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 *

61 related articles for article (PubMed ID: 691379)

  • 1. [Cystinuria and hyperlysinuria].
    Oyanagi K
    Nihon Rinsho; 1978 May; Suppl():1426-7. PubMed ID: 691379
    [No Abstract]   [Full Text] [Related]  

  • 2. [Cystinuria--familial lysinuria].
    Broyer M; Berger R
    Presse Med (1893); 1968 Mar; 76(16):754. PubMed ID: 5645015
    [No Abstract]   [Full Text] [Related]  

  • 3. [Metabolic errors of the cystinuria-lysinuria, cystinosis type detected in the newborn infant and child with renal and ocular diseases].
    Tănase-Mogoş I; Ciortoloman H; Petrescu L; Pâtea P; Popescu M; Ankăr V; Grigorescu G
    Physiologie; 1981; 18(3):187-95. PubMed ID: 6796978
    [No Abstract]   [Full Text] [Related]  

  • 4. Aminoaciduria and hyperaminoaciduria in childhood.
    Brodehl J; Bickel H
    Clin Nephrol; 1973; 1(3):149-68. PubMed ID: 4593448
    [No Abstract]   [Full Text] [Related]  

  • 5. [Combined cystinuria-lysinuria in 2 brothers with mental retardation and morphologic and neurologic anomalies].
    Thiriar MJ; Szliwowski HB; Vis HL
    Acta Neurol Psychiatr Belg; 1968 Mar; 68(3):216-27. PubMed ID: 4972603
    [No Abstract]   [Full Text] [Related]  

  • 6. [Cystinuria and lysinuria in Down's syndrome].
    Hyánek J; Goetz P; Hoza J; Kubík M; Seemanová E; Sedlácková M
    Cas Lek Cesk; 1970 Nov; 109(46):1088-92. PubMed ID: 4249168
    [No Abstract]   [Full Text] [Related]  

  • 7. [Cystinuria in children in the light of our observations].
    Hanicka M; Bernasowska-Knapczykowa K; Kos S
    Przegl Lek; 1966; 22(11):700-2. PubMed ID: 5959614
    [No Abstract]   [Full Text] [Related]  

  • 8. [The hyperaminoacidurias with special reference to cystinuria].
    Perfumo F; Basile G; Ginevri F; Gusmano R
    Minerva Med; 1979 Oct; 70(44):3065-74. PubMed ID: 386173
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Renal clearance of cystathionine in homozygous and heterozygous cystathioninuria, cystinuria, and the normal state.
    Frimpter GW; Greenberg AJ
    J Clin Invest; 1967 Jun; 46(6):975-82. PubMed ID: 6026103
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [On some aspects of renal tubule physiopathology in childhood].
    Bottone E; Macchia PA; Baldini G; Bani E
    Minerva Pediatr; 1973 Jul; 25(25):1073-118. PubMed ID: 4356737
    [No Abstract]   [Full Text] [Related]  

  • 11. [Primary and secondary hyperaminoaciduria in children (review of the literature)].
    Lebedev VP; Iur'eva EA; Mukhina IuG; Buravina TA; Koroleva IA
    Vopr Okhr Materin Det; 1970 Nov; 15(11):64-8. PubMed ID: 4928437
    [No Abstract]   [Full Text] [Related]  

  • 12. [Defects of renal tubular transport systems for amino acids].
    Gerok W
    Med Klin; 1975 Feb; 70(8):301-12. PubMed ID: 1091836
    [No Abstract]   [Full Text] [Related]  

  • 13. Genetics of renal transport disorders.
    Segal S
    Prog Clin Biol Res; 1989; 305():101-9. PubMed ID: 2668967
    [No Abstract]   [Full Text] [Related]  

  • 14. Cystinuria phenotyping by oral lysine and arginine loading.
    de Sanctis L; Bonetti G; Bruno M; De Luca F; Bisceglia L; Palacin M; Dianzani I; Ponzone A
    Clin Nephrol; 2001 Dec; 56(6):467-74. PubMed ID: 11770798
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Primary tubulopathies].
    Gerok W
    Acta Med Austriaca; 1975; 2(5):162-7. PubMed ID: 1220514
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Genetic bases of metabolic tubular nephropathies].
    Savi M
    Minerva Med; 1979 Oct; 70(44):3001-13. PubMed ID: 386171
    [No Abstract]   [Full Text] [Related]  

  • 17. [Cystinuria-lysinuria with dwarfism, facial dysmorphy, muscle hypoplasia and psychomotor retardation].
    See G; Lejeune J; Dayras JC; Raoul
    Ann Pediatr (Paris); 1970 Nov; 17(11):846-52. PubMed ID: 5484626
    [No Abstract]   [Full Text] [Related]  

  • 18. [Hereditary forms of tubular kidney disease: advances in diagnosis and therapy].
    Bickel H
    Monatsschr Kinderheilkd (1902); 1966 Apr; 114(4):193-8. PubMed ID: 5985792
    [No Abstract]   [Full Text] [Related]  

  • 19. [Disorders of renal tubular transport of amino acids, hexose and phosphate].
    Hasegawa H; Takayanagi K; Mitarai T
    Nihon Rinsho; 2006 Feb; 64 Suppl 2():522-7. PubMed ID: 16523947
    [No Abstract]   [Full Text] [Related]  

  • 20. Disorders of renal amino acid transport.
    Segal S
    N Engl J Med; 1976 May; 294(19):1044-51. PubMed ID: 943698
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.