Results 51 to 60 of about 138,072 (341)

Serum bile acids as a prognostic biomarker in biliary atresia following Kasai portoenterostomy

open access: yesHepatology, EarlyView., 2022
Serum bile acid levels predict outcomes in patients with biliary atresia who achieve normalized bilirubin levels after Kasai portoenterostomy. Abstract Background and Aims In biliary atresia, serum bilirubin is commonly used to predict outcomes after Kasai portoenterostomy (KP).
Sanjiv Harpavat   +22 more
wiley   +1 more source

Understanding Splenomegaly in Myelofibrosis: Association with Molecular Pathogenesis

open access: yesInternational Journal of Molecular Sciences, 2018
Myelofibrosis (MF) is a clinical manifestation of chronic BCR-ABL1-negative chronic myeloproliferative neoplasms. Splenomegaly is one of the major clinical manifestations of MF and is directly linked to splenic extramedullary hematopoiesis (EMH).
Moo‐Kon Song, Byeong-Bae Park, J. Uhm
semanticscholar   +1 more source

High-fat, high-sugar diet induces splenomegaly that is ameliorated with exercise and genistein treatment

open access: yesBMC Research Notes, 2018
We tested the effect of exercise training and genistein treatment on splenomegaly in mice fed a high-fat, high-sugar diet (HFSD). Male and female C57BL6 mice fed HFSD containing 60% fat along with drinking water containing 42 g/L sugar (55% sucrose/45 ...
Levi Buchan   +7 more
semanticscholar   +1 more source

Differentiating Benign from Malignant Causes of Splenomegaly: Is Acoustic Radiation Force Impulse Elastography Helpful?

open access: yesDiseases
Purpose: To evaluate the ability of acoustic radiation force impulse (ARFI) elastography in differentiating benign from malignant etiologies of splenomegaly based on differences in splenic stiffness.
Amjad Alhyari   +6 more
doaj   +1 more source

The Key Role of Splenectomy in Fever of unknown Origin which Resulted to be B-cell primary Splenic Lymphoma.

open access: yesAlbanian Journal of Trauma and Emergency Surgery, 2023
Background: The term ‘fever of unknown origin’ (FUO) was first introduced by Petersdorf and Beeson in 1961, and it is defined as recurrent fever >38.3°C, lasting for >3 weeks, remaining undiagnosed after 1 week of in-hospital evaluation.
Ermira Muco   +5 more
doaj   +1 more source

Risk factors for in-hospital mortality of visceral leishmaniasis patients in eastern Uganda. [PDF]

open access: yes, 2009
OBJECTIVE: To identify risk factors for in-hospital mortality in patients treated for visceral leishmaniasis (VL) in Uganda. METHODS: Retrospective analysis of VL patients' clinical data collected for project monitoring by Médecins Sans Frontières in ...
Bern   +20 more
core   +3 more sources

Spleen size evaluation in children: Time to define splenomegaly for pediatric surgeons and pediatricians

open access: yesPLoS ONE, 2018
Background We determined the range of normal spleen dimensions evaluated by ultrasonography (US) in children according to sex and age and the relationship between splenic measurements, auxological data and body proportions, in order to define ...
G. Pelizzo   +7 more
semanticscholar   +1 more source

Hairy cell lymphoma: a potentially under-recognized entity

open access: yesRare Tumors, 2017
Hairy cell leukemia (HCL) is a low grade B-cell lymphoproliferative disorder that typically presents with splenomegaly, cytopenias, and diffuse bone marrow infiltration.
William A. Hammond   +3 more
doaj   +1 more source

Clinical Analysis of Oxaliplatin-related Thrombocytopenia in Patients with Digestive System Malignancy

open access: yesZhongliu Fangzhi Yanjiu, 2021
Objective To investigate the changing trend and correlation of platelet count and spleen diameter in patients with digestive system malignancy receiving oxaliplatin-based chemotherapy. Methods We retrospectively analyzed clinical data of 72 patients with
DAI Yuhong   +5 more
doaj   +1 more source

Gaucher Disease and Myelofibrosis: A Combined Disease or a Misdiagnosis? [PDF]

open access: yes, 2018
Background: Gaucher disease (GD) and primary myelofibrosis (PMF) share similar clinical and laboratory features, such as cytopenia, hepatosplenomegaly, and marrow fibrosis, often resulting in a misdiagnosis.
Cardarelli, L   +5 more
core   +1 more source

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