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Minerva Pediatrica|March 1, 1997
[Ectopic neuroglial tissue associated with intrapulmonary congenital cystic adenomatoid malformation]T Rizzuti, S Ferrarese, G Varesi, et al.Pathologica|October 20, 2011
Autoptic and echocardiographic findings in seven foetuses with congenital heart anomalies, lung lobation defects and normal visceroatrial arrangementF Angiero, V Fesslova, T Rizzuti, et al.Prenatal Diagnosis|September 22, 1998
Prenatal diagnosis of genetic syndromes may be facilitated by serendipitous findings at fetal blood samplingF Lalatta, S Salmona, R Fogliani, et al.Prenatal Diagnosis|October 1, 1993
Prenatal diagnosis of anatomical connections in conjoined twins by use of contrast magnetic resonance imagingC Zoppini, A Vanzulli, A Kustermann, et al.The Journal of Comparative Neurology|July 9, 1999
Development of layer I of the human cerebral cortex after midgestation: architectonic findings, immunocytochemical identification of neurons and glia, and in situ labeling of apoptotic cellsR Spreafico, P Arcelli, C Frassoni, et al.Clinical Dysmorphology|September 15, 2004
Nasopharyngeal teratoma and diaphragmatic hernia: a non random association?F Natacci, M Moschetta, M F Bedeschi, et al.Journal of Inherited Metabolic Disease|January 27, 2005
Severe neonatal onset of glycogenosis type IV: clinical and laboratory findings leading to diagnosis in two siblingsB Giuffrè, R Parini, T Rizzuti, et al.Minerva Pediatrica|June 26, 2012
Atypical onset and course in a child with fulminant myocarditisA Rocchi, M Mazzoni, G Bertolozzi, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 3, 2010
Phenotype of five cases of prenatally diagnosed campomelic dysplasia harboring novel mutations of the SOX9 geneB Gentilin, F Forzano, M F Bedeschi, et al.Pageof 1