Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sarah Dürr"'
Autor:
Brooke M. Talbot, Julie A. Clennon, Miarintsoa Fara Nantenaina Rakotoarison, Lydia Rautman, Sarah Durry, Leo J. Ragazzo, Patricia C. Wright, Thomas R. Gillespie, Timothy D. Read
Publikováno v:
PeerJ, Vol 12, p e17805 (2024)
Background Tracking the spread of antibiotic resistant bacteria is critical to reduce global morbidity and mortality associated with human and animal infections. There is a need to understand the role that wild animals in maintenance and transfer of
Externí odkaz:
https://doaj.org/article/2ee8d7a49ab84519aa90e8860e69a0e6
Autor:
Lars Englberger, Valentin Gisler, Thierry Carrel, Irina Irincheeva, Sara Droz, Parham Sendi, Sarah Dürr, Andreas Limacher
Background Bacterial growth in cultures of resected heart valves of patients with infective endocarditis (IE) is influenced by pre-operative antibiotic treatment (preop-AT). Objectives This study sought to evaluate the time dependency of valve cultur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12dd92ff52f460834dc03a262f5c392b
Autor:
Kelvin Kering, Yuke Wang, Cecilia Mbae, Michael Mugo, Beatrice Ongadi, Georgina Odityo, Peter Muturi, Habib Yakubu, Pengbo Liu, Sarah Durry, Aniruddha Deshpande, Wondwossen Gebreyes, Christine Moe, Samuel Kariuki
Publikováno v:
PLOS Global Public Health, Vol 4, Iss 8 (2024)
Externí odkaz:
https://doaj.org/article/ef9004f81a09421180f1963947ced3a9
Autor:
Edward J. Bellfield, Jacqueline Chan, Sarah Durrin, Valerie Lindgren, Zohra Shad, Claudia Boucher-Berry
Publikováno v:
Case Reports in Endocrinology, Vol 2016 (2016)
We present the first reported case of an infant with 18p deletion syndrome with anterior pituitary aplasia secondary to a ring chromosome. Endocrine workup soon after birth was reassuring; however, repeat testing months later confirmed central hypopi
Externí odkaz:
https://doaj.org/article/3236166eacd04af385d4a77956d133bd
Autor:
Edgardo Corral, Andres Barrios, Monica Isnard, Pascale Saugier-Veber, Sophie M. Fortier, Sarah Durrin, Waldo Sepulveda
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2015 (2015)
X-linked hydrocephaly is a rare sex-linked genetic recessive condition occurring in 1/30,000 deliveries. Adduction of thumbs and mental retardation are additional associated clinical findings. We describe two cases of X-linked hydrocephaly with assoc
Externí odkaz:
https://doaj.org/article/e4ff97e3c4cd4b2c888cb2900beb0e6b