Results 51 to 60 of about 743,133 (291)

Immunological and laboratory features of HIV infection in infants of the first year of life

Журнал инфектологии, 2014
To study the characteristics of laboratory tests of infants born to HIV-positive women and left without parental care in the dynamics analyzed blood samples using methods of immunological and serological diagnosis of HIV infection, the qualitative and ...
V. N. Timchenko, Yu. A. Arkhipova, N. D. Dzhangavadze   +2 more
doaj   +1 more source

Broadband microwave burst produced by electron beams

, 2007
Theoretical and experimental study of fast electron beams attracts a lot of attention in the astrophysics and laboratory. In the case of solar flares the problem of reliable beam detection and diagnostics is of exceptional importance. This paper explores
A. T. Altyntsev, Ding M.-D., G. D. Fleishman, G.‐L. Huang, Getmantsev G. G., Ginzburg V. L., Ginzburg V. L., Klein K.-L., Korchak A. A., Korchak A. A., Nakajima H., Torii C., V. F. Melnikov, Yoshimori M.   +13 more
core   +1 more source

A new targeted CFTR mutation panel based on next-generation sequencing technology [PDF]

, 2017
Searching for mutations in the cystic fibrosis transmembrane conductance regulator gene (CFTR) is a key step in the diagnosis of and neonatal and carrier screening for cystic fibrosis (CF), and it has implications for prognosis and personalized therapy ...
Alberti, Luisella, Biffignandi, Alice, Bruno, Sabina Maria, Colombo, Carla, Corbetta, Carlo, Costantino, Lucy, Giannone, Valentina, Lucarelli, Marco, Porcaro, Luigi, Seia, Manuela, Torresani, Erminio   +10 more
core   +2 more sources

Germline TP53 Mutations Causing Diamond–Blackfan Anemia: A French Report

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Diamond–Blackfan anemia is a rare congenital erythroblastopenia typically caused by mutations in ribosomal protein genes. Recently, gain‐of‐function mutations in TP53 have been identified as a novel cause of Diamond–Blackfan anemia. We report two French patients who both harbored a heterozygous TP53 deletion (NM_000546.5: c.1077delA; p ...
Rafael Moisan, Lydie Da Costa, Ludivine David Nguyen, Heloise Chosseler, Audrey Riquet, Benedicte Bruno, Melissa Barbati   +6 more
wiley   +1 more source

A new 147-56 hPa water vapor product from the UARS Microwave Limb Sounder [PDF]

, 2004
Measurements of H2O in the tropopause region have been obtained by production of a new data set from the Microwave Limb Sounder (MLS) on the Upper Atmosphere Research Satellite (UARS).
Barath, Bauer, Borysow, D. L. Wu, Dagg, Goyette, H. C. Pumphrey, Hervig, J. W. Waters, Jarnot, Lahoz, List, Livesey, Oltmans, Pardo, Pawson, Pumphrey, Pumphrey, Randel, Randel, Read, Read, Reber, Rind, Russell, W. G. Read, Waters, Zeng   +27 more
core   +2 more sources

Laboratory diagnostics in acute poisoning: critical overview [PDF]

, 2017
Laboratory diagnostics play an important role in the treatment of patients with acute poisoning. The classical clinical chemistry and hematology tests help initiate supportive treatment, and specialized methods enable elucidation of the poisons involved.
Rentsch, Katharina M.
core  

Development of rapid, automated diagnostics for infectious disease: advances and challenges [PDF]

, 2009
The last 2 years has seen an exponential rise in the amount of research funding made available for the development of rapid diagnostic devices for infectious agents of medical importance. This review reports on several such projects.
Ince, J, McNally, A
core   +1 more source

Blinatumomab Utilization in Pediatric B‐Cell Acute Lymphoblastic Leukemia: Experience From the Mountain West

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Blinatumomab is a bispecific T‐cell engager approved for the treatment of pediatric B‐cell acute lymphoblastic leukemia (B‐ALL). Outpatient home infusion reduces hospitalization burden and optimizes resource utilization, but is logistically challenging.
Angela Parra del Riego, Kellee Parker, William C. Thomsen, James B. Ford, Mallorie B. Heneghan, David Spencer Mangum, Jennifer L. McNeer, Luke D. Maese, Claire E. F. Miller, Richard Lemons, Taumoha Ghosh   +10 more
wiley   +1 more source

Ethnic Differences in the Association Between SOD2 rs4880 and Hepatotoxicity in Pediatric Acute Lymphoblastic Leukemia: A Report From the REDIAL Consortium

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Treatment‐associated hepatotoxicity (TAH) is a common complication of pediatric acute lymphoblastic leukemia (ALL) treatment, but genetic risk factors remain poorly understood. We evaluated the SOD2 rs4880 variant in 544 children with ALL at Texas Children's Hospital. After adjusting for demographic and clinical covariates, the rs4880 C allele
Emily J. Mason, John P. Woodhouse, Joanna S. Yi, M. Monica Gramatges, Olga A. Taylor, Veronica A. Morales, Shalini Dhamodharan, Marley Roberts, Karen R. Rabin, Philip J. Lupo, Michael E. Scheurer, Van Huynh, Steven D. Mittelman, Etan Orgel, Austin L. Brown   +14 more
wiley   +1 more source

Some aspects of laboratory diagnostics of ophthalmodemodecosis

Acta Biomedica Scientifica
Demodicosis occupies a leading position among all dermatoses. According to ICD-10, it is not distinguished as a separate disease; it belongs to the class of parasitic diseases.
D. A. Popova, Yu. V. Kursakova
doaj   +1 more source