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.
134 related articles for article (PubMed ID: 5796364)
1. Cellular transport of L-histidine in Hartnup disease. Halvorsen S; Hygstedt O; Jagenburg R; Sjaastad O J Clin Invest; 1969 Aug; 48(8):1552-9. PubMed ID: 5796364 [TBL] [Abstract][Full Text] [Related]
2. Studies on intestinal absorption of amino acids and a dipeptide in a case of Hartnup disease. Navab F; Asatoor AM Gut; 1970 May; 11(5):373-9. PubMed ID: 4246731 [TBL] [Abstract][Full Text] [Related]
3. Intestinal absorption of carnosine and its constituent amino acids in man. Asatoor AM; Bandoh JK; Lant AF; Milne MD; Navab F Gut; 1970 Mar; 11(3):250-4. PubMed ID: 5423906 [TBL] [Abstract][Full Text] [Related]
5. Tryptophan load and uptake of tryptophan by leukocytes in Hartnup disease. Tada K; Morikawa T; Arakawa T Tohoku J Exp Med; 1966 Dec; 90(4):337-46. PubMed ID: 4226466 [No Abstract] [Full Text] [Related]
6. Absorption of amino acids and peptides in a child with a variant of Hartnup disease and coexistent coeliac disease. Tarlow MJ; Seakins JW; Lloyd JK; Matthews DM; Cheng B; Thomas AJ Arch Dis Child; 1972 Oct; 47(255):798-803. PubMed ID: 5086513 [TBL] [Abstract][Full Text] [Related]
7. Intestinal absorption and biopsy transport of peptides and amino acids in Hartnup disease. Tarlow MJ; Seakins JW; Lloyd JK; Matthews DM; Cheng B; Thomas AJ Clin Sci; 1970 Dec; 39(6):18P-19P. PubMed ID: 5493936 [No Abstract] [Full Text] [Related]
8. A clinicobiochemical study of tryptophan and other plasma and urinary amino acids in the family with Hartnup disease. Milovanović DD Adv Exp Med Biol; 2003; 527():325-35. PubMed ID: 15206746 [TBL] [Abstract][Full Text] [Related]
9. The Hartnup phenotype: Mendelian transport disorder, multifactorial disease. Scriver CR; Mahon B; Levy HL; Clow CL; Reade TM; Kronick J; Lemieux B; Laberge C Am J Hum Genet; 1987 May; 40(5):401-12. PubMed ID: 3578280 [TBL] [Abstract][Full Text] [Related]
10. The absorption of oral L-histidine in dystrophia myotonica. Jagenburg OR; Sjaastad O Acta Neurol Scand; 1966; 42(5):551-7. PubMed ID: 5959821 [No Abstract] [Full Text] [Related]
11. Absorption of amino acids and the dipeptide, carnosine, from the gut in normal subjects and a case of Hartnup disease. Asatoor AM; Bandoh JK; Lant AF; Milne MD; Navab F Clin Sci; 1969 Oct; 37(2):568. PubMed ID: 5359019 [No Abstract] [Full Text] [Related]
12. N-acetylhistaminuria in dystrophia myotonica. Sjaastad O Eur Neurol; 1968; 1(2):112-21. PubMed ID: 5696599 [No Abstract] [Full Text] [Related]
15. Studies of intestinal transport defect in Hartnup disease. Shih VE; Bixby EM; Alpers DH; Bartoscas CS; Thier SO Gastroenterology; 1971 Oct; 61(4):445-53. PubMed ID: 5157127 [No Abstract] [Full Text] [Related]
16. Transport of dibasic amino acids, cystine, and tryptophan by cultured human fibroblasts: absence of a defect in cystinuria and Hartnup disease. Groth U; Rosenberg LE J Clin Invest; 1972 Aug; 51(8):2130-42. PubMed ID: 5054467 [TBL] [Abstract][Full Text] [Related]
18. Transport of amino acids and peptides in the gut and the kidney. Milne MD Sci Basis Med Annu Rev; 1971; ():161-77. PubMed ID: 4933913 [No Abstract] [Full Text] [Related]
19. Hartnup disease. Oyanagi K; Takagi M; Kitabatake M; Nakao T Tohoku J Exp Med; 1967 Apr; 91(4):383-95. PubMed ID: 4228120 [No Abstract] [Full Text] [Related]
20. Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease. Seakins JW; Ersser RS Arch Dis Child; 1967 Dec; 42(226):682-8. PubMed ID: 6073838 [No Abstract] [Full Text] [Related] [Next] [New Search]