382 related articles for article (PubMed ID: 12102461)
1. Assessment and evaluation of hereditary sensory and autonomic neuropathies with autonomic and neurophysiological examinations.
Hilz MJ
Clin Auton Res; 2002 May; 12 Suppl 1():I33-43. PubMed ID: 12102461
[TBL] [Abstract][Full Text] [Related]
2. Sympathetic skin response differentiates hereditary sensory autonomic neuropathies III and IV.
Hilz MJ; Stemper B; Axelrod FB
Neurology; 1999 May; 52(8):1652-7. PubMed ID: 10331694
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. Hereditary sensory and autonomic neuropathies: types II, III, and IV.
Axelrod FB; Gold-von Simson G
Orphanet J Rare Dis; 2007 Oct; 2():39. PubMed ID: 17915006
[TBL] [Abstract][Full Text] [Related]
5. Inherited autonomic neuropathies.
Axelrod FB; Hilz MJ
Semin Neurol; 2003 Dec; 23(4):381-90. PubMed ID: 15088259
[TBL] [Abstract][Full Text] [Related]
6. From genes to pain: nerve growth factor and hereditary sensory and autonomic neuropathy type V.
Capsoni S
Eur J Neurosci; 2014 Feb; 39(3):392-400. PubMed ID: 24494679
[TBL] [Abstract][Full Text] [Related]
7. Hereditary sensory and autonomic neuropathy types 4 and 5: Review and proposal of a new rehabilitation method.
Yozu A; Haga N; Funato T; Owaki D; Chiba R; Ota J
Neurosci Res; 2016 Mar; 104():105-11. PubMed ID: 26562335
[TBL] [Abstract][Full Text] [Related]
8. Single-Fiber Recordings of Nociceptive Fibers in Patients With HSAN Type V With Congenital Insensitivity to Pain.
Sagafos D; Kleggetveit IP; Helås T; Schmidt R; Minde J; Namer B; Schmelz M; Jørum E
Clin J Pain; 2016 Jul; 32(7):636-42. PubMed ID: 27270876
[TBL] [Abstract][Full Text] [Related]
9. Genetics of congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV. Clinical, biological and molecular aspects of mutations in TRKA(NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor.
Indo Y
Clin Auton Res; 2002 May; 12 Suppl 1():I20-32. PubMed ID: 12102460
[TBL] [Abstract][Full Text] [Related]
10. Absent innervation of skin and sweat glands in congenital insensitivity to pain with anhidrosis.
Nolano M; Crisci C; Santoro L; Barbieri F; Casale R; Kennedy WR; Wendelschafer-Crabb G; Provitera V; Di Lorenzo N; Caruso G
Clin Neurophysiol; 2000 Sep; 111(9):1596-601. PubMed ID: 10964070
[TBL] [Abstract][Full Text] [Related]
11. The painless eye: Neurotrophic keratitis in a child suffering from hereditary sensory autonomic neuropathy type IV.
Sethi A; Ramasubramanian S; Swaminathan M
Indian J Ophthalmol; 2020 Oct; 68(10):2270-2272. PubMed ID: 32971688
[TBL] [Abstract][Full Text] [Related]
12. Arthropathy-related pain in a patient with congenital impairment of pain sensation due to hereditary sensory and autonomic neuropathy type II with a rare mutation in the WNK1/HSN2 gene: a case report.
Yamada K; Yuan J; Mano T; Takashima H; Shibata M
BMC Neurol; 2016 Oct; 16(1):201. PubMed ID: 27765018
[TBL] [Abstract][Full Text] [Related]
13. [Congenital insensitivity to pain: clinical and neurophysiological study in three sisters of a Moroccan family].
Kissani N; Krrati H; Alarcon G; Belaaidi H; Ouazzani R
Arch Pediatr; 2013 Nov; 20(11):1219-1224. PubMed ID: 24094759
[TBL] [Abstract][Full Text] [Related]
14. [Hereditary sensory and autonomic neuropathy type IV: a report on two cases].
Achouri E; Gribaa M; Bouguila J; Haddad S; Souayeh N; Saad A; Essoussi AS
Arch Pediatr; 2011 Apr; 18(4):390-3. PubMed ID: 21397470
[TBL] [Abstract][Full Text] [Related]
15. Familial insensitivity to pain (HSAN V) and a mutation in the NGFB gene. A neurophysiological and pathological study.
Minde J; Toolanen G; Andersson T; Nennesmo I; Remahl IN; Svensson O; Solders G
Muscle Nerve; 2004 Dec; 30(6):752-60. PubMed ID: 15468048
[TBL] [Abstract][Full Text] [Related]
16. [Hereditary sensory and autonomic neuropathy type II A: early neurological and skeletal findings].
Esmer C; Díaz Zambrano S; Santos Díaz MA; González Huerta LM; Cuevas Covarrubias SA; Bravo Oro A
An Pediatr (Barc); 2014 Apr; 80(4):254-8. PubMed ID: 23831200
[TBL] [Abstract][Full Text] [Related]
17. Late-onset hereditary ataxia with global thermoanalgesia and absence of fungiform papillae on the tongue in a Japanese family.
Fukutake T; Kita K; Sakakibara R; Takagi K; Tokumaru Y; Kojima S; Hattori T; Hirayama K
Brain; 1996 Jun; 119 ( Pt 3)():1011-21. PubMed ID: 8673478
[TBL] [Abstract][Full Text] [Related]
18. Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.
Altassan R; Saud HA; Masoodi TA; Dosssari HA; Khalifa O; Al-Zaidan H; Sakati N; Rhabeeni Z; Al-Hassnan Z; Binamer Y; Alhashemi N; Wade W; Al-Zayed Z; Al-Sayed M; Al-Muhaizea MA; Meyer B; Al-Owain M; Wakil SM
Am J Med Genet A; 2017 Apr; 173(4):1009-1016. PubMed ID: 28328124
[TBL] [Abstract][Full Text] [Related]
19. Neurophysiologic studies in congenital insensitivity to pain with anhidrosis.
Shorer Z; Moses SW; Hershkovitz E; Pinsk V; Levy J
Pediatr Neurol; 2001 Nov; 25(5):397-400. PubMed ID: 11744315
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 15534759
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
