Recent landmark publications from our research group outline a transformative approach to defining, studying and treating amyotrophic lateral sclerosis (ALS). Rather than approaching ALS as a single entity, we advocate targeting therapies to distinct “clusters” of patients based on their specific genomic and molecular features. Our findings point to the existence of a molecular taxonomy for ALS, bringing us a step closer to the establishment of a precision medicine approach in neurology practice
Caroline Eykens,1,2 Wim Robberecht1–31Research Group Experimental Neurology, Department of Neu...
Amyotrophic lateral sclerosis (ALS) belongs to the group of motor neuron diseases, in which the dege...
Objective markers of disease sensitive to the clinical activity, symptomatic progression, and underl...
Advances in diagnostic techniques and high-throughput biotechnologies provide a compelling opportuni...
Amyotrophic lateral sclerosis (ALS) is an incurable disease, caused by the loss of the upper and low...
Since amyotrophic lateral sclerosis (ALS) was discovered and described in 1869 as a neurodegenerativ...
Although the past two decades have produced exciting discoveries in the genetics and pathology of am...
Amyotrophic Lateral Sclerosis (ALS), more commonly referred to as Lou Gehrig’s disease, is a progres...
AbstractGenetic discoveries in ALS have a significant impact on deciphering molecular mechanisms of ...
Amyotrophic Lateral Sclerosis (ALS) is characterized by the degeneration of upper and lower motor ne...
Amyotrophic lateral sclerosis (ALS) is the most common form of motor neuron disease (MND). It is cur...
Amyotrophic lateral sclerosis (ALS) is a rare neurodegenerative disease that primarily affects motor...
The term motor neuron disease refers to several diseases affecting the motor neurons and is sometime...
Purpose of review Amyotrophic lateral sclerosis (ALS) is an archetypal complex disease wherein d...
Abstracts: Amyotrophic Lateral Sclerosis (ALS) is a progressive and disabling neurodegenerative diso...
Caroline Eykens,1,2 Wim Robberecht1–31Research Group Experimental Neurology, Department of Neu...
Amyotrophic lateral sclerosis (ALS) belongs to the group of motor neuron diseases, in which the dege...
Objective markers of disease sensitive to the clinical activity, symptomatic progression, and underl...
Advances in diagnostic techniques and high-throughput biotechnologies provide a compelling opportuni...
Amyotrophic lateral sclerosis (ALS) is an incurable disease, caused by the loss of the upper and low...
Since amyotrophic lateral sclerosis (ALS) was discovered and described in 1869 as a neurodegenerativ...
Although the past two decades have produced exciting discoveries in the genetics and pathology of am...
Amyotrophic Lateral Sclerosis (ALS), more commonly referred to as Lou Gehrig’s disease, is a progres...
AbstractGenetic discoveries in ALS have a significant impact on deciphering molecular mechanisms of ...
Amyotrophic Lateral Sclerosis (ALS) is characterized by the degeneration of upper and lower motor ne...
Amyotrophic lateral sclerosis (ALS) is the most common form of motor neuron disease (MND). It is cur...
Amyotrophic lateral sclerosis (ALS) is a rare neurodegenerative disease that primarily affects motor...
The term motor neuron disease refers to several diseases affecting the motor neurons and is sometime...
Purpose of review Amyotrophic lateral sclerosis (ALS) is an archetypal complex disease wherein d...
Abstracts: Amyotrophic Lateral Sclerosis (ALS) is a progressive and disabling neurodegenerative diso...
Caroline Eykens,1,2 Wim Robberecht1–31Research Group Experimental Neurology, Department of Neu...
Amyotrophic lateral sclerosis (ALS) belongs to the group of motor neuron diseases, in which the dege...
Objective markers of disease sensitive to the clinical activity, symptomatic progression, and underl...