4 results for author:"Rosenbloom A.L." in Literature citations
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| Intrauterine and postnatal growth failure with normal GH/IGF1 axis and insulin-resistant diabetes in a consanguineous kinship. Guevara-Aguirre J., Guevara-Aguirre M., Hwa V., Procel P., Saavedra J., Ostrer H., Fang P., Rosenfeld R.G., Kerns S., Rosenbloom A.L. Eur. J. Endocrinol. 166:521-529(2012) · Mapped (14) |
| Effects of heterozygosity for the E180 splice mutation causing growth hormone receptor deficiency in Ecuador on IGF-I, IGFBP-3, and stature. Guevara-Aguirre J., Rosenbloom A.L., Guevara-Aguirre M., Yariz K., Saavedra J., Baumbach L., Shuster J. Growth Horm. IGF Res. 17:261-264(2007) · Mapped (28) |
| Arterial thrombosis resulting in amputation in a child with poorly controlled type 1 diabetes and heterozygous Factor V Leiden mutation. Haller M.J., Valladares A., Rosenbloom A.L. Pediatr Diabetes 7:229-231(2006) · Mapped (3) |
| Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS. Bastepe M., Froehlich L.F., Hendy G.N., Indridason O.S., Josse R.G., Koshiyama H., Koerkkoe J., Nakamoto J.M., Rosenbloom A.L., Slyper A.H. et al. J. Clin. Invest. 112:1255-1263(2003) · UniProtKB (5) |