Literature DB >> 4744406

Iminoglycinuria in a child in Czechoslovakia.

B Blehová, N Păzoutová, J Hyánek, J Jirásek.   

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Year:  1973        PMID: 4744406     DOI: 10.1007/bf00282197

Source DB:  PubMed          Journal:  Humangenetik        ISSN: 0018-7348


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  8 in total

1.  [Familial disease with associated convulsions with very early onset, excess albumin in the cerebrospinal fluid & hyperaminoaciduria].

Authors:  R JOSEPH; M RIBIERRE; J C JOB; M GIRAULT
Journal:  Arch Fr Pediatr       Date:  1958

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.  Familial iminoglycinuria. An inborn error of renal tubular transport.

Authors:  L E Rosenberg; J L Durant; L J Elsas
Journal:  N Engl J Med       Date:  1968-06-27       Impact factor: 91.245

4.  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

5.  Impaired intestinal transport of proline in a patient with familial iminoaciduria.

Authors:  S I Goodman; C A McIntyre; D O'Brien
Journal:  J Pediatr       Date:  1967-08       Impact factor: 4.406

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

Authors:  T Morikawa; K Tada; T Ando; T Yoshida; Y Yokoyama; T Arakawa
Journal:  Tohoku J Exp Med       Date:  1966-10       Impact factor: 1.848

7.  Prolinuria: a new renal tubular defect in transport of proline and glycine.

Authors:  K Tada; T Morikawa; T Ando; T Yoshida; A Minagawa
Journal:  Tohoku J Exp Med       Date:  1965-11-25       Impact factor: 1.848

8.  Amino acid transport: evidence for genetic control of two types in human kidney.

Authors:  C R Scriver; O H Wilson
Journal:  Science       Date:  1967-03-17       Impact factor: 47.728

  8 in total

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