Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gina Capodanno"'
Autor:
Carla Janzen, Margarida Y Y Lei, Il Seok D Jeong, Amit Ganguly, Peggy Sullivan, Vladislava Paharkova, Gina Capodanno, Hiromi Nakamura, Alix Perry, Bo-Chul Shin, Kuk-Wha Lee, Sherin U Devaskar
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0193583 (2018)
Intrauterine growth restriction (IUGR) results from a lack of nutrients transferred to the developing fetus, particularly oxygen and glucose. Increased expression of the cytoprotective mitochondrial peptide, humanin (HN), and the glucose transporter
Externí odkaz:
https://doaj.org/article/4d7a940141884c81a716a9c8f0eff9d4
Autor:
Janet Y. Lee, Bo Fan, Gabrielle Montenegro, Roger K. Long, Srinath Sanda, Gina Capodanno, Anne L. Schafer, Andrew J. Burghardt, Stephen M. Rosenthal, Ellen B. Fung
Publikováno v:
Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry. 25(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5943e848acee43ca2badbb35c57c8b05
https://pubmed.ncbi.nlm.nih.gov/35941040
https://pubmed.ncbi.nlm.nih.gov/35941040
Autor:
Joseph T. Shieh, Pierre-Marie Martin, Norah Alsaleh, Daniah Beleford, Zuhair Rahbeeni, Shannon Rego, Fowzan S. Alkuraya, Jessica Van Ziffle, Alyssa Huang, Aya Abu-El-Haija, Anne Slavotinek, Bryce A. Mendelsohn, Neil Risch, Gina Capodanno
Publikováno v:
American Journal of Medical Genetics Part A. 182:513-520
We describe an 11-year old boy with severe global developmental delays, failure to thrive and growth retardation, refractory seizures with recurrent status epilepticus, hypogammaglobulinemia, hypergonadotropic hypogonadism, and duodenal strictures. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85683d2e04a6c1090f0b0a094508e047
https://doi.org/10.1002/ajmg.a.61450
https://doi.org/10.1002/ajmg.a.61450
Autor:
Ayca Erkin-Cakmak, Gina Capodanno, Stephen E. Gitelman, Christine T. Ferrara, Hannah Chesser, Joseph T. Shieh
Publikováno v:
Journal of the Endocrine Society
Background: Congenital hyperinsulinism (HI) is the leading cause of severe, persistent hypoglycemia in infants. Transient HI seen at risk neonates due to prenatal stress and some of the congenital HI cases due to mutations in K-ATPase channel are res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5ec2c08774e12ab258b90129cb52adb
http://europepmc.org/articles/PMC7207411
http://europepmc.org/articles/PMC7207411
Disruptions of growth and puberty are typically the first signs of an endocrine disorder. Using vignettes and a question-and-answer format, this chapter discusses common and uncommon cases of hormone dysfunction presenting from infancy through adoles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d307b17c4307c5b838dee6122e3c802e
https://doi.org/10.1093/med/9780190848712.003.0012
https://doi.org/10.1093/med/9780190848712.003.0012
Publikováno v:
Journal of the Endocrine Society
Background: Perinatal Hypophosphatasia (HPP) is a rare and lethal disorder associated with a 50–100% mortality rate, usually due to respiratory complications. HPP occurs due to a loss-of-function mutation in the ALPL gene, responsible for the funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce6c7ef7b50cc0fab5487ffc0dc275e1
https://doi.org/10.1210/jendso/bvab048.359
https://doi.org/10.1210/jendso/bvab048.359
Publikováno v:
Journal of the Endocrine Society
Background: In 2012, our pediatric hospital transitioned to an electronic medical record system and delegated all inpatient insulin ordering duties to the pediatric endocrine division. This led to a deficit in resident knowledge of blood glucose mana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a5493a81b61cf303b698047a3dee8e7
https://doi.org/10.1210/js.2019-sat-269
https://doi.org/10.1210/js.2019-sat-269
Autor:
Margarida Y.Y. Lei, Kuk-Wha Lee, Vladislava Paharkova, Carla Janzen, Peggy S. Sullivan, Il Seok D. Jeong, Amit Ganguly, Alix Perry, Sherin U. Devaskar, Hiromi Nakamura, Bo-Chul Shin, Gina Capodanno
Publikováno v:
PloS one, vol 13, iss 3
PLoS ONE, Vol 13, Iss 3, p e0193583 (2018)
PLoS ONE
PLoS ONE, Vol 13, Iss 3, p e0193583 (2018)
PLoS ONE
Background Intrauterine growth restriction (IUGR) results from a lack of nutrients transferred to the developing fetus, particularly oxygen and glucose. Increased expression of the cytoprotective mitochondrial peptide, humanin (HN), and the glucose t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b85f10ab25e4a596bb47f990c834e5cb
https://escholarship.org/uc/item/8qb5s83v
https://escholarship.org/uc/item/8qb5s83v