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3. 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]
4. Cystinuria with mental retardation and paroxysmal dyskinesia in 2 brothers. Cavanagh NP; Bicknell J; Howard F Arch Dis Child; 1974 Aug; 49(8):662-4. PubMed ID: 4421405 [No Abstract] [Full Text] [Related]
5. The excretion of amino acids by cystinuric patients and their relatives. Crawhall JC; Purkiss P; Watts RW; Young EP Ann Hum Genet; 1969 Oct; 33(2):149-69. PubMed ID: 5383982 [No Abstract] [Full Text] [Related]
6. Urinary amino acid patterns in cystinuric families. Kato T; Sugiura J Nagoya J Med Sci; 1974 Mar; 36(2):71-8. PubMed ID: 4855341 [No Abstract] [Full Text] [Related]
7. Cystinuria: genetic heterogeneity and allelism. Rosenberg LE Science; 1966 Dec; 154(3754):1341-3. PubMed ID: 5925065 [TBL] [Abstract][Full Text] [Related]
8. [Isolated cystinuria (without lysin-, ornithinand argininuria) in a family with hypocalcemic tetany]. Brodehl J; Gellissen K; Kowalewski S Monatsschr Kinderheilkd (1902); 1967 Apr; 115(4):317-20. PubMed ID: 5592547 [No Abstract] [Full Text] [Related]
9. Amino acid excretion studies in a cystinuric family. Leaf G; Alston WC; Bruce J Clin Chim Acta; 1973 Sep; 48(1):5-8. PubMed ID: 4746729 [No Abstract] [Full Text] [Related]
10. [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]
12. A quantitative study of amino aciduria in dachshunds with a history of cystine urolithiasis. Cornelius CE; Bishop JA; Schaffer MH Cornell Vet; 1967 Apr; 57(2):177-83. PubMed ID: 6068134 [No Abstract] [Full Text] [Related]
13. Lysine infusion in cystinuria: theoretical renal thresholds for lysine. Lester FT; Cusworth DC Clin Sci; 1973 Feb; 44(2):99-111. PubMed ID: 4723291 [No Abstract] [Full Text] [Related]
14. Urinary excretion of total cystine and the dibasic amino acids arginine, lysine and ornithine in relation to genetic findings in patients with cystinuria treated with sulfhydryl compounds. Fjellstedt E; Harnevik L; Jeppsson JO; Tiselius HG; Söderkvist P; Denneberg T Urol Res; 2003 Dec; 31(6):417-25. PubMed ID: 14586528 [TBL] [Abstract][Full Text] [Related]
15. Amino acid excretion patterns in the offspring of a 'doubly-heterozygous' cystine stone former. Kelly S; Copeland W; Leikhim E Experientia; 1970 Dec; 26(12):1389-90. PubMed ID: 5492238 [No Abstract] [Full Text] [Related]
16. Heterozygotes for cystinuria. Crawhall JC; Saunders EP; Thompson CJ Ann Hum Genet; 1966 Mar; 29(3):257-69. PubMed ID: 5951406 [No Abstract] [Full Text] [Related]
17. [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]
18. The incidence of cystinuria in Japan. Ito H; Murakami M; Miyauchi T; Mori I; Yamaguchi K; Usui T; Shimazaki J J Urol; 1983 May; 129(5):1012-4. PubMed ID: 6406687 [TBL] [Abstract][Full Text] [Related]
19. [Observation and treatment of 2 cases of cystinuria with recurring lithiasis. Trial of D-pencillamine]. Bischops G; Dodinval P; Willems C J Urol Nephrol (Paris); 1968 Mar; 74(3):223-39. PubMed ID: 5646975 [No Abstract] [Full Text] [Related]
20. [Physiopathological considerations on the limits of detection of certain metabolic syndromes of the cystinuria-cystinosis type. Possibilities of rapid diagnosis]. Pâtea P; Tănase-Mogos I; Ciortoloman H; Petrescu L; Ciucă C; Orăşeanu D; Jemna M; Meila P Physiologie; 1980; 17(2):113-20. PubMed ID: 6770383 [No Abstract] [Full Text] [Related] [Next] [New Search]