Results 211 to 220 of about 14,184,553 (374)

Estudio familiar de las hemofilias A y B: 5 años de experiencia en la detección de portadoras Family study of hemophilia A and B: 5 years of experience in carrier detection

open access: yesRevista Cubana de Hematología, Inmunología y Hemoterapia, 2010
La hemofilia se caracteriza por ser una enfermedad congénita del trastorno de la coagulación y constituye un desorden recesivo ligado al cromosoma X. El estudio molecular se realiza por estudios indirectos por ser causada por mutaciones heterogéneas en ...
Yaixa Piloto Roque   +6 more
doaj  

Modelling of a double‐scattering proton therapy nozzle using the FLUKA Monte Carlo code and analysis of linear energy transfer in patients treated for prostate cancer

open access: yesJournal of Applied Clinical Medical Physics, EarlyView.
Abstract Background The dose‐averaged linear energy transfer (LETD) in proton therapy (PT) has in pre‐clinical studies been linked to the relative biological effectiveness (RBE) of protons. Until recently, the most common PT delivery method in prostate cancer has been double‐scattered PT, with LETD only available through dedicated Monte Carlo (MC ...
Rasmus Klitgaard   +7 more
wiley   +1 more source

Closing the gap in plan quality: Leveraging deep‐learning dose prediction for adaptive radiotherapy

open access: yesJournal of Applied Clinical Medical Physics, Volume 26, Issue 5, May 2025.
Abstract Purpose Balancing quality and efficiency has been a challenge for online adaptive therapy. Most systems start the online re‐optimization with the original planning goals. While some systems allow planners to modify the planning goals, achieving a high‐quality plan within time constraints remains a common barrier.
Sean J. Domal   +9 more
wiley   +1 more source

Modified Factor VIII and Factor IX recombinant products

open access: yesHemaSphere, 2018
Elena Santagostino, Maria Elisa Mancuso
doaj   +1 more source

Genetic variation of rs438601 marker in the Iranian Population: An informative marker for molecular diagnosis of hemophilia B

open access: yesMajallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, 2014
Introduction: Hemophilia B is an X-linked recessive genetic disease caused by mutations in the coagulation Factor IX gene. Mutations in the Factor IX gene result in dysfunction or deficiency of coagulation factor of IX.
P Dorri, A Karimi , S Vallian boroujeni
doaj  

Impact of acceleration treatment on treatment plan and delivery qualities in tomotherapy for lung cancer

open access: yesJournal of Applied Clinical Medical Physics, Volume 26, Issue 5, May 2025.
Abstract Background Acceleration treatment (AT) is a novel treatment planning parameter introduced in the tomotherapy‐dedicated treatment planning system, Precision. This study explores the effects of AT on tomotherapy plans using helical (TomoHelical) and direct (TomoDirect) irradiation techniques.
Ryosuke Shirata   +9 more
wiley   +1 more source

Characterization of the defect in activation of factor IX Chapel Hill by human factor XIa. [PDF]

open access: bronze, 1981
K M Braunstein   +4 more
openalex   +3 more sources

Bone‐wise rigid registration of femur, tibia, and fibula for the tracking of temporal changes

open access: yesJournal of Applied Clinical Medical Physics, Volume 26, Issue 5, May 2025.
Abstract Background Multiple myeloma (MM) induces temporal alterations in bone structure, such as osteolytic bone lesions, which are challenging to identify through manual image interpretation. The large variation in radiologists' assessments, even at expert centers, further complicates diagnosis.
Arttu Ruohola   +5 more
wiley   +1 more source

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