Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Alexa Kanwit Craig"'
Autor:
Alexa Kanwit Craig
Publikováno v:
Journal of Clinical and Translational Science, Vol 1, Pp 35-36 (2017)
OBJECTIVES/SPECIFIC AIMS: Congenital heart disease (CHD) is the most frequently occurring birth defect in the United States affecting about 40,000 infants born every year. Despite significant advances in postsurgical survival, developmental outcomes
Externí odkaz:
https://doaj.org/article/1413e944ba054b05ab59140067e4208e
Publikováno v:
Journal of Clinical and Translational Science, Vol 2, Pp 43-43 (2018)
OBJECTIVES/SPECIFIC AIMS: Therapeutic hypothermia (TH) is a neuroprotective therapy regularly used in newborn infants following traumatic births. The infant’s temperature is maintained at 33.5°C for 72 hours by a cooling blanket upon which the inf
Externí odkaz:
https://doaj.org/article/8c19641156514a88acd6682943b37964
Autor:
Alexa Kanwit Craig
Publikováno v:
Journal of Clinical and Translational Science. 1:35-36
OBJECTIVES/SPECIFIC AIMS: Congenital heart disease (CHD) is the most frequently occurring birth defect in the United States affecting about 40,000 infants born every year. Despite significant advances in postsurgical survival, developmental outcomes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d2a3de5eaf968c0d9ffd5142ebbcb5c
https://doi.org/10.1017/cts.2017.131
https://doi.org/10.1017/cts.2017.131
Publikováno v:
Journal of child neurology. 29(3)
We describe 2 patients with X-linked Charcot-Marie-Tooth disease, type 1 (CMTX1) disease and central nervous system manifestations and review 19 cases from the literature. Our first case had not been previously diagnosed with Charcot-Marie-Tooth dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::445818c468e24fc4410c134bd7f21584
https://pubmed.ncbi.nlm.nih.gov/23400245
https://pubmed.ncbi.nlm.nih.gov/23400245
Publikováno v:
Mitochondrion. 11:639
Purpose To review our cohort of patients with Dravet syndrome and determine if patients with SCN1A mutations can also express mitochondrial disease due to electron transport chain dysfunction. Methods A retrospective chart review was used to describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::611a504c18aed9ea6c122e55ec93b73c
https://doi.org/10.1016/j.mito.2011.03.017
https://doi.org/10.1016/j.mito.2011.03.017