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51. Patterns and Predictors of Metastatic Spread to the Neck in Pediatric Thyroid Carcinoma.

63. Hereditary Mucin Deficiency Caused by Biallelic Loss-of-Function of MUC5B Defines a Novel Category of Lung Disease

72. Dieulafoy lesions and PHACE syndrome

81. Atypical Hepatic Mesenchymal Hamartoma: Histologic Appearance, Immunophenotype, and Molecular Findings.

82. NUT midline carcinoma of the larynx: an international series and review of the literature

87. The effects of STAT1 dysfunction on the gut

89. Epididymal melanotic neuroectodermal tumor of infancy: A rare cause of scrotal mass in an infant.

90. Posttransplant lymphoproliferative disorder in pediatric patients: Survival rates according to primary sites of occurrence and a proposed clinical categorization

91. Pediatric thyroid nodules: ultrasonographic characteristics and inter-observer variability in prediction of malignancy

92. The effects of STAT1 dysfunction on the gut

94. A case of pancreatitis, panniculitis and polyarthritis syndrome: Elucidating the pathophysiologic mechanisms of a rare condition

96. Mutations in tetratricopeptide repeat domain 7A (TTC7A) are associated with combined immunodeficiency with dendriform lung ossification but no intestinal atresia

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