Results 51 to 60 of about 75,889 (190)

Non-surgical interventions for paediatric pes planus

open access: yes, 2007
This is the protocol for a review and there is no abstract. The objectives are as follows: The aim of this review is to evaluate the evidence from randomised controlled trials for the non-surgical intervention of paediatric pes ...
Evans, A   +5 more
core   +2 more sources

Association between pediatric obesity and foot morphology: insights from a large-scale cross-sectional study using photogrammetry

open access: yesBMC Pediatrics
Background Childhood obesity is a critical public health concern with implications for musculoskeletal development. Foot posture abnormalities—particularly pes planus—may be associated with obesity and could serve as early diagnostic indicators. Aim This
Hakan Büyükçelebi   +5 more
doaj   +1 more source

Modulation of Lower Limb Biomechanics and Muscle Activation by Midsole Hardness in Children During Running

open access: yesJournal of Foot and Ankle Research, Volume 19, Issue 3, September 2026.
ABSTRACT Introduction Children's developing musculoskeletal systems are highly sensitive to mechanical stimuli. This study investigated the effects of running shoe midsole hardness (MH) (soft midsole [SM], medium midsole [MM], and hard midsole [HM]) on lower‐limb biomechanics and muscle activation during the running stance phase in children.
Zhaolong Ye   +14 more
wiley   +1 more source

Effect of barefoot walking on foot arch structure in Tribal children

open access: yesAsian Journal of Medical Sciences, 2016
Background: The anatomy of human foot owes its adaptation to bipedal locomotion. Support and propulsion are the two main activities of foot which are possible due to segmental nature of foot.
Shanmukha Varalakshmi Vangara
doaj   +1 more source

USP34 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes

open access: yesClinical Genetics, Volume 110, Issue 3, Page 315-324, September 2026.
Heterozygous loss‐of‐function variants in USP34 cause a novel neurodevelopmental disorder characterized by global developmental delay, speech impairment, autism, hypotonia, craniofacial dysmorphism, and distal limb anomalies. Disrupted Wnt/β‐catenin signaling via reduced Axin stabilization refines gene‐specific contributions within 2p15p16.1 ...
Helena Wigoda   +10 more
wiley   +1 more source

Biallelic SCO2 Variants Presenting as Motor‐Predominant Axonal Neuropathy With Complex IV Deficiency

open access: yesJournal of the Peripheral Nervous System, Volume 31, Issue 3, September 2026.
ABSTRACT Background and Aims SCO2 encodes a mitochondrial copper chaperone required for cytochrome c oxidase (COX) assembly and is classically associated with severe multisystem mitochondrial disease. We characterize a motor‐predominant axonal neuropathy presentation associated with biallelic SCO2 variants.
Adriana P. Rebelo   +5 more
wiley   +1 more source

Evaluation Of YouTube Information Quality About Pes Planus [PDF]

open access: yes, 2023
Background: The aim of this study was to measure the quality of information about “flatfoot” and “pes planus” presented online on the social media site YouTube and to determine the trends of viewers to medical information on YouTube.
Olcar, Hacı Ali   +9 more
core   +1 more source

Effects of CAD/CAM insoles and exercise on medial longitudinal arch and foot function in adolescents with flexible pes planus

open access: yesTurkish Journal of Kinesiology
The aim of our study was to investigate the effects of CAD/CAM-produced insoles and exercise on foot function and medial longitudinal arch (MLA) flexibility in adolescents aged 10-19 years diagnosed with painful flexible pes planus.
İbrahim Bulut   +4 more
doaj   +1 more source

Neuropathy With Demyelinating Features in a Patient With Biallelic HARS1 Variants

open access: yesJournal of the Peripheral Nervous System, Volume 31, Issue 3, September 2026.
ABSTRACT Background and Aims The HARS1 gene encodes cytoplasmic histidyl‐tRNA synthetase, which catalyzes the ligation of histidine to tRNAHIS in the cytoplasm as an early step in protein biosynthesis and is essential for cell viability. Pathogenic variants in HARS1 have been associated with three phenotypes: autosomal dominant Charcot–Marie–Tooth (CMT)
Christina Del Greco   +5 more
wiley   +1 more source

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1783-1798, August 2026.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet   +10 more
wiley   +1 more source

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