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Journal Abstract Search
129 related items for PubMed ID: 643293
1. [Renal glycosuria with loss of phosphate (author's transl)]. Schabel F, Glatzl J, Irnberger E. Padiatr Padol; 1978; 13(2):159-63. PubMed ID: 643293 [Abstract] [Full Text] [Related]
2. Complete absence of tubular glucose reabsorption: a new type of renal glucosuria (type 0). Oemar BS, Byrd DJ, Brodehl J. Clin Nephrol; 1987 Mar; 27(3):156-60. PubMed ID: 3568462 [Abstract] [Full Text] [Related]
3. [Renal glycosuria: dominant or recessive autosome anomaly? Mode of hereditary transmission based on the analysis of a 3-generation family tree]. De Marchi S, Proto G, Jengo A, Collinassi P, Basile A. Minerva Med; 1983 Feb 25; 74(7):301-6. PubMed ID: 6828258 [Abstract] [Full Text] [Related]
4. [Tubular secretion of phosphate in the human kidney (author's transl)]. Schabel F. Padiatr Padol; 1978 Feb 25; 13(4):385-90. PubMed ID: 714486 [Abstract] [Full Text] [Related]
5. [Kidney tubular transport disorders. Renal tubule defects in glucose transport--renal glycosuria]. Ogura Y, Tsuji H, Sakurai I, Ishida Y. Nihon Rinsho; 1989 Jul 25; 47(7):1589-96. PubMed ID: 2810811 [No Abstract] [Full Text] [Related]
6. Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion. Calado J, Sznajer Y, Metzger D, Rita A, Hogan MC, Kattamis A, Scharf M, Tasic V, Greil J, Brinkert F, Kemper MJ, Santer R. Nephrol Dial Transplant; 2008 Dec 25; 23(12):3874-9. PubMed ID: 18622023 [Abstract] [Full Text] [Related]
7. Type O renal glucosuria. Bagga A, Shankar V, Moudgil A, Srivastava RN. Acta Paediatr Scand; 1991 Jan 25; 80(1):116-9. PubMed ID: 2028783 [Abstract] [Full Text] [Related]
8. Urinary loss of glucose, phosphate, and protein by diffusion into proximal straight tubules injured by D-serine and maleic acid. Carone FA, Nakamura S, Goldman B. Lab Invest; 1985 Jun 25; 52(6):605-10. PubMed ID: 3925238 [Abstract] [Full Text] [Related]
9. [Renal tubular dysplastic glycosuria. Present knowledge]. Nurra P, Oliveri M, Nurra V, Basso L. Arch Sci Med (Torino); 1980 Jun 25; 137(4):649-54. PubMed ID: 7247685 [No Abstract] [Full Text] [Related]
10. Familial renal glycosuria: a genetic reappraisal of hexose transport by kidney and intestine. Elsas LJ, Rosenberg LE. J Clin Invest; 1969 Oct 25; 48(10):1845-54. PubMed ID: 5822589 [Abstract] [Full Text] [Related]
11. [Regulation of the renal excretion of phosphates. Use of isolated vesicles of luminal membranes for the study of phosphate transport]. Angielski S. Postepy Biochem; 1984 Oct 25; 30(3-4):273-94. PubMed ID: 6443024 [No Abstract] [Full Text] [Related]
12. Renal glycosuria (a family study). Dash R, Mishra K, Das PC, Das RK, Mohakur AC, Padhi PK, Mishra D. J Indian Med Assoc; 1984 Aug 25; 82(8):287-9. PubMed ID: 6491338 [No Abstract] [Full Text] [Related]
13. [Disorders of renal tubular transport of amino acids, hexose and phosphate]. Hasegawa H, Takayanagi K, Mitarai T. Nihon Rinsho; 2006 Feb 25; 64 Suppl 2():522-7. PubMed ID: 16523947 [No Abstract] [Full Text] [Related]
19. Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2). van den Heuvel LP, Assink K, Willemsen M, Monnens L. Hum Genet; 2002 Dec 20; 111(6):544-7. PubMed ID: 12436245 [Abstract] [Full Text] [Related]
20. Renal glucosuria due to SGLT2 mutations. Kleta R, Stuart C, Gill FA, Gahl WA. Mol Genet Metab; 2004 May 20; 82(1):56-8. PubMed ID: 15110322 [Abstract] [Full Text] [Related] Page: [Next] [New Search]