Results 161 to 170 of about 37,969 (302)
Congenital cervical spinal muscular atrophy: a non-familial, non progressive condition of the upper limbs. [PDF]
G. Hageman +3 more
openalex +1 more source
Objective Identifying modifiable factors influencing amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) risk is important for prevention. Blood biomarkers, particularly cholesterol, have been associated with neurodegenerative risk, but findings in ALS are inconsistent, and data on FTD are limited.
Christos V. Chalitsios +5 more
wiley +1 more source
Demographic, clinical and genetic characteristics of patients with amyotrophic lateral sclerosis from two specialised centres in Austria. [PDF]
Keritam O +19 more
europepmc +1 more source
Objective Amyotrophic lateral sclerosis (ALS) has a very specific neuroimaging signature, but the molecular underpinnings of the strikingly selective anatomic involvement have not elucidated to date. Accordingly, a large neuroimaging study was conducted with 258 participants to evaluate associations between patterns of neurodegeneration and focal ...
Marlene Tahedl +10 more
wiley +1 more source
Case of Progressive Muscular Atrophy, with Bulbar Paralysis [PDF]
A. W. Fox
openalex +1 more source
The Epidemiology of Primary Lateral Sclerosis: Results from a Population‐Based Cohort
Objective In this population‐based study, we described the epidemiology of primary lateral sclerosis (PLS) in northern Italy and compared the clinical characteristics of patients with PLS to those with predominant upper motor neuron (PUMN) involvement and classic amyotrophic lateral sclerosis (ALS).
Rosario Vasta +17 more
wiley +1 more source
Scoliosis correction in spinal muscular atrophy : the influence of genetic severity, functional level, and disease-modifying agents on postoperative outcomes. [PDF]
Çiftci S +6 more
europepmc +1 more source

