Results 171 to 180 of about 466,653 (340)
INF2‐Related Charcot–Marie–Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights
ABSTRACT Background INF2 mutations cause focal segmental glomerulosclerosis (FSGS) and Charcot–Marie–Tooth disease (CMT). Accurate genetic diagnosis is critical, as INF2‐related FSGS is typically resistant to immunotherapy yet rarely recurs after transplantation, and its associated neuropathy can mimic treatable immune‐mediated disorders such as ...
Chikashi Yano +27 more
wiley +1 more source
Chronic kidney disease progression, long-term nursing care burden and habitual physical activity: an observational study in Japan. [PDF]
Ohashi Y +6 more
europepmc +1 more source
A Study on the Expectation and Awareness of Anti-Bribety Management Systyem Certification in Korea [PDF]
Byoungho Jun
openalex +1 more source
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco +18 more
wiley +1 more source
L’introduction d’une certification étrangère en Allemagne. L’exemple du DELF scolaire en Rhénanie du Nord-Westphalie [PDF]
Henny Rönneper
openalex +1 more source
ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini +13 more
wiley +1 more source
How to achieve high-quality participation in voluntary environmental regulation: Influencing factors and decision mechanism. [PDF]
Pan F, Xu Y, Wang L.
europepmc +1 more source

