Results 161 to 170 of about 475,736 (375)
ABSTRACT The Clinical Assessment Scale in Autoimmune Encephalitis (CASE) tracks disease severity in autoimmune encephalitis (AE), but no threshold for significant change exists. We aimed to determine the minimally clinically important difference (MCID) for CASE.
Yihui Goh +8 more
wiley +1 more source
Study of the Influence of the Dental System Pathology on the Cerebral Blood Circulation
In Europe currently a quarter of the population suffers from brain diseases. In Russia cerebrovascular disease is one of the leading causes of death and disability.
Yurii I. Nyashin +2 more
doaj
Editorial: Journal of Negative Results in Biomedicine [PDF]
Christian P. Pfeffer, Bjørn R. Olsen
openalex +1 more source
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce +72 more
wiley +1 more source
A Depolarizing Leak in Sodium Bicarbonate Cotransporter NBCe1 Causes Brain Edema
ABSTRACT Objectives SLC4A4 encodes electrogenic sodium bicarbonate cotransporter NBCe1, prominently expressed in kidney and brain. Recessive loss‐of‐function variants in SLC4A4 cause proximal renal tubular acidosis, no brain edema. In the brain, NBCe1 is expressed by astrocytes, where it regulates pH and mediates astrocyte volume changes.
Quinty Bisseling +16 more
wiley +1 more source
Law and modern medicine: issues and prospects
Background. The study discusses the key problems of organizing healthcare in the Russian Federation, as well as the prospects for their legal resolution due to the emer-gence of innovative technologies (biomedicine, genomic medicine, digital medicine ...
G.B. Romanovskiy, O.V. Romanovskaya
doaj +1 more source
SPG4 and Dementia: Expanding the Clinical Spectrum
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza +19 more
wiley +1 more source
Semantic technologies for the automation of research in biomedicine
Ross D. King
openalex +2 more sources
Is the chronicity of HIV/AIDS fragile? Biomedicine, politics and sociability in an online social network [PDF]
Lucas Pereira de Melo +2 more
openalex +1 more source
Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone +8 more
wiley +1 more source

