van Diggelen OP

References (9)

Title : Juvenile-onset neuronal ceroid lipofuscinosis with infantile CLN1 mutation and palmitoyl-protein thioesterase deficiency - Kalviainen_2007_Eur.J.Neurol_14_369
Author(s) : Kalviainen R , Eriksson K , Losekoot M , Sorri I , Harvima I , Santavuori P , Jarvela I , Autti T , Vanninen R , Salmenpera T , van Diggelen OP
Ref : Eur Journal of Neurology , 14 :369 , 2007
Abstract :
PubMedSearch : Kalviainen_2007_Eur.J.Neurol_14_369
PubMedID: 17388982
Gene_locus related to this paper: human-PPT1

Title : [From gene to disease\; from CLN1, CLN2 and CLN3 to neuronal ceroid lipofuscinosis] - Taschner_2005_Ned.Tijdschr.Geneeskd_149_300
Author(s) : Taschner PE , Losekoot M , Breuning MH , Hofman I , van Diggelen OP
Ref : Ned Tijdschr Geneeskd , 149 :300 , 2005
Abstract :
PubMedSearch : Taschner_2005_Ned.Tijdschr.Geneeskd_149_300
PubMedID: 15730038
Gene_locus related to this paper: human-PPT1

Title : Palmitoyl protein thioesterase 1 is targeted to the axons in neurons - Ahtiainen_2003_J.Comp.Neurol_455_368
Author(s) : Ahtiainen L , van Diggelen OP , Jalanko A , Kopra O
Ref : Journal of Comparative Neurology , 455 :368 , 2003
Abstract :
PubMedSearch : Ahtiainen_2003_J.Comp.Neurol_455_368
PubMedID: 12483688
Gene_locus related to this paper: human-PPT1

Title : Adult neuronal ceroid lipofuscinosis with palmitoyl-protein thioesterase deficiency: first adult-onset patients of a childhood disease - van Diggelen_2001_Ann.Neurol_50_269
Author(s) : van Diggelen OP , Thobois S , Tilikete C , Zabot MT , Keulemans JL , van Bunderen PA , Taschner PE , Losekoot M , Voznyi YV
Ref : Annals of Neurology , 50 :269 , 2001
Abstract :
PubMedSearch : van Diggelen_2001_Ann.Neurol_50_269
PubMedID: 11506414
Gene_locus related to this paper: human-PPT1

Title : New mutations in the neuronal ceroid lipofuscinosis genes - Mole_2001_Eur.J.Paediatr.Neurol_5 Suppl A_7
Author(s) : Mole SE , Zhong NA , Sarpong A , Logan WP , Hofmann S , Yi W , Franken PF , van Diggelen OP , Breuning MH , Moroziewicz D , Ju W , Salonen T , Holmberg V , Jarvela I , Taschner PE
Ref : Eur J Paediatr Neurol , 5 Suppl A :7 , 2001
Abstract :
PubMedSearch : Mole_2001_Eur.J.Paediatr.Neurol_5 Suppl A_7
PubMedID: 11589012
Gene_locus related to this paper: human-PPT1

Title : A new simple enzyme assay for pre- and postnatal diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) and its variants - Voznyi_1999_J.Med.Genet_36_471
Author(s) : Voznyi YV , Keulemans JL , Mancini GM , Catsman-Berrevoets CE , Young E , Winchester B , Kleijer WJ , van Diggelen OP
Ref : Journal of Medical Genetics , 36 :471 , 1999
Abstract :
PubMedSearch : Voznyi_1999_J.Med.Genet_36_471
PubMedID: 10874636
Gene_locus related to this paper: human-PPT1

Title : Molecular defects underlying Wolman disease appear to be more heterogeneous than those resulting in cholesteryl ester storage disease - Lohse_1999_J.Lipid.Res_40_221
Author(s) : Lohse P , Maas S , Sewell AC , van Diggelen OP , Seidel D
Ref : J Lipid Res , 40 :221 , 1999
Abstract :
PubMedSearch : Lohse_1999_J.Lipid.Res_40_221
PubMedID: 9925650
Gene_locus related to this paper: human-LIPA

Title : First-trimester diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) using PPT enzyme assay and CLN1 mutation analysis - de Vries_1999_Prenat.Diagn_19_559
Author(s) : de Vries BB , Kleijer WJ , Keulemans JL , Voznyi YV , Franken PF , Eurlings MC , Galjaard RJ , Losekoot M , Catsman-Berrevoets CE , Breuning MH , Taschner PE , van Diggelen OP
Ref : Prenat Diagn , 19 :559 , 1999
Abstract :
PubMedSearch : de Vries_1999_Prenat.Diagn_19_559
PubMedID: 10416973
Gene_locus related to this paper: human-PPT1

Title : Cathepsin A deficiency in galactosialidosis: studies of patients and carriers in 16 families - Kleijer_1996_Pediatr.Res_39_1067
Author(s) : Kleijer WJ , Geilen GC , Janse HC , van Diggelen OP , Zhou XY , Galjart NJ , Galjaard H , d'Azzo A
Ref : Pediatr Res , 39 :1067 , 1996
Abstract :
PubMedSearch : Kleijer_1996_Pediatr.Res_39_1067
PubMedID: 8725271
Gene_locus related to this paper: human-CTSA