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 *

141 related articles for article (PubMed ID: 3472424)

  • 1. Descriptive epidemiology of selected neuromuscular disorders in Benghazi, Libya.
    Radhakrishnan K; el-Mangoush MA; Gerryo SE
    Acta Neurol Scand; 1987 Feb; 75(2):95-100. PubMed ID: 3472424
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prevalence and incidence of neuromuscular conditions in the UK between 2000 and 2019: A retrospective study using primary care data.
    Carey IM; Banchoff E; Nirmalananthan N; Harris T; DeWilde S; Chaudhry UAR; Cook DG
    PLoS One; 2021; 16(12):e0261983. PubMed ID: 34972157
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The prevalence of hereditary neuromuscular disorders in Northern Norway.
    Müller KI; Ghelue MV; Lund I; Jonsrud C; Arntzen KA
    Brain Behav; 2021 Jan; 11(1):e01948. PubMed ID: 33185984
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary motor and sensory neuropathies in Swedish children. I. Prevalence and distribution by disability groups.
    Hagberg B; Westerberg B
    Acta Paediatr Scand; 1983 May; 72(3):379-83. PubMed ID: 6576612
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort.
    Megarbane A; Bizzari S; Deepthi A; Sabbagh S; Mansour H; Chouery E; Hmaimess G; Jabbour R; Mehawej C; Alame S; Hani A; Hasbini D; Ghanem I; Koussa S; Al-Ali MT; Obeid M; Talea DB; Lefranc G; Lévy N; Leturcq F; El Hayek S; Delague V; Urtizberea JA
    J Neuromuscul Dis; 2022; 9(1):193-210. PubMed ID: 34602496
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood.
    Ouvrier RA; McLeod JG; Conchin TE
    Brain; 1987 Feb; 110 ( Pt 1)():121-48. PubMed ID: 3467805
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prevalence of hereditary motor and sensory neuropathy in Cantabria.
    Combarros O; Calleja J; Polo JM; Berciano J
    Acta Neurol Scand; 1987 Jan; 75(1):9-12. PubMed ID: 3472423
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Clinico-epidemiological aspects of hereditary neuromuscular diseases in the Krasnodar territory].
    Krivopusk ME
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(9):3-5. PubMed ID: 1664610
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Descriptive epidemiology of motor neuron disease in Benghazi, Libya.
    Radhakrishnan K; Ashok PP; Sridharan R; Mousa ME
    Neuroepidemiology; 1986; 5(1):47-54. PubMed ID: 3489194
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Descriptive epidemiology of some rare neurological diseases in Benghazi, Libya.
    Radhakrishnan K; Thacker AK; Maloo JC; Gerryo SE; Mousa ME
    Neuroepidemiology; 1988; 7(3):159-64. PubMed ID: 3405368
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A clinical, epidemiological and genetic study of hereditary motor neuropathies in Benghazi, Libya.
    Radhakrishnan K; Thacker AK; Maloo JC
    J Neurol; 1988 Sep; 235(7):422-4. PubMed ID: 3221247
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epidemiology of neuromuscular diseases, including the postpolio sequelae, in a Swedish county.
    Ahlström G; Gunnarsson LG; Leissner P; Sjödén PO
    Neuroepidemiology; 1993; 12(5):262-9. PubMed ID: 8309501
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prevalence and pattern of spinocerebellar degenerations in northeastern Libya.
    Sridharan R; Radhakrishnan K; Ashok PP; Mousa ME
    Brain; 1985 Dec; 108 ( Pt 4)():831-43. PubMed ID: 4075075
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Cardiac involvement in neuromuscular diseases].
    Posada Rodríguez IJ; Gutiérrez-Rivas E; Cabello A
    Rev Esp Cardiol; 1997 Dec; 50(12):882-901. PubMed ID: 9470454
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Progressive muscular dystrophy in Denmark. Natural history, prevalence and incidence.
    Leth A; Wulff K; Corfitsen M; Elmgreen J
    Acta Paediatr Scand; 1985 Nov; 74(6):881-5. PubMed ID: 4090963
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A population-based epidemiologic study of adult neuromuscular disease in the Republic of Ireland.
    Lefter S; Hardiman O; Ryan AM
    Neurology; 2017 Jan; 88(3):304-313. PubMed ID: 27927941
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [AMP-aminohydrolase of skeletal muscles in muscular diseases].
    Niebrój-Dobosz I; Strumień M
    Neurol Neurochir Pol; 1979; 13(4):383-7. PubMed ID: 481690
    [TBL] [Abstract][Full Text] [Related]  

  • 18. What we do not know about pregnancy in hereditary neuromuscular disorders.
    Argov Z; de Visser M
    Neuromuscul Disord; 2009 Oct; 19(10):675-9. PubMed ID: 19692244
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Childhood neuromuscular disorders: a decade's experience in Saudi Arabia.
    Salih MA; Mahdi AH; al-Jarallah AA; al Jarallah AS; al-Saadi M; Hafeez MA; Aziz SA
    Ann Trop Paediatr; 1996 Dec; 16(4):271-80. PubMed ID: 8985523
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Population frequencies of inherited neuromuscular diseases--a world survey.
    Emery AE
    Neuromuscul Disord; 1991; 1(1):19-29. PubMed ID: 1822774
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.