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Eugenio Taboada

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The American Journal of Forensic Medicine and Pathology|April 23, 2011
Large multifocal cardiac myxoma causing the sudden unexpected death of a 2-month-old infant--a rapidly growing, acquired lesion versus a congenital process?: a case reportKiyoe Kure, Daniel Lingamfelter, Eugenio Taboada
American Journal of Perinatology|October 3, 2002
Fetal hydrops and familial pulmonary lymphatic hypoplasiaDonald W Thibeault, Philip Black, Eugenio Taboada
American Journal of Medical Genetics. Part A|March 3, 2004
Eye abnormalities in Fryns syndromeDiane M Pierson, Eugenio Taboada, Merlin G Butler
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 11, 2002
Newborn with anophthalmia and features of Fryns syndromeDiane M Pierson, Antonio Subtil, Eugenio Taboada, et al.
Biomed Research International|February 15, 2014
Altered pulmonary lymphatic development in infants with chronic lung diseaseEmily M McNellis, Sherry M Mabry, Eugenio Taboada, et al.
Molecular & Cellular Oncology|June 16, 2017
YAP and the Hippo pathway in pediatric cancerAtif A Ahmed, Abdalla D Mohamed, Melissa Gener, et al.
American Journal of Medical Genetics. Part A|December 24, 2017
Arthrogryposis and pterygia as lethal end manifestations of genetically defined congenital myopathiesAtif A Ahmed, Priya Skaria, Nicole P Safina, et al.
Neuroscience Letters|February 25, 2006
Altered expression of pro-inflammatory and developmental genes in the fetal brain in a mouse model of maternal infectionChristopher S Liverman, Harold A Kaftan, Lisa Cui, et al.
Journal of Pediatric Hematology/Oncology|April 12, 2019
Neuroblastoma in Adolescents and Children Older than 10 Years: Unusual Clinicopathologic and Biologic FeaturesLaura C McCarthy, Katherine Chastain, Terrie G Flatt, et al.
Pathology, Research and Practice|August 28, 2019
Clinical and molecular characterization of novel deletions causing epsilon gamma delta beta thalassemia: Report of two casesElena Repnikova, Jennifer Roberts, Sarah Mc Dermott, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
The American Journal of Forensic Medicine and Pathology|April 23, 2011
Large multifocal cardiac myxoma causing the sudden unexpected death of a 2-month-old infant--a rapidly growing, acquired lesion versus a congenital process?: a case reportKiyoe Kure, Daniel Lingamfelter, Eugenio Taboada
American Journal of Perinatology|October 3, 2002
Fetal hydrops and familial pulmonary lymphatic hypoplasiaDonald W Thibeault, Philip Black, Eugenio Taboada
American Journal of Medical Genetics. Part A|March 3, 2004
Eye abnormalities in Fryns syndromeDiane M Pierson, Eugenio Taboada, Merlin G Butler
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 11, 2002
Newborn with anophthalmia and features of Fryns syndromeDiane M Pierson, Antonio Subtil, Eugenio Taboada, et al.
Biomed Research International|February 15, 2014
Altered pulmonary lymphatic development in infants with chronic lung diseaseEmily M McNellis, Sherry M Mabry, Eugenio Taboada, et al.
Molecular & Cellular Oncology|June 16, 2017
YAP and the Hippo pathway in pediatric cancerAtif A Ahmed, Abdalla D Mohamed, Melissa Gener, et al.
American Journal of Medical Genetics. Part A|December 24, 2017
Arthrogryposis and pterygia as lethal end manifestations of genetically defined congenital myopathiesAtif A Ahmed, Priya Skaria, Nicole P Safina, et al.
Neuroscience Letters|February 25, 2006
Altered expression of pro-inflammatory and developmental genes in the fetal brain in a mouse model of maternal infectionChristopher S Liverman, Harold A Kaftan, Lisa Cui, et al.
Journal of Pediatric Hematology/Oncology|April 12, 2019
Neuroblastoma in Adolescents and Children Older than 10 Years: Unusual Clinicopathologic and Biologic FeaturesLaura C McCarthy, Katherine Chastain, Terrie G Flatt, et al.
Pathology, Research and Practice|August 28, 2019
Clinical and molecular characterization of novel deletions causing epsilon gamma delta beta thalassemia: Report of two casesElena Repnikova, Jennifer Roberts, Sarah Mc Dermott, et al.
Pageof 2