Results 71 to 80 of about 10,443,238 (288)

The Implication of Substance P in the Development of Tendinopathy: A Case Control Study. [PDF]

open access: yes, 2017
It was reported that substance P had beneficial effects in the healing of acute tendon injury. However, the relationship between substance P and degenerative tendinopathy development remains unclear. The purpose of this study was to determine the role of
Ahn, Heejung   +13 more
core   +1 more source

NRASQ61R Expression in Lymphatic Endothelial Cells Causes Enlarged Vessels, Hemorrhagic Chylous Effusions, and High Mortality in a Mouse Model of Kaposiform Lymphangiomatosis

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Kaposiform lymphangiomatosis (KLA) is an aggressive complex lymphatic anomaly. Patients exhibit malformed lymphatic vessels and often develop hemorrhagic effusions and elevated angiopoietin‐2 (Ang‐2) levels. A somatic NRAS p.Q61R (NRASQ61R) mutation has been associated with KLA.
C. Griffin McDaniel   +3 more
wiley   +1 more source

Evaluation of Hepatitis A Outbreak in Boroujerd during 2019: A Case-Control Study

open access: yesمجله اپیدمیولوژی ایران, 2021
Background and Objectives: Viral hepatitis is one of the most prevalent diseases and an important underlying cause of death and disability in the world. This case-control study was conducted to investigate the outbreak of hepatitis A in Boroujerd in 2019.
Mohammad Ali Derik   +6 more
doaj  

Additional file 1: of Factors affecting fistula failure in patients on chronic hemodialysis: a populationâ based caseâ control study

open access: yes, 2018
Table S1. Analysis of factors affecting late fistula failure in patients on chronic hemodialysis. (DOCX 17 kb)
Cheng-Chieh Yen   +6 more
openaire   +1 more source

Social and spatial heterogeneity in psychosis proneness in a multilevel case-prodrome-control study [PDF]

open access: yes, 2014
To test whether spatial and social neighbourhood patterning of people at ultra-high risk (UHR) of psychosis differs from first-episode psychosis (FEP) participants or controls and to determine whether exposure to different social environments is evident ...
Aguilar, E   +10 more
core   +1 more source

Pulmonary Dysfunction Is Associated With Sleep Study Abnormalities in Children With Sickle Cell Disease: A Multicenter Study

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Introduction Pulmonary dysfunction and sleep abnormalities are common in children with sickle cell disease (SCD) and are associated with worse clinical outcomes. Whether spirometry abnormalities are associated with polysomnography (PSG) findings remains unclear.
Ammar Saadoon Alishlash   +4 more
wiley   +1 more source

How to Select and Report the Appropriate Study Design

open access: yesKerala Journal of Psychiatry
A clear understanding of study designs is essential for planning research and critically evaluating evidence. The choice of design depends on the research question, with multiple designs often suitable for a single question.
Samir Kumar Praharaj, Shahul Ameen
doaj   +1 more source

MOESM1 of Risk factors for human brucellosis in agro-pastoralist communities of south western Uganda: a caseâ control study

open access: yes, 2015
Additional file 1. Questionnaire: Risk Factors for Human Brucellosis in Agro-Pastoralist Communities of Nyabushozi County, South Western Uganda: A Case-Control Study.
Benon Asiimwe   +2 more
openaire   +1 more source

Involvement of deprivation and environmental lead in neural tube defects:a matched case-control study. [PDF]

open access: yes, 2009
OBJECTIVE. To analyse the prevalence of neural tube defects in small geographical areas and seek to explain any spatial variations with reference to environmental lead and deprivation. SETTING.
Awwad, Fuad   +4 more
core   +1 more source

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

open access: yesPediatric 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   +6 more
wiley   +1 more source

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