Cover Image

30‐sit‐to‐stand power is a better tool than isometric knee extensor strength to detect motor impairment in people with haemophilic arthropathy

Fuente: Wiley Open Access

Saved in:

Bibliographic Details
Main Authors:	Carlos Cruz‐Montecinos, María Moena‐León, Antonio Durán‐Ovalle, Aracelli Lizama‐Jofré, Verónica Soto, Andrés Oyarzún, Claudio Tapia, Sandro R. Freitas, Ronei S. Pinto, Rodrigo Núñez‐Cortés, Carla Daffunchio
Format:	Artículo Open Access
Published:	Wiley 2024
Subjects:	Haemophilia
Online Access:	Acceder al recurso
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Democratisation of physiotherapy for people with haemophilia
by: Carlos Cruz‐Montecinos, et al.
Published: (2024)

Accuracy and clinical role of digital templating for total knee arthroplasty performed on haemophilic knees
by: Arman Vahabi, et al.
Published: (2024)

Comparison of the kinematic analysis of indoor and outdoor gait in people with haemophilia and total knee replacement
by: Carlos Cruz‐Montecinos, et al.
Published: (2024)

Effects of resistance training on muscle strength in adults with haemophilia: A systematic review and meta‐analysis
by: Rodrigo Núñez‐Cortés, et al.
Published: (2024)

Pathogenesis of osteoarthritis, rheumatoid arthritis, and hemophilic arthropathy: The role of angiogenesis
by: Laura Caliogna, et al.
Published: (2024)

Self‐conducted sonographic monitoring of the knee in patients with haemophilia—A feasibility study
by: Anna Christina Strauss, et al.
Published: (2024)

Non‐surgical correction of knee flexion deformity in persons with haemophilia: A staged multidisciplinary approach
by: Merlyn Tilak, et al.
Published: (2024)

Multimodal Exercise Program of Balance and Strength Improves Dynamic Balance, Strength and Functionality and Decreases the Risk of Falls in Adults With Haemophilia
by: Ana Chimeno‐Hernández, et al.
Published: (2025)

Dental management of people with complex or rare inherited bleeding disorders
by: Lochana Nanayakkara, et al.
Published: (2024)

Association between cognitive impairment and functional limitations in everyday life in patients with haemophilia in Hong Kong
by: Yin Ting Cheung, et al.
Published: (2024)

Retrospective chart review of GI bleeding in people with von Willebrand disease
by: Jonathan C. Roberts, et al.
Published: (2024)

Assessing the factors affecting the accessibility of primary dental care for people with haemophilia
by: Kitti Sipos, et al.
Published: (2024)

Treatment of thrombotic cardiovascular diseases in people with haemophilia: A Japanese consensus study
by: Azusa Nagao, et al.
Published: (2024)

Preference of treatment characteristics among people with haemophilia or their caregivers, and physicians in the Japanese healthcare environment
by: Teruhisa Fujii, et al.
Published: (2024)

Functional clinical motor performance tests to assess potential fall risks in patients with haemophilia: A case‐control study
by: Fabian Tomschi, et al.
Published: (2024)

Race and ethnicity and the success of immune tolerance induction among people with severe haemophilia A in the United States
by: Stacey A. Fedewa, et al.
Published: (2024)

Pain attitudes and pain outcomes among people with bleeding disorders: Results from community voices in research
by: Corey Pierce, et al.
Published: (2024)

Expert United Kingdom consensus on the preservation of joint health in people with moderate and severe haemophilia A: A modified Delphi panel
by: Mike Laffan, et al.
Published: (2024)

Acute neuromuscular and perceptual responses to blood flow restriction exercise in adults with severe haemophilia: A pilot study
by: Daniel C. Ogrezeanu, et al.
Published: (2024)

Development of the coreHEM mental health patient‐reported outcome measure – A novel mental health outlook measure for people with haemophilia
by: Elizabeth Clearfield, et al.
Published: (2024)

Factor V haemostatic diathesis impairing thrombin activation, membrane binding and circulating antigen level due to a novel compound heterozygous mutation, Leu1821Ser and Gly2192Cys
by: Kimberley Talbot, et al.
Published: (2024)

Developing a Two‐Sided Decision Box to Facilitate Shared Decision‐Making for Switching From Conventional to Pharmacokinetic‐Tailored Prophylaxis in Haemophilia
by: Arun Keepanasseril, et al.
Published: (2025)

Competence and Confidence: An Evaluation of Physiotherapists' Knowledge and Self‐Perception About Physical Activity and Exercise in Patients With Haemophilia
by: Ozge Ozkutlu, et al.
Published: (2025)

The Humanitarian and Medical Crisis in Palestinian Territories: The Plight of Patients With Congenital Bleeding Disorders and Health Care Under Siege
by: Alessandro Gringeri, et al.
Published: (2026)

HEAD‐US Score and Cartilage Biomarkers in Patients With Severe Haemophilia A Who Receive Low‐Dose Factor VIII Prophylaxis
by: Arpanan Pramualratthakarn, et al.
Published: (2026)

Canadian clinical experience on switching from standard half‐life recombinant factor VIII (rFVIII), octocog alfa, to extended half‐life rFVIII, damoctocog alfa pegol, in persons with haemophilia A ≥ 12 years followed in a Comprehensive Hemophilia Care Program in Canada
by: Davide Matino, et al.
Published: (2024)

EAHAD statement on the ISTH clinical practice guideline for treatment of congenital haemophilia A and B
by: Pratima Chowdary, et al.
Published: (2024)

Comprehensive laboratory assessment of lonoctocog alfa versus octocog alfa in severe haemophilia A
by: Jens Müller, et al.
Published: (2024)

Differences and similarities in patient‐reported outcomes among men and women with haemophilia
by: Christine L. Kempton, et al.
Published: (2024)

Women and girls’ participation in haemophilia clinical trials
by: Stacey A. Fedewa, et al.
Published: (2024)

Acquired bleeding disorders
by: Andreas Tiede, et al.
Published: (2024)

UK Infected Blood Inquiry–An Historical Appraisal
by: Christopher A. Ludlam
Published: (2026)

Monitoring Extended Half‐Life Factor VIII and IX Concentrates: Performance in Routine Clotting‐and Thrombin Generation Assays
by: An K. Stroobants, et al.
Published: (2026)

Coagulation Factor Consumption and Medium‐ to Long‐Term Outcomes of Achilles Tendon Lengthening With and Without External Fixation in Haemophilia
by: Ze Chen, et al.
Published: (2025)

Real‐World Unmet Treatment Needs for Patients With Haemophilia: Results From the Global Adelphi Disease Specific Programme Database
by: Víctor Jiménez Yuste, et al.
Published: (2026)

Blood Group O Does Not Increase the Risk of Inhibitors in Severe Haemophilia A: Data from the PedNet Study Group
by: Marloes de Kovel, et al.
Published: (2025)

Identification and Analysis of Mitochondria‐Related Proteins in Haemophilic Arthritis Synovial Membranes Based on Proteomic Analysis
by: Haitao Ma, et al.
Published: (2025)

Effect of etranacogene dezaparvovec on quality of life for severe and moderately severe haemophilia B participants: Results from the phase III HOPE‐B trial 2 years after gene therapy
by: Robbin Itzler, et al.
Published: (2024)

Weight‐Bearing Lunge Test in Young Patients With Haemophilia and Limited Joint Damage: Reliability and Functional Associations for Ankle Assessment
by: Firat Tan, et al.
Published: (2026)

Prevalence and Impact of Heavy Menstrual Bleeding in Women With von Willebrand Disease Across Age Groups: A Retrospective Study
by: Anna Olsson, et al.
Published: (2025)