Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

4 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Are substitutions in the first hypervariable region of the mitochondrial DNA displacement-loop in sudden infant death syndrome due to maternal inheritance?
Arnestad M, Opdal SH, Musse MA, Vege A, Rognum TO. Arnestad M, et al. Among authors: musse ma. Acta Paediatr. 2002;91(10):1060-4. doi: 10.1080/080352502760311557. Acta Paediatr. 2002. PMID: 12434891
Possible role of mtDNA mutations in sudden infant death.
Opdal SH, Vege A, Egeland T, Musse MA, Rognum TO. Opdal SH, et al. Among authors: musse ma. Pediatr Neurol. 2002 Jul;27(1):23-9. doi: 10.1016/s0887-8994(02)00384-3. Pediatr Neurol. 2002. PMID: 12160969
Mitochondrial tRNA genes and flanking regions in sudden infant death syndrome.
Opdal SH, Vege A, Arnestad M, Musse MA, Rognum TO. Opdal SH, et al. Among authors: musse ma. Acta Paediatr. 2007 Feb;96(2):211-4. doi: 10.1111/j.1651-2227.2007.00085.x. Acta Paediatr. 2007. PMID: 17429907
Estimation of time since death by vitreous humor hypoxanthine, potassium, and ambient temperature.
Rognum TO, Holmen S, Musse MA, Dahlberg PS, Stray-Pedersen A, Saugstad OD, Opdal SH. Rognum TO, et al. Among authors: musse ma. Forensic Sci Int. 2016 May;262:160-5. doi: 10.1016/j.forsciint.2016.03.001. Epub 2016 Mar 9. Forensic Sci Int. 2016. PMID: 26994446
Feedback