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Microdeletion in a FAAH pseudogene identified in a patient with high anandamide concentrations and pain insensitivityBRITISH JOURNAL OF ANAESTHESIAIF9.22019-08-0185OAAI
A novel human pain insensitivity disorder caused by a point mutation in ZFHX2BRAINIF11.72017-12-1430OAAI
Rare NaV1.7 variants associated with painful diabetic peripheral neuropathyPAINIF5.52017-11-22111OAAI
Stratifying patients with peripheral neuropathic pain based on sensory profiles: algorithm and sample size recommendationsPAINIF5.52017-05-02148OAAI
The Pain in Neuropathy Study (PiNS): a cross-sectional observational study determining the somatosensory phenotype of painful and painless diabetic neuropathyPAINIF5.52016-05-01239OAAI
NULL MUTATION IN SCN9A IN WHICH NOXIOUS STIMULI CAN BE DETECTED IN THE ABSENCE OF PAINNEUROLOGYIF8.52014-10-215OAAI
Sensory, psychological, and metabolic dysfunction in HIV-associated peripheral neuropathy: A cross-sectional deep profiling studyPAINIF5.52014-09-0177OAAI
Novel Mutations Mapping to the Fourth Sodium Channel Domain of Nav1.7 Result in Variable Clinical Manifestations of Primary ErythromelalgiaNEUROMOLECULAR MEDICINEIF3.92013-01-0655OAAI
Intermediate Charcot-Marie-Tooth disease due to a novel Trp101Stop myelin protein zero mutation associated with debilitating neuropathic painPAINIF5.52012-08-0116OA
Imaging the neural correlates of neuropathic pain and pleasurable relief associated with inherited erythromelalgia in a single subject with quantitative arterial spin labellingPAINIF5.52012-05-0127OAAI
A Gain-of-Function Mutation in TRPA1 Causes Familial Episodic Pain SyndromeNEURONIF152010-06-01394OAAI
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