Lindor NM - Search Results

1

The spectrum, management and clinical outcome of Ehlers-Danlos syndrome type IV: a 30-year experience.

Oderich GS, Panneton JM, Bower TC, Lindor NM, Cherry KJ, Noel AA, Kalra M, Sullivan T, Gloviczki P. Oderich GS, et al. Among authors: lindor nm. J Vasc Surg. 2005 Jul;42(1):98-106. doi: 10.1016/j.jvs.2005.03.053. J Vasc Surg. 2005. PMID: 16012458 Free article.

2

Tenascin-X deficiency in autosomal recessive Ehlers-Danlos syndrome.

Lindor NM, Bristow J. Lindor NM, et al. Am J Med Genet A. 2005 May 15;135(1):75-80. doi: 10.1002/ajmg.a.30671. Am J Med Genet A. 2005. PMID: 15793839

3

Increased risk for cancer in patients with the Peutz-Jeghers syndrome.

Boardman LA, Thibodeau SN, Schaid DJ, Lindor NM, McDonnell SK, Burgart LJ, Ahlquist DA, Podratz KC, Pittelkow M, Hartmann LC. Boardman LA, et al. Among authors: lindor nm. Ann Intern Med. 1998 Jun 1;128(11):896-9. doi: 10.7326/0003-4819-128-11-199806010-00004. Ann Intern Med. 1998. PMID: 9634427

4

Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome.

Lindor NM, Furuichi Y, Kitao S, Shimamoto A, Arndt C, Jalal S. Lindor NM, et al. Am J Med Genet. 2000 Jan 31;90(3):223-8. doi: 10.1002/(sici)1096-8628(20000131)90:3<223::aid-ajmg7>3.0.co;2-z. Am J Med Genet. 2000. PMID: 10678659

5

Germline TGF-beta receptor mutations and skeletal fragility: a report on two patients with Loeys-Dietz syndrome.

Kirmani S, Tebben PJ, Lteif AN, Gordon D, Clarke BL, Hefferan TE, Yaszemski MJ, McGrann PS, Lindor NM, Ellison JW. Kirmani S, et al. Among authors: lindor nm. Am J Med Genet A. 2010 Apr;152A(4):1016-9. doi: 10.1002/ajmg.a.33356. Am J Med Genet A. 2010. PMID: 20358619

6

Visual impairment due to macular disciform scars in a 20-year-old man with Smith-Magenis syndrome: another ophthalmologic complication.

Babovic-Vuksanovic D, Jalal SM, Garrity JA, Robertson DM, Lindor NM. Babovic-Vuksanovic D, et al. Among authors: lindor nm. Am J Med Genet. 1998 Dec 4;80(4):373-6. doi: 10.1002/(sici)1096-8628(19981204)80:4<373::aid-ajmg13>3.0.co;2-m. Am J Med Genet. 1998. PMID: 9856566

7

Germline E-cadherin gene mutations: is prophylactic total gastrectomy indicated?

Chun YS, Lindor NM, Smyrk TC, Petersen BT, Burgart LJ, Guilford PJ, Donohue JH. Chun YS, et al. Among authors: lindor nm. Cancer. 2001 Jul 1;92(1):181-7. doi: 10.1002/1097-0142(20010701)92:1<181::aid-cncr1307>3.0.co;2-j. Cancer. 2001. PMID: 11443625 Review.

8

Desmoid tumors in familial adenomatous polyposis: a pilot project evaluating efficacy of treatment with pirfenidone.

Lindor NM, Dozois R, Nelson H, Wolff B, King J, Boardman L, Wilson M, Greene MH, Karnes W, Mesa R, Welch T, Edmonson J, Limburg P. Lindor NM, et al. Am J Gastroenterol. 2003 Aug;98(8):1868-74. doi: 10.1111/j.1572-0241.2003.07479.x. Am J Gastroenterol. 2003. PMID: 12907346

9

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.

Ensenauer RE, Adeyinka A, Flynn HC, Michels VV, Lindor NM, Dawson DB, Thorland EC, Lorentz CP, Goldstein JL, McDonald MT, Smith WE, Simon-Fayard E, Alexander AA, Kulharya AS, Ketterling RP, Clark RD, Jalal SM. Ensenauer RE, et al. Among authors: lindor nm. Am J Hum Genet. 2003 Nov;73(5):1027-40. doi: 10.1086/378818. Epub 2003 Oct 2. Am J Hum Genet. 2003. PMID: 14526392 Free PMC article.

10

Selective antibody immune deficiency in a patient with Smith-Lemli-Opitz syndrome.

Babovic-Vuksanovic D, Jacobson RM, Lindor NM, Weiler CR. Babovic-Vuksanovic D, et al. Among authors: lindor nm. J Inherit Metab Dis. 2005;28(2):181-6. doi: 10.1007/s10545-005-5515-3. J Inherit Metab Dis. 2005. PMID: 15877207

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