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 *

201 related articles for article (PubMed ID: 10369826)

  • 1. Autosomal dominant burning feet syndrome.
    Stögbauer F; Young P; Kuhlenbäumer G; Kiefer R; Timmerman V; Ringelstein EB; Wang JF; Schröder JM; Van Broeckhoven C; Weis J
    J Neurol Neurosurg Psychiatry; 1999 Jul; 67(1):78-81. PubMed ID: 10369826
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A second family with autosomal dominant burning feet syndrome.
    Kuhlenbäumer G; Young P; Kiefer R; Timmerman V; Wang JF; Schroeder JM; Weis J; Ringelstein EB; Van Broeckhoven C; Stoegbauer F
    Ann N Y Acad Sci; 1999 Sep; 883():445-8. PubMed ID: 10586269
    [No Abstract]   [Full Text] [Related]  

  • 3. A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci.
    Bellone E; Rodolico C; Toscano A; Di Maria E; Cassandrini D; Pizzuti A; Pigullo S; Mazzeo A; Macaione V; Girlanda P; Vita G; Ajmar F; Mandich P
    Neuromuscul Disord; 2002 Mar; 12(3):286-91. PubMed ID: 11801401
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I).
    Houlden H; King R; Blake J; Groves M; Love S; Woodward C; Hammans S; Nicoll J; Lennox G; O'Donovan DG; Gabriel C; Thomas PK; Reilly MM
    Brain; 2006 Feb; 129(Pt 2):411-25. PubMed ID: 16364956
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [The genetics of type 1 Charcot-Marie-Tooth disease, the hereditary focal neuropathies and the hereditary distal motor neuropathies].
    Sevilla T
    Rev Neurol; 2000 Jan 1-15; 30(1):71-9. PubMed ID: 10743001
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness.
    Dubourg O; Barhoumi C; Azzedine H; Birouk N; Brice A; Bouche P; Leguern E
    Muscle Nerve; 2000 Oct; 23(10):1508-14. PubMed ID: 11003785
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. "Burning feet" as the only manifestation of dominantly inherited sensory neuropathy.
    Dyck PJ; Low PA; Stevens JC
    Mayo Clin Proc; 1983 Jul; 58(7):426-9. PubMed ID: 6575233
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hereditary sensory and autonomic neuropathy type I in a Chinese family: British C133W mutation exists in the Chinese.
    Bi H; Gao Y; Yao S; Dong M; Headley AP; Yuan Y
    Neuropathology; 2007 Oct; 27(5):429-33. PubMed ID: 18018475
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An hereditary sensory and autonomic neuropathy transmitted as an X-linked recessive trait.
    Jestico JV; Urry PA; Efphimiou J
    J Neurol Neurosurg Psychiatry; 1985 Dec; 48(12):1259-64. PubMed ID: 3866836
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 11310631
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Molecular genetics of inherited neuropathies].
    Takashima H
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel RAB7 mutation associated with ulcero-mutilating neuropathy.
    Houlden H; King RH; Muddle JR; Warner TT; Reilly MM; Orrell RW; Ginsberg L
    Ann Neurol; 2004 Oct; 56(4):586-90. PubMed ID: 15455439
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary sensory neuropathy: biopsy study of an autosomal dominant variety.
    Danon MJ; Carpenter S
    Neurology; 1985 Aug; 35(8):1226-9. PubMed ID: 3860748
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal dominant inherited neuropathies with prominent sensory loss and mutilations: a review.
    Auer-Grumbach M; De Jonghe P; Verhoeven K; Timmerman V; Wagner K; Hartung HP; Nicholson GA
    Arch Neurol; 2003 Mar; 60(3):329-34. PubMed ID: 12633143
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary sensory and autonomic neuropathy with ataxia and late onset.
    Marbini A; Pavesi G; Cenacchi G; Mazzucchi A; Preda P; Gemignani F
    Clin Neurol Neurosurg; 1994 May; 96(2):191-6. PubMed ID: 7924091
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family.
    De Jonghe P; Timmerman V; FitzPatrick D; Spoelders P; Martin JJ; Van Broeckhoven C
    J Neurol Neurosurg Psychiatry; 1997 Jun; 62(6):570-3. PubMed ID: 9219740
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary thermosensitive neuropathy: an autosomal dominant disorder of the peripheral nervous system.
    Magy L; Birouk N; Vallat JM; Gouider R; Maisonobe T; Bouche P; Lyon-Caen O; Fontaine B
    Neurology; 1997 Jun; 48(6):1684-90. PubMed ID: 9191787
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary sensory and autonomic neuropathy type IID caused by an SCN9A mutation.
    Yuan J; Matsuura E; Higuchi Y; Hashiguchi A; Nakamura T; Nozuma S; Sakiyama Y; Yoshimura A; Izumo S; Takashima H
    Neurology; 2013 Apr; 80(18):1641-9. PubMed ID: 23596073
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [From gene to disease; Charcot-Marie-Tooth disease or the hereditary motor and sensory neuropathies].
    Verhamme C; Baas F
    Ned Tijdschr Geneeskd; 2005 Jul; 149(27):1505-9. PubMed ID: 16032995
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.