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Tumor detection rates in screening of individuals with SDHx-related hereditary paraganglioma-pheochromocytoma syndrome.
Greenberg SE, Jacobs MF, Wachtel H, Anson A, Buchmann L, Cohen DL, Bonanni M, Bennett B, Naumer A, Schaefer AM, Kohlmann W, Nathanson KL, Else T, Fishbein L. Greenberg SE, et al. Among authors: nathanson kl. Genet Med. 2020 Dec;22(12):2101-2107. doi: 10.1038/s41436-020-0921-3. Epub 2020 Aug 3. Genet Med. 2020. PMID: 32741965 Free PMC article.
Pheochromocytoma: the expanding genetic differential diagnosis.
Bryant J, Farmer J, Kessler LJ, Townsend RR, Nathanson KL. Bryant J, et al. Among authors: nathanson kl. J Natl Cancer Inst. 2003 Aug 20;95(16):1196-204. doi: 10.1093/jnci/djg024. J Natl Cancer Inst. 2003. PMID: 12928344 Review.
Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer.
Maxwell KN, Wubbenhorst B, D'Andrea K, Garman B, Long JM, Powers J, Rathbun K, Stopfer JE, Zhu J, Bradbury AR, Simon MS, DeMichele A, Domchek SM, Nathanson KL. Maxwell KN, et al. Among authors: nathanson kl. Genet Med. 2015 Aug;17(8):630-8. doi: 10.1038/gim.2014.176. Epub 2014 Dec 11. Genet Med. 2015. PMID: 25503501 Free PMC article.
Muscle oxidative phosphorylation quantitation using creatine chemical exchange saturation transfer (CrCEST) MRI in mitochondrial disorders.
DeBrosse C, Nanga RPR, Wilson N, D'Aquilla K, Elliott M, Hariharan H, Yan F, Wade K, Nguyen S, Worsley D, Parris-Skeete C, McCormick E, Xiao R, Cunningham ZZ, Fishbein L, Nathanson KL, Lynch DR, Stallings VA, Yudkoff M, Falk MJ, Reddy R, McCormack SE. DeBrosse C, et al. Among authors: nathanson kl. JCI Insight. 2016 Nov 3;1(18):e88207. doi: 10.1172/jci.insight.88207. JCI Insight. 2016. PMID: 27812541 Free PMC article.
386 results