25 citations
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May 2004 in “Prenatal Diagnosis” This study suggests that prenatal genetic diagnosis of MELAS syndrome using amniotic cells may not reliably predict fetal outcomes due to phenotypic diversity observed in siblings with similar levels of mutant mtDNA.
17 citations
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June 2017 in “Gene” This is the first report of the FOXN1 p.R255X mutation from India, demonstrating the global spread of this genetic mutation previously found only in an Italian community.
August 2017 in “Journal of biotechnology” This review found that topical corticosteroids hold the highest level of evidence as a first-line treatment for pediatric alopecia areata, but further trials are needed to explore additional therapies.
39 citations
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June 1982 in “The BMJ” Blood tests confirmed a baby in the womb had a CMV infection.
1 citations
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October 2015 in “Actas Dermo-Sifiliográficas”