Results 131 to 140 of about 744 (162)
European Journal of Pain, Volume 30, Issue 8, September 2026.ABSTRACT Introduction Erythromelalgia is a rare disorder characterised by burning pain, erythema and increased skin temperature in the extremities. Its pathophysiological heterogeneity, together with variable treatment responses, complicates management in the absence of evidence‐based guidelines.
Camille Racca +8 more
wiley +1 more source
International Medical Case Reports JournalArash Jelodari,1 Laleh Hosseini21Clinical Psychology, Islamic Azad University of Ahvaz, Ahvaz, Iran; 2Rehabilitation Counselling, Payam Noor University of Isfahan, Isfahan, IranCorrespondence: Arash Jelodari, Email Arash.Jelodari@gmx.usAim: Hereditary ...
Jelodari A, Hosseini L
doaj
The regulation of stem cell fate and its application in neural regeneration
Interdisciplinary Medicine, Volume 4, Issue 5, September 2026.Regulating stem cell fate is crucial for neural regeneration. This review summarizes key physical, biological, and chemical strategies and their applications in repairing nerve injuries, providing new insights for regenerative medicine. Abstract Regulating the fate of stem cells (SCs) is a key technical problem in the field of regenerative medicine and
Yuexin He +3 more
wiley +1 more source
Hereditary sensory autonomic neuropathy type VI in the age of genetic testing
Background Hereditary sensory and autonomic neuropathy type VI (HSAN VI) is a rare recessive genetic disorder caused by mutations in the human dystonin (DST) gene.
Lekshmi Peringassery Sateesh +5 more
core +1 more source
Diabetes Distress in People at Risk for Diabetes‐Related Foot Disease in Primary Health Care
Journal of Foot and Ankle Research, Volume 19, Issue 3, September 2026.ABSTRACT Introduction Diabetes‐related distress (DRD) is exacerbated in people at risk of Diabetes‐related Foot Disease (DFD); however, knowledge on this topic is still limited, especially in Primary Health Care (PHC), which focuses on prevention and monitoring.
Thallita Cláudia Moraes Barbosa +7 more
wiley +1 more source
Journal of Inherited Metabolic Disease, Volume 49, Issue 5, September 2026.ABSTRACT Phosphomannomutase 2 congenital disorder of glycosylation (PMM2‐CDG) is a rare, autosomal recessive disease caused by PMM2 deficiency, which impairs conversion of mannose‐6‐phosphate into mannose‐1‐phosphate (M1P) and disrupts N‐linked glycosylation.
Mercedes Serrano +3 more
wiley +1 more source
Migraine: Epidemiology, Risk Factors, Pathophysiology, and Treatment
MedComm, Volume 7, Issue 9, September 2026.Migraine is a highly prevalent, female‐predominant, and disabling brain disorder shaped by genetic susceptibility, hormonal influences, modifiable attack factors, and comorbidity‐related progression. This review integrates current evidence on migraine epidemiology, phase‐specific neurovascular and neuroglial mechanisms, including CGRP signaling and ...
Weiwei Lu +9 more
wiley +1 more source
Ergothioneine: Biosynthesis, Molecular Mechanisms, Physiological Function, and Role in Disease
MedComm, Volume 7, Issue 9, September 2026.Ergothioneine is a natural thione antioxidant with significant biomedical potential. By reducing oxidative stress, inflammation, mitochondrial dysfunction, and cellular injury, ergothioneine may support interventions for aging‐related disorders, neurodegeneration, metabolic diseases, and skin protection.
Guojuan Yi +6 more
wiley +1 more source
, 2002 The aim of this study was to evaluate A-delta fibre function in a patient with hereditary sensory-autonomic neuropathy (HSAN). We used the mixed and cutaneous silent period techniques in addition to a conventional electromyographic investigation in a ...
G. Piazza +5 more
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