Found: 7
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A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation.
- Published in:
- Genetics Research, 2019, v. 101, p. N.PAG, doi. 10.1017/S0016672319000041
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- Publication type:
- Article
Low plasma haptoglobin is a risk factor for life-threatening childhood severe malarial anemia and not an exclusive consequence of hemolysis.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-35944-w
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- Publication type:
- Article
Exome Sequencing Identifies Two Variants of the Alkylglycerol Monooxygenase Gene as a Cause of Relapses in Visceral Leishmaniasis in Children, in Sudan.
- Published in:
- 2017
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- Publication type:
- journal article
A Functional IL22 Polymorphism (rs2227473) Is Associated with Predisposition to Childhood Cerebral Malaria.
- Published in:
- Scientific Reports, 2017, p. 41636, doi. 10.1038/srep41636
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- Publication type:
- Article
Potential Use of Interleukin-10 Blockade as a Therapeutic Strategy in Human Cutaneous Leishmaniasis.
- Published in:
- 2015
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- Publication type:
- journal article
IL-17 and IL-22 are associated with protection against human kala azar caused by Leishmania donovani.
- Published in:
- 2009
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- Publication type:
- journal article
A functional promoter variant in IL12B predisposes to cerebral malaria.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 14, p. 2190, doi. 10.1093/hmg/ddn118
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- Publication type:
- Article