Research output per year
Research output per year
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Dive into the research topics where Eva Kretz is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Functional validation of ABHD12 mutations in the neurodegenerative disease PHARC
Tingaud-Sequeira, A., Raldúa, D., Lavie, J., Mathieu, G., Bordier, M., Knoll-Gellida, A., Rambeau, P., Coupry, I., André, M., Malm, E., Möller, C., Andreasson, S., Rendtorff, N. D., Tranebjærg, L., Koenig, M., Lacombe, D., Goizet, C. & Babin, P. J., 2017 Feb 1, In: Neurobiology of Disease. 98, p. 36-51 16 p.Research output: Contribution to journal › Article › peer-review
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Alteration of rod and cone function in children with Usher syndrome.
Malm, E., Ponjavic, V., Möller, C., Kimberling, W. J., Stone, E. S. & Andréasson, S., 2011, In: European Journal of Ophthalmology. Jul 1, p. 30-38Research output: Contribution to journal › Article › peer-review
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Phenotypes in Defined Genotypes Including Siblings with Usher Syndrome.
Malm, E., Ponjavic, V., Möller, C., Kimberling, W. J. & Andréasson, S., 2011, In: Ophthalmic Genetics. 32, p. 65-74Research output: Contribution to journal › Article › peer-review
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Retinal function in deaf-blind syndromes
Malm, E., 2011, Department of Clinical Sciences, Lund University. 110 p.Research output: Thesis › Doctoral Thesis (compilation)
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Full-field electroretinography and marked variability in clinical phenotype of Alström syndrome.
Malm, E., Ponjavic, V., Nishina, P. M., Naggert, J. K., Hinman, E. G., Andréasson, S., Marshall, J. D. & Möller, C., 2008, In: Archives of Ophthalmology. 126, 1, p. 51-57Research output: Contribution to journal › Article › peer-review
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