Title : 3-Methylglutaconic aciduria, a frequent but underrecognized finding in carbamoyl phosphate synthetase I deficiency - Rokicki_2017_Clin.Chim.Acta_471_95 |
Author(s) : Rokicki D , Pajdowska M , Trubicka J , Thong MK , Ciara E , Piekutowska-Abramczuk D , Pronicki M , Sikora R , Haidar R , Oltarzewski M , Jablonska E , Muthukumarasamy P , Sthaneswar P , Gan CS , Krajewska-Walasek M , Carrozzo R , Verrigni D , Semeraro M , Rizzo C , Taurisano R , Alhaddad B , Kovacs-Nagy R , Haack TB , Dionisi-Vici C , Pronicka E , Wortmann SB |
Ref : Clinica Chimica Acta , 471 :95 , 2017 |
Abstract : |
PubMedSearch : Rokicki_2017_Clin.Chim.Acta_471_95 |
PubMedID: 28526534 |
Title : New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre - Pronicka_2016_J.Transl.Med_14_174 |
Author(s) : Pronicka E , Piekutowska-Abramczuk D , Ciara E , Trubicka J , Rokicki D , Karkucinska-Wieckowska A , Pajdowska M , Jurkiewicz E , Halat P , Kosinska J , Pollak A , Rydzanicz M , Stawinski P , Pronicki M , Krajewska-Walasek M , Ploski R |
Ref : J Transl Med , 14 :174 , 2016 |
Abstract : |
PubMedSearch : Pronicka_2016_J.Transl.Med_14_174 |
PubMedID: 27290639 |
Gene_locus related to this paper: human-SERAC1 |
Title : Eyes on MEGDEL: distinctive basal ganglia involvement in dystonia deafness syndrome - Wortmann_2015_Neuropediatrics_46_98 |
Author(s) : Wortmann SB , van Hasselt PM , Baric I , Burlina A , Darin N , Horster F , Coker M , Ucar SK , Krumina Z , Naess K , Ngu LH , Pronicka E , Riordan G , Santer R , Wassmer E , Zschocke J , Schiff M , de Meirleir L , Alowain MA , Smeitink JA , Morava E , Kozicz T , Wevers RA , Wolf NI , Willemsen MA |
Ref : Neuropediatrics , 46 :98 , 2015 |
Abstract : |
PubMedSearch : Wortmann_2015_Neuropediatrics_46_98 |
PubMedID: 25642805 |
Gene_locus related to this paper: human-SERAC1 |
Title : Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness - Wortmann_2012_Nat.Genet_44_797 |
Author(s) : Wortmann SB , Vaz FM , Gardeitchik T , Vissers LE , Renkema GH , Schuurs-Hoeijmakers JH , Kulik W , Lammens M , Christin C , Kluijtmans LA , Rodenburg RJ , Nijtmans LG , Grunewald A , Klein C , Gerhold JM , Kozicz T , van Hasselt PM , Harakalova M , Kloosterman W , Baric I , Pronicka E , Ucar SK , Naess K , Singhal KK , Krumina Z , Gilissen C , van Bokhoven H , Veltman JA , Smeitink JA , Lefeber DJ , Spelbrink JN , Wevers RA , Morava E , de Brouwer AP |
Ref : Nat Genet , 44 :797 , 2012 |
Abstract : |
PubMedSearch : Wortmann_2012_Nat.Genet_44_797 |
PubMedID: 22683713 |
Gene_locus related to this paper: human-SERAC1 |
Title : Increased reactive oxygen species (ROS) production and low catalase level in fibroblasts of a girl with MEGDEL association (Leigh syndrome, deafness, 3-methylglutaconic aciduria) - Karkucinska-Wieckowska_2011_Folia.Neuropathol_49_56 |
Author(s) : Karkucinska-Wieckowska A , Lebiedzinska M , Jurkiewicz E , Pajdowska M , Trubicka J , Szymanska-Debinska T , Suski J , Pinton P , Duszynski J , Pronicki M , Wieckowski MR , Pronicka E |
Ref : Folia Neuropathol , 49 :56 , 2011 |
Abstract : |
PubMedSearch : Karkucinska-Wieckowska_2011_Folia.Neuropathol_49_56 |
PubMedID: 21455844 |