Carla Andreia Teixeira

Author

Also Known As

C Teixeira, C. Teixeira, C.A. Teixeira, C.A.F. Teixeira, Carla A. Teixeira, Carla Andreia Teixeira, Carla Noura Teixeira, Carla Teixeira

Publications

405

Citations

H-Index

Concepts

All Affiliations

Universidade do Porto Centro de Genética Clínica Hospital de Santo António Duke University Hospital Duke Medical Center

About

Carla Andreia Teixeira is an author at Universidade do Porto specializing in medicine, cell biology, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	292
2	Engineering	1	1	33
3	Natural Sciences	1	1	17
4	Social Sciences	1	1	82
5	Biomedical Engineering	1	1	26

Carla Andreia Teixeira

Publications

359

Citations

H-Index

Page 1

	Year	Citations
CNS Axons Globally Increase Axonal Transport after Peripheral Conditioning Fernando Milhazes Mar, Anabel R. Simões, Sérgio Carvalho Leite, Journal of Neuroscience Peripheral BranchPeripheral Nerve InjuryCytoskeletonPeripheral NerveCellular Physiology	2014	82
Early axonal loss accompanied by impaired endocytosis, abnormal axonal transport, and decreased microtubule stability occur in the model of Krabbe's disease Carla Andreia Teixeira, Catarina Oliveira Miranda, Vera Sousa, Neurobiology of Disease Early Axonal LossMicrotubule StabilityPathologyCytoskeletonNeuropathology	2014	62
Novel mutations in the CLN6 gene causing a variant late infantile neuronal ceroid lipofuscinosis Carla Andreia Teixeira, Janice A. Espinola, Liang Huo, Human Mutation	2003	50
Clinicopathological and molecular characterization of neuronal ceroid lipofuscinosis in the Portuguese population Carla Andreia Teixeira, Ant�nio Guimar�es, Carlos Bessa, Journal of Neurology Neuro-oncologyMolecular CharacterizationPathologyNeurologyNeuropathology	2003	41
Two novel CLN5 mutations in a Portuguese patient with vLINCL: Insights into molecular mechanisms of CLN5 deficiency Carlos Bessa, Carla Andreia Teixeira, M. Mangas, Molecular Genetics and Metabolism Cln5 DeficiencyMendelian DisorderGenetic DisorderGeneticsPathogenesis	2006	38
CLN2/TPP1 deficiency: The novel mutation IVS7-10A>G causes intron retention and is associated with a mild disease phenotype Carlos Bessa, Carla Andreia Teixeira, Ana Cristi Basile Dias, Molecular Genetics and Metabolism EngineeringGenetic DisorderMedicineGeneticsGenetic Epidemiology	2007	33
Systemic Delivery of Bone Marrow-Derived Mesenchymal Stromal Cells Diminishes Neuropathology in a Mouse Model of Krabbe's Disease Catarina Oliveira Miranda, Carla Andreia Teixeira, Márcia A. Liz, Stem Cells Cell TherapyImmunologyPeripheral NerveBiomedical EngineeringPeripheral Nerves	2011	26
Gene expression profiling in vLINCL CLN6-deficient fibroblasts: Insights into pathobiology Carla Andreia Teixeira, Simon Lin, M. Mangas, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease Signaling PathwayCell RegulationNatural SciencesMolecular BiologyCellular Biology	2006	17
Primary Bone Marrow Mesenchymal Stromal Cells Rescue the Axonal Phenotype of Twitcher Mice Catarina Oliveira Miranda, Carla Andreia Teixeira, Vera Sousa, Cell Transplantation Adult Stem CellImmunologyRegenerative MedicineNeuroregenerationStem Cell Transplantation	2013	10

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