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23. Interval breath hydrogen test in glucose-galactose malabsorption. Douwes AC; van Caillie M; Fernandes J; Bijleveld CM; Desjeux JF Eur J Pediatr; 1981 Nov; 137(3):273-6. PubMed ID: 7318838 [TBL] [Abstract][Full Text] [Related]
24. Nephrolithiasis in a child with glucose-galactose malabsorption. Tasic V; Slaveska N; Blau N; Santer R Pediatr Nephrol; 2004 Feb; 19(2):244-6. PubMed ID: 14673631 [TBL] [Abstract][Full Text] [Related]
25. [Intestinal malabsorption of glucose and galactose. Study of a family]. Grasset E; Evans LA; Dumontier AM; Heyman M; Faverge B; Beau JP; Desjeux JF Arch Fr Pediatr; 1982 Dec; 39 Suppl 2():729-33. PubMed ID: 7165473 [TBL] [Abstract][Full Text] [Related]
26. Diagnostic problems in glucose-galactose malabsorption. A case report. Kaijser K; Ockerman PA Acta Paediatr Scand; 1970 Mar; 59(2):214-6. PubMed ID: 5442433 [No Abstract] [Full Text] [Related]
27. [Glucose-galactose malabsorption. The first reported case in Denmark]. Boisen KA; Hjelt K Ugeskr Laeger; 1999 Jun; 161(26):4008-9. PubMed ID: 10402938 [TBL] [Abstract][Full Text] [Related]
28. Prenatal identification of a heterozygous status in two fetuses at risk for glucose-galactose malabsorption. Martín MG; Turk E; Kerner C; Zabel B; Wirth S; Wright EM Prenat Diagn; 1996 May; 16(5):458-62. PubMed ID: 8844006 [TBL] [Abstract][Full Text] [Related]
29. Nutrition management of congenital glucose-galactose malabsorption: a case study. Abad-Sinden A; Borowitz S; Meyers R; Sutphen J J Am Diet Assoc; 1997 Dec; 97(12):1417-21. PubMed ID: 9404340 [TBL] [Abstract][Full Text] [Related]
33. [Some hereditary disorders of intestinal resorption with renal dysfunction]. Clifton JA Internist (Berl); 1976 Jul; 17(7):325-35. PubMed ID: 780307 [No Abstract] [Full Text] [Related]
34. The genetics of intestinal carbohydrate intolerance. Eggermont E Prog Med Genet; 1969; 6():241-79. PubMed ID: 4897153 [No Abstract] [Full Text] [Related]
35. Absorption of glucose and maltose in congenital glucose-galactose malabsorption. Fairclough PD; Clark ML; Dawson AM; Silk DB; Milla PJ; Harries JT Pediatr Res; 1978 Dec; 12(12):1112-4. PubMed ID: 745864 [TBL] [Abstract][Full Text] [Related]
36. [A new case of glucose-galactose malabsorption]. La Selve P; Regent P; Duquesne A; Gueho A; Guibaud P; Larbre F Pediatrie; 1986 Jun; 41(4):329-32. PubMed ID: 3808842 [TBL] [Abstract][Full Text] [Related]
37. [Absorption studies in hereditary mono- and disaccharide malabsorptions]. Schaumlöffel E; Linneweh F; Graul EH Nucl Med (Stuttg); 1967; ():23-8. PubMed ID: 5601744 [No Abstract] [Full Text] [Related]
38. Congenital glucose-galactose malabsorption: a novel deletion within the SLC5A1 gene. Vallaeys L; Van Biervliet S; De Bruyn G; Loeys B; Moring AS; Van Deynse E; Cornette L Eur J Pediatr; 2013 Mar; 172(3):409-11. PubMed ID: 22843301 [TBL] [Abstract][Full Text] [Related]
39. Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1. Soylu OB; Ecevit C; Altinöz S; Oztürk AA; Temizkan AK; Maeda M; Kasahara M Eur J Pediatr; 2008 Dec; 167(12):1395-8. PubMed ID: 18288487 [TBL] [Abstract][Full Text] [Related]
40. Carbohydrate malabsorption in kwashiorkor. Habte D; Hyvarinen A; Sterky G Ethiop Med J; 1973 Jan; 11(1):33-40. PubMed ID: 4782006 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]