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 *

118 related articles for article (PubMed ID: 5618050)

  • 1. [Hypotonias in newborn and older infants].
    Hennequet A
    Ann Pediatr (Paris); 1967; 14(6):521-3. PubMed ID: 5618050
    [No Abstract]   [Full Text] [Related]  

  • 2. [Current views on the diagnosis, etiology and genetics of the most frequent non-metabolic congenital myopathies].
    Herrmann V
    Padiatr Grenzgeb; 1983; 22(1):27-45. PubMed ID: 6866527
    [No Abstract]   [Full Text] [Related]  

  • 3. The myopathies.
    Dubowitz V
    Physiotherapy; 1968 Nov; 54(11):384-9. PubMed ID: 5701438
    [No Abstract]   [Full Text] [Related]  

  • 4. [The hypotonic infant].
    Ueda K; Ito T; Matsumoto K; Nakata T; Ohara T
    Nihon Rinsho; 1968 Nov; 26(11):3231-56. PubMed ID: 4886807
    [No Abstract]   [Full Text] [Related]  

  • 5. [Diagnosis and nosographic classification of muscular hypotonia in infancy].
    Cazzato G
    Riv Sper Freniatr Med Leg Alien Ment; 1968 Apr; 92(2):525-51. PubMed ID: 5715887
    [No Abstract]   [Full Text] [Related]  

  • 6. [Clinical-genetic classification of muscular dystrophies].
    López de Munain A; Andoni Urtizberea J
    Med Clin (Barc); 1998 Sep; 111(6):226-35. PubMed ID: 9789230
    [No Abstract]   [Full Text] [Related]  

  • 7. [The floppy infant syndrome].
    Zellweger H
    Klin Padiatr; 1972 Sep; 184(5):344-9. PubMed ID: 4264047
    [No Abstract]   [Full Text] [Related]  

  • 8. [For the anatomo-clinical diagnosis of primary muscular dystrophy of neonatal onset: apropos of a case].
    Bruni G; Zalla PG
    Arch De Vecchi Anat Patol; 1968 Mar; 51(1):435-45. PubMed ID: 5737308
    [No Abstract]   [Full Text] [Related]  

  • 9. [Progressive muscular spinal atrophy of Werdnig-Hoffmann].
    Galimberti A; Graziano L; Airò R
    Folia Hered Pathol (Milano); 1968; ():113-26. PubMed ID: 5760545
    [No Abstract]   [Full Text] [Related]  

  • 10. [Waning and waxing phenomena in neuromuscular diseases in children].
    Segawa M; Nihei K; Aoyama M
    Shinkei Kenkyu No Shimpo; 1970; 14(3):527-32. PubMed ID: 4250543
    [No Abstract]   [Full Text] [Related]  

  • 11. Pathology of the muscular dystrophies and the congenital nonprogressive myopathies.
    Armbrustmacher VW
    Pathol Annu; 1980; 15(Pt 1):301-33. PubMed ID: 7443308
    [No Abstract]   [Full Text] [Related]  

  • 12. Differentiating Congenital Myopathy from Congenital Muscular Dystrophy.
    Harmelink M
    Clin Perinatol; 2020 Mar; 47(1):197-209. PubMed ID: 32000926
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Muscular defects.
    Gucker T
    Pediatr Clin North Am; 1967 May; 14(2):439-60. PubMed ID: 5337116
    [No Abstract]   [Full Text] [Related]  

  • 14. [Atlas of myohistochemistry. 12. Congenital myopathy. 2].
    Kinoshita M
    No To Shinkei; 1971 Apr; 23(4):348-51. PubMed ID: 4323911
    [No Abstract]   [Full Text] [Related]  

  • 15. [Diagnosis of the Werdnig-Hoffman syndrome in the newborn age. (Apropos of a case)].
    Allemand F; Ottaviano S; Sacchettoni Logroscino G; Iannetti P
    Minerva Pediatr; 1976 Sep; 28(29):1763-72. PubMed ID: 1012213
    [No Abstract]   [Full Text] [Related]  

  • 16. [Hereditary myelopathy].
    Sugita H; Furukawa T
    Nihon Rinsho; 1967 Oct; 25(8):1630-7. PubMed ID: 4868958
    [No Abstract]   [Full Text] [Related]  

  • 17. [Congenital myopathies. 9 case reports and general review].
    Larbrisseau A; Brochu P; Vanasse M; Jasmin G; Geoffroy G
    Union Med Can; 1980 Feb; 109(2):256-76. PubMed ID: 6998072
    [No Abstract]   [Full Text] [Related]  

  • 18. [Congenital muscular dystrophy].
    Mumenthaler M
    Z Kinderheilkd; 1969; 106(2):131-62. PubMed ID: 5802055
    [No Abstract]   [Full Text] [Related]  

  • 19. [Karyologic studies in muscle diseases].
    Badurska B; Prot J
    Pol Tyg Lek; 1969 Mar; 24(13):476-8. PubMed ID: 5790554
    [No Abstract]   [Full Text] [Related]  

  • 20. [Unusual causes of the hypotonic syndrome in the newborn infant].
    Vajda P; Benko J; Cajková E; Szabová I
    Cesk Neurol; 1969 May; 32(3):157-61. PubMed ID: 5770742
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.