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 *

103 related articles for article (PubMed ID: 22426684)

  • 21. Split Hand Associated With Monomelic Amyotrophy: A Challenging Diagnosis.
    Karaahmet OZ; Gurcay E; Unlu E; Cakci A; Odabasi Z
    J Clin Neuromuscul Dis; 2015 Sep; 17(1):34-5. PubMed ID: 26301379
    [No Abstract]   [Full Text] [Related]  

  • 22. Clinical improvement of monomelic amyotrophy after avoidance of sustained neck flexion.
    Quinn C; Paganoni S; Cochrane T
    J Clin Neuromuscul Dis; 2014 Jun; 15(4):191-2. PubMed ID: 24872219
    [No Abstract]   [Full Text] [Related]  

  • 23. [Questionnaire survey conducted on the parents of patients with spinal muscular atrophy type 1 in Japan regarding switch devices, language development, upper extremity function and QOL].
    Sakai S; Maki M; Sakai N; Sudoh A; Kato M; Saitoh S
    No To Hattatsu; 2012 Nov; 44(6):465-71. PubMed ID: 23240528
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Proximal monomelic amyotrophy of the upper limb.
    Amir D; Magora A; Vatine JJ
    Arch Phys Med Rehabil; 1987 Jul; 68(7):450-1. PubMed ID: 3606370
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Electromyography in distal atrophy of the upper limbs with segmental spinal muscular atrophy: Hirayama's disease].
    García-Solana MI; García-Rodríguez V; Rodrigo-Sesma A; Lloret-Alcañiz MA; Medrano-Tovar L; Mora-Rodríguez E
    Rev Neurol; 2006 May 1-15; 42(9):570-2. PubMed ID: 16676281
    [No Abstract]   [Full Text] [Related]  

  • 26. A clinical and genetic study of spinal muscular atrophy.
    Mishra VN; Kalita J; Kesari A; Mitta B; Shankar SK; Misra UK
    Electromyogr Clin Neurophysiol; 2004; 44(5):307-12. PubMed ID: 15378871
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Study of association between hyperIgEaemia and Hirayama disease].
    Fu Y; Sun QL; Han HB; Hou C; Zhang J; Kang DX; Fan DS
    Zhonghua Yi Xue Za Zhi; 2010 Oct; 90(37):2629-32. PubMed ID: 21162930
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Monomelic amyotrophy: a rare disease with unusual features (Hirayama disease).
    Kulkarni C; Naqvi WM
    Pan Afr Med J; 2022; 42():48. PubMed ID: 35949470
    [No Abstract]   [Full Text] [Related]  

  • 29. [Infantile spinal amyotrophy with myotonia. Electromyographic study].
    Renault F
    Neurophysiol Clin; 1989 May; 19(2):155-61. PubMed ID: 2725454
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Altered axonal excitability properties in juvenile muscular atrophy of distal upper extremity (Hirayama disease).
    Sawai S; Misawa S; Kanai K; Isose S; Shibuya K; Noto Y; Fujimaki Y; Sekiguchi Y; Nasu S; Nomura F; Kuwabara S
    Clin Neurophysiol; 2011 Jan; 122(1):205-9. PubMed ID: 20624687
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical features of Hirayama disease in mainland China.
    Zhou B; Chen L; Fan D; Zhou D
    Amyotroph Lateral Scler; 2010; 11(1-2):133-9. PubMed ID: 19412815
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Clinical profile of Monomelic Amyotrophy (MMA) and role of persistent viral infection.
    Vibha D; Behari M; Goyal V; Shukla G; Bhatia R; Srivastava AK; Vivekanandhan S
    J Neurol Sci; 2015 Dec; 359(1-2):4-7. PubMed ID: 26671077
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Genotypic and clinical features of spinal muscular atrophy type 3].
    Wang YY; Feng SW; Cao JQ; Yang J; Li YQ; Li J; Zhang C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr; 29(2):218-21. PubMed ID: 22487838
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Familial polymorphism of spinal amyotrophy in childhood].
    Badalian LO; Temin PA; Arkhipov BA; Zavadenko NN; Bulaeva NV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(11):123-6. PubMed ID: 2624041
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Benign monomelic amyotrophy with proximal upper limb involvement: case report.
    Neves MA; Freitas MR; Mello MP; Dumard CH; Freitas GR; Nascimento OJ
    Arq Neuropsiquiatr; 2007 Jun; 65(2B):524-7. PubMed ID: 17665029
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Progressive spinal amyotrophy type I or Werdnig-Hoffman disease. Apropos of 5 cases in Dakar (Senegal)].
    Ndiaye O; Sall G; Sylla A; Diouf S; Diagne I; Kuakuvi N
    Bull Soc Pathol Exot; 2002 Jun; 95(2):81-2. PubMed ID: 12145964
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Contractures of the upper extremities in spinal muscular atrophy type II. Descriptive clinical study with retrospective data collection.
    Fujak A; Kopschina C; Gras F; Forst R; Forst J
    Ortop Traumatol Rehabil; 2010; 12(5):410-9. PubMed ID: 21057148
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Waterskier's Hirayama syndrome.
    Bede P; Bokde AL; Byrne SC; Elamin M; Walsh RJ; Hardiman O
    J Neurol; 2011 Nov; 258(11):2078-9. PubMed ID: 21503827
    [No Abstract]   [Full Text] [Related]  

  • 39. Familial monomelic amyotrophy: a case report from India.
    Nalini A; Lokesh L; Ratnavalli E
    J Neurol Sci; 2004 May; 220(1-2):95-8. PubMed ID: 15140613
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Exome sequencing identifies KIAA1377 and C5orf42 as susceptibility genes for monomelic amyotrophy.
    Lim YM; Koh I; Park YM; Kim JJ; Kim DS; Kim HJ; Baik KH; Choi HY; Yang GS; Also-Rallo E; Tizzano EF; Gamez J; Park K; Yoo HW; Lee JK; Kim KK
    Neuromuscul Disord; 2012 May; 22(5):394-400. PubMed ID: 22264561
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.