Results 241 to 250 of about 16,288,597 (342)

Simulation‐free workflow for lattice radiation therapy using deep learning predicted synthetic computed tomography: A feasibility study

Journal of Applied Clinical Medical Physics, EarlyView.
Abstract Purpose Lattice radiation therapy (LRT) is a form of spatially fractionated radiation therapy that allows increased total dose delivery aiming for improved treatment response without an increase in toxicities, commonly utilized for palliation of bulky tumors.
Libing Zhu, Nathan Y. Yu, Safia K. Ahmed, Jonathan B. Ashman, Diego Santos Toesca, Michael P. Grams, Christopher L. Deufel, Jingwei Duan, Quan Chen, Yi Rong   +9 more
wiley   +1 more source

Assessing the influence of rapid diagnostic test (RDT) accuracy on malaria misdiagnosis and antimalarial resistance in Nigeria. [PDF]

Ann Med Surg (Lond)
Okereke PU, Ayodeji BM, Bolarinwa RT, Ayodeji OD, Popoola IO, Okereke WO, Ogamba N, Nworah LU, Umeh CV, Okpechukwu CP, Ibekwe SN, Emeka E, Tola OS.   +12 more
europepmc   +1 more source

Mitochondrial DNA disorders in neuromuscular diseases in diverse populations

Annals of Clinical and Translational Neurology, EarlyView.
Abstract Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite
Fei Gao, Katherine R Schon, Jana Vandrovcova, Özlem Yayıcı Köken, Sharika Raga, Kireshnee Naidu, Maryke Schoonen, Nimita Rani, Pedro Tomaselli, Dipti Baskar, Musambo Kapapa, Ipek Polat, Lindsay A Wilson, Kumarasamy Thangaraj, Uluç Yiş, Bevinahalli N Nandeesh, David Bearden, Michelle Kvalsund, Franclo Henning, Seena Vengalil, Atchayaram Nalini, Claudia F. R. Sobreira, Wilson Marques, Haluk Topoloğlu, Michael G Hanna, Sireesha Yareeda, Venugopalan Y Vishnu, Francois H van der Westhuizen, Izelle Smuts, Surita Meldau, Jo Wilmshurst, Büşranur Çavdarlı, Jeannine Heckmann, Patrick F Chinnery, Rita Horvath   +34 more
wiley   +1 more source

Towards a diagnostic test for sporadic ALS utilising deep learning and SNP microarrays

Hu J, Pain O, Khleifat AA, Shatunov A, Andersen PM, Başak NA, Cooper-Knock J, Corcia P, Couratier P, de Carvalho M, Drory V, Gotkine M, Landers JE, Glass JD, McLaughlin R, Mora Pardina JS, Morrison KE, Pinto S, Povedano M, Shaw CE, Shaw PJ, Silani V, Ticozzi N, van Damme P, van den Berg LH, Vourc’h P, Weber M, Hardiman O, Veldink JH, Project MinE ALS Sequencing Consortium, Dobson RJ, Schönhuth A, Al-Chalabi A, Iacoangeli A.   +33 more
europepmc   +1 more source

Determination of the performance of a novel diagnostic test for <i>Clostridioides difficile</i> toxins A and B using latent class analysis. [PDF]

J Clin Microbiol
Li J, Dendukuri N, Longtin Y, Banz A, Frenette C, Gervais P, Miller MA, Bourgault A-M, Dawang NL, Loo VG.   +9 more
europepmc   +1 more source

LINC00323 variant is associated with increased risk of essential tremor

Annals of Clinical and Translational Neurology, EarlyView.
Abstract Essential tremor (ET) is a common adult movement disorder, with accumulating evidence suggesting that genetic factors primarily account for ET risk. However, replication studies on the genetic variants have yielded inconsistent results. In our case–control study, we show that the LINC00323 variant, identified in a European GWAS study, is ...
Brendan Tan, Ebonne Ng, Qiao Yang Sun, Aaron Mai, Ling‐Ling Chan, Thomas Welton, Kumar M. Prakash, Kay Yaw Tay, Wing Lok Au, Louis C.S. Tan, Eng‐King Tan, Bin Xiao   +11 more
wiley   +1 more source

The Value of Labial Gland Biopsies as a Diagnostic Test for Sjögren's Syndrome. [PDF]

Head Neck Pathol
Clark M, Walsh H, Stephens-Laborde I, Khurram SA.   +3 more
europepmc   +1 more source

A Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra, Sara Bernal, David Almenta, Josefina Pérez‐Blanco, Valle Camacho, Isabel Sala, Mª Belén Sánchez‐Saudinós, Jesús García Castro, Judit Selma‐González, Miguel Ángel Santos‐Santos, Álvaro Carbayo, Janina Turon‐Sans, Ricard Rojas‐Garcia, Daniel Alcolea, Juan Fortea, Alberto Lleó, Oriol Dols‐Icardo, Ignacio Illán‐Gala   +17 more
wiley   +1 more source

Field evaluation of the Bioline Malaria Ag P.f/Pan rapid diagnostic test: causes of microscopy discordance and performance in Uganda. [PDF]

Malar J
Kabbale KD, Nsengimaana B, Semakuba FD, Kagurusi BA, Mwubaha C, Wiringilimaana I, Katairo T, Kiyaga S, Mbabazi M, Gonahasa S, Kamya MR, Tukwasibwe S, Nsobya SL, Asua V, Jjingo D, Agaba B, Maiteki-Sebuguzi C, Opigo J, Hilton K, Staedke SG, Dorsey G, Conrad MD, Greenhouse B, Ssewanyana I, Briggs J.   +24 more
europepmc   +1 more source

Design basis of the F9F grid-spaced FTR diagnostic assembly for irradiation tests in EBR-II

, 1973
S. Kaplan, D.B. Atcheson, J. S. Marron, W. Meinhardt   +3 more
openalex   +2 more sources