Sudden infant death syndrome (SIDS) - Standardised investigation and classification: Recommendations

Autor: Bajanowski, T., Vege, A., Byard, R.W., Krous, H.F., Arnestadt, M., Bachs, L., Banner, Jytte, Blair, P.S., Borthne, A., Dettmeyer, R., Flemming, P., Gaustadt, P., Gregersen, Markil Ebbe Gregers, Grogaard, J., Holter, E., Isaksen, C.V., Jorgensen, J.V., de Lange, C., Madea, B., Moore, I., Morland, J., Opdal, S.H., Rasten-Almqvist, P., Sclaud, M., Sidebotham, P., Skullerud, K., Stoltenburg-Didinger, G., Stray-Pedersen, A., Sveum, L., Rognum, T.O.

Publikováno v: Bajanowski, T, Vege, A, Byard, R W, Krous, H F, Arnestadt, M, Bachs, L, Banner, J, Blair, P S, Borthne, A, Dettmeyer, R, Flemming, P, Gaustadt, P, Gregersen, M E G, Grogaard, J, Holter, E, Isaksen, C V, Jorgensen, J V, de Lange, C, Madea, B, Moore, I, Morland, J, Opdal, S H, Rasten-Almqvist, P, Sclaud, M, Sidebotham, P, Skullerud, K, Stoltenburg-Didinger, G, Stray-Pedersen, A, Sveum, L & Rognum, T O 2007, ' Sudden infant death syndrome (SIDS)-Standardised investigation and classification: Recommendations ', Forensic Science International, vol. 165, no. 2-3, pp. 129-143 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pure_au_____::15cf7c5cb3e745b9cf3979d7aac0f4e6
https://pure.au.dk/portal/da/publications/sudden-infant-death-syndrome-sids--standardised-investigation-and-classification-recommendations(6b2ec5c0-e05d-11dc-9afb-000ea68e967b).html

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

Autor: 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

Publikováno v: 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 .

The Mohr-Tranebjaerg syndrome (MIM 304700) and the Jensen syndrome (MIM 311150) were previously reported as separate X-linked recessive deafness syndromes associated with progressive visual deterioration, dystonia, dementia, and psychiatric abnormali

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

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