete, D.; Feriozzi, S.; Gai, G.; Clementi, M.; La Manna, A.; Miglietti, N.; Mancini, R.; Mandrile, G.; Ghiggeri, G.M.; Piaggio, G.; Brancati, F.; Diano, L.; Frate, E.; Pinciaroli, A.R.; Giani, M.; Castorina, P.; Bresin, E.
Journal:
Clinical genetics
Issue:
Volume 86:Number 3(2014:Sep.)
Page Start:
252
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗