These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 29701257)

  • 1. Repeated hyperhidrosis and chilblain-like swelling with ulceration of the fingers and toes in hereditary sensory and autonomic neuropathy type II.
    Shima T; Yamamoto Y; Kanazawa N; Murata KY; Ito H; Kondo T; Yuan J; Hashiguchi A; Takashima H; Furukawa F
    J Dermatol; 2018 Nov; 45(11):e308-e309. PubMed ID: 29701257
    [No Abstract]   [Full Text] [Related]  

  • 2. Late-onset hereditary sensory and autonomic neuropathy type 2B caused by novel compound heterozygous mutations in FAM134B presenting as chronic recurrent ulcers on the soles.
    Luo ZY; Wang HJ; Zhao YK; Liu JH; Chen YM; Lin ZM; Luo DQ
    Indian J Dermatol Venereol Leprol; 2021; 87(3):455. PubMed ID: 33943063
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study.
    Yuan JH; Hashiguchi A; Yoshimura A; Sakai N; Takahashi MP; Ueda T; Taniguchi A; Okamoto S; Kanazawa N; Yamamoto Y; Saigoh K; Kusunoki S; Ando M; Hiramatsu Y; Okamoto Y; Takashima H
    Clin Genet; 2017 Dec; 92(6):659-663. PubMed ID: 28422281
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The coexistence of a novel WNK1 variant and a copy number variation causes hereditary sensory and autonomic neuropathy type IIA.
    Wang JJ; Yu B; Li Z
    BMC Med Genet; 2019 May; 20(1):91. PubMed ID: 31132985
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Plantar ulcers in hereditary sensory neuropathy. A plea for conservative treatment.
    Berginer V; Baruchin A; Ben-Yakar Y; Mahler D
    Int J Dermatol; 1984 Dec; 23(10):664-8. PubMed ID: 6597137
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel nonsense mutation in WNK1/HSN2 associated with sensory neuropathy and limb destruction in four siblings of a large Iranian pedigree.
    Rahmani B; Fekrmandi F; Ahadi K; Ahadi T; Alavi A; Ahmadiani A; Asadi S
    BMC Neurol; 2018 Nov; 18(1):195. PubMed ID: 30497409
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Non-healing ulcers in the foot.
    Shah SV; Bavdekar AV
    J Assoc Physicians India; 1984 Apr; 32(4):377-8. PubMed ID: 6589221
    [No Abstract]   [Full Text] [Related]  

  • 9. Hereditary Sensory and Autonomic Neuropathy Presenting With Mutilating Trophic Ulcers.
    Mathur DK; Prakash C; Bhargava P; Paliwal V; Mathur K
    Wounds; 2018 Mar; 30(3):E25-E28. PubMed ID: 29584606
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Progressive external ophthalmoplegia with hereditary sensory neuropathy: a rare association.
    Sahu PK; Rao VA; Srinivasan R; Tanikachalam S
    J Neuroophthalmol; 2005 Mar; 25(1):55-6. PubMed ID: 15756139
    [No Abstract]   [Full Text] [Related]  

  • 11. Osteoarthropathy in hereditary sensory radicular neuropathy. A case report.
    Ahmed SS; Kaji S; Samesima K; Tsuruta J; Namba K
    Acta Orthop Scand; 1990 Feb; 61(1):92-4. PubMed ID: 2336963
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci.
    Auer-Grumbach M; Wagner K; Timmerman V; De Jonghe P; Hartung HP
    Neurology; 2000 Jan; 54(1):45-52. PubMed ID: 10636124
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Recurrent abdominal pain in hereditary sensory autonomic neuropathy type II (HSAN-II).
    Alkaissi H; Al-Sibahee E; Baher H; Eggermann K; Al-Abayechi A; Kurth I
    Rev Neurol (Paris); 2021 Dec; 177(10):1307-1309. PubMed ID: 34229871
    [No Abstract]   [Full Text] [Related]  

  • 14. [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]  

  • 15. Hereditary sensory neuropathy with spastic paraplegia.
    Kherbaoui-Redouani L; Ploton D; Abely M; Bednarek N; Stourbe A; Sabouraud P; Motte J
    Eur J Paediatr Neurol; 2004; 8(2):95-9. PubMed ID: 15253057
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary sensory and autonomic neuropathy type IV.
    Karande S; Satam N
    Indian Pediatr; 2005 Jun; 42(6):608-9. PubMed ID: 15995280
    [No Abstract]   [Full Text] [Related]  

  • 17. New HSN2 mutation in Japanese patient with hereditary sensory and autonomic neuropathy type 2.
    Takagi M; Ozawa T; Hara K; Naruse S; Ishihara T; Shimbo J; Igarashi S; Tanaka K; Onodera O; Nishizawa M
    Neurology; 2006 Apr; 66(8):1251-2. PubMed ID: 16636245
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Late onset hereditary sensory and autonomic neuropathy with cognitive impairment associated with Y163X prion mutation.
    Themistocleous AC; Kennett R; Husain M; Palace J; Mead S; Bennett DL
    J Neurol; 2014 Nov; 261(11):2230-3. PubMed ID: 25287017
    [No Abstract]   [Full Text] [Related]  

  • 19. Hereditary sensory and autonomic neuropathy II due to novel mutation in the HSN2 gene in Mexican families.
    Pacheco-Cuellar G; González-Huerta LM; Valdés-Miranda JM; Peláez-González H; Zenteno-Bacheron S; Cazarin-Barrientos J; Cuevas-Covarrubias SA
    J Neurol; 2011 Oct; 258(10):1890-2. PubMed ID: 21625937
    [No Abstract]   [Full Text] [Related]  

  • 20. A novel biallelic single base insertion in WNK1 in a Pakistani family with congenital insensitivity to pain.
    Pastore S; Harripaul R; Azam M; Vincent JB
    J Hum Genet; 2020 May; 65(5):493-496. PubMed ID: 32127623
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.