Results 61 to 70 of about 3,257 (143)

Pseudo‐Dystonic Gait in a Preschool Child: Foot Posturing Contralateral to a Cuboid Fracture

Movement Disorders Clinical Practice, EarlyView.
Allison J. Chirigos, Donald L. Gilbert, Barbara E. Hallinan, Jes Marchbank, Alberto J. Espay   +4 more
wiley   +1 more source

Tackling Anxiety‐ and Stress‐Related Freezing of Gait in People With Parkinson's Disease (TACKLING‐FOG): Study Protocol for a Randomized Controlled Trial

European Journal of Neuroscience, Volume 63, Issue 12, June 2026.
Participants undergo baseline assessment followed by randomization to either the intervention or a waitlist control condition. The intervention group receives four sessions immediately, while the waitlist group enters a 4‐week waiting period. Post‐intervention assessment is conducted in both groups, after which the waitlist group crosses over to ...
Gijs Vissers, Anouk Tosserams, Annelien A. Duits, Anouk van der Heide, Bastiaan R. Bloem, Rick C. Helmich, William R. Young, Jorik Nonnekes   +7 more
wiley   +1 more source

A Difficult‐to‐Manage Case of Primary Idiopathic Erythromelalgia—Case Report

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Erythromelalgia is a rare condition with symptoms of erythema, warmth, and painful extremities exacerbated by warmth and relieved by cooling. Pain management is often challenging. The sodium channel blocker, lacosamide, was most effective in this patient.
Sarah Wide, Rajish S. K. Shil, Bernhard Frank, Viraj Bharambe   +3 more
wiley   +1 more source

¿Caminan de manera diferente los niños con trastorno por déficit de atención hiperactividad (TDAH)? Relación entre marcha de puntillas idiopática y TDAH

Anales de Pediatría, 2018
Resumen: Introducción: La marcha de puntillas idiopática (MPI) se describe como el patrón de marcha sin apoyo del talón en niños mayores de 3 años.
Víctor Soto Insuga, Beatriz Moreno Vinués, Rebeca Losada del Pozo, María Rodrigo Moreno, Marta Martínez González, Raquel Cutillas Ruiz, Carmen Mateos Carmen   +6 more
doaj   +1 more source

Pycnodysostosis With Papilledema and Isolated Low Parathyroid Hormone Levels in an Eight‐Year‐Old Girl: A Genetically Confirmed Case Report

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Pycnodysostosis is a rare autosomal recessive skeletal dysplasia resulting from pathogenic variants in the CTSK gene, which encodes cathepsin K, a lysosomal cysteine protease expressed in osteoclasts. Deficiency of this enzyme leads to defective bone resorption and generalized osteosclerosis.
Meghana Krishna Kesineni, Naveen Jagadish Kandregula, Sameer Kumar Majety, Yulia Alekseevna Pimenova, Bhargav Kadali, Vineeth Potluri, Prudhvi Lekkala   +6 more
wiley   +1 more source

The Interplay Between IL‐6, Hepcidin, and BMPR2 Signalling in Pulmonary Arterial Hypertension: Mechanistic Insights Into Vascular Remodelling

Pulmonary Circulation, Volume 16, Issue 2, April 2026.
ABSTRACT Pulmonary arterial hypertension (PAH) is characterized by excessive pulmonary vasoconstriction and vascular remodelling, with mutations in bone morphogenetic protein receptor type 2 (BMPR2) being the most common genetic alteration associated with the disease.
Quezia K. Toe, Theo Issitt, Gregory J. Quinlan, S. John Wort   +3 more
wiley   +1 more source

Sotatercept in TBX4 Associated Heritable Pulmonary Arterial Hypertension: A Case Report of a Super Responder

Pulmonary Circulation, Volume 16, Issue 2, April 2026.
ABSTRACT Pulmonary arterial hypertension (PAH) is a life‐threatening disease of the pulmonary arteries. Progressively increasing pulmonary artery pressure may lead to fatal failure of the right ventricle, necessitating aggressive drug treatment. Sotatercept, a novel drug for PAH‐targeted therapy, shows promising results in clinical trials. Nevertheless,
Jop W. Schneijdenberg, Annemien E. van den Bosch, Miriam E. Kap, Robert M. Kauling, Prewesh P. Chandoesing, Leon M. van den Toorn, Bas J. Mathot, Thomas Koudstaal, Karin A. Boomars   +8 more
wiley   +1 more source

Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay in Two Half‐Siblings

Annals of Clinical and Translational Neurology, Volume 13, Issue 2, Page 413-417, February 2026.
ABSTRACT Autosomal recessive spastic ataxia of Charlevoix‐Saguenay (ARSACS) is caused by biallelic pathogenic variants in the SACS gene. We report the clinical, radiologic and neurophysiologic features of a pair of half‐siblings who presented with progressive cerebellar ataxia, peripheral neuropathy and upper motor neuron signs.
Dennis Yeow, Matthew Katz, Jonathan Rodgers, Mark Davis, Thomas Robertson, R. J. McKinlay Gardner, Pamela A. McCombe   +6 more
wiley   +1 more source

Neurodevelopment in preschool idiopathic toe-walkers

Neurología (English Edition), 2017
Introduction: Idiopathic toe walking, a differential diagnosis for neurological and orthopaedic disorders, has been associated with neurodevelopmental alterations.
P. Martín-Casas, R. Ballestero-Pérez, A. Meneses-Monroy, J.V. Beneit-Montesinos, M.A. Atín-Arratibel, J.A. Portellano-Pérez   +5 more
doaj   +1 more source

Returning to Marathons: Complete Restoration of Exercise with Runner's Dystonia After Globus Pallidus Internus Deep Brain Stimulation

Movement Disorders, Volume 41, Issue 7, Page 1902-1903, July 2026.
Arthur Thevathasan, Kristian Bulluss, Katya Kotschet, Wesley Thevathasan   +3 more
wiley   +1 more source