Birgit Schwalenstöcker

Author

Universität Ulm

Also Known As

B. SCHWALENSTOCKER, B. Schwalenstocker, B. Schwalenstöcker, Birgit Schwalenstocker, Birgit Schwalenstöcker

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Universität Ulm Université de Strasbourg Inserm Humboldt-Universität zu Berlin Mécanismes Centraux et Périphériques de la Neurodégénérescence

About

Birgit Schwalenstöcker is an author at Universität Ulm specializing in medicine, neurodegenerative diseases, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	847
2	Social Sciences	5	5	303
3	Natural Sciences	1	1	23
4	Biochemistry	1	1	23
5	Biomedical Engineering	1	1	122

Birgit Schwalenstöcker

Publications

989

Citations

H-Index

Page 1

	Year	Citations
Guidelines for preclinical animal research in ALS/MND: A consensus meeting Albert C. Ludolph, Caterina Bendotti, Eran Blaugrund, Amyotrophic Lateral Sclerosis Neurological DisorderTranslational MedicineExperimental NeuropathologySean F. ScottAnimal Models	2010	311
The RNA of the glutamate transporter EAAT2 is variably spliced in amyotrophic lateral sclerosis and normal individuals Thomas Meyer, Andrea Fromm, Christoph Münch, Journal of the Neurological Sciences Amyotrophic Lateral SclerosisMolecular NeuroscienceNeurochemical BiomarkersNeurologyNeuroscience	1999	127
Intrathecal application of neuroectodermally converted stem cells into a mouse model of ALS: limited intraparenchymal migration and survival narrows therapeutic effects Hansjörg Habisch, Mirosław Janowski, Donat Binder, Journal of Neural Transmission Regenerative MedicineDevelopmental BiologyIntrathecal ApplicationMedicineAdult Stem Cell	2007	122
PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis J. W. Eschbach, Birgit Schwalenstöcker, Selma M. Soyal, Human Molecular Genetics NeurogenomicsNeurological DisorderGeneticsIndependent Als PopulationsNeurochemical Biomarkers	2013	76
Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron disease Luc Dupuis, Anissa Fergani, Kerstin E. Braunstein, Experimental Neurology Neurodegenerative DiseasesMolecular NeuroscienceGenetic DisorderGeneticsDegenerative Disease	2008	68
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons Kerstin E. Braunstein, Judith Eschbach, Krisztina Ròna-Vörös, Human Molecular Genetics	2010	61
Alternative splicing of the 5′‐sequences of the mouse EAAT2 glutamate transporter and expression in a transgenic model for amyotrophic lateral sclerosis Christoph Münch, M. Ebstein, Ulrich Seefried, Journal of Neurochemistry	2002	43
The dynactin p150 subunit: cell biology studies of sequence changes found in ALS/MND and Parkinsonian Syndromes Marianne Stockmann, Marie Meyer-Ohlendorf, Kevin Achberger, Journal of Neural Transmission Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMolecular NeuroscienceMotor DysfunctionDynactin P150 Subunit	2012	36
Neuroprotective Function of Cellular Prion Protein in a Mouse Model of Amyotrophic Lateral Sclerosis Petra Steinacker, A. Hawlik, Stefan Lehnert, American Journal Of Pathology Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMedicineCellular Prion ProteinPrion Disease	2010	30
Differential regulation of 5′ splice variants of the glutamate transporter EAAT2 in an in vivo model of chemical hypoxia induced by 3‐nitropropionic acid Christoph Münch, binggen Zhu, Annette Leven, Journal of Neuroscience Research	2003	24

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