المؤلفون: Ignjatovic, D., Sund, S., Stimec, B., Bergamaschi, R.

المصدر: Techniques in Coloproctology: Official Journal of the Italian Society of Colo-Rectal Surgery (SICCR), Mediterranean Society of Coloproctology (MSCP), Israel Society of Colon and Rectal Surgery (ISCRS), Mexican Society of Coloproctology, North-Northeastern Society of Coloproctology. September 2007 11(3):247-250

المؤلفون: Zeller, B., Storm-Mathisen, I., Smevik, B., Sund, S., Danielsen, K., Lie, S. O.

المصدر: European Journal of Pediatrics. October 1997 156(11):841-844

المؤلفون: Worden, H, Beer, R, Bowman, K, Eldering, A, Luo, M, Osterman, G, Sund, S, Worden, J, Steck, T

URL الوصول: https://ntrs.nasa.gov/citations/20060030462

المؤلفون: Worden, H, Steck, T, Beer, R, Bowman, K, Eldering, A, Luo, M, Osterman, G, Sund, S, Worden, J

URL الوصول: https://ntrs.nasa.gov/citations/20060031444

المؤلفون: Gran, J. T., Sund, S., Langholm, R.

المصدر: Clinical Rheumatology. December 1994 13(4):628-630

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المؤلفون: Van Ghelue M, Elgjo K, Jensen Pk, Warburg M, Sund S, Fuglsang-Frederiksen A, Skullerud K, Jakobsen J, Lisbeth Tranebjærg, Lindal S, Cindy L. Vnencak-Jones

المصدر: Tranebjærg, L, Jensen, P K A, Ghelue, M V, Vnencak-Jones, C L, Sund, S, Elgjo, K, Jakobsen, J, Lindal, S, Warburg, M, Fuglsang-Frederiksen, A & Skullerud, K 2002, ' Neuronal cell death in the visual cortex is a prominent feature of the X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a gene ' Ophthalmic Genetics, pp. 518-4 .

مصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, Mitochondrial Diseases, X Chromosome, Adolescent, Genetic Linkage, DNA Mutational Analysis, Genes, Recessive, Biology, Deafness, medicine.disease_cause, Polymerase Chain Reaction, Electron Transport Complex IV, Immunoenzyme Techniques, Basal ganglia, Optic Nerve Diseases, otorhinolaryngologic diseases, medicine, Humans, Allele, Child, Genetics (clinical), X-linked recessive inheritance, Aged, Visual Cortex, Dystonia, Neurons, Mutation, Cell Death, Mohr–Tranebjærg syndrome, Proteins, Syndrome, Middle Aged, Spinal cord, medicine.disease, Pedigree, Ophthalmology, medicine.anatomical_structure, Phosphopyruvate Hydratase, Pediatrics, Perinatology and Child Health, Optic nerve, Evoked Potentials, Visual, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::876a04ab4a048cbb9e5ef9d61e5d4538
https://pubmed.ncbi.nlm.nih.gov/11803487