229 related articles for article (PubMed ID: 14976160)
21. Abnormal neutrophil chemotactic activity in children with congenital insensitivity to pain with anhidrosis (CIPA): the role of nerve growth factor.
Beigelman A; Levy J; Hadad N; Pinsk V; Haim A; Fruchtman Y; Levy R
Clin Immunol; 2009 Mar; 130(3):365-72. PubMed ID: 18955016
[TBL] [Abstract][Full Text] [Related]
22. No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type V.
Toscano E; Simonati A; Indo Y; Andria G
Ann Neurol; 2002 Aug; 52(2):224-7. PubMed ID: 12210794
[TBL] [Abstract][Full Text] [Related]
23. [Clinical and genetic aspects of congenital insensitivity to pain with anhidrosis].
Schwarzkopf R; Pinsk V; Weisel Y; Atar D; Gorzak Y
Harefuah; 2005 Jun; 144(6):433-7, 453, 452. PubMed ID: 15999564
[TBL] [Abstract][Full Text] [Related]
24. Polymorphic corneal amyloidosis: a disorder due to a novel mutation in the transforming growth factor beta-induced (BIGH3) gene.
Eifrig DE; Afshari NA; Buchanan HW; Bowling BL; Klintworth GK
Ophthalmology; 2004 Jun; 111(6):1108-14. PubMed ID: 15177960
[TBL] [Abstract][Full Text] [Related]
25. Congenital insensitivity to pain with anhydrosis. Report of two unrelated cases.
Vital A; Fontan D; Julien J; Talon P; Héron B; Routon MC; Ponsot G; Vital C
J Peripher Nerv Syst; 1998; 3(2):125-32. PubMed ID: 10959246
[TBL] [Abstract][Full Text] [Related]
26. In vitro receptor binding properties of a "painless" NGF mutein, linked to hereditary sensory autonomic neuropathy type V.
Covaceuszach S; Capsoni S; Marinelli S; Pavone F; Ceci M; Ugolini G; Vignone D; Amato G; Paoletti F; Lamba D; Cattaneo A
Biochem Biophys Res Commun; 2010 Jan; 391(1):824-9. PubMed ID: 19945432
[TBL] [Abstract][Full Text] [Related]
27. The effect of endoneurial nerve growth factor on calcitonin gene-related peptide expression in primary sensory neurons.
Ruiz G; Baños JE
Brain Res; 2005 Apr; 1042(1):44-52. PubMed ID: 15823252
[TBL] [Abstract][Full Text] [Related]
28. Stoichiometric alteration of PMP22 protein determines the phenotype of hereditary neuropathy with liability to pressure palsies.
Li J; Ghandour K; Radovanovic D; Shy RR; Krajewski KM; Shy ME; Nicholson GA
Arch Neurol; 2007 Jul; 64(7):974-8. PubMed ID: 17620487
[TBL] [Abstract][Full Text] [Related]
29. Rescue of NGF-deficient mice I: transgenic expression of NGF in skin rescues mice lacking endogenous NGF.
Harrison SM; Davis BM; Nishimura M; Albers KM; Jones ME; Phillips HS
Brain Res Mol Brain Res; 2004 Mar; 122(2):116-25. PubMed ID: 15010204
[TBL] [Abstract][Full Text] [Related]
30. Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.
Stalmans I
Verh K Acad Geneeskd Belg; 2005; 67(4):229-76. PubMed ID: 16334858
[TBL] [Abstract][Full Text] [Related]
31. Congenital insensitivity to pain with anhidrosis. Report of a case and review of the literature.
Theodorou SD; Klimentopoulou AE; Papalouka E
Acta Orthop Belg; 2000 Apr; 66(2):137-45. PubMed ID: 10842874
[TBL] [Abstract][Full Text] [Related]
32. [Hereditary sensory and autonomic neuropathies. The neurophysiological and pathological aspects of two cases with congenital insensitivity to pain].
Esteban-García A; Salinero-Paniagua E; Traba A; Prieto-Montalvo J; Polo-Arrondo AP; Godes-Medrano B; Fernández-Lorente J
Rev Neurol; 2004 Sep 16-30; 39(6):525-9. PubMed ID: 15467989
[TBL] [Abstract][Full Text] [Related]
33. Mutation analysis of congenital cataracts in Indian families: identification of SNPS and a new causative allele in CRYBB2 gene.
Santhiya ST; Manisastry SM; Rawlley D; Malathi R; Anishetty S; Gopinath PM; Vijayalakshmi P; Namperumalsamy P; Adamski J; Graw J
Invest Ophthalmol Vis Sci; 2004 Oct; 45(10):3599-607. PubMed ID: 15452067
[TBL] [Abstract][Full Text] [Related]
34. Congenital insensitivity to pain (hereditary sensory and autonomic neuropathy type V): a rare case report.
Singla S; Marwah N; Dutta S
J Dent Child (Chic); 2008; 75(2):207-11. PubMed ID: 18647521
[TBL] [Abstract][Full Text] [Related]
35. A missense point mutation in nerve growth factor (NGF
Yang W; Sung K; Xu W; Rodriguez MJ; Wu AC; Santos SA; Fang S; Uber RK; Dong SX; Guillory BC; Orain X; Raus J; Jolivalt C; Calcutt N; Rissman RA; Ding J; Wu C
Prog Neurobiol; 2020 Nov; 194():101886. PubMed ID: 32693191
[TBL] [Abstract][Full Text] [Related]
36. Transient receptor potential vanilloid 1, vanilloid 2 and melastatin 8 immunoreactive nerve fibers in human skin from individuals with and without Norrbottnian congenital insensitivity to pain.
Axelsson HE; Minde JK; Sonesson A; Toolanen G; Högestätt ED; Zygmunt PM
Neuroscience; 2009 Sep; 162(4):1322-32. PubMed ID: 19482060
[TBL] [Abstract][Full Text] [Related]
37. Central nervous system involvement in hereditary neuropathy with liability to pressure palsies: description of a large family with this association.
Sanahuja J; Franco E; Rojas-García R; Gallardo E; Combarros O; Begué R; Granés P; Illa I
Arch Neurol; 2005 Dec; 62(12):1911-4. PubMed ID: 16344349
[TBL] [Abstract][Full Text] [Related]
38. No involvement of the nerve growth factor gene locus in hypertension in spontaneously hypertensive rats.
Nemoto K; Sekimoto M; Fukamachi K; Kageyama H; Degawa M; Hamadai M; Hendley ED; Macrae IM; Clark JS; Dominiczak AF; Ueyama T
Hypertens Res; 2005 Feb; 28(2):155-63. PubMed ID: 16025743
[TBL] [Abstract][Full Text] [Related]
39. Behavioral and histological effects of endoneurial administration of nerve growth factor: possible implications in neuropathic pain.
Ruiz G; Ceballos D; Baños JE
Brain Res; 2004 Jun; 1011(1):1-6. PubMed ID: 15140639
[TBL] [Abstract][Full Text] [Related]
40. [Effect of nerve growth factor on the promotion of sensory recovery of large skin graft in patients].
Wu ZH; Huang J; Gao WH; Wang AL; Jia Q; Chen B; Xu S; Gu YH
Zhonghua Shao Shang Za Zhi; 2007 Dec; 23(6):440-3. PubMed ID: 18457257
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]