Literature DB >> 5971079

Prolinuria: defect in intestinal absorption of imino acids and glycine.

T Morikawa, K Tada, T Ando, T Yoshida, Y Yokoyama, T Arakawa.   

Abstract

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Year:  1966        PMID： 5971079     DOI： 10.1620/tjem.90.105

Source DB:  PubMed          Journal:  Tohoku J Exp Med        ISSN： 0040-8727            Impact factor:   1.848


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  6 in total

1.  Iminoglycinuria in a child in Czechoslovakia.

Authors:  B Blehová; N Păzoutová; J Hyánek; J Jirásek
Journal:  Humangenetik       Date:  1973-07-20

2.  Renal tubular transport of proline, hydroxyproline, and glycine. 3. Genetic basis for more than one mode of transport in human kidney.

Authors:  C R Scriver
Journal:  J Clin Invest       Date:  1968-04       Impact factor: 14.808

3.  Iminoglycinuria--a "harmless" inborn error of metabolism?

Authors:  G R Fraser; A I Friedmann; V M Patton; D N Wade; L I Woolf
Journal:  Humangenetik       Date:  1968

Review 4.  The molecular basis of neutral aminoacidurias.

Authors:  Angelika Bröer; Juleen A Cavanaugh; John E J Rasko; Stefan Bröer
Journal:  Pflugers Arch       Date:  2005-07-29       Impact factor: 3.657

5.  Familial renal glycosuria: a genetic reappraisal of hexose transport by kidney and intestine.

Authors:  L J Elsas; L E Rosenberg
Journal:  J Clin Invest       Date:  1969-10       Impact factor: 14.808

6.  Renal and intestinal hexose transport in familial glucose-galactose malabsorption.

Authors:  L J Elsas; R E Hillman; J H Patterson; L E Rosenberg
Journal:  J Clin Invest       Date:  1970-03       Impact factor: 14.808
  6 in total

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