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Items: 1 to 20 of 328

1.

Inherited autonomic neuropathies.

Axelrod FB, Hilz MJ.

Semin Neurol. 2003 Dec;23(4):381-90. Review.

PMID:
15088259
2.

Hereditary sensory and autonomic neuropathies: types II, III, and IV.

Axelrod FB, Gold-von Simson G.

Orphanet J Rare Dis. 2007 Oct 3;2:39. Review.

3.
4.

Sympathetic skin response differentiates hereditary sensory autonomic neuropathies III and IV.

Hilz MJ, Stemper B, Axelrod FB.

Neurology. 1999 May 12;52(8):1652-7.

PMID:
10331694
5.

Disease mechanisms in hereditary sensory and autonomic neuropathies.

Verpoorten N, De Jonghe P, Timmerman V.

Neurobiol Dis. 2006 Feb;21(2):247-55. Epub 2005 Sep 23. Review.

PMID:
16183296
7.

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
8.

[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. Spanish.

9.

Hereditary sensory and autonomic neuropathies. Familial dysautonomia and other HSANs.

Axelrod FB.

Clin Auton Res. 2002 May;12 Suppl 1:I2-14. Review. No abstract available.

PMID:
12102459
10.

Recent advances in hereditary sensory and autonomic neuropathies.

Verhoeven K, Timmerman V, Mauko B, Pieber TR, De Jonghe P, Auer-Grumbach M.

Curr Opin Neurol. 2006 Oct;19(5):474-80. Review.

PMID:
16969157
11.

A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V.

Houlden H, King RH, Hashemi-Nejad A, Wood NW, Mathias CJ, Reilly M, Thomas PK.

Ann Neurol. 2001 Apr;49(4):521-5.

PMID:
11310631
12.

Oral manifestations of hereditary sensory and autonomic neuropathy type IV. Congenital insensitivity to pain with anhidrosis.

Amano A, Akiyama S, Ikeda M, Morisaki I.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1998 Oct;86(4):425-31.

PMID:
9798226
13.

Pediatric autonomic disorders.

Axelrod FB, Chelimsky GG, Weese-Mayer DE.

Pediatrics. 2006 Jul;118(1):309-21. Review.

PMID:
16818580
14.

Not 'indifference to pain' but varieties of hereditary sensory and autonomic neuropathy.

Dyck PJ, Mellinger JF, Reagan TJ, Horowitz SJ, McDonald JW, Litchy WJ, Daube JR, Fealey RD, Go VL, Kao PC, Brimijoin WS, Lambert EH.

Brain. 1983 Jun;106 (Pt 2):373-90.

PMID:
6189547
15.

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
16.

[Hereditary sensory and autonomic neuropathy type 2: two cases report].

Sanvito WL, Cataldo BO, Costa AR.

Arq Neuropsiquiatr. 2003 Sep;61(3A):654-8. Epub 2003 Sep 16. Portuguese.

17.

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
18.

Hereditary sensory neuropathies.

Houlden H, Blake J, Reilly MM.

Curr Opin Neurol. 2004 Oct;17(5):569-77. Review.

PMID:
15367861
19.

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
20.

Hereditary sensory neuropathy type I.

Auer-Grumbach M.

Orphanet J Rare Dis. 2008 Mar 18;3:7. doi: 10.1186/1750-1172-3-7. Review.

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