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Annals of Oncology, ISSN 0923-7534, 2014, Volume 25, Issue 1, pp. 126 - 131
Background: There is scarce data available about epidermal growth factor receptor (EGFR) mutations other than common exon 19 deletions and exon 21 (L858R)... 
Non-small-cell lung cancer | Exon 20 mutations | Tyrosine-kinase inhibitors | Epidermal growth factor receptor mutations | Exon 18 mutations | epidermal growth factor receptor mutations | GEFITINIB | axon 18 mutations | exon 20 mutations | tyrosine-kinase inhibitors | TKIS | SENSITIVITY | CLASSIFICATION | SOMATIC MUTATIONS | CHEMOTHERAPY | TYROSINE KINASE INHIBITORS | GROWTH-FACTOR RECEPTOR | ONCOLOGY | NEVER SMOKERS | CLINICAL-RESPONSE | non-small-cell lung cancer | Lung Neoplasms - drug therapy | Receptor, Epidermal Growth Factor - genetics | Exons | Lung Neoplasms - mortality | Humans | Middle Aged | Male | Antineoplastic Agents - therapeutic use | Young Adult | Aged, 80 and over | Adult | Female | Adenocarcinoma - genetics | Antineoplastic Agents - pharmacology | Lung Neoplasms - genetics | Genetic Association Studies | Carcinoma, Non-Small-Cell Lung - genetics | Gene Frequency | Proportional Hazards Models | Adenocarcinoma - drug therapy | Carcinoma, Non-Small-Cell Lung - mortality | Disease-Free Survival | Drug Resistance, Neoplasm - genetics | Protein Kinase Inhibitors - therapeutic use | Receptor, Epidermal Growth Factor - antagonists & inhibitors | Aged | Protein Kinase Inhibitors - pharmacology | Carcinoma, Non-Small-Cell Lung - drug therapy | Adenocarcinoma - mortality | Life Sciences | Cancer | exon 18 mutations | Original
Journal Article
Annals of Neurology, ISSN 0364-5134, 01/2017, Volume 81, Issue 1, pp. 117 - 128
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2011, Volume 88, Issue 4, pp. 422 - 432
Journal Article
Journal Article
European Journal of Neurology, ISSN 1351-5101, 01/2017, Volume 24, Issue 1, pp. 37 - 45
Background and purpose The clinical characteristics of colony stimulating factor 1 receptor (CSF1R) related adult‐onset leukoencephalopathy with axonal... 
leukoencephalopathy | pigmented orthochromatic leukodystrophy | colony stimulating factor 1 receptor | adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia | hereditary diffuse leukoencephalopathy with spheroids | adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | HDLS | MRI | LEUKODYSTROPHY | INVOLVEMENT | NEUROSCIENCES | CLINICAL NEUROLOGY | FEATURES | IMPAIRMENT | PROGRESSIVE MULTIPLE-SCLEROSIS | HEREDITARY DIFFUSE LEUKOENCEPHALOPATHY | CORPUS-CALLOSUM | PATIENT | Leukoencephalopathies - genetics | Neuroglia - pathology | Humans | Leukoencephalopathies - diagnostic imaging | Middle Aged | Male | Young Adult | Receptors, Granulocyte-Macrophage Colony-Stimulating Factor - genetics | Aged, 80 and over | Adult | Female | Pyramidal Tracts - pathology | Leukoencephalopathies - pathology | Penetrance | Sex Characteristics | Mutation - genetics | White Matter - pathology | Corpus Callosum - diagnostic imaging | Magnetic Resonance Imaging | White Matter - diagnostic imaging | Movement Disorders - physiopathology | Pyramidal Tracts - diagnostic imaging | Axons - pathology | Corpus Callosum - pathology | Movement Disorders - etiology | Adolescent | Age of Onset | Heterozygote | Aged | Tyrosine | Genetic research | Genetic aspects | Leukoencephalopathy | Kinases | Age | Mutation | Original
Journal Article
Science, ISSN 0036-8075, 2014, Volume 343, Issue 6170, pp. 506 - 511
Journal Article
Journal Article
Journal Article