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 *

185 related articles for article (PubMed ID: 14879299)

  • 1. Infantile spinal progressive muscular atrophy in twins.
    POIRIER R; CORBET RC; BUCKWOLD AE
    Can Med Assoc J; 1951 Oct; 65(4):342-3. PubMed ID: 14879299
    [No Abstract]   [Full Text] [Related]  

  • 2. Case reports of progressive infantile muscular atrophy (Werdnig-Hoffmann) in fraternal twins.
    LEYRER RH
    AMA Am J Dis Child; 1954 Nov; 88(5):604-5. PubMed ID: 13206380
    [No Abstract]   [Full Text] [Related]  

  • 3. [Infantile spinal muscular atrophy : therapeutic (R)evolution].
    Daron A; Delstanche S; Dangouloff T; Servais L
    Rev Med Liege; 2019 Feb; 74(2):82-85. PubMed ID: 30793560
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Medical therapy in spinal muscular atrophy: a realistic expectation?
    Jennekens FG
    Clin Neurol Neurosurg; 1992; 94 Suppl():S89-92. PubMed ID: 1320532
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hereditary factors in infantile progressive muscular atrophy; study of 112 cases in 70 families.
    BRANDT S
    Am J Dis Child (1911); 1949 Aug; 78(2):226-36. PubMed ID: 18135521
    [No Abstract]   [Full Text] [Related]  

  • 6. [On the morphology, nosological position and pathogenesis of Oppenheim's myotonia congenita and Werdnig-Hoffmann's infantile spinal progressive muscular atrophy].
    GEILER G; GEILER G
    Virchows Arch Pathol Anat Physiol Klin Med; 1962; 335():654-67. PubMed ID: 13897523
    [No Abstract]   [Full Text] [Related]  

  • 7. Course and symptoms of progressive infantile muscular atrophy; a follow-up study of 112 cases in Denmark.
    BRANDT S
    Arch Neurol Psychiatry; 1950 Feb; 63(2):218-28. PubMed ID: 15404484
    [No Abstract]   [Full Text] [Related]  

  • 8. Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: a variant of infantile spinal muscular atrophy.
    Bertini E; Gadisseux JL; Palmieri G; Ricci E; Di Capua M; Ferriere G; Lyon G
    Am J Med Genet; 1989 Jul; 33(3):328-35. PubMed ID: 2801766
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity, and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of the joints or muscles in children].
    BRANDT S
    Nord Med; 1950 Sep; 44(37):1499. PubMed ID: 14806955
    [No Abstract]   [Full Text] [Related]  

  • 10. [On the problem of spinal muscular atrophy resembling progressive muscular dystrophy (Kugelberg-Welander's juvenile muscular atrophy)].
    GOLDSZTAJN M; ZEBROWSKI S
    Neurol Neurochir Psychiatr Pol; 1962; 12():669-73. PubMed ID: 13948828
    [No Abstract]   [Full Text] [Related]  

  • 11. [Catamnestic inquiries in conditions of hypertonia in early childhood. With a critical contribution to the differential diagnosis of infantile spinal progressive muscular atrophy (Werdnig-Hoffman disease--myatonia congenital Oppenheilm)].
    HORSTMANN W
    Z Kinderheilkd; 1959; 82():649-67. PubMed ID: 13848453
    [No Abstract]   [Full Text] [Related]  

  • 12. Familial progressive bulbar-spinal muscular atrophy.
    MAGEE KR
    Neurology; 1960 Mar; 10():295-305. PubMed ID: 14419783
    [No Abstract]   [Full Text] [Related]  

  • 13. Two early infantile hereditary cases of progressive muscular atrophy simulating dystrophy, but on a neural basis. 1891.
    Werdnig G
    Arch Neurol; 1971 Sep; 25(3):276-8. PubMed ID: 4952838
    [No Abstract]   [Full Text] [Related]  

  • 14. [Infantile spinal muscular atrophy. Description of 2 cases of Werdnig-Hoffmann disease].
    Priora U; Quaglia P; Vivalda M; Giachino-AmistĂ  MT; Domeneghetti G; Sardi R
    Minerva Pediatr; 1987 Sep; 39(17-18):709-14. PubMed ID: 3437861
    [No Abstract]   [Full Text] [Related]  

  • 15. [Progressive infantile spinal muscular atrophy. Report of 12 cases].
    Fontana MH; Pörtner MR; Salim PA; Bobek PR; Da Roza PR
    Arq Neuropsiquiatr; 1990 Mar; 48(1):26-31. PubMed ID: 2378573
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Infantile progressive spinal muscular atrophy in identical Negro twins.
    Marquardt JE; MacLowry J; Perry RE
    N Engl J Med; 1962 Aug; 267():386-8. PubMed ID: 14470139
    [No Abstract]   [Full Text] [Related]  

  • 17. Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.
    KUGELBERG E; WELANDER L
    AMA Arch Neurol Psychiatry; 1956 May; 75(5):500-9. PubMed ID: 13312732
    [No Abstract]   [Full Text] [Related]  

  • 18. [CASE OF MYELOPATHIC MUSCULAR ATROPHY THOUGHT AT FIRST TO BE PROGRESSIVE MUSCULAR DYSTROPHY--A VIEW OF THE RELATION BETWEEN KUGELBERG-WELANDER'S MUSCULAR ATROPHY AND WERDNIG-HOFFMANN DISEASE].
    FURUKAWA S; MAMIYA S
    Nihon Shonika Gakkai Zasshi; 1963 Nov; 67():745-8. PubMed ID: 14096316
    [No Abstract]   [Full Text] [Related]  

  • 19. Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance.
    Boylan KB; Cornblath DR
    Ann Neurol; 1992 Sep; 32(3):404-7. PubMed ID: 1416812
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Another milestone in childhood spinal muscular atrophy.
    Wokke JH
    Lancet Neurol; 2017 Jul; 16(7):491-492. PubMed ID: 28460890
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.