| Title : Cannabidiol's impact on drug-metabolization - Stollberger_2023_Eur.J.Intern.Med__ |
| Author(s) : Stollberger C , Finsterer J |
| Ref : Eur J Intern Med , : , 2023 |
| Abstract : |
| PubMedSearch : Stollberger_2023_Eur.J.Intern.Med__ |
| PubMedID: 37541924 |
| Title : Cannabidiol's impact on drug-metabolization - Stollberger_2023_Eur.J.Intern.Med__ |
| Author(s) : Stollberger C , Finsterer J |
| Ref : Eur J Intern Med , : , 2023 |
| Abstract : |
| PubMedSearch : Stollberger_2023_Eur.J.Intern.Med__ |
| PubMedID: 37541924 |
| Title : Cannabidiol's impact on drug-metabolization - Stollberger_2023_Eur.J.Intern.Med__ |
| Author(s) : Stollberger C , Finsterer J |
| Ref : Eur J Intern Med , : , 2023 |
| Abstract : |
| PubMedSearch : Stollberger_2023_Eur.J.Intern.Med__ |
| PubMedID: 37541924 |
| Title : MEGDEL Syndrome - Finsterer_2020_Pediatr.Neurol_110_25 |
| Author(s) : Finsterer J , Scorza FA , Fiorini AC , Scorza CA |
| Ref : Pediatr Neurol , 110 :25 , 2020 |
| Abstract : |
| PubMedSearch : Finsterer_2020_Pediatr.Neurol_110_25 |
| PubMedID: 32684373 |
| Gene_locus related to this paper: human-SERAC1 |
| Title : MEGDEL Syndrome - Finsterer_2020_Pediatr.Neurol_110_25 |
| Author(s) : Finsterer J , Scorza FA , Fiorini AC , Scorza CA |
| Ref : Pediatr Neurol , 110 :25 , 2020 |
| Abstract : |
| PubMedSearch : Finsterer_2020_Pediatr.Neurol_110_25 |
| PubMedID: 32684373 |
| Gene_locus related to this paper: human-SERAC1 |
| Title : MEGDEL Syndrome - Finsterer_2020_Pediatr.Neurol_110_25 |
| Author(s) : Finsterer J , Scorza FA , Fiorini AC , Scorza CA |
| Ref : Pediatr Neurol , 110 :25 , 2020 |
| Abstract : |
| PubMedSearch : Finsterer_2020_Pediatr.Neurol_110_25 |
| PubMedID: 32684373 |
| Gene_locus related to this paper: human-SERAC1 |
| Title : Dystonia is a Common Phenotypic Feature of MEGDEL Syndrome - Finsterer_2018_Tremor.Other.Hyperkinet.Mov.(N.Y)_8_568 |
| Author(s) : Finsterer J , Scorza FA , Fiorini AC , Scorza CA , Almeida AC |
| Ref : Tremor Other Hyperkinet Mov (N Y) , 8 :568 , 2018 |
| Abstract : |
| PubMedSearch : Finsterer_2018_Tremor.Other.Hyperkinet.Mov.(N.Y)_8_568 |
| PubMedID: 29971201 |
| Gene_locus related to this paper: human-SERAC1 |
| Title : Dystonia is a Common Phenotypic Feature of MEGDEL Syndrome - Finsterer_2018_Tremor.Other.Hyperkinet.Mov.(N.Y)_8_568 |
| Author(s) : Finsterer J , Scorza FA , Fiorini AC , Scorza CA , Almeida AC |
| Ref : Tremor Other Hyperkinet Mov (N Y) , 8 :568 , 2018 |
| Abstract : |
| PubMedSearch : Finsterer_2018_Tremor.Other.Hyperkinet.Mov.(N.Y)_8_568 |
| PubMedID: 29971201 |
| Gene_locus related to this paper: human-SERAC1 |
| Title : Dystonia is a Common Phenotypic Feature of MEGDEL Syndrome - Finsterer_2018_Tremor.Other.Hyperkinet.Mov.(N.Y)_8_568 |
| Author(s) : Finsterer J , Scorza FA , Fiorini AC , Scorza CA , Almeida AC |
| Ref : Tremor Other Hyperkinet Mov (N Y) , 8 :568 , 2018 |
| Abstract : |
| PubMedSearch : Finsterer_2018_Tremor.Other.Hyperkinet.Mov.(N.Y)_8_568 |
| PubMedID: 29971201 |
| Gene_locus related to this paper: human-SERAC1 |
| Title : Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance - Finsterer_2012_J.Neurol.Sci_318_1 |
| Author(s) : Finsterer J , Loscher W , Quasthoff S , Wanschitz J , Auer-Grumbach M , Stevanin G |
| Ref : Journal of Neurology Sci , 318 :1 , 2012 |
| Abstract : |
| PubMedSearch : Finsterer_2012_J.Neurol.Sci_318_1 |
| PubMedID: 22554690 |
| Gene_locus related to this paper: human-SPG21 |
| Title : Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance - Finsterer_2012_J.Neurol.Sci_318_1 |
| Author(s) : Finsterer J , Loscher W , Quasthoff S , Wanschitz J , Auer-Grumbach M , Stevanin G |
| Ref : Journal of Neurology Sci , 318 :1 , 2012 |
| Abstract : |
| PubMedSearch : Finsterer_2012_J.Neurol.Sci_318_1 |
| PubMedID: 22554690 |
| Gene_locus related to this paper: human-SPG21 |
| Title : Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance - Finsterer_2012_J.Neurol.Sci_318_1 |
| Author(s) : Finsterer J , Loscher W , Quasthoff S , Wanschitz J , Auer-Grumbach M , Stevanin G |
| Ref : Journal of Neurology Sci , 318 :1 , 2012 |
| Abstract : |
| PubMedSearch : Finsterer_2012_J.Neurol.Sci_318_1 |
| PubMedID: 22554690 |
| Gene_locus related to this paper: human-SPG21 |
| Title : Mitochondrial disorders, cognitive impairment and dementia - Finsterer_2009_J.Neurol.Sci_283_143 |
| Author(s) : Finsterer J |
| Ref : Journal of Neurology Sci , 283 :143 , 2009 |
| Abstract : |
| PubMedSearch : Finsterer_2009_J.Neurol.Sci_283_143 |
| PubMedID: 19268975 |
| Title : Mitochondrial disorders, cognitive impairment and dementia - Finsterer_2009_J.Neurol.Sci_283_143 |
| Author(s) : Finsterer J |
| Ref : Journal of Neurology Sci , 283 :143 , 2009 |
| Abstract : |
| PubMedSearch : Finsterer_2009_J.Neurol.Sci_283_143 |
| PubMedID: 19268975 |
| Title : Mitochondrial disorders, cognitive impairment and dementia - Finsterer_2009_J.Neurol.Sci_283_143 |
| Author(s) : Finsterer J |
| Ref : Journal of Neurology Sci , 283 :143 , 2009 |
| Abstract : |
| PubMedSearch : Finsterer_2009_J.Neurol.Sci_283_143 |
| PubMedID: 19268975 |
| Title : Cognitive decline as a manifestation of mitochondrial disorders (mitochondrial dementia) - Finsterer_2008_J.Neurol.Sci_272_20 |
| Author(s) : Finsterer J |
| Ref : Journal of Neurology Sci , 272 :20 , 2008 |
| Abstract : |
| PubMedSearch : Finsterer_2008_J.Neurol.Sci_272_20 |
| PubMedID: 18572195 |
| Title : Cognitive decline as a manifestation of mitochondrial disorders (mitochondrial dementia) - Finsterer_2008_J.Neurol.Sci_272_20 |
| Author(s) : Finsterer J |
| Ref : Journal of Neurology Sci , 272 :20 , 2008 |
| Abstract : |
| PubMedSearch : Finsterer_2008_J.Neurol.Sci_272_20 |
| PubMedID: 18572195 |
| Title : Cognitive decline as a manifestation of mitochondrial disorders (mitochondrial dementia) - Finsterer_2008_J.Neurol.Sci_272_20 |
| Author(s) : Finsterer J |
| Ref : Journal of Neurology Sci , 272 :20 , 2008 |
| Abstract : |
| PubMedSearch : Finsterer_2008_J.Neurol.Sci_272_20 |
| PubMedID: 18572195 |