BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

83 related articles for article (PubMed ID: 634661)

  • 1. [Hereditary familial spastic paraparesis (Strumpell-Lorraine disease)].
    Wróblewski T; Smoliński J
    Pediatr Pol; 1978 Feb; 53(2):211-3. PubMed ID: 634661
    [No Abstract]   [Full Text] [Related]  

  • 2. [Etiology and pathogenesis of familial spastic paraplegia (Strümpell-Lorrain disease)].
    Michałowicz R; Ignatowicz R; Kmieć T; Jóźwiak S
    Pol Tyg Lek; 1984 Aug; 39(32):1083-6. PubMed ID: 6504736
    [No Abstract]   [Full Text] [Related]  

  • 3. Hereditary spastic paraplegia.
    Charkabarti AK; Lloyd GH; Johnson SC
    J Indian Med Assoc; 1977 Oct; 69(7):141-6. PubMed ID: 611148
    [No Abstract]   [Full Text] [Related]  

  • 4. Familial spastic paraparesis, optic atrophy, and dementia. Clinical observations of affected kindred.
    Rothner AD; Yahr F; Yahr MD
    N Y State J Med; 1976 May; 76(5):756-8. PubMed ID: 1063327
    [No Abstract]   [Full Text] [Related]  

  • 5. [Classical Strumpell-Lorrain disease in a father and congenital diplegia in his son].
    Christodorescu D
    Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1977; 22(3):235-8. PubMed ID: 303794
    [No Abstract]   [Full Text] [Related]  

  • 6. [New variant of a rare neurocutaneous syndrome].
    Khannanova FK; Shamgunova SB; Ruzybakiev RM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1981; 81(3):338-42. PubMed ID: 7257675
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial spastic paraplegia.
    Rischbieth RH
    Proc Aust Assoc Neurol; 1973; 10(0):31-3. PubMed ID: 4792159
    [No Abstract]   [Full Text] [Related]  

  • 8. [Congenital autosomal-recessive familial spastic paraplegia].
    Badalian LO; Umakhanov RU; Temin PA; Arhipov BA; Bulaeva NV; Sakidebirov GM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(8):97-9. PubMed ID: 1661531
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Progressive spastic paraparesis, vitiligo, premature graying, and distinct facial appearance: a new genetic syndrome in 3 sibs.
    Lison M; Kornbrut B; Feinstein A; Hiss Y; Boichis H; Goodman RM
    Am J Med Genet; 1981; 9(4):351-7. PubMed ID: 7294071
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Familial spastic paraplegia in 3 families].
    Fujiwara H; Akabori O; Akashi K; Moriya S
    Seikei Geka; 1971; 22(6):471-6. PubMed ID: 5104423
    [No Abstract]   [Full Text] [Related]  

  • 11. [Spastic paraparesis and familial Addison's disease].
    Liaño H; Lousa M; García-Merino A; Pérez C; Barcelo B
    Arch Neurobiol (Madr); 1980; 43(4):249-60. PubMed ID: 7458543
    [No Abstract]   [Full Text] [Related]  

  • 12. [Involvement of the peripheral motor neuron in hereditary spastic paraplegia (author's transl)].
    Malin JP
    EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb; 1976 Sep; 7(3):140-5. PubMed ID: 829059
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Differential diagnosis of hereditary spastic spinal paralysis. Simultaneously a report on genetically independent type of recessive hereditary infantile spastic spinal paralysis].
    Malin JP
    Nervenarzt; 1976 Nov; 47(11):661-8. PubMed ID: 1004664
    [No Abstract]   [Full Text] [Related]  

  • 14. [Familial spastic diplegia (study of a Mexican family)].
    Gamboa I; Hernández Peniche J
    Rev Invest Clin; 1973; 25(1):47-50. PubMed ID: 4805167
    [No Abstract]   [Full Text] [Related]  

  • 15. [Clinical polymorphism and genetic heterogeneity of hereditary spastic ataxia].
    Dadali EL; Illarioshkin SN; Markova ED; Ivanova-Smolenskaia IA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1992; 92(4):10-3. PubMed ID: 1333696
    [TBL] [Abstract][Full Text] [Related]  

  • 16. X-linked hereditary spastic paraplegia.
    Raggio JF; Thurmon TF; Anderson EE
    J La State Med Soc; 1973 Jan; 125(1):4-5. PubMed ID: 4684346
    [No Abstract]   [Full Text] [Related]  

  • 17. Troyer syndrome: a recessively inherited form of spastic paraplegia with distal muscle wasting.
    Cross HE
    Birth Defects Orig Artic Ser; 1971 Feb; 7(1):211-3. PubMed ID: 5173362
    [No Abstract]   [Full Text] [Related]  

  • 18. [Late familial spastic paraparesis associated with osteoarticular and vasomotor disorders].
    Ionescu M
    Neurol Psihiatr Neurochir; 1969; 14(5):465-72. PubMed ID: 5380163
    [No Abstract]   [Full Text] [Related]  

  • 19. [Gonosomal recessive heredity of microcephaly with epilepsy and spastic quadruparesis. New variant of the so called Paine's dyndrome?].
    Seemanová E; Lesný I; Hyánek J; Brachfeld K; Rössler M; Prosková M
    Cesk Pediatr; 1973 Nov; 28(11):596-600. PubMed ID: 4769658
    [No Abstract]   [Full Text] [Related]  

  • 20. [Hereditary spastic paraplegia. Case report and review with special reference to current neurophysiologic examination methods].
    Urnes O
    Tidsskr Nor Laegeforen; 1983 May; 103(15):1249-51. PubMed ID: 6879555
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.