Results 71 to 80 of about 34,982 (211)

The Results of The Surgical Treatment of Idiopathic Adolescent Scoliosis

مجله دانشکده پزشکی اصفهان, 2009
Background: Adolescent idiopathic scoliosis is the most common form of scoliosis. However, there is a little information exists about the patient satisfaction who underwent the surgery of adolescent idiopathic scoliosis. Most of the surgeons rely on the
Mohammadreza Etemadifar, Arsalan Mahmoodian, Farshad Mahnam   +2 more
doaj  

A case of cardiac arrest due to air embolism during scoliosis surgery

Journal of Orthopaedic Surgery, 2019
Cardiac arrest during scoliosis surgery is rare in idiopathic scoliosis. We present a case of cardiorespiratory collapse during corrective surgery in a young patient with idiopathic scoliosis. A diagnosis of venous air embolism was made by exclusion.
Mohamad Zaki Haji Mohd Amin, James Tan Boon Beng, Brian Teo Yian Young, Nur Aida Faruk Seman, Teo Shu Ching, Wong Chung Chek   +5 more
doaj   +1 more source

Long-Term Effects of Untreated Adolescent Idiopathic Scoliosis: A Review of the Literature [PDF]

Asian Spine Journal, 2016
Currently, adolescent idiopathic scoliosis (AIS) is principally regarded as benign, but some researchers have cited serious or extreme effects, including severe pain, cardiopulmonary compromise, social isolation, and even early death.
Hans-Rudolf Weiss, Nikos Karavidas, Marc Moramarco, Kathryn Moramarco   +3 more
doaj   +1 more source

Inhibition of Hypersialylation in Human Intervertebral Disc Degeneration Modulates Inflammation and Metabolism

Advanced Science, Volume 13, Issue 6, 30 January 2026.
Glycosylation, specifically hypersialylation, is identified as a critical factor in human intervertebral disc (IVD) degeneration—a major cause of low back pain. This study demonstrates that inhibiting sialylation reduces inflammation and oxidative stress in IVD tissues, suggesting new therapeutic possibilities.
Kieran Joyce, Aert F. Scheper, Aung Myat Phyo, Roisin O’ Flaherty, Richard Drake, Aiden Devitt, Martina Marchetti‐Deschmann, Radka Saldova, Abhay Pandit   +8 more
wiley   +1 more source

The Influence of Genetics in the Early Development of Axial Postural Abnormalities in Parkinson's Disease

Movement Disorders Clinical Practice, Volume 13, Issue 1, Page 230-235, January 2026.
ABSTRACT Background Postural abnormalities (PA) can complicate Parkinson's disease (PD). While age and motor severity are established predictors, the genetic role remains underexplored. Objective To evaluate the influence of major genetic variants on PA development in PD over 4 years.
Ilaria A. Di Vico, Silvia Gallo, Eleonora Bertoncello, Claudia Ledda, Michele Tinazzi, Leonardo Lopiano, Carlo Alberto Artusi   +6 more
wiley   +1 more source

Psychometric validation of the EuroQoL 5-Dimension 5-Level (EQ-5D-5L) in Chinese patients with adolescent idiopathic scoliosis [PDF]

, 2016
Background: Scoliosis is a common spinal deformity that occurs often during adolescence. Previous studies suggested that adolescent idiopathic scoliosis (AIS) patients can have various aspects of their lives being affected, due to disease presentation ...
Cheung, JPY, Cheung, KMC, Cheung, WHP, Lam, CLK, Luk, KDK, Samartzis, D, Wong, CKH   +6 more
core   +1 more source

Analysis of a Modified Version of the Inventory of Non‐Ataxia Signs Over 12 Years in Patients with Friedreich's Ataxia in the EFACTS Study

Movement Disorders, Volume 41, Issue 1, Page 200-211, January 2026.
Abstract Background Friedreich's ataxia is a rare, neurodegenerative, multisystem disorder. While ataxia is a hallmark, non‐ataxia signs, including muscle weakness, spasticity, and dysphagia are equally disabling. The Inventory of Non‐Ataxia Signs (INAS) is a symptom list transformable to a 16‐item count.
Stella Andrea Lischewski, Imis Dogan, Paola Giunti, Michael H. Parkinson, Caterina Mariotti, Alexandra Durr, Claire Ewenczyk, Sylvia Boesch, Wolfgang Nachbauer, Thomas Klopstock, Claudia Stendel, Francisco Javier Rodríguez de Rivera Garrido, Ludger Schöls, Zofia Fleszar, Thomas Klockgether, Marcus Grobe‐Einsler, Ilaria Giordano, Myriam Rai, Massimo Pandolfo, Heike Jacobi, Ralf‐Dieter Hilgers, Jörg B. Schulz, Kathrin Reetz, on behalf of the EFACTS Study Group, Elisabetta Indelicato, Matthias Amprosi, Cinzia Gellera, Alessia Mongelli, Anna Castaldo, Mario Fichera, Enrico Bertini, Gessica Vasco, Marie Biet, Marie Lorraine Monin, Florian Holtbernd, Nikolina Brcina, Christian Hohenfeld, Florentine Radelfahr, Almut T. Bischoff, Stefanie N. Hayer, Georgios Koutsis, Marianthi Breza, Francesc Palau, Mar O'Callaghan, Gilbert Thomas‐Black, Katarina Manso, Nita Solanky, Robyn Labrum   +47 more
wiley   +1 more source

Expanding the Genetic and Phenotypic Spectrum of DYT‐VPS16: The Importance of Splice‐Site Variants

Movement Disorders, Volume 41, Issue 1, Page 84-94, January 2026.
Abstract Background DYT‐VPS16, an early‐onset isolated dystonia caused by variants in the VPS16 gene, has been reported in fewer than 70 patients. Methods We explored the clinical and genotypic spectrum of DYT‐VPS16 by investigating early‐onset dystonia patients with VPS16 variants discovered in our large Biodatabank and through gene‐matching ...
Ana Westenberger, Edgard Verdura, Mandy Radefeldt, Leslie E. Sanderson, Kornelia Tripolszki, Anna Marcé‐Grau, Ana Cazurro‐Gutiérrez, Anita Nikoncuk, Rebecca Herzog, Ruslan Al‐Ali, Mariana Ferreira, Ligia S. Almeida, Tainá Regina Damaceno Silveira, Suliman Khan, Raphael Doyle Maia, Péter Klivényi, András Salamon, Volkan Baltaci, Asli Subasioglu, Jeanette Prada‐Arismendy, Goran Čuturilo, Sebastian Loens, Vera Tadic, Isabelle Maystadt, Deniz Karadurmus, Barbara Leube, Jonathan De Winter, Alice Monticelli, Liesbeth De Waele, Jonathan Baets, Mateja Vinkšel, Aleš Maver, Lorena Tschopp, Gabriela Ziegler, Ana Sanguinetti, Katja Lohmann, Tahsin Stefan Barakat, Peter Bauer, Belén Perez‐Dueñas, Aida M. Bertoli‐Avella   +39 more
wiley   +1 more source

Whole Exome Sequencing in Patients With Developmental Delay/Intellectual Disability (DD/ID), Epilepsy and the First Turkish Patient Diagnosed With BCL11A‐Related Intellectual Disability

Molecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.
In this study, WES analysis was performed on patients with DD/ID, global developmental delay, epilepsy, and multiple congenital anomalies who could not be diagnosed through karyotype, CMA, and other examinations. Nineteen pathogenic/likely pathogenic (P/LP) variants were identified in 19 patients, and with the confirmation made in the parents and ...
Nejmiye Akkus, Abdullah Canbal, Seda Guneysu, Erkan Gokce, Pakize Duzgun, İbrahim Barıs   +5 more
wiley   +1 more source

An alternative to a randomised control design for assessing the efficacy and effectiveness of bracing in adolescent idiopathic scoliosis [PDF]

, 2015
Randomised controlled trials (RCTs) that assessed the efficacy of bracing for adolescent idiopathic scoliosis have suffered from small sample sizes, low compliance and lack of willingness to participate.
Cheung, KMC, Cheung, WY, Fong, DYT, Fu, ICY, Kuong, EEYL, Luk, KDK, Mak, KC, Samartzis, D, To, MKT, Wong, YW   +9 more
core   +1 more source