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 *

116 related articles for article (PubMed ID: 5540383)

  • 1. Amino acids of plasma and urine in diseases of muscle.
    Bank WJ; Rowland LP; Ipsen J
    Arch Neurol; 1971 Feb; 24(2):176-86. PubMed ID: 5540383
    [No Abstract]   [Full Text] [Related]  

  • 2. Amino acids of plasma and urine in muscular dystrophies.
    Bank WJ; Rowland LP; Ipsen J
    Trans Am Neurol Assoc; 1968; 93():185-7. PubMed ID: 5711014
    [No Abstract]   [Full Text] [Related]  

  • 3. [Hyperaminoaciduria in children suffering from progressive muscular dystrophy].
    Gusev EI
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1967; 67(7):971-8. PubMed ID: 5598794
    [No Abstract]   [Full Text] [Related]  

  • 4. [Pathological aminoaciduria in muscular dystrophy].
    Rubio Pérez P; Ramos F; Vivanco F
    Rev Clin Esp; 1972 Sep; 126(6):509-14. PubMed ID: 4658356
    [No Abstract]   [Full Text] [Related]  

  • 5. [Urinary amino acids in progressive muscular dystrophy and amyotonia congenita].
    BAUZA C
    Arch Pediatr Urug; 1959 Dec; 30():749-55. PubMed ID: 13797772
    [No Abstract]   [Full Text] [Related]  

  • 6. [Amino acid plotting charts in progressive muscular dystrophy. Family studies].
    Beckmann R; Ritter H
    Dtsch Med Wochenschr; 1966 Dec; 91(52):2231-5. PubMed ID: 5926730
    [No Abstract]   [Full Text] [Related]  

  • 7. [A clinico-experimental study of amino acid metabolism in progressive muscular dystrophy].
    Badalian LO; Bondarenko ES; Gusev EI; Lukoianov IuE; Revich GG
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1970; 70(9):1304-9. PubMed ID: 5511108
    [No Abstract]   [Full Text] [Related]  

  • 8. Urinary amino acid and peptide excretion patterns in patients with muscular dystrophy (Duchenne). A preliminary study with the autoanalyzer.
    Maskaleris ML; Gross S; Milhorat AT
    Clin Chem; 1969 Jul; 15(7):545-54. PubMed ID: 5794148
    [No Abstract]   [Full Text] [Related]  

  • 9. Paper chromatographic survey of urinary amino-acids in muscular dystrophy.
    Hurwitz LJ; McCormick D
    Br Med J; 1970 Jul; 3(5713):29-30. PubMed ID: 5427484
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Urinary excretion of methylamino acids in myogenic and neurogenic muscular atrophy (author's transl)].
    Inoue R
    Rinsho Shinkeigaku; 1980 Jul; 20(7):510-5. PubMed ID: 7460420
    [No Abstract]   [Full Text] [Related]  

  • 11. Biochemical studies on muscular dystrophy. Serum and urine creatine, creatinine and aminoacids.
    el-Nabawy M; Sakr R; el-Hawary MF
    J Egypt Med Assoc; 1968; 51(11):949-63. PubMed ID: 5714513
    [No Abstract]   [Full Text] [Related]  

  • 12. Catecholamines and indoleamines in patients with Duchenne muscular dystrophy.
    Mendell JR; Murphy DL; Engel WK; Chase TN; Gordon E
    Arch Neurol; 1972 Dec; 27(6):518-20. PubMed ID: 5083869
    [No Abstract]   [Full Text] [Related]  

  • 13. Sulfur-containing amino acids in the plasma and urine of homocystinurics.
    Perry TL; Hansen S; MacDougall L; Warrington PD
    Clin Chim Acta; 1967 Mar; 15(3):409-20. PubMed ID: 6034417
    [No Abstract]   [Full Text] [Related]  

  • 14. [Pathogenesis of creatinuria and aminoaciduria in neuromuscular diseases].
    Il'ina NA; Poliakova NF; Khokhlov AP
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1977; 77(7):1025-8. PubMed ID: 197760
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Proteins in the urine associated with Duchenne muscular dystrophy and other neuromuscular diseases.
    Frearson N; Taylor RD; Perry SV
    Clin Sci (Lond); 1981 Aug; 61(2):141-9. PubMed ID: 7261538
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Vodskov Project VII: the amino acids in plasma and urine determined by ion exchange chromatography in a selected patient material and in a normal material.
    Espersen O; Paaby P
    Dan Med Bull; 1971 Aug; 18(4):88-99. PubMed ID: 5570689
    [No Abstract]   [Full Text] [Related]  

  • 17. Increased taurine excretion in hereditary hyperprolinemia of the mouse.
    Blake RL; Grillo RV; Russell ES
    Life Sci; 1974 Apr; 14(7):1285-90. PubMed ID: 4823641
    [No Abstract]   [Full Text] [Related]  

  • 18. Some biochemical changes occurring in muscular dystrophy and their possible genetical significance.
    Monckton G; Nihei T
    Ann N Y Acad Sci; 1966 Sep; 138(1):329-41. PubMed ID: 5230213
    [No Abstract]   [Full Text] [Related]  

  • 19. [Chromatographic study of aminoaciduria in subjects with progressive muscular dystrophy and in healthy carriers of such a defect].
    Brunelli B; Falorni A; Cao A; Lungarotti MS; Tangheroni W
    Pediatria (Napoli); 1971; 79(2):168-80. PubMed ID: 5095771
    [No Abstract]   [Full Text] [Related]  

  • 20. Qualitative study of aminoaciduria in muscular dystrophy and myotonia dystrophica.
    BLAHD WH; BLOOM A; DRELL W
    Proc Soc Exp Biol Med; 1955 Dec; 90(3):704-6. PubMed ID: 13289881
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.