These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 8576798)

  • 1. Congenital sucrase-isomaltase deficiency.
    Treem WR
    J Pediatr Gastroenterol Nutr; 1995 Jul; 21(1):1-14. PubMed ID: 8576798
    [No Abstract]   [Full Text] [Related]  

  • 2. Congenital sucrase-isomaltase deficiency: summary of an evaluation in one family.
    Chumpitazi BP; Robayo-Torres CC; Opekun AR; Nichols BL; Naim HY
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2(0 2):S36. PubMed ID: 23103651
    [No Abstract]   [Full Text] [Related]  

  • 3. Congenital sucrase-isomaltase deficiency: heterogeneity of inheritance, trafficking, and function of an intestinal enzyme complex.
    Naim HY; Heine M; Zimmer KP
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2():S13-20. PubMed ID: 23103643
    [No Abstract]   [Full Text] [Related]  

  • 4. Clinical aspects and treatment of congenital sucrase-isomaltase deficiency.
    Treem WR
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2():S7-13. PubMed ID: 23103658
    [No Abstract]   [Full Text] [Related]  

  • 5. Congenital sucrase-isomaltase deficiency: identification of a common Inuit founder mutation.
    Marcadier JL; Boland M; Scott CR; Issa K; Wu Z; McIntyre AD; Hegele RA; Geraghty MT; Lines MA
    CMAJ; 2015 Feb; 187(2):102-107. PubMed ID: 25452324
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Breath hydrogen test and sucrase isomaltase deficiency.
    Ford RP; Barnes GL
    Arch Dis Child; 1983 Aug; 58(8):595-7. PubMed ID: 6614973
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Congenital sucrase-isomaltase deficiency: a rare cause of chronic or recurrent diarrhea in children].
    Délèze G; Spahr A
    Rev Med Suisse Romande; 1980 May; 100(5):441-2. PubMed ID: 7455469
    [No Abstract]   [Full Text] [Related]  

  • 8. Index of suspicion. Case 3. Congenital sucrase-isomaltase deficiency.
    Mahant S; Friedman J
    Pediatr Rev; 2000 Jan; 21(1):20, 24-5. PubMed ID: 10702073
    [No Abstract]   [Full Text] [Related]  

  • 9. 13C-breath tests for sucrose digestion in congenital sucrase isomaltase-deficient and sacrosidase-supplemented patients.
    Robayo-Torres CC; Opekun AR; Quezada-Calvillo R; Villa X; Smith EO; Navarrete M; Baker SS; Nichols BL
    J Pediatr Gastroenterol Nutr; 2009 Apr; 48(4):412-8. PubMed ID: 19330928
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Congenital sucrase-isomaltase deficiency in Türkiye; a single center experience.
    Barut D; Kıran Taşcı E; Kunay B; Güven B; Aksoy B; Çağan Appak Y; Karakoyun M; Çetin F; Selimoğlu A; Onay H; Aydoğdu S
    Scand J Gastroenterol; 2024 Jun; 59(6):647-651. PubMed ID: 38459691
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients.
    Gericke B; Amiri M; Scott CR; Naim HY
    Biochim Biophys Acta Mol Basis Dis; 2017 Mar; 1863(3):817-826. PubMed ID: 28062276
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sacrosidase therapy for congenital sucrase-isomaltase deficiency.
    Treem WR; McAdams L; Stanford L; Kastoff G; Justinich C; Hyams J
    J Pediatr Gastroenterol Nutr; 1999 Feb; 28(2):137-42. PubMed ID: 9932843
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency.
    Alfalah M; Keiser M; Leeb T; Zimmer KP; Naim HY
    Gastroenterology; 2009 Mar; 136(3):883-92. PubMed ID: 19121318
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical heterogeneity in congenital sucrase-isomaltase deficiency.
    Treem WR
    J Pediatr; 1996 Jun; 128(6):727-9. PubMed ID: 8648527
    [No Abstract]   [Full Text] [Related]  

  • 15. Differential Effects of Sucrase-Isomaltase Mutants on Its Trafficking and Function in Irritable Bowel Syndrome: Similarities to Congenital Sucrase-Isomaltase Deficiency.
    Husein DM; Rizk S; Naim HY
    Nutrients; 2020 Dec; 13(1):. PubMed ID: 33375084
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Frequency of sucrase deficiency in mucosal biopsies.
    Nichols BL; Adams B; Roach CM; Ma CX; Baker SS
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2():S28-30. PubMed ID: 23103647
    [No Abstract]   [Full Text] [Related]  

  • 17. [Peripheral gangrene in a congenital sucrase isomaltase deficiency (author's transl)].
    Méndez Aparicio FM
    An Esp Pediatr; 1980 Aug; 13(8):720-5. PubMed ID: 7436153
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital Sucrase-Isomaltase Deficiency: Same Mutation with Different Clinical Presentations.
    İryancı Fİ; Güven B; Çakır M
    Turk J Gastroenterol; 2024 Apr; 35(4):343-349. PubMed ID: 39128102
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Glucose polymer as a cause of protracted diarrhea in infants with unsuspected congenital sucrase-isomaltase deficiency.
    Newton T; Murphy MS; Booth IW
    J Pediatr; 1996 Jun; 128(6):753-6. PubMed ID: 8648532
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Four mutations in the SI gene are responsible for the majority of clinical symptoms of CSID.
    Uhrich S; Wu Z; Huang JY; Scott CR
    J Pediatr Gastroenterol Nutr; 2012 Nov; 55 Suppl 2():S34-5. PubMed ID: 23103650
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.