Showing results (791-800 of 1,238) with videos related to

Sort By:
Pageof 124
Fetal and Pediatric Pathology|February 17, 2016
Refining the Diagnosis of Congenital Nephrotic Syndrome on Long-term Stored Tissue: c.1097G>A (p.(Arg366His)) WT1 Mutation Causing Denys Drash SyndromeLisa Maria Hillen, Erik Jan Kamsteeg, Jeroen Schoots, et al.
Fetal and Pediatric Pathology|March 5, 2016
Retrospective Evaluation of Children with Congenital Pulmonary Airway Malformation: A Single Center Experience of 20 YearsRagip Ortac, Gulden Diniz, Hulya Tosun Yildirim, et al.
Fetal and Pediatric Pathology|December 17, 2013
Unsuspected Langerhans cell histiocytosis can be easily missed in a colonic biopsyBadr Abdullgaffar, Buthaina Al-Murbati, Mouza Al-Falasi, et al.
Fetal and Pediatric Pathology|August 26, 2014
Difficulties in the hemodynamic assessment of the newborn with prenatally treated congenital diaphragmatic herniaIwona Maroszyńska, Marta Niedźwiecka, Katarzyna Fortecka-Piestrzeniewicz, et al.
Fetal and Pediatric Pathology|June 17, 2016
The First 5-Year-Long Survey on Intrauterine Unexplained Sudden Deaths from the Northeast ItalyLuca Roncati, Teresa Pusiol, Francesco Piscioli, et al.
Fetal and Pediatric Pathology|June 17, 2016
Tetrasomy 18p in a Twin Pregnancy with Diverse Expression in Both FetusesCihan Inan, N Cenk Sayın, Emine Atlı, et al.
Fetal and Pediatric Pathology|May 26, 2016
MicroRNA-197 Mediates the Overgrowth and Anti-Apoptotic Effects by Downregulating Insulin-Like Growth Factor-Binding Protein-3 During Nephroblastoma TumorigenesisJinhua Hu, Guochang Liu, Zhang Zhao, et al.
Fetal and Pediatric Pathology|May 10, 2016
Prenatally Diagnosed Aggressive Intracranial Immature Teratoma-Clinicopathological CorrelationHiroki Nariai, Dana E Price, Ajit Jada, et al.
Fetal and Pediatric Pathology|May 10, 2016
Human Placental Histopathology in Preterm Stillbirth: One Center's ExperienceÖzgül Salihoğlu, Keziban Doğan, Nurten Sever, et al.
Fetal and Pediatric Pathology|December 6, 2017
Prenatal Diagnosis of Twin Fetuses with a Novel AR Gene Mutation in a Chinese Family of Complete Androgen Insensitivity SyndromeWeiqing Wu, Qian Geng, Yang Liu, et al.
Pageof 124