Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Amanda Moody"'
Publikováno v:
Studying Teacher Education. 18:40-60
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9203b7c930f6c00b0643c02b286c3b90
https://doi.org/10.1080/17425964.2021.1969227
https://doi.org/10.1080/17425964.2021.1969227
Autor:
Amanda Moody, Hee W Foo, Elizabeth G Bannister, Zornitza Stark, Natasha J Brown, Christopher M. Richmond, Anthea Greenway, Sebastian Lunke, Sally Campbell
Publikováno v:
Molecular Syndromology. 11:50-55
Heterozygous pathogenic variants in SPTB cause autosomal dominant hereditary spherocytosis, an important cause of neonatal nonimmune hemolytic anemia. Biallelic mutations are rarely reported, all with severe neonatal presentation. We describe rapid (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d66cf0f834d84050b0765ce121073ce
https://doi.org/10.1159/000505886
https://doi.org/10.1159/000505886
Autor:
Amanda Moody Maestranzi
Publikováno v:
Proceedings of the 2022 AERA Annual Meeting.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ee816ffc63561232e46f5486212da9f
https://doi.org/10.3102/1879933
https://doi.org/10.3102/1879933
Publikováno v:
Archives of Disease in Childhood - Fetal and Neonatal Edition. 108:206-207
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c60c687e45795f2b7411ca7b2a8ef0b0
https://doi.org/10.1136/archdischild-2021-323694
https://doi.org/10.1136/archdischild-2021-323694
Autor:
Natalie B Tan, Tiong Yang Tan, Ravi Savarirayan, Zornitza Stark, Amanda Moody, David J. Amor, Susan M. White, Melissa Martyn
Publikováno v:
Journal of Paediatrics and Child Health. 55:1309-1314
Aim To investigate the diagnostic and service impact of chromosomal microarray and whole exome sequencing (WES) in a neonatal intensive care unit (NICU). Methods This was a retrospective medical record review of NICU patients referred for genetics co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e6b2d826fe7ca214e7b855fd58ea4b8
https://doi.org/10.1111/jpc.14398
https://doi.org/10.1111/jpc.14398
Publikováno v:
Journal of Paediatrics and Child Health. 54:872-874
Aim Isolated oesophageal perforation in neonates is a rare but potentially life-threatening condition. Although management has historically been operative, conservative management (antibiotics, bowel rest, parenteral nutrition) is now more routinely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a6d9284cc3cff354edb9b901bd4bb8e
https://doi.org/10.1111/jpc.13905
https://doi.org/10.1111/jpc.13905
Autor:
Christopher M, Richmond, Sally, Campbell, Hee W, Foo, Sebastian, Lunke, Zornitza, Stark, Amanda, Moody, Elizabeth, Bannister, Anthea, Greenway, Natasha, Brown
Publikováno v:
Mol Syndromol
Heterozygous pathogenic variants in SPTB cause autosomal dominant hereditary spherocytosis, an important cause of neonatal nonimmune hemolytic anemia. Biallelic mutations are rarely reported, all with severe neonatal presentation. We describe rapid (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e165bd165cb6f73705b5beef6b32876f
https://pubmed.ncbi.nlm.nih.gov/32256302
https://pubmed.ncbi.nlm.nih.gov/32256302
Autor:
Kate, Hodgson, Andrea, Togo, Aideen M, Moore, Amanda, Moody, Sebastian K, King, Augusto, Zani
Publikováno v:
Journal of paediatrics and child health. 54(8)
Isolated oesophageal perforation in neonates is a rare but potentially life-threatening condition. Although management has historically been operative, conservative management (antibiotics, bowel rest, parenteral nutrition) is now more routinely used
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f9816b5e3593f0ff58f7f446e399c0d
https://pubmed.ncbi.nlm.nih.gov/29602257
https://pubmed.ncbi.nlm.nih.gov/29602257