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| Title : Neutral Lipid Storage Diseases: clinical\/genetic features and natural history in a large cohort of Italian patients - Pennisi_2017_Orphanet.J.Rare.Dis_12_90 |
| Author(s) : Pennisi EM , Arca M , Bertini E , Bruno C , Cassandrini D , D'Amico A , Garibaldi M , Gragnani F , Maggi L , Massa R , Missaglia S , Morandi L , Musumeci O , Pegoraro E , Rastelli E , Santorelli FM , Tasca E , Tavian D , Toscano A , Angelini C |
| Ref : Orphanet J Rare Dis , 12 :90 , 2017 |
| Abstract : Pennisi_2017_Orphanet.J.Rare.Dis_12_90 |
| ESTHER : Pennisi_2017_Orphanet.J.Rare.Dis_12_90 |
| PubMedSearch : Pennisi_2017_Orphanet.J.Rare.Dis_12_90 |
| PubMedID: 28499397 |
| Title : Late onset of neutral lipid storage disease due to novel PNPLA2 mutations causing total loss of lipase activity in a patient with myopathy and slight cardiac involvement - Missaglia_2017_Neuromuscul.Disord_27_481 |
| Author(s) : Missaglia S , Maggi L , Mora M , Gibertini S , Blasevich F , Agostoni P , Moro L , Cassandrini D , Santorelli FM , Gerevini S , Tavian D |
| Ref : Neuromuscular Disorders , 27 :481 , 2017 |
| Abstract : Missaglia_2017_Neuromuscul.Disord_27_481 |
| ESTHER : Missaglia_2017_Neuromuscul.Disord_27_481 |
| PubMedSearch : Missaglia_2017_Neuromuscul.Disord_27_481 |
| PubMedID: 28258942 |
| Title : Severe cardiomyopathy in a young patient with complete deficiency of adipose triglyceride lipase due to a novel mutation in PNPLA2 gene - |
| Author(s) : Pasanisi MB , Missaglia S , Cassandrini D , Salerno F , Farina S , Andreini D , Agostoni P , Morandi L , Mora M , Tavian D |
| Ref : Int J Cardiol , 207 :165 , 2016 |
| PubMedID: 26803235 |
| Title : Acitretin-responsive ichthyosis in Chanarin-Dorfman syndrome with a novel mutation in the ABHD5\/CGI-58 gene - Srinivasaraghavan_2014_Pediatr.Dermatol_31_612 |
| Author(s) : Srinivasaraghavan R , Krishnamurthy S , Chandar R , Cassandrini D , Mahadevan S , Bruno C , Santorelli FM |
| Ref : Pediatr Dermatol , 31 :612 , 2014 |
| Abstract : Srinivasaraghavan_2014_Pediatr.Dermatol_31_612 |
| ESTHER : Srinivasaraghavan_2014_Pediatr.Dermatol_31_612 |
| PubMedSearch : Srinivasaraghavan_2014_Pediatr.Dermatol_31_612 |
| PubMedID: 23756328 |
| Gene_locus related to this paper: human-ABHD5 |
| Title : Clinical and genetic characterization of Chanarin-Dorfman syndrome. - Bruno_2008_Biochem.Biophys.Res.Commun_369_1125 |
| Author(s) : Bruno C , Bertini E , Di Rocco M , Cassandrini D , Ruffa G , De Toni T , Seri M , Spada M , Li Volti G , D'Amico A , Trucco F , Arca M , Casali C , Angelini C , Dimauro S , Minetti C |
| Ref : Biochemical & Biophysical Research Communications , 369 :1125 , 2008 |
| Abstract : Bruno_2008_Biochem.Biophys.Res.Commun_369_1125 |
| ESTHER : Bruno_2008_Biochem.Biophys.Res.Commun_369_1125 |
| PubMedSearch : Bruno_2008_Biochem.Biophys.Res.Commun_369_1125 |
| PubMedID: 18339307 |
| Gene_locus related to this paper: human-ABHD5 |