Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Pain and NTRK1[original query] |
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Two novel mutant alleles of the gene encoding neurotrophic tyrosine kinase receptor type 1 (NTRK1) in a patient with congenital insensitivity to pain with anhidrosis: a splice junction mutation in intron 5 and cluster of four mutations in exon 15. Human mutation 2001 1 17 (1): 72. Bodzioch M, Lapicka K, Aslanidis C, Kacinski M, Schmitz |
Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. Brain : a journal of neurology 2009 Oct 132 (Pt 10): 2699-711. Rotthier Annelies, Baets Jonathan, De Vriendt Els, Jacobs An, Auer-Grumbach Michaela, Lévy Nicolas, Bonello-Palot Nathalie, Kilic Sara Sebnem, Weis Joachim, Nascimento Andrés, Swinkels Marielle, Kruyt Moyo C, Jordanova Albena, De Jonghe Peter, Timmerman Vince |
First evidence of a polygenic susceptibility to pain in a pediatric cohort. Anesthesia and analgesia 2013 Jan 116 (1): 170-7. Mamie Chantal, Rebsamen Michela C, Morris Michael A, Morabia Alfre |
Phenotypes and Genotypes in Five Children with Congenital Insensitivity to Pain with Anhidrosis. Pediatric neurology 2016 Apr . Wang Qing-Li, Guo Shanna, Duan Guangyou, Ying Ying, Huang Penghao, Liu Jing Yu, Zhang Xianw |
Variations in COMT and NTRK2 Influence Symptom Burden in Women Undergoing Breast Cancer Treatment. Biological research for nursing 2017 Jan 1099800417692877. Young Erin E, Kelly Debra Lynch, Shim Insop, Baumbauer Kyle M, Starkweather Angela, Lyon Debra |
Associations between single-nucleotide polymorphisms in the NTRK1 gene and basal pain sensitivity in young Han Chinese women. Neuroscience letters 2017 Oct . Li Ningbo, Duan Guangyou, Sun Jiaoli, Guo Shanna, Wang Qingli, Zheng Hua, Wang Cong, Zhu Changmao, Liu Yi, Zhang Xianw |
Exonic mutations in SCN9A (NaV1.7) are found in a minority of patients with erythromelalgia. Scandinavian journal of pain 2018 6 5 (4): 217-225. Zhang Zhiping, Schmelz Martin, Segerdahl Märta, Quiding Hans, Centerholt Carina, Juréus Anna, Carr Thomas Hedley, Whiteley Jessica, Salter Hugh, Kvernebo Mari Skylstad, Ørstavik Kristin, Helås Tormod, Kleggetveit Inge-Petter, Lunden Lars Kristian, Jørum Ell |
No Association of Polymorphisms in Nav1.7 or Nerve Growth Factor Receptor Genes with Trigeminal Neuralgia. Pain medicine (Malden, Mass.) 2018 Oct . Costa Grazielle Mara Ferreira, Rocha Luiz Paulo C, Siqueira Silvia Regina Dowgan Tesseroli de, Moreira Paula Rocha, Almeida-Leite Camila Mega |
Genotype, resilience and function and physical activity post hip fracture. International journal of orthopaedic and trauma nursing 2019 Mar . Resnick Barbara, Klinedinst N Jennifer, Yerges-Armstrong Laura, Magaziner Jay, Orwig Denise, Hochberg Marc C, Gruber-Baldini Ann L, Dorsey Susan |
Heterogeneity of clinical features and mutation analysis of NTRK1 in Han Chinese patients with congenital insensitivity to pain with anhidrosis. Journal of pain research 2019 2 12 453-465. Li Ningbo, Guo Shanna, Wang Qingli, Duan Guangyou, Sun Jiaoli, Liu Yi, Zhang Jin, Wang Cong, Zhu Changmao, Liu Jingyu, Zhang Xianw |
Congenital insensitivity to pain with anhidrosis syndrome: A series from Jordan. Clinical neurology and neurosurgery 2019 12 189 105636. Masri Amira, Shboul Mohammad, Khasawneh Aisha, Jadallah Rama, ALmustafa Asma, Escande-Beillard Nathalie, Hamamy Hanan, Bakri Faris, Reversade Bru |
Effects of genotype on TENS effectiveness in controlling knee pain in persons with mild to moderate osteoarthritis. European journal of pain (London, England) 2019 Oct . Govil Manika, Mukhopadhyay Nandita, Holwerda Teri, Sluka Kathleen, Rakel Barbara, Schutte Debra |
Molecular genetic analysis in 21 Chinese families with congenital insensitivity to pain with or without anhidrosis. European journal of neurology 2020 3 27 (8): 1697-1705. Zhao F, Mao B, Geng X, Ren X, Wang Y, Guan Y, Li S, Li L, Zhang S, You Y, Cao Y, Yang T, Zhao |
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- Page last updated:Apr 16, 2024
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