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Possible role of mtDNA mutations in sudden infant death.
Opdal SH, Vege A, Egeland T, Musse MA, Rognum TO. Opdal SH, et al. Pediatr Neurol. 2002 Jul;27(1):23-9. doi: 10.1016/s0887-8994(02)00384-3. Pediatr Neurol. 2002. PMID: 12160969
Vitreous humor hypoxanthine levels in SIDS and infectious death.
Vege A, Chen Y, Opdal SH, Saugstad OD, Rognum TO. Vege A, et al. Among authors: opdal sh. Acta Paediatr. 1994 Jun;83(6):634-9. doi: 10.1111/j.1651-2227.1994.tb13096.x. Acta Paediatr. 1994. PMID: 7919762
Is partial deletion of the complement C4 genes associated with sudden infant death?
Opdal SH, Vege A, Saugstad OD, Rognum TO. Opdal SH, et al. Eur J Pediatr. 1994 Apr;153(4):287-90. doi: 10.1007/BF01954522. Eur J Pediatr. 1994. PMID: 8194566
Hypoxanthine levels in vitreous humor: a study of influencing factors in sudden infant death syndrome.
Opdal SH, Rognum TO, Vege A, Saugstad OD. Opdal SH, et al. Pediatr Res. 1998 Aug;44(2):192-6. doi: 10.1203/00006450-199808000-00009. Pediatr Res. 1998. PMID: 9702913
Objective measurements of nicotine exposure in victims of sudden infant death syndrome and in other unexpected child deaths.
Milerad J, Vege A, Opdal SH, Rognum TO. Milerad J, et al. Among authors: opdal sh. J Pediatr. 1998 Aug;133(2):232-6. doi: 10.1016/s0022-3476(98)70225-2. J Pediatr. 1998. PMID: 9709711
SIDS--changes in the epidemiological pattern in eastern Norway 1984-1996.
Vege A, Rognum TO, Opdal SH. Vege A, et al. Among authors: opdal sh. Forensic Sci Int. 1998 May 11;93(2-3):155-66. doi: 10.1016/s0379-0738(98)00048-6. Forensic Sci Int. 1998. PMID: 9717266
Increased number of substitutions in the D-loop of mitochondrial DNA in the sudden infant death syndrome.
Opdal SH, Rognum TO, Vege A, Stave AK, Dupuy BM, Egeland T. Opdal SH, et al. Acta Paediatr. 1998 Oct;87(10):1039-44. doi: 10.1080/080352598750031347. Acta Paediatr. 1998. PMID: 9825969
The complement component C4 in sudden infant death.
Opdal SH, Vege A, Stave AK, Rognum TO. Opdal SH, et al. Eur J Pediatr. 1999 Mar;158(3):210-2. doi: 10.1007/s004310051051. Eur J Pediatr. 1999. PMID: 10094440
Mitochondrial DNA point mutations detected in four cases of sudden infant death syndrome.
Opdal SH, Rognum TO, Torgersen H, Vege A. Opdal SH, et al. Acta Paediatr. 1999 Sep;88(9):957-60. doi: 10.1080/08035259950168441. Acta Paediatr. 1999. PMID: 10519336
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: opdal sh. Acta Paediatr. 2002;91(10):1060-4. doi: 10.1080/080352502760311557. Acta Paediatr. 2002. PMID: 12434891
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