FAJANS SS - Search Results

1

POLYOSTOTIC FIBROUS DYSPLASIA AND ACROMEGALY.

SCURRY MT, BICKNELL JM, FAJANS SS. SCURRY MT, et al. Among authors: fajans ss. Arch Intern Med. 1964 Jul;114:40-5. doi: 10.1001/archinte.1964.03860070086008. Arch Intern Med. 1964. PMID: 14152128 No abstract available.

2

Human adrenal cortex after administration of ACTH and cortisone; morphologic changes.

O'DONNELL WM, FAJANS SS, WEINBAUM JG. O'DONNELL WM, et al. Among authors: fajans ss. AMA Arch Intern Med. 1951 Jul;88(1):28-35. doi: 10.1001/archinte.1951.03810070038005. AMA Arch Intern Med. 1951. PMID: 14837542 No abstract available.

3

A comparison of the duration of action of various long-acting ACTH preparations in human subjects.

WOLFSON WQ, FAJANS SS. WOLFSON WQ, et al. Among authors: fajans ss. N Engl J Med. 1952 Jun 26;246(26):1000-4. doi: 10.1056/NEJM195206262462603. N Engl J Med. 1952. PMID: 14941264 No abstract available.

4

MODY: history, genetics, pathophysiology, and clinical decision making.

Fajans SS, Bell GI. Fajans SS, et al. Diabetes Care. 2011 Aug;34(8):1878-84. doi: 10.2337/dc11-0035. Diabetes Care. 2011. PMID: 21788644 Free PMC article. Review. No abstract available.

5

Insufficient sensitivity of hemoglobin A(₁C) determination in diagnosis or screening of early diabetic states.

Fajans SS, Herman WH, Oral EA. Fajans SS, et al. Metabolism. 2011 Jan;60(1):86-91. doi: 10.1016/j.metabol.2010.06.017. Epub 2010 Aug 17. Metabolism. 2011. PMID: 20723948 Free PMC article.

6

Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60.

Fajans SS, Bell GI, Paz VP, Below JE, Cox NJ, Martin C, Thomas IH, Chen M. Fajans SS, et al. Transl Res. 2010 Jul;156(1):7-14. doi: 10.1016/j.trsl.2010.03.003. Epub 2010 Apr 23. Transl Res. 2010. PMID: 20621032 Free PMC article.

7

Hemoglobin A1c for the diagnosis of diabetes: practical considerations.

Herman WH, Fajans SS. Herman WH, et al. Among authors: fajans ss. Pol Arch Med Wewn. 2010;120(1-2):37-40. Pol Arch Med Wewn. 2010. PMID: 20150843 Free article. Review.

8

Neonatal diabetes mellitus with pancreatic agenesis in an infant with homozygous IPF-1 Pro63fsX60 mutation.

Thomas IH, Saini NK, Adhikari A, Lee JM, Kasa-Vubu JZ, Vazquez DM, Menon RK, Chen M, Fajans SS. Thomas IH, et al. Among authors: fajans ss. Pediatr Diabetes. 2009 Nov;10(7):492-6. doi: 10.1111/j.1399-5448.2009.00526.x. Epub 2009 Jun 3. Pediatr Diabetes. 2009. PMID: 19496967 Free PMC article.

9

Macrosomia and neonatal hypoglycaemia in RW pedigree subjects with a mutation (Q268X) in the gene encoding hepatocyte nuclear factor 4alpha (HNF4A).

Fajans SS, Bell GI. Fajans SS, et al. Diabetologia. 2007 Dec;50(12):2600-1. doi: 10.1007/s00125-007-0833-7. Epub 2007 Sep 22. Diabetologia. 2007. PMID: 17891372 No abstract available.

10

Phenotypic heterogeneity between different mutations of MODY subtypes and within MODY pedigrees.

Fajans SS, Bell GI. Fajans SS, et al. Diabetologia. 2006 May;49(5):1106-8. doi: 10.1007/s00125-006-0158-y. Epub 2006 Feb 25. Diabetologia. 2006. PMID: 16502298 Free article. No abstract available.

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