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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

468 related items for PubMed ID: 11423041

  • 1. [Neonatal hypotonia of muscular origin: analysis of 50 cases].
    Floriach-Robert M, Cabello A, Simón De Las Heras R, Mateos Beato F.
    Neurologia; 2001; 16(6):245-53. PubMed ID: 11423041
    [Abstract] [Full Text] [Related]

  • 2. The hypotonic infant: case study of central core disease.
    Castrodale V.
    Neonatal Netw; 2003; 22(1):53-9. PubMed ID: 12597091
    [Abstract] [Full Text] [Related]

  • 3. Clinical and skeletal muscle biopsy characteristics of 25 patients with floppy infant syndrome.
    Bing Q, Hu J, Li N, Shen HR, Zhao Z.
    Clin Neuropathol; 2013; 32(6):471-9. PubMed ID: 23743156
    [Abstract] [Full Text] [Related]

  • 4. [Congenital muscular dystrophy. Apropos of 4 cases].
    Posada IJ, Molina JA, Ramo C, Cabello A, Mateos F.
    An Esp Pediatr; 1988 Feb; 28(2):157-60. PubMed ID: 3281538
    [Abstract] [Full Text] [Related]

  • 5. The value of electromyography in the aetiological diagnosis of hypotonia in infants and toddlers.
    Cetin E, Cuisset JM, Tiffreau V, Vallée L, Hurtevent JF, Thevenon A.
    Ann Phys Rehabil Med; 2009 Feb; 52(7-8):546-55. PubMed ID: 19713169
    [Abstract] [Full Text] [Related]

  • 6. Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study.
    Flanigan KM, Kerr L, Bromberg MB, Leonard C, Tsuruda J, Zhang P, Gonzalez-Gomez I, Cohn R, Campbell KP, Leppert M.
    Ann Neurol; 2000 Feb; 47(2):152-61. PubMed ID: 10665485
    [Abstract] [Full Text] [Related]

  • 7. Role of EMG in congenital hypotonia with favorable outcome.
    Pisani F, Carboni P.
    Acta Biomed; 2005 Dec; 76(3):171-4. PubMed ID: 16676567
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Congenital myopathies: clinical and immunohistochemical study.
    Thaha F, Gayathri N, Nalini A.
    Neurol India; 2011 Dec; 59(6):879-83. PubMed ID: 22234203
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Spectrum of congenital myopathies: a single centre experience.
    Uppin MS, Meena AK, Sundaram C.
    Neurol India; 2013 Dec; 61(3):254-9. PubMed ID: 23860144
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood.
    Gamstorp I.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):72-81. PubMed ID: 5173129
    [Abstract] [Full Text] [Related]

  • 20. Electromyography (EMG) accuracy compared to muscle biopsy in childhood.
    Rabie M, Jossiphov J, Nevo Y.
    J Child Neurol; 2007 Jul; 22(7):803-8. PubMed ID: 17715269
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 24.