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Arndt Rolfs (1959-)

Arzt

Name	Arndt Rolfs
Time	1959- (Date of birth and death)
Place	Rostock (Wirkungsort) Deutschland
Gender	männlich
Academic degree	Prof. Dr. med.
Profession	Arzt (characteristic profession)
Variant	A. Rolfs
Related	Universität Rostock
Further information	seit 1997 Professor für Neurologie an der Klinik und Poliklinik für Neurologie an der Universität Rostock seit 2008 Professor für Neurorestauration am Albrecht-Kossel-Institut für Neuroregeneration an der Universität Rostock
Source	Internet Catalogus Professorum Rostochiensium: http://purl.uni-rostock.de/cpr/00001513
Record type	Person
GND-Identifier	136256864
Record ID	136256864
Involved in show all A Comprehensive Assessment of Qualitative and Quantitative Prodromal Parkinsonian Features in Carriers of Gaucher Disease-Identifying Those at the Greatest Risk PDA Indolylmaleimides Induce Anti-Tumor Effects in Prostate Carcinoma Cell Lines Through Mitotic Death Identification of Brain-Specific Treatment Effects in NPC1 Disease by Focusing on Cellular and Molecular Changes of Sphingosine-1-Phosphate Metabolism A therapy with miglustat, 2-hydroxypropyl-ß-cyclodextrin and allopregnanolone restores splenic cholesterol homeostasis in Niemann-pick disease type C1 A therapy with miglustat, 2-hydroxypropyl-ß-cyclodextrin and allopregnanolone restores splenic cholesterol homeostasis in Niemann-pick disease type C1 Funktionelle Charakterisierung von zerebellären Purkinjezellen eines Mausmodells des Morbus Niemann-Pick Typ C1 Multicenter Female Fabry Study (MFFS) - clinical survey on current treatment of females with Fabry disease Genetic variants in components of the NALCN–UNC80–UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies) A KAT6A variant in a family with autosomal dominantly inherited microcephaly and developmental delay Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes Correction: Broadening the phenotypic spectrum of pathogenic LARP7 variants: two cases with intellectual disability, variable growth retardation and distinct facial features Biallelic inactivating variants in the GTPBP2 gene cause a neurodevelopmental disorder with severe intellectual disability Auswirkungen von Miglustat bzw. einer Kombination aus Cyclodextrin, Allopregnanolon und Miglustat auf Verhalten, Motorik, Schmerzempfinden und Gewichtsentwicklung von BALB/c-Wildtypmäusen Beeinflussung der ER-assoziierten Proteostase zur Erhöhung der Aktivität mutanter α-Galaktosidase A und der Verbesserung der Pathophysiologie in Morbus Fabry Beschreibung und Vergleich der weltweit größten Kohorte mit Pantothenatkinase-assoziierter Neurodegeneration Die Wirkung von Trichostatin A in einem zellkultur-basierten Krankheitsmodell des Morbus Niemann-Pick Typ C Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke Untersuchung zur Gliose im Morbus Niemann-Pick Typ C unter Verwendung von induzierten pluripotenten Stammzellen 17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a case report AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability Wnt3a induces neuronal differentiation and crosstalk between Wnt/Ca2+-pathway and Wnt/β-catenin pathway Multicenter Female Fabry Study (MFFS) - clinical survey on current treatment of females with Fabry disease Cardiac troponin I: a valuable biomarker indicating the cardiac involvement in fabry disease Generierung, Charakterisierung und neurale Differenzierung von humanen induzierten pluripotenten Stammzellen : ein zelluläres Modell für Morbus Niemann-Pick Typ C1 Die antineoplastische Potenz des Indolylmaleimids PDA66 eine Studie zu Wirkmechanismen, Aktivität in verschiedenen Zellmodellen und Verträglichkeit im Tiermodell : eine Studie zu Wirkmechanismen, Aktivität in verschiedenen Zellmodellen und Verträglichkeit im Tiermodell Erythropoetin und die Rolle von Sauerstoff bei der Proliferation und Differenzierung der humanen mesenzephalen Progenitorzellen ReNcell VM The network of signaling pathways : analysis of the Notch and Wnt signaling pathway in the differentiation of human neural progenitor cells The role of gap junctional intercellular communication and connexins in the differentiation of human neural progenitor cells Defects in the retina of Niemann-pick type C 1 mutant mice Characterisation of novel α-galactosidase A mutations in Fabry disease based on in vitro, in vivo and pharmacological data Differentiation and survival of human neural progenitor cells in 3D scaffolds of self-assembling peptide hydrogels Persistent increase in cardiac troponin I in Fabry disease: a case report CAG Repeats Determine Brain Atrophy in Spinocerebellar Ataxia 17: A VBM Study Sequentielle Analyse der hypervariablen V2-Domäne der HIV-1 envelope-Genregion im Liquor cerebrospinalis PCR : clinical diagnostics and research PCR: Clinical Diagnostics and Research PCR topics : usage of polymerase chain reaction in genetic and infectious diseases PCR Topics : Usage of Polymerase Chain Reaction in Genetic and Infectious Diseases Hemmung der exokrinen Pankreassekretion beim Menschen durch Oxethazain, einem potenten Lokalanästhetikum, Hinweise für die Existenz eines enteropankreatischen Reflexbogen

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Katalog der Deutschen Nationalbibliothek

Arndt Rolfs (1959-)

A Comprehensive Assessment of Qualitative and Quantitative Prodromal Parkinsonian Features in Carriers of Gaucher Disease-Identifying Those at the Greatest Risk

PDA Indolylmaleimides Induce Anti-Tumor Effects in Prostate Carcinoma Cell Lines Through Mitotic Death

Identification of Brain-Specific Treatment Effects in NPC1 Disease by Focusing on Cellular and Molecular Changes of Sphingosine-1-Phosphate Metabolism

A therapy with miglustat, 2-hydroxypropyl-ß-cyclodextrin and allopregnanolone restores splenic cholesterol homeostasis in Niemann-pick disease type C1

A therapy with miglustat, 2-hydroxypropyl-ß-cyclodextrin and allopregnanolone restores splenic cholesterol homeostasis in Niemann-pick disease type C1

Funktionelle Charakterisierung von zerebellären Purkinjezellen eines Mausmodells des Morbus Niemann-Pick Typ C1

Multicenter Female Fabry Study (MFFS) - clinical survey on current treatment of females with Fabry disease

Genetic variants in components of the NALCN–UNC80–UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies)

A KAT6A variant in a family with autosomal dominantly inherited microcephaly and developmental delay

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Correction: Broadening the phenotypic spectrum of pathogenic LARP7 variants: two cases with intellectual disability, variable growth retardation and distinct facial features

Biallelic inactivating variants in the GTPBP2 gene cause a neurodevelopmental disorder with severe intellectual disability

Auswirkungen von Miglustat bzw. einer Kombination aus Cyclodextrin, Allopregnanolon und Miglustat auf Verhalten, Motorik, Schmerzempfinden und Gewichtsentwicklung von BALB/c-Wildtypmäusen

Beeinflussung der ER-assoziierten Proteostase zur Erhöhung der Aktivität mutanter α-Galaktosidase A und der Verbesserung der Pathophysiologie in Morbus Fabry

Beschreibung und Vergleich der weltweit größten Kohorte mit Pantothenatkinase-assoziierter Neurodegeneration

Die Wirkung von Trichostatin A in einem zellkultur-basierten Krankheitsmodell des Morbus Niemann-Pick Typ C

Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke

Untersuchung zur Gliose im Morbus Niemann-Pick Typ C unter Verwendung von induzierten pluripotenten Stammzellen

17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a case report

AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability

Wnt3a induces neuronal differentiation and crosstalk between Wnt/Ca2+-pathway and Wnt/β-catenin pathway

Multicenter Female Fabry Study (MFFS) - clinical survey on current treatment of females with Fabry disease

Cardiac troponin I: a valuable biomarker indicating the cardiac involvement in fabry disease

Generierung, Charakterisierung und neurale Differenzierung von humanen induzierten pluripotenten Stammzellen : ein zelluläres Modell für Morbus Niemann-Pick Typ C1

Die antineoplastische Potenz des Indolylmaleimids PDA66 eine Studie zu Wirkmechanismen, Aktivität in verschiedenen Zellmodellen und Verträglichkeit im Tiermodell : eine Studie zu Wirkmechanismen, Aktivität in verschiedenen Zellmodellen und Verträglichkeit im Tiermodell

Erythropoetin und die Rolle von Sauerstoff bei der Proliferation und Differenzierung der humanen mesenzephalen Progenitorzellen ReNcell VM

The network of signaling pathways : analysis of the Notch and Wnt signaling pathway in the differentiation of human neural progenitor cells

The role of gap junctional intercellular communication and connexins in the differentiation of human neural progenitor cells

Defects in the retina of Niemann-pick type C 1 mutant mice

Characterisation of novel α-galactosidase A mutations in Fabry disease based on in vitro, in vivo and pharmacological data

Differentiation and survival of human neural progenitor cells in 3D scaffolds of self-assembling peptide hydrogels

Persistent increase in cardiac troponin I in Fabry disease: a case report

CAG Repeats Determine Brain Atrophy in Spinocerebellar Ataxia 17: A VBM Study

Sequentielle Analyse der hypervariablen V2-Domäne der HIV-1 envelope-Genregion im Liquor cerebrospinalis

PCR : clinical diagnostics and research

PCR: Clinical Diagnostics and Research

PCR topics : usage of polymerase chain reaction in genetic and infectious diseases

PCR Topics : Usage of Polymerase Chain Reaction in Genetic and Infectious Diseases

Hemmung der exokrinen Pankreassekretion beim Menschen durch Oxethazain, einem potenten Lokalanästhetikum, Hinweise für die Existenz eines enteropankreatischen Reflexbogen