Zobrazeno 1 - 10
of 23
pro vyhledávání: '"DOL, day of life"'
Autor:
Kurt D. Piggott, Jason Turner, LaTasha Lewis, Song-Gui Yang, Cynthia Laviolette, Timothy W. Pettitt
Publikováno v:
JACC Case Reports
Pulmonary artery thrombosis is reported in neonates with risk factors for hypercoagulability. No consensus exists regarding standard therapy for this condition. We present a neonate, with no risk factors for thrombosis, who was admitted after birth t
Autor:
Anji T. Yetman, Ali N. Ibrahimiye, James M. Hammel, Taylor E. Katt, Robert L. Spicer, Jeffrey A. Robinson
Publikováno v:
JACC Case Reports
JACC: Case Reports, Vol 2, Iss 11, Pp 1716-1719 (2020)
JACC: Case Reports, Vol 2, Iss 11, Pp 1716-1719 (2020)
Williams syndrome (WS) is an arteriopathic derangement associated with supravalvular aortic stenosis and branch pulmonary stenosis. We describe double-outlet right ventricle with mitral atresia and aortic arch hypoplasia in an infant with WS. This ca
Autor:
Mari Charisse Trinidad, Sherif A. Shazly, Andre Terzic, Mikel Prieto, Brenda Schiltz, Victoria Novoa, David J. Sas, Simrit K. Warring, Rodrigo Ruano
Publikováno v:
Mayo Clinic Proceedings: Innovations, Quality & Outcomes, Vol 4, Iss 4, Pp 391-409 (2020)
Mayo Clinic Proceedings: Innovations, Quality & Outcomes
Mayo Clinic Proceedings: Innovations, Quality & Outcomes
The aim of this study was to investigate the effect of serial amnioinfusion therapy (SAT) for pulmonary hypoplasia in lower urinary tract obstruction (LUTO) or congenital renal anomalies (CRAs), introduce patient selection criteria, and present a cas
Autor:
Manoj K Gupta, Jesus C Jaile
Publikováno v:
JACC Case Reports
JACC: Case Reports, Vol 3, Iss 4, Pp 630-632 (2021)
JACC: Case Reports, Vol 3, Iss 4, Pp 630-632 (2021)
We describe the first case of atrial flutter requiring multiple cardioversions in a preterm infant. Direct current cardioversion is one of the best-understood treatment options, with a first-time success rate higher than 96%. The electrocardiograms p
Autor:
Jeremy W. Prokop, Heather Menden, Sherry M Mabry, Inamul Haque, Badal C. Roy, Aparna Venkatraman, Venkatesh Sampath, Wei Yu, Sheng Xia, Aron M. Geurts, Shahid Umar
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology
Cellular and Molecular Gastroenterology and Hepatology, Vol 13, Iss 2, Pp 425-440 (2022)
Cellular and Molecular Gastroenterology and Hepatology, Vol 13, Iss 2, Pp 425-440 (2022)
Background & Aims Single immunoglobulin interleukin-1–related receptor (SIGIRR) is a major inhibitor of Toll-like receptor signaling. Our laboratory identified a novel SIGIRR stop mutation (p.Y168X) in an infant who died of severe necrotizing enter
Publikováno v:
NeuroImage : Clinical
NeuroImage: Clinical, Vol 31, Iss, Pp 102678-(2021)
NeuroImage: Clinical, Vol 31, Iss, Pp 102678-(2021)
Highlights • Myelination is a developmental process that intensifies after birth during the first years of life. • We used a T2* mapping sequence to assess myelination in healthy and critically ill neonates with neonatal encephalopathy. • Birth
Autor:
Rossana Sanchez Russo, Charles M. Rowland, Chung Lee, Pranoot Tanpaiboon, Stephen D. Cederbaum, Inderneel Sahai, Denise Salazar, Derek Wong, Yue Huang, Felicitas Lacbawan, Rajesh Sharma, Juanita Neira, Susan Sklower Brooks, Annette Feigenbaum, Kelly E. Jackson
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 27, Iss, Pp 100735-(2021)
Molecular Genetics and Metabolism Reports, Vol 27, Iss, Pp 100735-(2021)
Arginase deficiency is a rare inborn error of metabolism that interrupts the final step of the urea cycle. Untreated individuals often present with episodic hyperammonemia, developmental delay, cognitive impairment, and spasticity in early childhood.
Autor:
Maïa Proisy, Isabelle Corouge, Antoine Legouhy, Valérie Charon, Nadia Mazille, Amélie Nicolas, Stéphanie Leroux, Bertrand Bruneau, Christian Barillot, Jean-Christophe Ferré
Publikováno v:
Neuroimage-Clinical
Neuroimage-Clinical, 2019, 101939, pp.1-31. ⟨10.1016/j.nicl.2019.101939⟩
SPR 2019-Annual Meeting & Postgraduate Course
SPR 2019-Annual Meeting & Postgraduate Course, Apr 2019, San Francisco, California, United States
Neuroimage-Clinical, Elsevier, 2019, 101939, pp.1-31. ⟨10.1016/j.nicl.2019.101939⟩
NeuroImage : Clinical
NeuroImage: Clinical, Vol 24, Iss, Pp-(2019)
HAL
Neuroimage-Clinical, 2019, 101939, pp.1-31. ⟨10.1016/j.nicl.2019.101939⟩
SPR 2019-Annual Meeting & Postgraduate Course
SPR 2019-Annual Meeting & Postgraduate Course, Apr 2019, San Francisco, California, United States
Neuroimage-Clinical, Elsevier, 2019, 101939, pp.1-31. ⟨10.1016/j.nicl.2019.101939⟩
NeuroImage : Clinical
NeuroImage: Clinical, Vol 24, Iss, Pp-(2019)
HAL
The primary objective of this study was to evaluate changes in cerebral blood flow (CBF) using arterial spin labeling MRI between day 4 of life (DOL4) and day 11 of life (DOL11) in neonates with hypoxic-ischemic encephalopathy (HIE) treated with hypo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::46ad882c706511f65ae7c2ed58c94b4a
https://www.hal.inserm.fr/inserm-02189386/document
https://www.hal.inserm.fr/inserm-02189386/document
Publikováno v:
Journal of Clinical & Translational Endocrinology, Vol 2, Iss 1, Pp 14-20 (2015)
Journal of Clinical & Translational Endocrinology
Journal of Clinical & Translational Endocrinology
Objective To describe the association of calcitriol treatment with the change in parathyroid hormone (PTH) and biochemical markers of bone disease in infants with metabolic bone disease of prematurity (MBD) and secondary hyperparathyroidism. Study de
Autor:
Mary L. Brandt, Sanjiv Harpavat, Mary Elizabeth M. Tessier, Benjamin L. Shneider, Dana N. Cerminara
Publikováno v:
Contemporary Clinical Trials Communications
Contemporary Clinical Trials Communications, Vol 15, Iss, Pp-(2019)
Contemporary Clinical Trials Communications, Vol 15, Iss, Pp-(2019)
Background: Biliary atresia (BA) is a life-threatening liver disease of infancy, characterized by extrahepatic biliary obstruction, bile retention, and progressive liver injury. The Kasai portoenterostomy (KP) is BA's only nontransplant treatment. It