Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 389

3.
4.

Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families.

Miura Y, Mardy S, Awaya Y, Nihei K, Endo F, Matsuda I, Indo Y.

Hum Genet. 2000 Jan;106(1):116-24. Erratum in: Hum Genet 2000 May;106(5):575.

PMID:
10982191
5.

Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis.

Indo Y, Tsuruta M, Hayashida Y, Karim MA, Ohta K, Kawano T, Mitsubuchi H, Tonoki H, Awaya Y, Matsuda I.

Nat Genet. 1996 Aug;13(4):485-8.

PMID:
8696348
6.

Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor.

Mardy S, Miura Y, Endo F, Matsuda I, Sztriha L, Frossard P, Moosa A, Ismail EA, Macaya A, Andria G, Toscano E, Gibson W, Graham GE, Indo Y.

Am J Hum Genet. 1999 Jun;64(6):1570-9.

8.

Nerve growth factor and the physiology of pain: lessons from congenital insensitivity to pain with anhidrosis.

Indo Y.

Clin Genet. 2012 Oct;82(4):341-50. doi: 10.1111/j.1399-0004.2012.01943.x. Epub 2012 Aug 13. Review.

PMID:
22882139
9.

Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis.

Huehne K, Zweier C, Raab K, Odent S, Bonnaure-Mallet M, Sixou JL, Landrieu P, Goizet C, Sarlangue J, Baumann M, Eggermann T, Rauch A, Ruppert S, Stettner GM, Rautenstrauss B.

Neuromuscul Disord. 2008 Feb;18(2):159-66. Epub 2008 Feb 20.

PMID:
18077166
10.

Nerve growth factor, interoception, and sympathetic neuron: lesson from congenital insensitivity to pain with anhidrosis.

Indo Y.

Auton Neurosci. 2009 May 11;147(1-2):3-8. doi: 10.1016/j.autneu.2009.01.008. Epub 2009 Feb 8. Review.

PMID:
19201660
11.

[Congenital insensitivity to pain with anhidrosis associated with congenital myasthenic syndrome].

Raspall-Chaure M, Del Toro-Riera M, Gratacós M, Cuenca-León E, Ferrer I, Indo Y, Roig-Quilis M, Macaya-Ruiz A.

Rev Neurol. 2005 Aug 16-31;41(4):218-22. Spanish.

12.

Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population.

Tüysüz B, Bayrakli F, DiLuna ML, Bilguvar K, Bayri Y, Yalcinkaya C, Bursali A, Ozdamar E, Korkmaz B, Mason CE, Ozturk AK, Lifton RP, State MW, Gunel M.

Neurogenetics. 2008 May;9(2):119-25. doi: 10.1007/s10048-008-0121-9. Epub 2008 Mar 6.

PMID:
18322713
14.

[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. Review. Hebrew.

PMID:
15999564
15.

Neurobiology of pain, interoception and emotional response: lessons from nerve growth factor-dependent neurons.

Indo Y.

Eur J Neurosci. 2014 Feb;39(3):375-91. doi: 10.1111/ejn.12448. Review.

PMID:
24494678
16.

Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV.

Verpoorten N, Claeys KG, Deprez L, Jacobs A, Van Gerwen V, Lagae L, Arts WF, De Meirleir L, Keymolen K, Ceuterick-de Groote C, De Jonghe P, Timmerman V, Nelis E.

Neuromuscul Disord. 2006 Jan;16(1):19-25. Epub 2005 Dec 20.

PMID:
16373086
17.

Skoura - a genetic island for congenital insensitivity to pain and anhidrosis among Moroccan Jews, as determined by a novel mutation in the NTRK1 gene.

Suriu C, Khayat M, Weiler M, Kfir N, Cohen C, Zinger A, Aslanidis C, Schmitz G, Falik-Zaccai TC.

Clin Genet. 2009 Mar;75(3):230-6. doi: 10.1111/j.1399-0004.2008.01143.x.

PMID:
19250380
18.

Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies.

Shatzky S, Moses S, Levy J, Pinsk V, Hershkovitz E, Herzog L, Shorer Z, Luder A, Parvari R.

Am J Med Genet. 2000 Jun 19;92(5):353-60.

PMID:
10861667
20.

The evaluation of autonomic nervous function in a patient with hereditary sensory and autonomic neuropathy type IV with novel mutations of the TRKA gene.

Ohto T, Iwasaki N, Fujiwara J, Ohkoshi N, Kimura S, Kawade K, Tanaka R, Matsui A.

Neuropediatrics. 2004 Oct;35(5):274-8.

PMID:
15534759

Supplemental Content

Support Center