Dagnino, M.
~ 300  results:
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1

Novel INF2 mutations in an Italian cohort of patients with ..:

Caridi, G. ; Lugani, F. ; Dagnino, M....
Nephrology Dialysis Transplantation.  29 (2014)  suppl 4 - p. iv80-iv86 , 2014
 
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2

A novel frame‐shift deletion causing analbuminaemia in an I..:

Dagnino, M. ; Caridi, G. ; Marsciani, M....
European Journal of Clinical Investigation.  40 (2010)  3 - p. 281-284 , 2010
 
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3

Lack of cardiac anomalies in children with NPHS2 mutations:

Caridi, G. ; Dagnino, M. ; Carrea, A....
Nephrology Dialysis Transplantation.  22 (2007)  5 - p. 1477-1479 , 2007
 
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4

Podocin-Related Mechanisms in Posttransplantation Recurrenc..:

Caridi, G. ; Dagnino, M. ; Sanna-Cherchi, S...
Transplantation Proceedings.  38 (2006)  10 - p. 3486-3490 , 2006
 
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5

Loss of heterozygosity for chromosome 1p in familial neurob..:

Tonini, G.P ; Lo Cunsolo, C ; Cusano, R...
European Journal of Cancer.  33 (1997)  12 - p. 1953-1956 , 1997
 
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8

Innovative technologies for intangible cultural heritage ed..:

Cozzani, G. ; Pozzi, F. ; Dagnino, F. M...
Personal and Ubiquitous Computing.  21 (2016)  2 - p. 253-265 , 2016
 
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9

Clonal haematopoiesis is not prevalent in survivors of chil..:

Collord, G ; Park, N ; Podestà, M...
https://www.repository.cam.ac.uk/handle/1810/263996.  , 2017
 
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10

Exome sequencing identified MYO1E and NEIL1 as candidate ge..:

Sanna Cherchi S ; Burgess KE ; Nees SN...
info:eu-repo/semantics/altIdentifier/wos/WOS:000293264900010.  , 2011
 
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11

Clinical features and long-term outcome of nephrotic syndro..:

Caridi G ; Gigante M ; Ravani P...
info:eu-repo/semantics/altIdentifier/wos/WOS:000266478600008.  , 2009
 
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12

Localization of a gene for nonsyndromic renal hypodysplasia..:

SANNA CHERCHI S ; CARIDI G ; WENG PL...
info:eu-repo/semantics/altIdentifier/wos/WOS:000244403300016.  , 2007
 
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13

Allelism of MCKD, FJHN and GCKD caused by impairment of uro..:

RAMPOLDI L ; CARIDI G ; SANTON D...
info:eu-repo/semantics/altIdentifier/wos/WOS:000187224200018.  , 2003
 
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