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Blueberry muffin baby: a pictoral differential diagnosis.
Mehta V, Balachandran C, Lonikar V. Mehta V, et al. Dermatol Online J. 2008 Feb 28;14(2):8. Dermatol Online J. 2008. PMID: 18700111 Free article. Review.
The term blueberry muffin baby was initially coined by pediatricians to describe cutaneous manifestations observed in newborns infected with rubella during the American epidemic of the 1960s. These children had generalized hemorrhagic purpuric eruptions that on histopathol …
The term blueberry muffin baby was initially coined by pediatricians to describe cutaneous manifestations observed in newborns infect …
Zika Virus Infection in a Cohort of Pregnant Women with Exanthematic Disease in Manaus, Brazilian Amazon.
Redivo EF, Bôtto Menezes C, da Costa Castilho M, Brock M, da Silva Magno E, Gomes Saraiva MDG, Alvarez Fernandes SS, Costa Antony de Andrade AB, Costa Alecrim MDG, Martinez-Espinosa FE. Redivo EF, et al. Viruses. 2020 Nov 28;12(12):1362. doi: 10.3390/v12121362. Viruses. 2020. PMID: 33260784 Free PMC article.

Severe adverse pregnancy outcomes (miscarriage, stillbirth, or microcephaly) were observed in both RT-PCR ZIKV-positive (5.0%) and ZIKV-negative (1.8%) cases (RR 3.1; 95% IC 1.4-7.3; p < 0.05), especially during the first trimester of pregnancy (RR 6.2, 95% IC 2.3-16.5;

Severe adverse pregnancy outcomes (miscarriage, stillbirth, or microcephaly) were observed in both RT-PCR ZIKV-positive (5.0%) and ZI …
Genetic syndromes mimic congenital infections.
Sanchis A, Cerveró L, Bataller A, Tortajada JL, Huguet J, Crow YJ, Ali M, Higuet LJ, Martínez-Frías ML. Sanchis A, et al. J Pediatr. 2005 May;146(5):701-5. doi: 10.1016/j.jpeds.2005.01.033. J Pediatr. 2005. PMID: 15870678
We describe two brothers born to consanguineous parents with clinical features suggestive of intrauterine infection but with negative serologic investigations. Our observations suggest that Aicardi-Goutieres syndrome (AGS) and pseudo-TORCH syndrome likely rep …
We describe two brothers born to consanguineous parents with clinical features suggestive of intrauterine infection but with negative serolo …
Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism.
Crow YJ, Black DN, Ali M, Bond J, Jackson AP, Lefson M, Michaud J, Roberts E, Stephenson JB, Woods CG, Lebon P. Crow YJ, et al. J Med Genet. 2003 Mar;40(3):183-7. doi: 10.1136/jmg.40.3.183. J Med Genet. 2003. PMID: 12624136 Free PMC article.
Cree encephalitis shows phenotypic overlap with AGS although the conditions have been considered distinct because of immunological abnormalities observed in Cree encephalitis. We report that levels of interferon alpha (IFN-alpha), a marker of AGS, are raised in Cree enceph …
Cree encephalitis shows phenotypic overlap with AGS although the conditions have been considered distinct because of immunological abnormali …
A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts.
Mochida GH, Ganesh VS, Felie JM, Gleason D, Hill RS, Clapham KR, Rakiec D, Tan WH, Akawi N, Al-Saffar M, Partlow JN, Tinschert S, Barkovich AJ, Ali B, Al-Gazali L, Walsh CA. Mochida GH, et al. Am J Hum Genet. 2010 Dec 10;87(6):882-9. doi: 10.1016/j.ajhg.2010.10.026. Epub 2010 Nov 25. Am J Hum Genet. 2010. PMID: 21109224 Free PMC article.
Their clinical presentation overlaps with some reported cases of pseudo-TORCH syndrome as well as with cases involving mutations in occludin, another component of the tight-junction complex. ...Homozygosity mapping identified the disease locus in this family on chro …
Their clinical presentation overlaps with some reported cases of pseudo-TORCH syndrome as well as with cases involving mutatio …