Diagnosis of neurofibromatosis type 1 (NF1) requires a combination of clinical assessment, genetic testing, and imaging studies. 1 NF1 is a rare genetic disorder characterized by the development of ...

The ratio of posterior wall thickness to the minimum voltage of QRS complexes in limb leads and several parameters derived from electrocardiography could independently predict ATTR-CM. The ratio of ...

Between 21.4% and 57.8% of patients from a real-world ATTR-CM cohort would have been eligible to take part in clinical trials testing disease-modifying therapies. Inclusion and exclusion criteria used ...

The devices are available for patients aged 17 years and older at no extra cost and can be used after receiving training from a healthcare professional. Two new medical devices that will facilitate ...

POEMS syndrome remains a diagnostic challenge due to its variable presentation and overlap with other demyelinating neuropathies, such as CIDP. Cases of polyneuropathy, organomegaly, endocrinopathy, ...

NMOSD is a rare autoimmune disorder characterized by inflammation and demyelination of nerves in the central nervous system (CNS), particularly the optic nerves and spinal cord. It typically manifests ...

The combination strategy of LXH254 and trametinib effectively overcame adaptive and acquired resistance to MEK inhibition. Combined inhibition of B/CRAF and mitogen-activated extracellular ...

The AI ECG amyloid algorithm screening tool may provide decision support for clinicians and improve the diagnosis and survival of patients with ATTR-CM. A new study seeks to test an artificial ...

In all 6 CANVAS cases where SRAR was calculable, values exceeded 0.33 despite sometimes misleading length-dependent patterns. The sural/radial amplitude ratio (SRAR) as a valuable electrophysiological ...

Although a pregnant patient may exhibit a favorable response to IVIG treatment in one FNAIT-affected pregnancy, this does not ensure the success of IVIG therapy in subsequent pregnancies. A favorable ...