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 *

114 related articles for article (PubMed ID: 20083254)

  • 1. Hereditary sensory ataxic neuropathy associated with proximal muscle weakness in the lower extremities.
    Murakami T; Fukai Y; Rikimaru M; Henmi S; Ohsawa Y; Sunada Y
    J Neurol Sci; 2010 Apr; 291(1-2):121-3. PubMed ID: 20083254
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinicopathological features of acute autonomic and sensory neuropathy.
    Koike H; Atsuta N; Adachi H; Iijima M; Katsuno M; Yasuda T; Fukada Y; Yasui K; Nakashima K; Horiuchi M; Shiomi K; Fukui K; Takashima S; Morita Y; Kuniyoshi K; Hasegawa Y; Toribe Y; Kajiura M; Takeshita S; Mukai E; Sobue G
    Brain; 2010 Oct; 133(10):2881-96. PubMed ID: 20736188
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sensory neuropathy in infantile onset spinocerebellar ataxia (IOSCA).
    Koskinen T; Sainio K; Rapola J; Pihko H; Paetau A
    Muscle Nerve; 1994 May; 17(5):509-15. PubMed ID: 8159181
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary motor and sensory neuropathy with proximal dominancy in the lower extremities, urinary disturbance, and paroxysmal dry cough.
    Miura S; Shibata H; Kida H; Noda K; Tomiyasu K; Yamamoto K; Iwaki A; Ayabe M; Aizawa H; Taniwaki T; Fukumaki Y
    J Neurol Sci; 2008 Oct; 273(1-2):88-92. PubMed ID: 18662816
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sensory neuronopathy in ataxia with oculomotor apraxia type 2.
    Gazulla J; Benavente I; López-Fraile IP; Tordesillas C; Modrego P; Alonso I; Pinto-Basto J
    J Neurol Sci; 2010 Nov; 298(1-2):118-20. PubMed ID: 20869730
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Chronic hereditary ataxic polyneuropathy].
    Nogués M; Leiguarda R; Sevlever G; García H
    Medicina (B Aires); 2000; 60(3):316-20. PubMed ID: 11050807
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations.
    Sivakumar K; Kyriakides T; Puls I; Nicholson GA; Funalot B; Antonellis A; Sambuughin N; Christodoulou K; Beggs JL; Zamba-Papanicolaou E; Ionasescu V; Dalakas MC; Green ED; Fischbeck KH; Goldfarb LG
    Brain; 2005 Oct; 128(Pt 10):2304-14. PubMed ID: 16014653
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Clinical and electrophysiological findings in various hereditary sensory neuropathies].
    Caruso G; Santoro L; Perretti A
    Acta Neurol (Napoli); 1992; 14(4-6):345-62. PubMed ID: 1293978
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hereditary motor sensory neuropathy type II with neurofilament accumulation: new finding or new disorder?
    Vogel P; Gabriel M; Goebel HH; Dyck PJ
    Ann Neurol; 1985 May; 17(5):455-61. PubMed ID: 3859241
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new type of hereditary motor and sensory neuropathy linked to chromosome 3.
    Takashima H; Nakagawa M; Nakahara K; Suehara M; Matsuzaki T; Higuchi I; Higa H; Arimura K; Iwamasa T; Izumo S; Osame M
    Ann Neurol; 1997 Jun; 41(6):771-80. PubMed ID: 9189038
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Clinical, multimodal electrophysiological study of a family with progressive cerebellar ataxia and late deafness and an autosomal recessive inheritance].
    Ragno M; Curatola L; Rossi R; Salvolini U
    Acta Neurol (Napoli); 1992; 14(4-6):431-9. PubMed ID: 1293986
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new variant of sensory ataxic neuropathy with autosomal dominant inheritance.
    van Dijk GW; Wokke JH; Oey PL; Franssen H; Ippel PF; Veldman H
    Brain; 1995 Dec; 118 ( Pt 6)():1557-63. PubMed ID: 8595484
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Clinical report of hereditary motor and sensory neuropathy with proximal dominance in Shiga prefecture].
    Takahashi M; Mitsui Y; Yorifuji S; Nakamura Y; Tsukamoto Y; Nishimoto K
    Rinsho Shinkeigaku; 2007 Sep; 47(9):571-6. PubMed ID: 18018614
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
    Bouhouche A; Birouk N; Azzedine H; Benomar A; Durosier G; Ente D; Muriel MP; Ruberg M; Slassi I; Yahyaoui M; Dubourg O; Ouazzani R; LeGuern E
    Brain; 2007 Apr; 130(Pt 4):1062-75. PubMed ID: 17347251
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A case with posterior column ataxia associated with cerebellar ataxia and sensory neuropathy].
    Kikuchi Y; Ogawa M; Shigetoh H; Kawai M; Satoyoshi E
    Rinsho Shinkeigaku; 1999 Sep; 39(9):944-7. PubMed ID: 10614159
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Recurrent Guillain Barre' syndrome.
    Das A; Kalita J; Misra UK
    Electromyogr Clin Neurophysiol; 2004 Mar; 44(2):95-102. PubMed ID: 15061403
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cranial nerves palsy as an initial feature of an early onset distal hereditary motor neuropathy--a new distal hereditary motor neuropathy phenotype.
    Haberlová J; Claeys KG; De Jonghe P; Seeman P
    Neuromuscul Disord; 2009 Jun; 19(6):427-8. PubMed ID: 19409784
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Electrodiagnostic changes of the lower limbs in subjects with chronic complete cervical spinal cord injury.
    Kirshblum S; Lim S; Garstang S; Millis S
    Arch Phys Med Rehabil; 2001 May; 82(5):604-7. PubMed ID: 11346835
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clincial and pathological study of distal motor neuropathy with N88S mutation in BSCL2.
    Chen B; Zheng R; Luan X; Zhang W; Wang Z; Yuan Y
    Neuropathology; 2009 Oct; 29(5):543-7. PubMed ID: 19323790
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neuronal intranuclear hyaline inclusion disease showing motor-sensory and autonomic neuropathy.
    Sone J; Hishikawa N; Koike H; Hattori N; Hirayama M; Nagamatsu M; Yamamoto M; Tanaka F; Yoshida M; Hashizume Y; Imamura H; Yamada E; Sobue G
    Neurology; 2005 Nov; 65(10):1538-43. PubMed ID: 16301479
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.