Publications

2017

Zouboulis CC, Theodoridis A, Brunner M, Magro CM. Benign atrophic papulosis (Köhlmeier-Degos disease): the wedge-shaped dermal necrosis can resolve with time. J Eur Acad Dermatol Venereol. 2017;31(10):1753-1756.
Yanagida K, Liu CH, Faraco G, Galvani S, Smith HK, Burg N, et al. Size-selective opening of the blood-brain barrier by targeting endothelial sphingosine 1-phosphate receptor 1. Proc Natl Acad Sci U S A. 2017;114(17):4531-4536.
DeSimone RA, Schwartz J, Schneiderman J. Extracorporeal photopheresis in pediatric patients: Practical and technical considerations. J Clin Apher. 2017;32(6):543-552.
Greenblatt MB, Tsai JN, Wein MN. Bone Turnover Markers in the Diagnosis and Monitoring of Metabolic Bone Disease. Clin Chem. 2017;63(2):464-474.
Gratzinger D, Jaffe ES, Chadburn A, Chan JK, de Jong D, Goodlad JR, et al. Primary/Congenital Immunodeficiency: 2015 SH/EAHP Workshop Report-Part 5. Am J Clin Pathol. 2017;147(2):204-216.
Goel R, Snow J, Pri-Paz SM, Cushing M, Vasovic LV. Intrauterine transfusions for severe fetal anemia and hydrops due to de novo εγδβ-thalassemia. Transfusion. 2017;57(4):876.
Marchionni L, Netto GJ, Hoque MO, Argani P. MicroRNAs, promising biomarkers in the diagnosis of Xp11 translocation RCC-reply. Hum Pathol. 2017;68:206-207.
Yantiss RK, Cui I, Panarelli NC, Jessurun J. Idiopathic Myointimal Hyperplasia of Mesenteric Veins: An Uncommon Cause of Ischemic Colitis With Distinct Mucosal Features. Am J Surg Pathol. 2017;41(12):1657-1665.
Hung PJ, Chen B-, George R, Liberman C, Morales AJ, Colon-Ortiz P, et al. Deficiency of XLF and PAXX prevents DNA double-strand break repair by non-homologous end joining in lymphocytes. Cell Cycle. 2017;16(3):286-295.

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