Results 21 to 30 of about 388 (169)

Transthyretin levels in the vitreous correlate with change in visual acuity after vitrectomy [PDF]

open access: yes, 2009
Background/aim: Little is known about biochemical markers related to change in visual acuity after vitrectomy. The potential use of transthyretin (TTR), a carrier of the retinol/retinol-binding protein, as a biochemical marker protein, was investigated ...
De Letter, Els   +7 more
core   +3 more sources

A dedicated protocol and environment for central venous catheter removal in pediatric patients affected by oncohematological diseases [PDF]

open access: yes, 2014
The removal of long-term central venous catheters (CVCs) is not performed according to evidence-based guidelines, thus conveying the message that it is a procedure of secondary importance.
Atti, Mlcd   +10 more
core   +1 more source

Drugs for preventing red blood cell dehydration in people with sickle cell disease. [PDF]

open access: yes, 2016
BACKGROUND: Sickle cell disease is an inherited disorder of hemoglobin, resulting in abnormal red blood cells. These are rigid and may block blood vessels leading to acute painful crises and other complications.
Ballas, Samir K., Nagalla, Srikanth
core   +2 more sources

Renal Thrombotique microangiopathy: An unusual renal involvement in Niemann‐Pick disease type B

open access: yesClinical Case Reports, Volume 8, Issue 12, Page 3315-3320, December 2020., 2020
Renal involvement in Niemann‐Pick disease type B is very rare. Kidney check‐up and renal biopsy should be performed in any patient presented with hypertension and kidney disease. Histology identifies the lesion, the prognosis, and guide treatment. Abstract Renal involvement in Niemann‐Pick disease type B is very rare.
Mouna Jerbi   +6 more
wiley   +1 more source

Erythrocyte-erythrocyte aggregation dynamics under shear flow [PDF]

open access: yes, 2020
Red blood cells (RBCs) -- erythrocytes -- suspended in plasma tend to aggregate and form rouleaux. During aggregation the first stage consists in the formation of RBC doublets [Blood cells, molecules, and diseases 25, 339 (1999)].
Abbasi, Mehdi   +4 more
core   +2 more sources

Conceptual graph-based knowledge representation for supporting reasoning in African traditional medicine [PDF]

open access: yes, 2013
Although African patients use both conventional or modern and traditional healthcare simultaneously, it has been proven that 80% of people rely on African traditional medicine (ATM).
Diallo, Gayo   +2 more
core   +3 more sources

Gender-Related Differences in Sickle Cell Disease in a Pediatric Cohort: A Single-Center Retrospective Study

open access: yesFrontiers in Molecular Biosciences, 2019
Sickle cell disease (SCD) is one of the most common monogenic disease worldwide. The incidence of SCD is not strictly gender-related as it is transmitted as an autosomal recessive disorder.
Giulia Ceglie   +10 more
doaj   +1 more source

Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease [PDF]

open access: yes, 2015
Background: Globally, about five per cent of children are born with congenital or genetic disorders. The most common autosomal recessive conditions are thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease, with higher carrier rates in
Abbot   +89 more
core   +1 more source

Drugs for preventing red blood cell dehydration in people with sickle cell disease. [PDF]

open access: yes, 2012
BACKGROUND: Sickle cell disease is an inherited disorder of hemoglobin, resulting in abnormal red blood cells. These are rigid and may block blood vessels leading to acute painful crises and other complications.
Ballas, Samir K, Nagalla, Srikanth
core   +2 more sources

In Vitro Biological Activities of Drepanoalpha® Ethanolic Extract, A Justicia Secunda and Moringa Oleifera-Based Phytomedicine Proposed for The Symptomatic Treatment of Sickle Cell Disease [PDF]

open access: yes, 2023
Sickle cell disease (SCD) is an autosomal recessive blood disorder characterized by red blood cells that assume an abnormal, rigid sickle shape under low-oxygen conditions.
Duez, Pierre   +9 more
core   +2 more sources

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