Gorin MB - Search Results

1

Ophthalmologic manifestations of type B Niemann-Pick diseases.

Filling-Katz MR, Fink JK, Gorin MB, Caruso R, Carl JB, Fitzgibbon EJ, Barton NW, Katz NN. Filling-Katz MR, et al. Among authors: gorin mb. Metab Pediatr Syst Ophthalmol (1985). 1992;15(1-3):16-20. Metab Pediatr Syst Ophthalmol (1985). 1992. PMID: 1484498

2

von Hippel-Lindau disease: radiologic screening for visceral manifestations.

Choyke PL, Filling-Katz MR, Shawker TH, Gorin MB, Travis WD, Chang R, Seizinger BR, Dwyer AJ, Linehan WM. Choyke PL, et al. Among authors: gorin mb. Radiology. 1990 Mar;174(3 Pt 1):815-20. doi: 10.1148/radiology.174.3.2305064. Radiology. 1990. PMID: 2305064

3

Radiologic screening for von Hippel-Lindau disease: the role of Gd-DTPA enhanced MR imaging of the CNS.

Filling-Katz MR, Choyke PL, Patronas NJ, Gorin MB, Barba D, Chang R, Doppman JL, Seizinger B, Oldfield EH. Filling-Katz MR, et al. Among authors: gorin mb. J Comput Assist Tomogr. 1989 Sep-Oct;13(5):743-55. doi: 10.1097/00004728-198909000-00001. J Comput Assist Tomogr. 1989. PMID: 2778131

4

Central nervous system involvement in Von Hippel-Lindau disease.

Filling-Katz MR, Choyke PL, Oldfield E, Charnas L, Patronas NJ, Glenn GM, Gorin MB, Morgan JK, Linehan WM, Seizinger BR, et al. Filling-Katz MR, et al. Among authors: gorin mb. Neurology. 1991 Jan;41(1):41-6. doi: 10.1212/wnl.41.1.41. Neurology. 1991. PMID: 1985294

5

Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration.

Stefko ST, Zhang K, Gorin MB, Traboulsi EI. Stefko ST, et al. Among authors: gorin mb. Am J Ophthalmol. 2000 Aug;130(2):203-8. doi: 10.1016/s0002-9394(00)00562-6. Am J Ophthalmol. 2000. PMID: 11004295

6

Tamoxifen-associated eye disease. A review.

Nayfield SG, Gorin MB. Nayfield SG, et al. Among authors: gorin mb. J Clin Oncol. 1996 Mar;14(3):1018-26. doi: 10.1200/JCO.1996.14.3.1018. J Clin Oncol. 1996. PMID: 8622006 Review.

7

Screening for von Hippel-Lindau disease by DNA polymorphism analysis.

Glenn GM, Linehan WM, Hosoe S, Latif F, Yao M, Choyke P, Gorin MB, Chew E, Olfield E, Manolatos C, et al. Glenn GM, et al. Among authors: gorin mb. JAMA. 1992 Mar 4;267(9):1226-31. JAMA. 1992. PMID: 1347089 Free article.

8

Localization of the von Hippel-Lindau disease gene to a small region of chromosome 3.

Hosoe S, Brauch H, Latif F, Glenn G, Daniel L, Bale S, Choyke P, Gorin M, Oldfield E, Berman A, et al. Hosoe S, et al. Genomics. 1990 Dec;8(4):634-40. doi: 10.1016/0888-7543(90)90249-t. Genomics. 1990. PMID: 2276737

9

Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locus.

Glenn GM, Daniel LN, Choyke P, Linehan WM, Oldfield E, Gorin MB, Hosoe S, Latif F, Weiss G, Walther M, et al. Glenn GM, et al. Among authors: gorin mb. Hum Genet. 1991 Jun;87(2):207-10. doi: 10.1007/BF00204184. Hum Genet. 1991. PMID: 2066108

10

VON HIPPEL-LINDAU DISEASE: Update on Pathogenesis and Systemic Aspects.

Aronow ME, Wiley HE, Gaudric A, Krivosic V, Gorin MB, Shields CL, Shields JA, Jonasch EW, Singh AD, Chew EY. Aronow ME, et al. Among authors: gorin mb. Retina. 2019 Dec;39(12):2243-2253. doi: 10.1097/IAE.0000000000002555. Retina. 2019. PMID: 31095066 Review.

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