Results 31 to 40 of about 799,164 (305)

MicroRNA expression in multiple myeloma is associated with genetic subtype, isotype and survival [PDF]

, 2011
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work
Hatton, CSR, Taylor Steve, Taylor, Stephen, Taylor, S, Lawrie Charles H, Saunders, NJ, Steve Taylor, Pezzella Francesco, Saunders Nigel J, Tramonti, D, Lawrie, CH, Wainscoat James S, Kusec, R, Pezzella, F, Tramonti Daniela, Nigel J Saunders, Hatton Christian SR, Chen, XH, Hatton, CS, Charles H Lawrie, Rajko Kušec, Littlewood, T, Erica Ballabio, Deborah Hay, Timothy Littlewood, Chi, J, Jacqueline Boultwood, Boultwood Jacqueline, Kušec Rajko, Jianxiang Chi, Chen Xiao-He, James S Wainscoat, Ballabio, E, Ballabio Erica, Chi Jianxiang, Xiao-He Chen, Littlewood Timothy, Francesco Pezzella, Christian SR Hatton, Wainscoat, JS, Hay Deborah, Pezzella, Francesco, Boultwood, Jacqueline, Hay, D, Boultwood, J, Daniela Tramonti   +45 more
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Multiple ocular abnormalities associated with trisomy 4p [PDF]

, 2008
Ocular features associated with trisomy 4p have rarely been described. The authors have experienced multiple ocular abnormalities (bilateral cataracts, posterior synechiae, and posterior segment changes) associated with this chromosomal abnormality.
홍사민, 성공제, 강성용, 김찬윤   +3 more
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Prognostic implications of abnormalities of chromosome 13 and the presence of multiple cytogenetic high-risk abnormalities in newly diagnosed multiple myeloma [PDF]

, 2017
Fluorescence in situ hybridization evaluation is essential for initial risk stratification in multiple myeloma. While the presence of specific cytogenetic high-risk abnormalities (HRA) is known to confer a poor prognosis, less is known about the ...
M Binder, P T Greipp, S R Hayman, P Kapoor, F K Buadi, S R Zeldenrust, S K Kumar, M A Gertz, R P Ketterling, M Q Lacy, S J Russell, R A Kyle, A Dispenzieri, J A Lust, S V Rajkumar, Y L Hwa, R S Go, N Leung, W I Gonsalves   +18 more
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Clinical Significance of TP53 Abnormalities in Newly Diagnosed Multiple Myeloma

Turkish Journal of Hematology, 2021
Objective: This study aimed to identify the clinical significance of TP53 and common cytogenetic abnormalities. Materials and Methods: A total of 114 patients with newly diagnosed multiple myeloma (MM) and TP53 abnormalities were selected from two large ...
Fang Ye, Tongtong Wang, Aijun Liu, Yanchen Li, Ningning Li, Huan Wang, Wenming Chen   +6 more
doaj   +1 more source

Beta1 integrin deficiency results in multiple abnormalities of the knee joint [PDF]

, 2009
The lack of beta1 integrins on chondrocytes leads to severe chondrodysplasia associated with high mortality rate around birth. To assess the impact of beta1 integrin-mediated cell-matrix interactions on the function of adult knee joints, we conditionally
Hunziker, Ernst B, Drosse, Inga, Raducanu, A., Drosse, I., Raducanu, Aurelia, Aszódi, Attila, Hunziker, E. B., Aszodi, A.   +7 more
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Evidence for grey matter MTR abnormality in minimally disabled patients with early relapsing-remitting multiple sclerosis [PDF]

, 2004
Objectives: To establish whether magnetisation transfer ratio (MTR) histograms are sensitive to change in normal appearing grey matter (NAGM) in early relapsing-remitting multiple sclerosis (RRMS) in the absence of significant disability; and to assess ...
Griffin, C M B, Kapoor, R., Miller, D.H., Chard, D T, Hadjiprocopis, A., Ramio-Torrenta, L, Barker, G J; id_orcid, Davies, G.R., Ramió-Torrentà, L., Griffin, C.M.B., Rashid, W., Chard, D.T., Davies, G R, Miller, D H, Rashid, W, Thompson, A.J., Kapoor, R, Thompson, A J, Barker, G.J., Hadjiprocopis, A   +19 more
core   +1 more source

Neuroimaging Evidence of Major Morpho-Anatomical and Functional Abnormalities in the BTBR T+TF/J Mouse Model of Autism [PDF]

, 2013
BTBR T+tf/J (BTBR) mice display prominent behavioural deficits analogous to the defining symptoms of autism, a feature that has prompted a widespread use of the model in preclinical autism research.
Scattoni, Maria Luisa, Gozzi, Alessandro, Sotirios A Tsaftsaris, Tsaftsaris Sotirios A., Angelo Bifone (232236), Bifone Angelo, Mario Damiano (471358), Scattoni Maria Luisa, Bifone, Angelo, Alberto Galbusera (471359), Maria Luisa Scattoni (270655), Dodero Luca, Luca Dodero (471357), Gozzi Alessandro, Galbusera Alberto, Damiano Mario, Mario Damiano, Alberto Galbusera, Angelo Bifone, Alessandro Gozzi (232210), Tsaftaris, Sotirios A., Damiano, Mario, Galbusera, Alberto, Sotirios A. Tsaftsaris (471360), Luca Dodero, Maria Luisa Scattoni, Dodero, Luca, Alessandro Gozzi, Sforazzini, Francesco   +28 more
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Lipid Profile Abnormalities in ß-Thalassemia Patients with Multiple Blood Transfusions

Journal of Bahria University Medical and Dental College, 2023
Objective: To determine lipid profile abnormalities in ß -thalassemia patients with multiple blood transfusions in tertiary care hospital.   Study design and setting: This cross-sectional study was conducted in Chemical Pathology section ...
Syeda Sabahat Haidar, Mehvish Sana, Rukhsana Tumrani, Farwa Shafqat   +3 more
doaj   +1 more source

Genomic Diversity and Clinical Variability in Pediatric Primary Cutaneous Anaplastic Large Cell Lymphoma: A Case Series

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Primary cutaneous anaplastic large cell lymphoma (pcALCL) is a rare pediatric CD30‐positive T‐cell lymphoproliferative disorder with an excellent prognosis, but its genomic drivers are poorly defined. We report three children with skin‐limited disease demonstrating striking molecular heterogeneity, including NPM::ALK, NUP214::FRK, and a novel ...
Shoshana Greenberger, Efrat Bar‐Ilan, Victoria Marcu, Evgeny Grishin, Rinat Yacobi, Aviv Barzilai, Hana Golan, Assaf Arie Barg   +7 more
wiley   +1 more source

A longitudinal study of abnormalities on MRI and disability from multiple sclerosis [PDF]

, 2002
Background: In patients with isolated syndromes that are clinically suggestive of multiple sclerosis, such as optic neuritis or brain-stem or spinal cord syndromes, the presence of lesions as determined by T2-weighted magnetic resonance imaging (MRI) of ...
Ciccarelli, O., Thompson, A.J., Miller, D.H., Brex, P.A., O'Riordan, J.I., Sailer, M.   +5 more
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