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2. Phenotypic variance in childhood coeliac disease and the HLA-DQ/DR dose effect. Vermeulen BA; Hogen Esch CE; Yuksel Z; Koning F; Verduijn W; Doxiadis II; Schreuder GM; Mearin ML Scand J Gastroenterol; 2009; 44(1):40-5. PubMed ID: 18932050 [TBL] [Abstract][Full Text] [Related]
3. Different genotypes in a large Italian family with recurrent hereditary fructose intolerance. Caciotti A; Donati MA; Adami A; Guerrini R; Zammarchi E; Morrone A Eur J Gastroenterol Hepatol; 2008 Feb; 20(2):118-21. PubMed ID: 18188031 [TBL] [Abstract][Full Text] [Related]
5. The diagnosis of hereditary fructose intolerance. Steinmann B; Gitzelmann R Helv Paediatr Acta; 1981 Sep; 36(4):297-316. PubMed ID: 6268573 [TBL] [Abstract][Full Text] [Related]
6. Hereditary fructose intolerance in a patient with phenylketonuria. Coşkun T; Ozalp I; Tekinalp G Turk J Pediatr; 1991; 33(3):181-4. PubMed ID: 1792698 [TBL] [Abstract][Full Text] [Related]
7. HLA genotyping is useful in the evaluation of the risk for coeliac disease in the 1st-degree relatives of patients with coeliac disease. Karinen H; Kärkkäinen P; Pihlajamäki J; Janatuinen E; Heikkinen M; Julkunen R; Kosma VM; Naukkarinen A; Laakso M Scand J Gastroenterol; 2006 Nov; 41(11):1299-304. PubMed ID: 17060123 [TBL] [Abstract][Full Text] [Related]
8. Molecular analysis of aldolase B genes in the diagnosis of hereditary fructose intolerance in the United Kingdom. Cross NC; Cox TM Q J Med; 1989 Nov; 73(271):1015-20. PubMed ID: 2623136 [TBL] [Abstract][Full Text] [Related]
9. Hereditary fructose intolerance in early childhood: a major diagnostic challenge. Survey of 20 symptomatic cases. Baerlocher K; Gitzelmann R; Steinmann B; Gitzelmann-Cumarasamy N Helv Paediatr Acta; 1978 Dec; 33(6):465-87. PubMed ID: 738900 [TBL] [Abstract][Full Text] [Related]
10. Analysis of HLA and non-HLA alleles can identify individuals at high risk for celiac disease. Romanos J; van Diemen CC; Nolte IM; Trynka G; Zhernakova A; Fu J; Bardella MT; Barisani D; McManus R; van Heel DA; Wijmenga C Gastroenterology; 2009 Sep; 137(3):834-40, 840.e1-3. PubMed ID: 19454285 [TBL] [Abstract][Full Text] [Related]
15. [Adults with hereditary fructose intolerance: risks of fructose infusion]. Steegmanns I; Rittmann M; Bayerl JR; Gitzelmann R Dtsch Med Wochenschr; 1990 Apr; 115(14):539-41. PubMed ID: 1969793 [TBL] [Abstract][Full Text] [Related]
16. Daily Fructose Traces Intake and Liver Injury in Children with Hereditary Fructose Intolerance. Di Dato F; Spadarella S; Puoti MG; Caprio MG; Pagliardini S; Zuppaldi C; Vallone G; Fecarotta S; Esposito G; Iorio R; Parenti G; Spagnuolo MI Nutrients; 2019 Oct; 11(10):. PubMed ID: 31591370 [TBL] [Abstract][Full Text] [Related]
17. [Death following fructose and sorbitol infusions]. Wagner K; Wolf AS Anaesthesist; 1984 Nov; 33(11):573-8. PubMed ID: 6517265 [TBL] [Abstract][Full Text] [Related]
18. Frequencies of genetic polymorphisms of TLR4 and CD14 and of HLA-DQ genotypes in children with celiac disease, type 1 diabetes mellitus, or both. Dezsofi A; Szebeni B; Hermann CS; Kapitány A; Veres G; Sipka S; Körner A; Madácsy L; Korponay-Szabó I; Rajczy K; Arató A J Pediatr Gastroenterol Nutr; 2008 Sep; 47(3):283-7. PubMed ID: 18728522 [TBL] [Abstract][Full Text] [Related]
19. Six novel alleles identified in Italian hereditary fructose intolerance patients enlarge the mutation spectrum of the aldolase B gene. Esposito G; Santamaria R; Vitagliano L; Ieno L; Viola A; Fiori L; Parenti G; Zancan L; Zagari A; Salvatore F Hum Mutat; 2004 Dec; 24(6):534. PubMed ID: 15532022 [TBL] [Abstract][Full Text] [Related]
20. Hereditary fructose intolerance: functional study of two novel ALDOB natural variants and characterization of a partial gene deletion. Esposito G; Imperato MR; Ieno L; Sorvillo R; Benigno V; Parenti G; Parini R; Vitagliano L; Zagari A; Salvatore F Hum Mutat; 2010 Dec; 31(12):1294-303. PubMed ID: 20848650 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]