Matches in Nanopublications for { ?s ?p "[Familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a rare, autosomal recessive disease of unregulated insulin secretion, defined by elevations in serum insulin despite severe hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_assertion description "[Familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a rare, autosomal recessive disease of unregulated insulin secretion, defined by elevations in serum insulin despite severe hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323679.RABMN45g4rbCSwTZHq3vA3FqABKubl_OmXeJa0zvDK1OU130_provenance.
- NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_assertion description "[Familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a rare, autosomal recessive disease of unregulated insulin secretion, defined by elevations in serum insulin despite severe hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323678.RAsHr65DUPwYhbBK2oQ4kRJ---6afw0jbo0tgyxn2fdFk130_provenance.
- NP1323680.RAsaqTA6Wt4OW0W3jBVimjupO7l1pVj411ZTWWmbSa_9Q130_assertion description "[Familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a rare, autosomal recessive disease of unregulated insulin secretion, defined by elevations in serum insulin despite severe hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323680.RAsaqTA6Wt4OW0W3jBVimjupO7l1pVj411ZTWWmbSa_9Q130_provenance.
- NP8543.RAKMZ0eZRaVKobehOSB58lwoo7yo4Vbnx5ftvYv_zC5Ns130_assertion description "[Familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a rare, autosomal recessive disease of unregulated insulin secretion, defined by elevations in serum insulin despite severe hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8543.RAKMZ0eZRaVKobehOSB58lwoo7yo4Vbnx5ftvYv_zC5Ns130_provenance.