Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jennifer Vethamuthu"'
Autor:
Jennifer Vethamuthu, R. Cassim, Melise A. Keays, C. van Walraven, Michael P. Leonard, V. Grandpierre, Luke T. Lavallée, Luis Guerra, K. McAlpine, Kerri Highmore
Publikováno v:
Journal of pediatric urology. 15(5)
Summary Introduction Asymptomatic, or incidental, pediatric kidney stones detected on abdominal imaging pose a clinical challenge as their significance and expected outcome are not well described. Objective Our primary objective was to estimate the i
Autor:
Gabrielle Weiler, Jennifer Vethamuthu, Vy Hong-Diep Kim, Eyal Grunebaum, Elizabeth Nizalik, Anne Pham-Huy
Publikováno v:
LymphoSign Journal. 2:195-199
Inherited defects in the ubiquitous adenosine deaminase (ADA) enzyme disrupt the function of the immune system as well as many other organs and tissues. Some patients may also suffer from kidney damage. Here we report on an ADA-deficient patient who
Publikováno v:
Pediatric Transplantation. 16:E5-E9
Kutilek S, Skalova S, Vethamuthu J, Geier P, Feber J. Transient hyperphosphatasemia in pediatric renal transplant patients – Is there a need for concern and when? Pediatr Transplantation 2012: 16: E5–E9. © 2010 John Wiley & Sons A/S. Abstract: T
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 20, Iss 5, Pp 831-834 (2009)
Acute renal failure (ARF) is a rare but potentially fatal complication of diabetic ketoacidosis (DKA). Early recognition and aggressive treatment of ARF during DKA may im-prove the prognosis of these patients. We present a case report of a 12 year ol
Publikováno v:
The Journal of Pediatrics. 145:71-76
To assess the efficacy of the anti-estrogens tamoxifen and raloxifen in the medical management of persistent pubertal gynecomastia.Retrospective chart review of 38 consecutive patients with persistent pubertal gynecomastia who presented to a pediatri
Infant nephrolithiasis and nephrocalcinosis: Natural history and predictors of surgical intervention
Autor:
Michael P. Leonard, Jennifer Vethamuthu, Luis Guerra, Kenneth Tang, Kerri Highmore, Veridiana Andrioli, Melise A. Keays, Victoria Meyers, Katrina J. Sullivan
Publikováno v:
Journal of Pediatric Urology. 13:355.e1-355.e6
Summary Introduction Renal stone disease diagnosed in the first year of life is relatively uncommon. While risk factors such as low birth weight, furosemide exposure, and metabolic disorders are well established, there exists little information regar
Autor:
Sylva Skálová, Amani Roushdi, Pavel Geier, Jennifer Vethamuthu, Gabrielle Weiler, Janusz Feber
Publikováno v:
Pediatric nephrology (Berlin, Germany). 27(12)
We analyzed the impact of immunoglobulin M (IgM) positivity on the relapse-free interval post completed course of cyclophosphamide (CYC) treatment in patients with steroid-dependent nephrotic syndrome (SDNS) and minimal change disease (MCD). This was
Publikováno v:
Pediatric transplantation. 16(1)
TH of infancy and early childhood is characterized by transiently increased S-ALP, predominantly its bone or liver isoforms. There are neither signs of metabolic bone disease or hepatopathy corresponding to the increased S-ALP, nor a common underlyin
Publikováno v:
Pediatric transplantation. 11(3)
Few studies report Ganciclovir or Valganciclovir levels in children. Single-center, retrospective study of all available Ganciclovir levels in transplanted children. Ganciclovir monitoring was performed as previously described [G. Filler (1998); Pedi
Publikováno v:
The Journal of Pediatrics. 146:576-577