Schmidt LS - Search Results

1

A diagnosis of Birt-Hogg-Dubé syndrome in individuals with Smith-Magenis syndrome: Recommendation for cancer screening.

Vocke CD, Fleming LR, Piskorski AM, Amin A, Phornphutkul C, de la Monte S, Vilboux T, Duncan F, Pellegrino J, Braddock B, Middelton LA, Schmidt LS, Merino MJ, Cowen EW, Introne WJ, Linehan WM, Smith ACM. Vocke CD, et al. Among authors: schmidt ls. Am J Med Genet A. 2023 Feb;191(2):490-497. doi: 10.1002/ajmg.a.63049. Epub 2022 Dec 13. Am J Med Genet A. 2023. PMID: 36513625 Free PMC article.

2

Molecular and genetic characterization and physical mapping of 11 new markers detecting multiallele restriction fragment length polymorphisms on the short arm of human chromosome 3.

Latif F, Modi WS, Duh FM, Schmidt L, Li H, Geil L, Orcutt ML, Heppell-Parton A, Rabbitts PH, Linehan WM, et al. Latif F, et al. Hum Genet. 1992 Sep-Oct;90(1-2):17-22. doi: 10.1007/BF00210739. Hum Genet. 1992. PMID: 1358787

3

A microsatellite, D8S602, adjacent to the MSR gene.

Schmidt L, Pozzatti R, Li H, Wei MH, Vocke C, Linehan WM, Tory K. Schmidt L, et al. Hum Mol Genet. 1994 Apr;3(4):679. doi: 10.1093/hmg/3.4.679. Hum Mol Genet. 1994. PMID: 8069323 No abstract available.

4

Hereditary papillary renal cell carcinoma.

Zbar B, Tory K, Merino M, Schmidt L, Glenn G, Choyke P, Walther MM, Lerman M, Linehan WM. Zbar B, et al. J Urol. 1994 Mar;151(3):561-6. doi: 10.1016/s0022-5347(17)35015-2. J Urol. 1994. PMID: 8308957 Review.

5

Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomas.

Zhuang Z, Park WS, Pack S, Schmidt L, Vortmeyer AO, Pak E, Pham T, Weil RJ, Candidus S, Lubensky IA, Linehan WM, Zbar B, Weirich G. Zhuang Z, et al. Nat Genet. 1998 Sep;20(1):66-9. doi: 10.1038/1727. Nat Genet. 1998. PMID: 9731534

6

Novel mutations of the MET proto-oncogene in papillary renal carcinomas.

Schmidt L, Junker K, Nakaigawa N, Kinjerski T, Weirich G, Miller M, Lubensky I, Neumann HP, Brauch H, Decker J, Vocke C, Brown JA, Jenkins R, Richard S, Bergerheim U, Gerrard B, Dean M, Linehan WM, Zbar B. Schmidt L, et al. Oncogene. 1999 Apr 8;18(14):2343-50. doi: 10.1038/sj.onc.1202547. Oncogene. 1999. PMID: 10327054

7

Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype.

Lubensky IA, Schmidt L, Zhuang Z, Weirich G, Pack S, Zambrano N, Walther MM, Choyke P, Linehan WM, Zbar B. Lubensky IA, et al. Am J Pathol. 1999 Aug;155(2):517-26. doi: 10.1016/S0002-9440(10)65147-4. Am J Pathol. 1999. PMID: 10433944 Free PMC article.

8

Hereditary papillary renal carcinoma: pathology and pathogenesis.

Schmidt L, Lubensky I, Linehan WM, Zbar B. Schmidt L, et al. Contrib Nephrol. 1999;128:11-27. doi: 10.1159/000059982. Contrib Nephrol. 1999. PMID: 10597374 Review. No abstract available.

9

Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2.

Schmidt LS, Warren MB, Nickerson ML, Weirich G, Matrosova V, Toro JR, Turner ML, Duray P, Merino M, Hewitt S, Pavlovich CP, Glenn G, Greenberg CR, Linehan WM, Zbar B. Schmidt LS, et al. Am J Hum Genet. 2001 Oct;69(4):876-82. doi: 10.1086/323744. Epub 2001 Aug 30. Am J Hum Genet. 2001. PMID: 11533913 Free PMC article.

10

Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dubé syndrome.

Zbar B, Alvord WG, Glenn G, Turner M, Pavlovich CP, Schmidt L, Walther M, Choyke P, Weirich G, Hewitt SM, Duray P, Gabril F, Greenberg C, Merino MJ, Toro J, Linehan WM. Zbar B, et al. Cancer Epidemiol Biomarkers Prev. 2002 Apr;11(4):393-400. Cancer Epidemiol Biomarkers Prev. 2002. PMID: 11927500

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