Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Julie L. Gardner"'
Autor:
Andrew W. Lee, Julie L. Gardner, Heather L. Platt, Peter E. Silas, Shanjun Helian, Edward Zissman
Publikováno v:
Hum Vaccin Immunother
The varicella vaccine passage extension (VAR-PE) process was undertaken to extend the availability of varicella zoster virus (VZV)-containing vaccines. This study (V210-A03; NCT03239873) assessed the immunogenicity, safety, and tolerability of VAR-PE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a3d18f130bec80e2d43e39e5cb75c13
https://europepmc.org/articles/PMC7733937/
https://europepmc.org/articles/PMC7733937/
Autor:
Keith S. Reisinger, Jon E. Stek, Barbara J. Kuter, Julie L. Gardner, Myron J. Levin, Edgardo A. Malacaman, William Wang, Elizabeth Richardson
Publikováno v:
Vaccine. 37(38)
Objective VARIVAX® (varicella virus vaccine, live Oka/Merck, Merck & Co., Inc., Kenilworth, NJ, USA) was originally licensed as a frozen formulation. A refrigerator-stable formulation of VARIVAX was subsequently developed to allow for increased avai
Autor:
Shelly Senders, Jerry D. Twiggs, Jonathan Hartzel, Rowan Valenzuela, Frans A. Helmond, Gary S. Marshall, Darcy A. Hille, Jon E. Stek, Julie L. Gardner, Julie Shepard
Vaccination against measles, mumps, rubella, and varicella is recommended for all children in the US. Limitations manufacturing Oka/Merck strain varicella-zoster virus have hampered the availability of the combination vaccine (MMRV) against these 4 v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ed2ca6d3778258080e5b00a7c354c9c
https://europepmc.org/articles/PMC4994724/
https://europepmc.org/articles/PMC4994724/
Autor:
Roger Baxter, Barbara J. Kuter, Ouzama Nicholson, Wendy R. Williams, Michael Brockley, Stephanie O. Klopfer, Vicky Leamy, Julie L. Gardner, Florian Schödel, James Trammel, Michael Leonardi, Kenneth Bromberg
Publikováno v:
Pediatrics. 128:e1387-e1394
OBJECTIVE: We assessed the immunogenicity and safety of a combination measles, mump, rubella, and varicella vaccine (MMRV) (ProQuad [Merck & Co, Inc, West Point, PA]) administered to healthy children concomitantly with a pneumococcal 7-valent conjuga
Autor:
Gavin Hudson, Robert W. Taylor, Emma L. Blakely, Julie L. Gardner, Douglass M. Turnbull, John H. Walter, Langping He, Imelda Hughes
Publikováno v:
Neuromuscular Disorders. 18:557-560
Mitochondrial DNA depletion syndromes are a heterogeneous group of childhood neurological disorders characterised by a quantitative abnormality of mitochondrial DNA. We describe two siblings who presented at 8 months and 14 months with myopathy, whic
Publikováno v:
Bioscience Reports. 27:139-150
An extensive range of molecular defects have been identified in the human mitochondrial genome (mtDNA), causing a range of clinical phenotypes characterized by mitochondrial respiratory chain dysfunction. Sadly, given the complexities of mitochondria
Autor:
Anthony D. Grosso, Jon E. Stek, Barbara J. Kuter, Julie L. Gardner, Steven Black, Stephanie O. Klopfer, Maria Petrecz, Keith S. Reisinger, Florian Schödel, Ouzama Nicholson, Michelle G. Goveia, Michelle L Brown
Publikováno v:
Vaccine. 32(52)
Background In randomized clinical studies, over 11,800 children, 12 months to 6 years of age, were administered ProQuad ® , a combination measles, mumps, rubella, and varicella vaccine (MMRV). This paper describes the safety following a 2-dose regim
Autor:
Julie L. Gardner, Ronald G. Haller, Robert W. Taylor, Jane Newman, Andrew M. Schaefer, Tanja Taivassalo, Martin J. Barron, Douglass M. Turnbull
Publikováno v:
Brain : a journal of neurology. 129(Pt 12)
At present there are limited therapeutic interventions for patients with mitochondrial myopathies. Exercise training has been suggested as an approach to improve physical capacity and quality of life but it is uncertain whether it offers a safe and e
Autor:
D. T. Brown, Patrick F. Chinnery, Mary Herbert, Lynsey M. Cree, Robert N. Lightowlers, Lyndsey Craven, Julie L. Gardner, VK Lamb, Robert W. Taylor, Douglass M. Turnbull
Publikováno v:
Lancet (London, England). 368(9529)
87 Defects of mitochondrial function are increasingly recognised as important causes of disease. The clinical phenotype of mitochondrial diseases is extremely variable, aff ecting patients at any age and in a wide variety of tissues. 1 Patients are r
Autor:
Patrick F. Chinnery, Stephen Lynn, Douglass M. Turnbull, Robert W. Taylor, C Hayes, Julie L. Gardner, Mark Walker, Martin J. Barron, Robert McFarland, Andrew M. Schaefer
Publikováno v:
Annals of neurology. 55(4)
We have defined the genetic defect in a large family first described in one of the earliest reports of suspected mitochondrial myopathy, as the mutation T14709C in the mitochondrial transfer RNA(Glu) (mt-tRNA(Glu)) gene. Extraordinarily, this mutatio