Results 51 to 60 of about 140,078 (149)

Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly

open access: yesGenetics in Medicine, 2018
To estimate diagnostic yield and genotype-phenotype correlations in a cohort of 811 patients with lissencephaly or subcortical band heterotopia. We collected DNA from 756 children with lissencephaly over 30 years.
N. Donato   +20 more
semanticscholar   +1 more source

A videolaparoscopia no diagnóstico e tratamento do schwannoma abdominal

open access: yesRevista do Colégio Brasileiro de Cirurgiões
The authors present two patients with solid tumours (benign Schwannoma), which were found during abdominal ultra-sonography. One of them was located adjacent to the hepatic artery, near its origin at the celiac axis.
Nelson Ary Brandalise   +2 more
doaj   +1 more source

Clinical Implications of Tacrolimus Time in Therapeutic Range and Intrapatient Variability in Urban Renal Transplant Recipients Undergoing Early Corticosteroid Withdrawal

open access: yesTransplantation Direct, 2021
Background. Tacrolimus demonstrates wide intrapatient and interpatient variability requiring therapeutic drug monitoring. The utility of tacrolimus time in therapeutic range (TTR) after renal transplantation (RT) under an early corticosteroid withdrawal (
Dana R. Pierce, PharmD   +6 more
doaj   +1 more source

Case Report: Superior Vena Cava Resection and Reconstruction for Invasive Thyroid Cancer: Report of Three Cases and Literature Review

open access: yesFrontiers in Surgery, 2021
Background: Thyroid cancer with massive invasion into the cervical and mediastinal great veins is extremely rare, and the surgical treatment is controversial, thus posing a great challenge for head and neck surgeons.
Wenjie Chen   +6 more
doaj   +1 more source

Lesões abdominais nos traumatizados com fraturas de bacia

open access: yesRevista do Colégio Brasileiro de Cirurgiões
OBJETIVO: Analisar as lesões abdominais e seu impacto no prognóstico dos traumatizados com fraturas de bacia MÉTODO: Avaliamos retrospectivamente todos os prontuários das vítimas de trauma fechado com fraturas de bacia admitidos de 1996 a 2000.
José Gustavo Parreira   +2 more
doaj   +1 more source

Qualidade de vida após a cardiomiotomia à Heller-Dor

open access: yesRevista do Colégio Brasileiro de Cirurgiões
OBJETIVOS: Avaliar os resultados da cardiomiotomia de Heller associada à fundoplicatura de Dor por Laparoscopia (HDL) no tratamento cirúrgico da acalásia do esôfago, através de escores de qualidade de vida e dados da esofagomanometria.
Fernando A.V. Madureira   +3 more
doaj   +1 more source

Investigation of the leaching mechanism of NMC 811 (LiNi0.8Mn0.1Co0.1O2) by hydrochloric acid for recycling lithium ion battery cathodes

open access: yesRSC Advances, 2019
This paper investigates the reactions involved when LiNi0.8Mn0.1Co0.1O2 (NMC 811), which is one of the most promising positive electrodes for the next generation of lithium-ion batteries, is leached by hydrochloric acid.
Wen Xuan, A. Otsuki, A. Chagnes
semanticscholar   +1 more source

Avaliação do fluxo arterial mesentérico em humanos durante o exercício

open access: yesRevista do Colégio Brasileiro de Cirurgiões
O aumento da atividade simpática durante o exercício dinâmico progressivo associa-se à resposta da concentração de lactato sangüíneo. Com o objetivo de testar a hipótese de que a diminuição do fluxo da artéria mesentérica superior também tenha relação ...
Adamastor Humberto Pereira   +5 more
doaj   +1 more source

Spatio-temporal characterization of S- and M/L-cone degeneration in the Rd1 mouse model of retinitis pigmentosa

open access: yesBMC Neuroscience, 2019
The Pde6brd1 (Rd1) mouse is widely used as a murine model for human retinitis pigmentosa. Understanding the spatio-temporal patterns of cone degeneration is important for evaluating potential treatments.
Daniel S Narayan   +4 more
semanticscholar   +1 more source

DZNep inhibits H3K27me3 deposition and delays retinal degeneration in the rd1 mice

open access: yesCell Death and Disease, 2018
Retinitis pigmentosa (RP) is a group of inherited retinal degenerative diseases causing progressive loss of photoreceptors. Numerous gene mutations are identified to be related with RP, but epigenetic modifications may also be involved in the ...
Shijie Zheng   +7 more
semanticscholar   +1 more source

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