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International Journal of Pediatric Otorhinolaryngology
|
August 30, 2005
Otolaryngological manifestations of posttransplant lymphoproliferative disorder in pediatric thoracic transplant patients
Brian W Herrmann, Stuart C Sweet, Robert J Hayashi, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
May 24, 2005
Sialidosis presenting as severe nonimmune fetal hydrops is associated with two novel mutations in lysosomal alpha-neuraminidase
David J Loren, Yvan Campos, Alessandra d'Azzo, et al.
American Journal of Respiratory Cell and Molecular Biology
|
July 22, 2020
Functional Genomics of <i>ABCA3</i> Variants
Jennifer A Wambach, Ping Yang, Daniel J Wegner, et al.
Pediatric Research
|
April 28, 2006
Surfactant composition and function in patients with ABCA3 mutations
Tami H Garmany, Michael A Moxley, Frances V White, et al.
Journal of Pediatric Surgery
|
June 21, 2011
Bacterial DNA content in the intestinal wall from infants with necrotizing enterocolitis
Brian T Bucher, Lucas A McDuffie, Nurmohammad Shaikh, et al.
Inflammatory Bowel Diseases
|
October 13, 2007
Granulocyte macrophage colony-stimulating factor ameliorates DSS-induced experimental colitis
Satheesh K Sainathan, Eyad M Hanna, Qingqing Gong, et al.
Human Mutation
|
March 21, 2020
Functional characterization of four ATP-binding cassette transporter A3 gene (ABCA3) variants
June Y Hu, Ping Yang, Daniel J Wegner, et al.
American Journal of Medical Genetics. Part A
|
May 21, 2014
Two deletions overlapping a distant FOXF1 enhancer unravel the role of lncRNA LINC01081 in etiology of alveolar capillary dysplasia with misalignment of pulmonary veins
Przemyslaw Szafranski, Avinash V Dharmadhikari, Jennifer A Wambach, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology
|
June 16, 2021
The common ABCA3<sup>E292V</sup> variant disrupts AT2 cell quality control and increases susceptibility to lung injury and aberrant remodeling
Yaniv Tomer, Jennifer Wambach, Lars Knudsen, et al.
American Journal of Medical Genetics. Part A
|
February 22, 2020
Phenotypic expansion of KMT2D-related disorder: Beyond Kabuki syndrome
Dustin Baldridge, Rebecca C Spillmann, Daniel J Wegner, et al.
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of 5
Search research articles
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Showing results (21-30 of 43) with videos related to
Sort By:
Page
of 5
International Journal of Pediatric Otorhinolaryngology
|
August 30, 2005
Otolaryngological manifestations of posttransplant lymphoproliferative disorder in pediatric thoracic transplant patients
Brian W Herrmann, Stuart C Sweet, Robert J Hayashi, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
May 24, 2005
Sialidosis presenting as severe nonimmune fetal hydrops is associated with two novel mutations in lysosomal alpha-neuraminidase
David J Loren, Yvan Campos, Alessandra d'Azzo, et al.
American Journal of Respiratory Cell and Molecular Biology
|
July 22, 2020
Functional Genomics of <i>ABCA3</i> Variants
Jennifer A Wambach, Ping Yang, Daniel J Wegner, et al.
Pediatric Research
|
April 28, 2006
Surfactant composition and function in patients with ABCA3 mutations
Tami H Garmany, Michael A Moxley, Frances V White, et al.
Journal of Pediatric Surgery
|
June 21, 2011
Bacterial DNA content in the intestinal wall from infants with necrotizing enterocolitis
Brian T Bucher, Lucas A McDuffie, Nurmohammad Shaikh, et al.
Inflammatory Bowel Diseases
|
October 13, 2007
Granulocyte macrophage colony-stimulating factor ameliorates DSS-induced experimental colitis
Satheesh K Sainathan, Eyad M Hanna, Qingqing Gong, et al.
Human Mutation
|
March 21, 2020
Functional characterization of four ATP-binding cassette transporter A3 gene (ABCA3) variants
June Y Hu, Ping Yang, Daniel J Wegner, et al.
American Journal of Medical Genetics. Part A
|
May 21, 2014
Two deletions overlapping a distant FOXF1 enhancer unravel the role of lncRNA LINC01081 in etiology of alveolar capillary dysplasia with misalignment of pulmonary veins
Przemyslaw Szafranski, Avinash V Dharmadhikari, Jennifer A Wambach, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology
|
June 16, 2021
The common ABCA3<sup>E292V</sup> variant disrupts AT2 cell quality control and increases susceptibility to lung injury and aberrant remodeling
Yaniv Tomer, Jennifer Wambach, Lars Knudsen, et al.
American Journal of Medical Genetics. Part A
|
February 22, 2020
Phenotypic expansion of KMT2D-related disorder: Beyond Kabuki syndrome
Dustin Baldridge, Rebecca C Spillmann, Daniel J Wegner, et al.
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of 5