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- [1] CACNA1D De Novo Mutations in Autism Spectrum Disorders Activate Cav1.3 L-Type Calcium ChannelsBIOLOGICAL PSYCHIATRY, 2015, 77 (09) : 816 - 822Pinggera, Alexandra论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, Austria Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, AustriaLieb, Andreas论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, Austria Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, AustriaBenedetti, Bruno论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, Austria Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, AustriaLampert, Michaela论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, Austria Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, AustriaMonteleone, Stefania论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Inst Gen Inorgan & Theoret Chem, A-6020 Innsbruck, Austria Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, AustriaLiedl, Klaus R.论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Inst Gen Inorgan & Theoret Chem, A-6020 Innsbruck, Austria Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, AustriaTuluc, Petronel论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, Austria Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, AustriaStriessnig, Joerg论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, Austria Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, Austria
- [2] Cav1.3 missense mutations associated with neurodevelopmental disorders lead to gain-of-function in single-channel gatingNAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2024, 397 : S39 - S39论文数: 引用数: h-index:机构:Toeroek, F.论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Pharm, Dept Pharmacol & Toxicol, Ctr Mol Biosci, Innsbruck, Austria Univ Cologne, Ctr Pharmacol, Cologne, GermanyZanetti, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Pharm, Dept Pharmacol & Toxicol, Ctr Mol Biosci, Innsbruck, Austria Univ Cologne, Ctr Pharmacol, Cologne, GermanyOrtner, N. J.论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Pharm, Dept Pharmacol & Toxicol, Ctr Mol Biosci, Innsbruck, Austria Univ Cologne, Ctr Pharmacol, Cologne, GermanyStriessnig, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Pharm, Dept Pharmacol & Toxicol, Ctr Mol Biosci, Innsbruck, Austria Univ Cologne, Ctr Pharmacol, Cologne, GermanyMatthes, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Ctr Pharmacol, Cologne, Germany Univ Cologne, Ctr Pharmacol, Cologne, Germany
- [3] Cav1.3 (CACNA1D) L-type Ca2+ channel dysfunction in CNS disordersJOURNAL OF PHYSIOLOGY-LONDON, 2016, 594 (20): : 5839 - 5849Pinggera, Alexandra论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Dept Pharmacol & Toxicol, Ctr Mol Biosci, Innrain 80-82, A-6020 Innsbruck, Austria Univ Innsbruck, Dept Pharmacol & Toxicol, Ctr Mol Biosci, Innrain 80-82, A-6020 Innsbruck, AustriaStriessnig, Joerg论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Dept Pharmacol & Toxicol, Ctr Mol Biosci, Innrain 80-82, A-6020 Innsbruck, Austria Univ Innsbruck, Dept Pharmacol & Toxicol, Ctr Mol Biosci, Innrain 80-82, A-6020 Innsbruck, Austria
- [4] Loss of Cav1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafnessNATURE NEUROSCIENCE, 2011, 14 (01) : 77 - U107Baig, Shahid M.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Biotechnol & Genet Engn, Human Mol Genet Lab, Hlth Biotechnol Div, Faisalabad, Pakistan Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyKoschak, Alexandra论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Inst Pharm, A-6020 Innsbruck, Austria Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyLieb, Andreas论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Inst Pharm, A-6020 Innsbruck, Austria Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyGebhart, Mathias论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Inst Pharm, A-6020 Innsbruck, Austria Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyDafinger, Claudia论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Cologne, Inst Human Genet, Cologne, Germany Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyNuernberg, Gudrun论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom, Cologne, Germany Univ Cologne, Inst Genet, Cologne, Germany Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyAli, Amjad论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Biotechnol & Genet Engn, Human Mol Genet Lab, Hlth Biotechnol Div, Faisalabad, Pakistan Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyAhmad, Ilyas论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Biotechnol & Genet Engn, Human Mol Genet Lab, Hlth Biotechnol Div, Faisalabad, Pakistan Univ Hosp Cologne, Inst Human Genet, Cologne, GermanySinnegger-Brauns, Martina J.论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Inst Pharm, A-6020 Innsbruck, Austria Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyBrandt, Niels论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Physiol 2, Tubingen, Germany Univ Tubingen, Tubingen Hearing Res Ctr, Tubingen, Germany Univ Saarland, Dept Biophys, D-6650 Homburg, Germany Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyEngel, Jutta论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Inst Physiol 2, Tubingen, Germany Univ Tubingen, Tubingen Hearing Res Ctr, Tubingen, Germany Univ Saarland, Dept Biophys, D-6650 Homburg, Germany Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyMangoni, Matteo E.论文数: 0 引用数: 0 h-index: 0机构: Univ Montpellier 1 & 2, CNRS, Inst Genom Fonct,Dept Physiol,UMR 5203,U661, Montpellier, France Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyFarooq, Muhammad论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Biotechnol & Genet Engn, Human Mol Genet Lab, Hlth Biotechnol Div, Faisalabad, Pakistan Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyKhan, Habib U.论文数: 0 引用数: 0 h-index: 0机构: Khyber Teaching Hosp, Dept Pathol, Peshawar, Pakistan Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyNuernberg, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom, Cologne, Germany Univ Cologne, Inst Genet, Cologne, Germany Univ Cologne, Cologne Excellence Cluster Cellular Stress Respon, Cologne, Germany Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyStriessnig, Joerg论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Inst Pharm, A-6020 Innsbruck, Austria Univ Hosp Cologne, Inst Human Genet, Cologne, GermanyBolz, Hanno J.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Cologne, Inst Human Genet, Cologne, Germany Bioscientia, Ctr Human Genet, Ingelheim, Germany Univ Hosp Cologne, Inst Human Genet, Cologne, Germany
- [5] Loss of Cav1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafnessNature Neuroscience, 2011, 14 : 77 - 84Shahid M Baig论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionAlexandra Koschak论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionAndreas Lieb论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionMathias Gebhart论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionClaudia Dafinger论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionGudrun Nürnberg论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionAmjad Ali论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionIlyas Ahmad论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionMartina J Sinnegger-Brauns论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionNiels Brandt论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionJutta Engel论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionMatteo E Mangoni论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionMuhammad Farooq论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionHabib U Khan论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionPeter Nürnberg论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionJörg Striessnig论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology DivisionHanno J Bolz论文数: 0 引用数: 0 h-index: 0机构: Human Molecular Genetics Laboratory,Health Biotechnology Division
- [6] A Novel De Novo Gain-of-Function CACNA1D Variant in Neurodevelopmental Disease With Congenital Tremor, Seizures, and HypotoniaNEUROLOGY-GENETICS, 2024, 10 (05)Dannenberg, Fabian论文数: 0 引用数: 0 h-index: 0机构: Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, Germany Charite Univ Med Berlin, Ctr Chronically Sick Children, Berlin, Germany Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanyVon Moers, Arpad论文数: 0 引用数: 0 h-index: 0机构: DRK Kliniken Berlin Westend, Dept Pediat, Berlin, Germany Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanyBittigau, Petra论文数: 0 引用数: 0 h-index: 0机构: Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, Germany Charite Univ Med Berlin, Ctr Chronically Sick Children, Berlin, Germany Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanyLange, Joern论文数: 0 引用数: 0 h-index: 0机构: VAMED Klin Hohenstucken, Dept Neuropediat, Brandenburg, Germany Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanyWiegand, Sylvia论文数: 0 引用数: 0 h-index: 0机构: VAMED Klin Hohenstucken, Dept Neuropediat, Brandenburg, Germany Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanyToeroek, Ferenc论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Pharm, Ctr Mol Biosci Innsbruck, Dept Pharmacol & Toxicol, Innsbruck, Austria Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanyStoelting, Gabriel论文数: 0 引用数: 0 h-index: 0机构: Charite Univ Med Berlin, Ctr Funct Genom, Berlin Inst Hlth, Hessische Str 4A, Berlin, Germany Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanyStriessnig, Joerg论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Pharm, Ctr Mol Biosci Innsbruck, Dept Pharmacol & Toxicol, Innsbruck, Austria Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanyMotazacker, M. Mahdi论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Dept Human Genet, Amsterdam UMC, Amsterdam, Netherlands Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanyBroekema, Marjoleine F.论文数: 0 引用数: 0 h-index: 0机构: Univ Amsterdam, Dept Human Genet, Amsterdam UMC, Amsterdam, Netherlands Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanySchuelke, Markus论文数: 0 引用数: 0 h-index: 0机构: Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, Germany Charite Univ Med Berlin, Ctr Chronically Sick Children, Berlin, Germany Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanyKaindl, Angela M.论文数: 0 引用数: 0 h-index: 0机构: Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, Germany Charite Univ Med Berlin, Ctr Chronically Sick Children, Berlin, Germany Charite Univ Med Berlin, Inst Cell Biol & Neurobiol, Berlin, Germany Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanyScholl, Ute I.论文数: 0 引用数: 0 h-index: 0机构: Charite Univ Med Berlin, Ctr Funct Genom, Berlin Inst Hlth, Hessische Str 4A, Berlin, Germany Charite Univ Med Berlin, Dept Nephrol & Med Intens Care, Berlin, Germany Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, GermanyOrtner, Nadine J.论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Inst Pharm, Ctr Mol Biosci Innsbruck, Dept Pharmacol & Toxicol, Innsbruck, Austria Charite Univ Med Berlin, Dept Pediat Neurol, Berlin, Germany
- [7] Neurodevelopmental response to nifedipine treatment in an infant with Congenital Hyperinsulinism due to de novo gain-of-function CACNA1D variantHORMONE RESEARCH IN PAEDIATRICS, 2024, 97 : 134 - 135Pujari, Divya论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Sick Children, Dept Paediat Endocrinol & Diabet, London, England Great Ormond St Hosp Sick Children, Dept Paediat Endocrinol & Diabet, London, EnglandConlon, Alison论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Sick Children, Dept Paediat Endocrinol & Diabet, London, England Great Ormond St Hosp Sick Children, Dept Paediat Endocrinol & Diabet, London, EnglandWakeling, Emma论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Sick Children, Dept Clin Genet, London, England Great Ormond St Hosp Sick Children, Dept Paediat Endocrinol & Diabet, London, EnglandHoughton, Jayne论文数: 0 引用数: 0 h-index: 0机构: Royal Devon Univ Healthcare NHS Trust, Exeter Genom Lab, Exeter, Devon, England Great Ormond St Hosp Sick Children, Dept Paediat Endocrinol & Diabet, London, EnglandFlanagan, Sarah论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter, Dept Biomed & Clin Sci, Sch Med, Exeter, Devon, England Great Ormond St Hosp Sick Children, Dept Paediat Endocrinol & Diabet, London, EnglandEldred, Carey论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Sick Children, Dept Physiotherapy, London, England Great Ormond St Hosp Sick Children, Dept Paediat Endocrinol & Diabet, London, EnglandStarling, Luke论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Sick Children, Ctr Inherited Cardiovasc Dis, London, England Great Ormond St Hosp Sick Children, Dept Paediat Endocrinol & Diabet, London, EnglandKaliakatsos, Marios论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Inst Child Hlth, Dept Neurol, London, England UCL, Dept Neurol, London, England Great Ormond St Hosp Sick Children, Dept Paediat Endocrinol & Diabet, London, EnglandDastamani, Antonia论文数: 0 引用数: 0 h-index: 0机构: Great Ormond St Hosp Sick Children, Dept Paediat Endocrinol & Diabet, London, England Great Ormond St Hosp Sick Children, Dept Paediat Endocrinol & Diabet, London, England
- [8] A de novo CACNA1D missense mutation in a patient with congenital hyperinsulinism, primary hyperaldosteronism and hypotoniaCHANNELS, 2020, 14 (01) : 175 - 180De Mingo Alemany, Maria Carmen论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ La Fe, Pediat Endocrinol Unit, Valencia, Spain Hosp Univ La Fe, Pediat Endocrinol Unit, Valencia, SpainMifsud Grau, Luis论文数: 0 引用数: 0 h-index: 0机构: Hosp La Plana, Primary Care, Vilareal, Spain Hosp Univ La Fe, Pediat Endocrinol Unit, Valencia, SpainMoreno Macian, Francisca论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ La Fe, Pediat Endocrinol Unit, Valencia, Spain Hosp Univ La Fe, Pediat Endocrinol Unit, Valencia, SpainFerrer Lorente, Belen论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ La Fe, Pediat Endocrinol Unit, Valencia, Spain Hosp Univ La Fe, Pediat Endocrinol Unit, Valencia, SpainLeon Carinena, Sara论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ La Fe, Pediat Endocrinol Unit, Valencia, Spain Hosp Univ La Fe, Pediat Endocrinol Unit, Valencia, Spain
- [9] New gain-of-function mutation shows CACNA1D as recurrently mutated gene in autism spectrum disorders and epilepsyHUMAN MOLECULAR GENETICS, 2017, 26 (15) : 2923 - 2932Pinggera, Alexandra论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Dept Pharmacol & Toxicol, Ctr Mol Biosci, A-6020 Innsbruck, Austria MRC Lab Mol Biol, Cambridge Biomed Campus, Cambridge CB2 0QH, England Univ Innsbruck, Dept Pharmacol & Toxicol, Ctr Mol Biosci, A-6020 Innsbruck, AustriaMackenroth, Luisa论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Dresden, Inst Klin Genet, D-01307 Dresden, Germany Univ Innsbruck, Dept Pharmacol & Toxicol, Ctr Mol Biosci, A-6020 Innsbruck, Austria论文数: 引用数: h-index:机构:Schallner, Jens论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Dresden, Med Fak Carl Gustav Carus, Abt Neuropadiatrie, D-01307 Dresden, Germany Univ Innsbruck, Dept Pharmacol & Toxicol, Ctr Mol Biosci, A-6020 Innsbruck, AustriaBeleggia, Filippo论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Cologne, Dept Internal Med 1, D-50923 Cologne, Germany Univ Innsbruck, Dept Pharmacol & Toxicol, Ctr Mol Biosci, A-6020 Innsbruck, AustriaWollnik, Bernd论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Gottingen, Inst Human Genet, D-37073 Gottingen, Germany Univ Innsbruck, Dept Pharmacol & Toxicol, Ctr Mol Biosci, A-6020 Innsbruck, AustriaStriessnig, Joerg论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Dept Pharmacol & Toxicol, Ctr Mol Biosci, A-6020 Innsbruck, Austria Univ Innsbruck, Dept Pharmacol & Toxicol, Ctr Mol Biosci, A-6020 Innsbruck, Austria
- [10] Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic EpilepsyINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (22)Rinne, Susanne论文数: 0 引用数: 0 h-index: 0机构: Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, Germany Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, GermanyStallmeyer, Birgit论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Muenster, Inst Genet Heart Dis IfGH, D-48149 Munster, Germany Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, GermanyPinggera, Alexandra论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, Austria Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, GermanyNetter, Michael F.论文数: 0 引用数: 0 h-index: 0机构: Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, Germany Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, GermanyMatschke, Lina A.论文数: 0 引用数: 0 h-index: 0机构: Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, Germany Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, GermanyDittmann, Sven论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Muenster, Inst Genet Heart Dis IfGH, D-48149 Munster, Germany Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, GermanyKirchhefer, Uwe论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Muenster, Inst Pharmacol & Toxicol, D-48149 Munster, Germany Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, GermanyNeudorf, Ulrich论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Essen, Klin Kinderheilkunde Bereich Kardiol 3, Zentrum Kinder & Jugendmed, D-45147 Essen, Germany Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, GermanyOpp, Joachim论文数: 0 引用数: 0 h-index: 0机构: Ev Krankenhaus Oberhausen, D-46047 Oberhausen, Germany Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, GermanyStriessnig, Joerg论文数: 0 引用数: 0 h-index: 0机构: Univ Innsbruck, Ctr Mol Biosci, Dept Pharmacol & Toxicol, A-6020 Innsbruck, Austria Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, Germany论文数: 引用数: h-index:机构:Schulze-Bahr, Eric论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Muenster, Inst Genet Heart Dis IfGH, D-48149 Munster, Germany Univ Marburg, Inst Physiol & Pathophysiol, Vegetat Physiol, D-35037 Marburg, Germany