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 *

88 related articles for article (PubMed ID: 5362973)

  • 1. [Experiences with the Berry screening test].
    Janousek O
    Cesk Pediatr; 1969 Dec; 24(12):1126-9. PubMed ID: 5362973
    [No Abstract]   [Full Text] [Related]  

  • 2. [Paper samples in detection and confirmation of some anomalies of amino acid metabolism].
    Charpentier C; Lemonnier A
    Ann Biol Clin (Paris); 1969; 27(5):297-323. PubMed ID: 4897889
    [No Abstract]   [Full Text] [Related]  

  • 3. The hyperphenylalaninemias in Israel.
    Cohen BE; Szeinberg A; Pollak S; Peled I; Likverman S; Crispin M
    Isr J Med Sci; 1973; 9(9):1393-5. PubMed ID: 4775121
    [No Abstract]   [Full Text] [Related]  

  • 4. [Mass screening of genetic metabolic abnormalities with special reference to amino acid metabolism disorders, using chemical methods].
    Lubs H; Knapp A
    Z Arztl Fortbild (Jena); 1970 May; 64(10):516-9. PubMed ID: 5520559
    [No Abstract]   [Full Text] [Related]  

  • 5. Urinary metabolic screening in children with psycho-neurological diseases. Evaluation of different screening tests.
    Hambraeus L; Holmgren G
    Ups J Med Sci Suppl; 1974; 15():1-23. PubMed ID: 4274307
    [No Abstract]   [Full Text] [Related]  

  • 6. [Difficulties in interpreting a pathological aminoaciduria].
    Farriaux JP; Dautrevaux M; Adam E; Gosselin B; Fontaine G
    Acta Paediatr Belg; 1968; 22(1):5-28. PubMed ID: 5759454
    [No Abstract]   [Full Text] [Related]  

  • 7. [Progress in the early detection of inborn errors of metabolism].
    Bozkowa K; Cabalska B; Duczyńska N; Grodzka Z; Sendecka E; Nowakowska A; Lenartowska I; Kasperska-Dworak A; Helwich E
    Probl Med Wieku Rozwoj; 1981; 10():69-85. PubMed ID: 7349406
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Studies of inborn errors of amino acid metabolism and urinary excretion of -phenylethylamine, using screening methods].
    Berio A
    Minerva Pediatr; 1972 Jun; 24(32):937-41. PubMed ID: 5050421
    [No Abstract]   [Full Text] [Related]  

  • 9. [Amino acid composition in blood and urine from healthy newborn infants: screening test for the detection of enxymopathies].
    Adrienne S
    Orv Hetil; 1969 Jun; 110(23):1315-20. PubMed ID: 5794637
    [No Abstract]   [Full Text] [Related]  

  • 10. A simple screening test for histidinuria.
    Gerber MG; Gerber DA
    Pediatrics; 1969 Jan; 43(1):40-3. PubMed ID: 5764066
    [No Abstract]   [Full Text] [Related]  

  • 11. [Multiple screening test for the detection of inborn errors of metabolism : experiment of mass-screening test with ultra-micro amino acid analysis method in dried blood spot (author's transl)].
    Sumi K; Konishi K; Shimizu S; Mimura K; Uemura I; Matsuoka A
    Rinsho Byori; 1978 Jun; 26(6):532-6. PubMed ID: 691784
    [No Abstract]   [Full Text] [Related]  

  • 12. [Screening of newborn infants for inborn errors of metabolism].
    Halvorsen S; Skjelkvåle L
    Tidsskr Nor Laegeforen; 1970 Jan; 90(2):233-5. PubMed ID: 5430194
    [No Abstract]   [Full Text] [Related]  

  • 13. Diagnosis and treatment: interpreting the positive screening test in the newborn infant.
    Scriver CR
    Pediatrics; 1967 May; 39(5):764-8. PubMed ID: 6026878
    [No Abstract]   [Full Text] [Related]  

  • 14. [Results of a survey of search of amino-acidopathies in the north of France. Apropos of 8,433 children].
    Fontaine G; Farriaux JP; Delecour M
    Ann Pediatr (Paris); 1970; 17(6):487-9. PubMed ID: 5421331
    [No Abstract]   [Full Text] [Related]  

  • 15. [Inborn errors of amino acid metabolism].
    Endo F
    Nihon Rinsho; 2004 Nov; 62 Suppl 11():562-6. PubMed ID: 15628476
    [No Abstract]   [Full Text] [Related]  

  • 16. [Histidenemia (a review of the literature)].
    Nikolaeva EA
    Vopr Okhr Materin Det; 1980 Jan; 25(1):56-62. PubMed ID: 6992428
    [No Abstract]   [Full Text] [Related]  

  • 17. [Results of screening for inborn errors of aminoacid metabolism in adult and infant patients from psychiatric institutions (author's transl)].
    Hyánek J; Turek S; Kríz J; Trísková J; Homolka J; Kopejtková H
    Cas Lek Cesk; 1975 Mar; 114(10-11):307-8. PubMed ID: 1139573
    [No Abstract]   [Full Text] [Related]  

  • 18. Studies on the metabolism of the phenolic acids in hereditary tyrosinemia by a gas-liquid chromatographic method.
    Gentz J; Lindblad B; Lindstedt S; Zetterström R
    J Lab Clin Med; 1969 Aug; 74(2):185-202. PubMed ID: 5799507
    [No Abstract]   [Full Text] [Related]  

  • 19. [Organization of a screening test program for congenital metabolic disorders in newborn infants in Berlin--problems, results and experiences. 2. Screening tests for amino-acid metabolism].
    Ahlbehrendt I; Wagenknecht C
    Z Med Lab Diagn; 1978; 19(3):157-63. PubMed ID: 695812
    [No Abstract]   [Full Text] [Related]  

  • 20. Benign hyperaminoacidaemia and hyperaminoaciduria.
    Hyánek J
    Acta Univ Carol Med Monogr; 1977; (79 Pt 3):23-9. PubMed ID: 615478
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.