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2. Familial iminoglycinuria. An inborn error of renal tubular transport. Rosenberg LE; Durant JL; Elsas LJ N Engl J Med; 1968 Jun; 278(26):1407-13. PubMed ID: 5652624 [No Abstract] [Full Text] [Related]
3. Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype". Statter M; Ben-Zvi A; Shina A; Schein R; Russell A Helv Paediatr Acta; 1976 Aug; 31(2):173-82. PubMed ID: 955941 [TBL] [Abstract][Full Text] [Related]
4. Cystathioninuria and renal iminoglycinuria in a pedigree. Whelan DT; Scriver CR N Engl J Med; 1968 Apr; 278(17):924-7. PubMed ID: 5644557 [No Abstract] [Full Text] [Related]
5. Ontogeny of amino acid reabsorption in human kidney. Evidence from the homozygous infant with familial renal iminoglycinuria for multiple proline and glycine systems. Lasley L; Scriver CR Pediatr Res; 1979 Jan; 13(1):65-70. PubMed ID: 432003 [TBL] [Abstract][Full Text] [Related]
6. [Renal clearance of amino acid in a hyperprolinemic child]. Dodinval P; Willems C; Heusden AM; Hainaut H; Gottschalk C J Genet Hum; 1969 Oct; 17(3):297-315. PubMed ID: 5387412 [No Abstract] [Full Text] [Related]
10. Iminoglycinuria: a benign type of inherited aminoaciduria. Coşkun T; Ozalp I; Tokatli A Turk J Pediatr; 1993; 35(2):121-5. PubMed ID: 7504361 [TBL] [Abstract][Full Text] [Related]
11. [Prolinuria]. Tada K Saishin Igaku; 1969 Jun; 24(6):1226-34. PubMed ID: 5805578 [No Abstract] [Full Text] [Related]
12. Renal imino acid and glycine transport system ontogeny and involvement in developmental iminoglycinuria. Vanslambrouck JM; Bröer A; Thavyogarajah T; Holst J; Bailey CG; Bröer S; Rasko JE Biochem J; 2010 May; 428(3):397-407. PubMed ID: 20377526 [TBL] [Abstract][Full Text] [Related]
13. Hyperprolinemia: clinical and biochemical family study. Woody NC; Snyder CH; Harris JA Pediatrics; 1969 Oct; 44(4):554-63. PubMed ID: 5346634 [No Abstract] [Full Text] [Related]
14. [Results of a period of research (1967-1974) in the field of disorders of transport amino acid and metabolism using chromatographic, electrophoretic and dosimetric methods]. Berio A; Allegranza A; Scapaticci E; Cadoni M; Camozzi C; Cavallo V; Di Stefano A; Santos JG Minerva Pediatr; 1975 Sep; 27(30):1609-23. PubMed ID: 1177852 [No Abstract] [Full Text] [Related]
15. [Hyperprolinemia and hydroxyprolinemia]. Berger R; Broyer M Presse Med (1893); 1969 May; 77(26):957-8. PubMed ID: 5795142 [No Abstract] [Full Text] [Related]
17. [Primary and secondary hyperaminoaciduria in children (review of the literature)]. Lebedev VP; Iur'eva EA; Mukhina IuG; Buravina TA; Koroleva IA Vopr Okhr Materin Det; 1970 Nov; 15(11):64-8. PubMed ID: 4928437 [No Abstract] [Full Text] [Related]
18. [On some aspects of renal tubule physiopathology in childhood]. Bottone E; Macchia PA; Baldini G; Bani E Minerva Pediatr; 1973 Jul; 25(25):1073-118. PubMed ID: 4356737 [No Abstract] [Full Text] [Related]
19. Iminodipeptiduria: a genetic defect in recycling collagen; a method for determining prolidase in erythrocytes. Jackson SH; Dennis AW; Greenberg M Can Med Assoc J; 1975 Oct; 113(8):759, 762-3. PubMed ID: 803128 [TBL] [Abstract][Full Text] [Related]
20. Cystathioninuria, renal iminoglycinuria and...alpha 1-antitrypsin...deficiency in the same family: relevance in medical practice. Halal F; Scriver CR; Cox DW; Jaber L; Varsano I Can Med Assoc J; 1979 Jul; 121(1):64-8. PubMed ID: 313837 [No Abstract] [Full Text] [Related] [Next] [New Search]