Klein, Christine
كريستين كلاين
Klein, Christine, 1969-
Klein, Christine, sophrologue
Klein-Lataud, Christine
Klein, Cristine
VIAF ID: 9321152381815301950005 (Personal)
Permalink: http://viaf.org/viaf/9321152381815301950005
Preferred Forms
- 200 _ | ‡a Klein ‡b Cristine
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- 100 1 _ ‡a Klein, Christine
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- 100 1 _ ‡a Klein, Christine
- 100 1 _ ‡a Klein, Christine
- 100 1 _ ‡a Klein, Christine ‡d 1969-
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- 100 1 _ ‡a Klein, Christine, ‡d 1969-
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- 100 1 _ ‡a Klein-Lataud, Christine
- 100 0 _ ‡a كريستين كلاين
4xx's: Alternate Name Forms (7)
5xx's: Related Names (3)
- 551 _ _ ‡a Hamburg ‡4 ortg ‡4 https://d-nb.info/standards/elementset/gnd#placeOfBirth
- 551 _ _ ‡a Lübeck ‡4 ortw ‡4 https://d-nb.info/standards/elementset/gnd#placeOfActivity
- 500 1 _ ‡a Schinkmann, Christine
Works
Title | Sources |
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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 | |
Charakterisierung von mit der synaptischen Verbindung assoziierten Proteinen der Ratte | |
COVID-19 Vaccine-Associated Cerebral Venous Thrombosis in Germany | |
Dissection of TAF1 neuronal splicing and implications for neurodegeneration in X-linked dystonia-parkinsonism | |
Dokumente zur Telemann-Rezeption 1767 bis 1907 | |
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias | |
Ma bulle bien-être du soir : rituels de yoga, automassages, pilates et sophro | |
Motor complications in patients form the German Competence Network on Parkinson's disease and the DRD3 Ser9Gly polymorphism | |
Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variants | |
Movement disorders in 2011: Translating new research findings into clinical practice | |
Multi-omic landscaping of human midbrains identifies disease-relevant molecular targets and pathways in advanced-stage Parkinson's disease | |
Munchausen syndrome by genetics: Next-generation challenges for clinicians | |
Musician's dystonia and comorbid anxiety: two sides of one coin? | |
Mutant Parkin impairs mitochondrial function and morphology in human fibroblasts | |
Mutations in GNAL: a novel cause of craniocervical dystonia | |
Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study. | |
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice | |
Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness. | |
Mutations in TUBB4A and spastic paraplegia. | |
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects. | |
Mutations in VPS26A are not a frequent cause of Parkinson's disease. | |
Myoclonus-dystonia due to maternal uniparental disomy | |
Myopathy causing camptocormia in idiopathic Parkinson's disease: a multidisciplinary approach. | |
Nanopore Single-Molecule Sequencing for Mitochondrial DNA Methylation Analysis: Investigating Parkin-Associated Parkinsonism as a Proof of Concept | |
Needle in a Haystack: The Common Can Inform the Rare in Restless Legs Syndrome | |
Neuroanatomical changes extend beyond striatal atrophy in X-linked dystonia parkinsonism. | |
Neurogenetics | |
Neuroimaging abnormalities in individuals exhibiting Parkinson's disease risk markers | |
Neurophysiological fingerprints of X-linked dystonia-parkinsonism: A model basal ganglia disease. | |
Neuropsychiatric symptoms and intelligence quotient in autosomal dominant Segawa disease. | |
New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3). | |
Next-generation phenotyping and genomic incidental findings--reply | |
Next-generation phenotyping using the parkin example: time to catch up with genetics | |
Next generation sequencing and the future of genetic diagnosis | |
Niemann-Pick type C1 patient-specific induced pluripotent stem cells display disease specific hallmarks | |
No association between NOD2 variants and Parkinson's disease | |
No association of the BDNF val66met polymorphism with implicit associative vocabulary and motor learning | |
No evidence for differential methylation of α-synuclein in leukocyte DNA of Parkinson's disease patients | |
No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia | |
Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force. | |
Non-motor phenotype of dopa-responsive dystonia and quality of life assessment. | |
Nonmotor and diagnostic findings in subjects with de novo Parkinson disease of the DeNoPa cohort. | |
Nonmotor symptoms in Parkin gene-related parkinsonism. | |
Nonsteroidal Anti-Inflammatory Use and LRRK2 Parkinson's Disease Penetrance | |
A novel APTX variant and ataxia with oculomotor apraxia type 1 | |
Novel GNAL mutations in two German patients with sporadic dystonia. | |
Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans | |
Novel NAXE variants as a cause for neurometabolic disorder: implications for treatment | |
NR4A2 mutations are rare among European patients with familial Parkinson's disease | |
Osteoclast imbalance in primary familial brain calcification: evidence for its role in brain calcification | |
Pallidal and thalamic deep brain stimulation in myoclonus-dystonia. | |
Parkin gene alterations in hepatocellular carcinoma | |
Parkin Interacts with Apoptosis-Inducing Factor and Interferes with Its Translocation to the Nucleus in Neuronal Cells | |
Parkin-linked Parkinson's disease: From clinical insights to pathogenic mechanisms and novel therapeutic approaches | |
Parkin Type of Early-Onset Parkinson Disease | |
Parkingene modifies the effect ofRLS4on the age at onset of restless legs syndrome (RLS) | |
Parkinson disease, 10 years after its genetic revolution: multiple clues to a complex disorder | |
Parkinson disease: genetic testing in Parkinson disease-who should be assessed? | |
Parkinson disease(s): is "Parkin disease" a distinct clinical entity? | |
Parkinson's disease in the Western Pacific Region | |
Paroxysmal cervical myoclonus | |
Personality profiles are different in musician's dystonia and other isolated focal dystonias | |
Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson's disease | |
Phenomenology and classification of dystonia: a consensus update | |
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study | |
Phenotypes and genetic architecture of focal primary torsion dystonia | |
Phenotypic insights into ADCY5-associated disease. | |
Phenotypic spectrum of musician's dystonia: a task-specific disorder? | |
Phenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family | |
Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene | |
Phosphatase and tensin homolog (PTEN)-induced putative kinase 1 (PINK1)-dependent ubiquitination of endogenous Parkin attenuates mitophagy: study in human primary fibroblasts and induced pluripotent stem cell-derived neurons | |
PINK1-dependent mitophagy is driven by the UPS and can occur independently of LC3 conversion | |
PINK1-Interacting Proteins: Proteomic Analysis of Overexpressed PINK1. | |
PINK1 loss-of-function mutations affect mitochondrial complex I activity via NdufA10 ubiquinone uncoupling | |
PINK1 p.Leu347Pro mutations in Malays: Prevalence and illustrative cases | |
PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism. | |
PLA2G6mutations and Parkinsonism: Long-term follow-up of clinical features and neuropathology | |
Plasmid-Based Generation of Induced Neural Stem Cells from Adult Human Fibroblasts | |
Le rouge et le noir - Stendhal : analyse critique | |
Sophro du matin : partir à la découverte de l'intelligence du corps | |
Sophro du soir : décompresser en fin de journée pour laisser place à un sommeil de qualité | |
Sophrologie pratique : exercices pour tous les jours | |
Stem Cells and Organoid Technology in Precision Medicine in Inflammation : Are We There Yet? | |
Untersuchung zur Gliose im Morbus Niemann-Pick Typ C unter Verwendung von induzierten pluripotenten Stammzellen | |
An unusual neurological syndrome of crawling gait, dystonia, pyramidal signs, and limited speech | |
Wirkung von Trichostatin A in einem zellkultur-basierten Krankheitsmodell des Morbus Niemann-Pick Typ C |