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344 results
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von Hippel-Lindau disease.
Couch V, Lindor NM, Karnes PS, Michels VV. Couch V, et al. Among authors: lindor nm. Mayo Clin Proc. 2000 Mar;75(3):265-72. doi: 10.4065/75.3.265. Mayo Clin Proc. 2000. PMID: 10725953 Review.
A genetic review of complete and partial hydatidiform moles and nonmolar triploidy.
Lindor NM, Ney JA, Gaffey TA, Jenkins RB, Thibodeau SN, Dewald GW. Lindor NM, et al. Mayo Clin Proc. 1992 Aug;67(8):791-9. doi: 10.1016/s0025-6196(12)60805-2. Mayo Clin Proc. 1992. PMID: 1434919 Review.
Initial assessment of infants and children with suspected inborn errors of metabolism.
Lindor NM, Karnes PS. Lindor NM, et al. Mayo Clin Proc. 1995 Oct;70(10):987-8. doi: 10.4065/70.10.987. Mayo Clin Proc. 1995. PMID: 7564553 No abstract available.
Asplenia in two father-son pairs.
Lindor NM, Smithson WA, Ahumada CA, Michels VV, Opitz JM. Lindor NM, et al. Am J Med Genet. 1995 Mar 13;56(1):10-1. doi: 10.1002/ajmg.1320560104. Am J Med Genet. 1995. PMID: 7747770 Review.
Mutations in the RET protooncogene in sporadic pheochromocytomas.
Lindor NM, Honchel R, Khosla S, Thibodeau SN. Lindor NM, et al. J Clin Endocrinol Metab. 1995 Feb;80(2):627-9. doi: 10.1210/jcem.80.2.7852530. J Clin Endocrinol Metab. 1995. PMID: 7852530
Genetic testing in the diagnosis and management of multiple endocrine neoplasia type II.
Ledger GA, Khosla S, Lindor NM, Thibodeau SN, Gharib H. Ledger GA, et al. Among authors: lindor nm. Ann Intern Med. 1995 Jan 15;122(2):118-24. doi: 10.7326/0003-4819-122-2-199501150-00008. Ann Intern Med. 1995. PMID: 7992986 Review.
A new syndrome of Crohn's disease and pachydermoperiostosis in a family.
Compton RF, Sandborn WJ, Yang H, Lindor NM, Tremaine WJ, Davis MD, Khalil AA, Tountas NA, Tyan DB, Landers CJ, Taylor KD, Viggiano TR, Matteson EL, Schroeter AL, Plevy SE, Cominelli F, Targan SR, Rotter JI. Compton RF, et al. Among authors: lindor nm. Gastroenterology. 1997 Jan;112(1):241-9. doi: 10.1016/s0016-5085(97)70241-5. Gastroenterology. 1997. PMID: 8978365
Genetic testing in medullary thyroid carcinoma syndromes: mutation types and clinical significance.
Heshmati HM, Gharib H, Khosla S, Abu-Lebdeh HS, Lindor NM, Thibodeau SN. Heshmati HM, et al. Among authors: lindor nm. Mayo Clin Proc. 1997 May;72(5):430-6. doi: 10.4065/72.5.430. Mayo Clin Proc. 1997. PMID: 9146685
Mitomycin C chromosome stress test to identify hypersensitivity to bifunctional alkylating agents in patients with Fanconi anemia or aplastic anemia.
Kuffel DG, Lindor NM, Litzow MR, Zinsmeister AR, Dewald GW. Kuffel DG, et al. Among authors: lindor nm. Mayo Clin Proc. 1997 Jun;72(6):579-80. doi: 10.4065/72.6.579. Mayo Clin Proc. 1997. PMID: 9179145 No abstract available.
A new autosomal dominant disorder of pyogenic sterile arthritis, pyoderma gangrenosum, and acne: PAPA syndrome.
Lindor NM, Arsenault TM, Solomon H, Seidman CE, McEvoy MT. Lindor NM, et al. Mayo Clin Proc. 1997 Jul;72(7):611-5. doi: 10.1016/S0025-6196(11)63565-9. Mayo Clin Proc. 1997. PMID: 9212761
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