Results 71 to 80 of about 1,103,541 (343)
Turkish Journal of Hematology, 2018 Hereditary factor X (FX) deficiency is a rare bleeding disorder more prevalent in countries with high rates of consanguineous marriage. In a prospective, open-label, multicenter phase 3 study, 25 IU/kg plasmaderived factor X (pdFX) was administered as on-
Ahmet F. Öner +4 more
doaj +1 more source
Acquired Factor X Deficiency in Light Chain Amyloidosis: A Report of 2 Korean Cases [PDF]
Amyloidosis is a heterogeneous group of diseases in which misfolding of extracellular proteins is the pathogenic factor. Light chain amyloidosis (AL) is the most common form of amyloidosis, and the causative proteins in AL are the immunoglobulin light ...
Adam +11 more
core +2 more sources
An analysis of 8 cases of factor X deficiency [PDF]
Indian Journal of Hematology and Blood Transfusion, 2008 Factor X deficiency is a rare coagulation defect. There are occasional reports of factor X deficiency from India. Difficulty in accurate diagnosis and non-availability of ideal treatment is discussed.Eight cases of factor X deficiency, diagnosed from 1992 to 2007 are reported hereSeven were male while one was female.
Nilam M. Shah, Ashwin P. Patel
openaire +3 more sources
Chandra Observations of the Three Most Metal-Deficient Blue Compact Dwarf Galaxies known in the Local Universe, SBS 0335-052, SBS 0335-052W, and I Zw 18 [PDF]
Astrophys.J. 606 (2004) 213-220, 2004 We present an X-ray study of the three most metal-deficient blue compact dwarf (BCD) galaxies known in the local Universe, based on deep Chandra observations of SBS 0335-052 (0.025 solar abundance), SBS 0335-052W (0.02 solar abundance) and I Zw 18 (0.02 solar abundance).
arxiv +1 more source
Population Ecology, EarlyView.In this study, we compared three methods for kinship identification using different algorithms in samples of wild Pacific bluefin tuna and generated genotyping data. The three methods resulted in different numbers of inferred kinship pairs for both generated and actual data. Particularly for the half‐sibling pairs, considerable number of false‐positive
Yohei Tsukahara +5 more
wiley +1 more source
Superconductivity induced by oxygen deficiency in Sr-doped LaOFeAs [PDF]
Phys. Rev. B 78, 092503 (2008)., 2008 We synthesized Sr-doped $La_{0.85}Sr_{0.15}OFeAs$ sample with single phase, and systematically studied the effect of oxygen deficiency in the Sr-doped LaOFeAs system. It is found that substitution of Sr for La indeed induces the hole carrier evidenced by positive thermoelectric power (TEP), but no bulk superconductivity is observed.
arxiv +1 more source
Asian Journal of Transfusion Science, 2021 Hemophilia A is an X-linked recessive bleeding disorder occurs due to deficiency of factor VIII (FVIII). The disease manifests exclusively in males though it rarely occurs in females due to complex pathophysiological mechanisms. We present a rare case of
Sanooja Pinki +3 more
doaj +1 more source
Management of a Giant Renal Artery Aneurysm in a Patient with Severe Hemophilia A [PDF]
, 2022 Patient: Male, 54-year-old Final Diagnosis: Giant right renal artery aneurysm Symptoms: Bilateral leg edema Medication: — Clinical Procedure: — Specialty: Hematology • Radiology • Urology OBJECTIVE: Rare coexistence of disease or pathology BACKGROUND ...
Freimanis, Arvis +4 more
core +1 more source
Congenital factor X deficiency in Japan.
The Tohoku Journal of Experimental Medicine, 1981 Congenital factor X deficiency is a very rare inherited coagulation abnormality. There have been reported 43 cases of this disorder in the world and only 2 cases in Japan. Recently, we have hemostatically and immunologically examined as many as 3 cases of this rare disease, 18-year-old male, 11-year-old male and 6-year-old female.
Noboru Nakano +6 more
openaire +4 more sources
Insights into PI3K/AKT signaling in B cell development and chronic lymphocytic leukemia
FEBS Letters, EarlyView.This Review explores how the phosphoinositide 3‐kinase and protein kinase B pathway shapes B cell development and drives chronic lymphocytic leukemia, a common blood cancer. It examines how signaling levels affect disease progression, addresses treatment challenges, and introduces novel experimental strategies to improve therapies and patient outcomes.
Maike Buchner
wiley +1 more source