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Journal Abstract Search
212 related items for PubMed ID: 5104075
21. [Diagnosis of hereditary saccharose-isomaltose-malabsorption]. Beyreiss K, Winkler U, Theile H. Kinderarztl Prax; 1971 Aug; 39(8):345-56. PubMed ID: 5137363 [No Abstract] [Full Text] [Related]
22. [Growth of patients with hereditary fructose intolerance or hereditary saccharose-isomaltose malabsorption]. Nüssli R. Helv Paediatr Acta; 1971 Dec; 26(5):637-47. PubMed ID: 5142943 [No Abstract] [Full Text] [Related]
24. [Intestinal disaccharidases enzyme activity. Its reduction in enteropathy caused by gluten and in other conditions of malabsorption]. De Larrechea I, Sampayo RR, Sosa Miatello C, Ibarra R. Prensa Med Argent; 1966 Jul 01; 53(26):1421-5. PubMed ID: 5999675 [No Abstract] [Full Text] [Related]
25. [HEREDITARY SACCHAROSE AND ISOMALTOSE MALABSORPTION]. PRADER A, AURICCHIO S, SEMENZA G. Monatsschr Kinderheilkd (1902); 1964 Apr 01; 112():177-80. PubMed ID: 14203475 [No Abstract] [Full Text] [Related]
26. Diets in disaccharidase deficiency and defective monosaccharide absorption. Lindquist B, Meeuwisse G. J Am Diet Assoc; 1966 Apr 01; 48(4):307-10. PubMed ID: 5906665 [No Abstract] [Full Text] [Related]
28. Trehalase deficiency in a family. Madzarovovà-Nohejlova J. Gastroenterology; 1973 Jul 01; 65(1):130-3. PubMed ID: 4737205 [No Abstract] [Full Text] [Related]
29. [General problems in the diagnosis of disaccharidase deficiency]. Fodor O, Dumitraşcu D. Med Interna (Bucur); 1970 May 01; 22(5):515-22. PubMed ID: 4913181 [No Abstract] [Full Text] [Related]
37. [Structural and functional changes caused by diet and gefarnate in the intestinal mucosa in malabsorption syndromes in the infantile age]. Mastella G, Marcer V, Buffatti GA, Mariotti M. Minerva Pediatr; 1970 Jun 09; 22(23):1157-74. PubMed ID: 5477004 [No Abstract] [Full Text] [Related]