BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 13785363)

  • 1. [A newborn child with Werdnig-Hoffmann's disease (infantile spinal muscular atrophy)].
    WILLEMSE J
    Ned Tijdschr Geneeskd; 1961 Feb; 105():243-5. PubMed ID: 13785363
    [No Abstract]   [Full Text] [Related]  

  • 2. [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]  

  • 3. [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]  

  • 4. [Two cases of a proximal spinal muscular atrophy (Werdnig-Hoffmann's disease) in one family].
    Nurbekova UA
    Zh Nevrol Psikhiatr Im S S Korsakova; 2014; 114(10):106-7. PubMed ID: 25591528
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Werdnig-Hoffmann disease with congenital hypothyroidism.
    Gunes T; Akcakus M; Cetin N; Kurtoğlu S; Kumandaş S
    Ann Trop Paediatr; 2003 Dec; 23(4):301-4. PubMed ID: 14738578
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Studies on Werdnig-Hoffmann's disease. 3. Anatomo-pathological and histochemical contribution].
    Mercante G; Crosta C
    Riv Anat Patol Oncol; 1967; 30(2):115-47. PubMed ID: 5608996
    [No Abstract]   [Full Text] [Related]  

  • 7. Infantile spinal muscular atrophy (morbus Werdnig-Hoffmann) causing neonatal asphyxia.
    Kyllerman M
    Neuropadiatrie; 1977 Feb; 8(1):53-6. PubMed ID: 576732
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neuronal RNA metabolism in infantile spinal muscular atrophy (Werdnig-Hoffmann's disease) studied by radioautography: a new technic in the investigation of neurological disease.
    Hogenhuis LA; Spaulding SW; Engel WK
    J Neuropathol Exp Neurol; 1967 Apr; 26(2):335-41. PubMed ID: 6022173
    [No Abstract]   [Full Text] [Related]  

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

  • 10. [Clinical picture, pathogenesis and geneology of hereditary progressive spinal muscular atrophies].
    Nesterov LN; Sushcheva GP; Viatkina SIa; Novikova NP
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(3):321-30. PubMed ID: 6326437
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Werdnig-Hoffmann's congenital spinal atrophy in nursing infants].
    Kutafin IuF; Osipov SM; Osipov ES
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(3):15-8. PubMed ID: 1646528
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Infantile muscular atrophy: an eleven year experience.
    BYERS RK; BANKER BQ
    Trans Am Neurol Assoc; 1960; 85():10-4. PubMed ID: 13875293
    [No Abstract]   [Full Text] [Related]  

  • 13. Infantile muscular atrophy.
    BYERS RK; BANKER BQ
    Arch Neurol; 1961 Aug; 5():140-64. PubMed ID: 13689565
    [No Abstract]   [Full Text] [Related]  

  • 14. HISTOCHEMISTRY OF MUSCLE IN INFANTILE SPINAL MUSCULAR ATROPHY.
    FENICHEL GM; ENGEL WK
    Neurology; 1963 Dec; 13():1059-66. PubMed ID: 14134179
    [No Abstract]   [Full Text] [Related]  

  • 15. [Werdnig-Hoffmann's disease. Study on 53 cases (author's transl)].
    López-Terradas JM; Pascual Castroviejo I; Gutiérrez Molina M; Rodríguez Costa T
    An Esp Pediatr; 1975; 8(4):371-84. PubMed ID: 1147411
    [No Abstract]   [Full Text] [Related]  

  • 16. Cerebral distribution of beta-lipotropin and beta-endorphin in infantile progressive spinal muscular atrophy of Werdnig and Hoffman disease.
    Pasi A; Mehraein P; Pedrinis E; Hartmann H; Gramsch C; Külling P; Pagnamenta F; Messiha FS
    Res Commun Chem Pathol Pharmacol; 1987 Jun; 56(3):401-8. PubMed ID: 2957764
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Adult-onset motor neuron disease and infantile Werdnig-Hoffmann disease (spinal muscular atrophy type 1) in the same family.
    Shaw PJ; Ince PG; Goodship J; Burn J; Slade J; Bates D; Medwin DG
    Neurology; 1992 Aug; 42(8):1477-80. PubMed ID: 1641139
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cardiac involvement in Werdnig-Hoffmann's spinal muscular atrophy.
    Finsterer J; Stöllberger C
    Cardiology; 1999; 92(3):178-82. PubMed ID: 10754348
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Werdnig-Hoffmann's disease (etiopathogenetic, clinical and anatomo-pathological considerations)].
    Bigotti A; Alù A; Lalli F; Lotti A
    Policlinico Med; 1967 Jun; 74(3):153-69. PubMed ID: 5606257
    [No Abstract]   [Full Text] [Related]  

  • 20. [Infantile neurogenic amyotrophies with prolonged course: the problem of their nosologic classification in relation to Werdnig-Hoffmann's disease].
    Lugaresi E; Giovanardi-Rossi P; Gambetti P
    Riv Sper Freniatr Med Leg Alien Ment; 1965 Jun; 89(3):594-619. PubMed ID: 5845541
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.