Unknown

Dataset Information

0

Eliminating barriers to personalized medicine: learning from neurofibromatosis type 1.


ABSTRACT: With the emergence of high-throughput discovery platforms, robust preclinical small-animal models, and efficient clinical trial pipelines, it is becoming possible to envision a time when the treatment of human neurologic diseases will become personalized. The emergence of precision medicine will require the identification of subgroups of patients most likely to respond to specific biologically based therapies. This stratification only becomes possible when the determinants that contribute to disease heterogeneity become more fully elucidated. This review discusses the defining factors that underlie disease heterogeneity relevant to the potential for individualized brain tumor (optic pathway glioma) treatments arising in the common single-gene cancer predisposition syndrome, neurofibromatosis type 1 (NF1). In this regard, NF1 is posited as a model genetic condition to establish a workable paradigm for actualizing precision therapeutics for other neurologic disorders.

SUBMITTER: Gutmann DH 

PROVIDER: S-EPMC4132567 | biostudies-literature | 2014 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Eliminating barriers to personalized medicine: learning from neurofibromatosis type 1.

Gutmann David H DH  

Neurology 20140627 5


With the emergence of high-throughput discovery platforms, robust preclinical small-animal models, and efficient clinical trial pipelines, it is becoming possible to envision a time when the treatment of human neurologic diseases will become personalized. The emergence of precision medicine will require the identification of subgroups of patients most likely to respond to specific biologically based therapies. This stratification only becomes possible when the determinants that contribute to dis  ...[more]

Similar Datasets

| S-EPMC4264975 | biostudies-literature
| S-EPMC8931211 | biostudies-literature
| S-EPMC6437674 | biostudies-literature
| S-EPMC8604218 | biostudies-literature
| S-EPMC3513204 | biostudies-literature
| PRJNA606620 | ENA
| PRJNA606621 | ENA
| S-EPMC4634358 | biostudies-literature
| S-EPMC10233311 | biostudies-literature
| S-EPMC7149555 | biostudies-literature