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Genetic mutations as a cause of hyperinsulinemic hypoglycemia in children.
Thomas PM. Thomas PM. Endocrinol Metab Clin North Am. 1999 Sep;28(3):647-56, viii. doi: 10.1016/s0889-8529(05)70092-x. Endocrinol Metab Clin North Am. 1999. PMID: 10500935 Review.
A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.
Otonkoski T, Ammälä C, Huopio H, Cote GJ, Chapman J, Cosgrove K, Ashfield R, Huang E, Komulainen J, Ashcroft FM, Dunne MJ, Kere J, Thomas PM. Otonkoski T, et al. Among authors: thomas pm. Diabetes. 1999 Feb;48(2):408-15. doi: 10.2337/diabetes.48.2.408. Diabetes. 1999. PMID: 10334322
Persistent hyperinsulinemic hypoglycemia of infancy.
Thomas PM, Cote GJ. Thomas PM, et al. Cancer Treat Res. 1997;89:347-63. doi: 10.1007/978-1-4615-6355-6_16. Cancer Treat Res. 1997. PMID: 9204200 Review. No abstract available.
The molecular basis for familial persistent hyperinsulinemic hypoglycemia of infancy.
Thomas PM, Cote GJ, Wohllk N, Mathew PM, Gagel RF. Thomas PM, et al. Proc Assoc Am Physicians. 1996 Jan;108(1):14-9. Proc Assoc Am Physicians. 1996. PMID: 8834059
Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancy.
Thomas PM, Wohllk N, Huang E, Kuhnle U, Rabl W, Gagel RF, Cote GJ. Thomas PM, et al. Am J Hum Genet. 1996 Sep;59(3):510-8. Am J Hum Genet. 1996. PMID: 8751851 Free PMC article.
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy.
Thomas PM, Cote GJ, Wohllk N, Haddad B, Mathew PM, Rabl W, Aguilar-Bryan L, Gagel RF, Bryan J. Thomas PM, et al. Science. 1995 Apr 21;268(5209):426-9. doi: 10.1126/science.7716548. Science. 1995. PMID: 7716548
Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy.
Thomas PM, Cote GJ, Hallman DM, Mathew PM. Thomas PM, et al. Am J Hum Genet. 1995 Feb;56(2):416-21. Am J Hum Genet. 1995. PMID: 7847376 Free PMC article.
Targeted detection and quantitation of histone modifications from 1,000 cells.
Abshiru NA, Sikora JW, Camarillo JM, Morris JA, Compton PD, Lee T, Neelamraju Y, Haddox S, Sheridan C, Carroll M, Cripe LD, Tallman MS, Paietta EM, Melnick AM, Thomas PM, Garrett-Bakelman FE, Kelleher NL. Abshiru NA, et al. Among authors: thomas pm. PLoS One. 2020 Oct 26;15(10):e0240829. doi: 10.1371/journal.pone.0240829. eCollection 2020. PLoS One. 2020. PMID: 33104722
Development of novel methods for non-canonical myeloma protein analysis with an innovative adaptation of immunofixation electrophoresis, native top-down mass spectrometry, and middle-down de novo sequencing.
Deighan WI, Winton VJ, Melani RD, Anderson LC, McGee JP, Schachner LF, Barnidge D, Murray D, Alexander HD, Gibson DS, Deery MJ, McNicholl FP, McLaughlin J, Kelleher NL, Thomas PM. Deighan WI, et al. Among authors: thomas pm. Clin Chem Lab Med. 2020 Oct 20:/j/cclm.ahead-of-print/cclm-2020-1072/cclm-2020-1072.xml. doi: 10.1515/cclm-2020-1072. Online ahead of print. Clin Chem Lab Med. 2020. PMID: 33079696
Chemical composition of material extractives influences microbial growth and dynamics on wetted wood materials.
Zhao D, Cardona C, Gottel N, Winton VJ, Thomas PM, Raba DA, Kelley ST, Henry C, Gilbert JA, Stephens B. Zhao D, et al. Among authors: thomas pm. Sci Rep. 2020 Sep 2;10(1):14500. doi: 10.1038/s41598-020-71560-3. Sci Rep. 2020. PMID: 32879425 Free PMC article.
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