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 *

138 related articles for article (PubMed ID: 38459691)

  • 21. Functional variants in the sucrase-isomaltase gene associate with increased risk of irritable bowel syndrome.
    Henström M; Diekmann L; Bonfiglio F; Hadizadeh F; Kuech EM; von Köckritz-Blickwede M; Thingholm LB; Zheng T; Assadi G; Dierks C; Heine M; Philipp U; Distl O; Money ME; Belheouane M; Heinsen FA; Rafter J; Nardone G; Cuomo R; Usai-Satta P; Galeazzi F; Neri M; Walter S; Simrén M; Karling P; Ohlsson B; Schmidt PT; Lindberg G; Dlugosz A; Agreus L; Andreasson A; Mayer E; Baines JF; Engstrand L; Portincasa P; Bellini M; Stanghellini V; Barbara G; Chang L; Camilleri M; Franke A; Naim HY; D'Amato M
    Gut; 2018 Feb; 67(2):263-270. PubMed ID: 27872184
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Congenital sucrase-isomaltase deficiency: an under-diagnosed disease in Chinese children.
    Geng L; Li DY; Ou W; Yang Q; Fang T; Chen P; Yang M; Gong S
    BMC Pediatr; 2014 Jan; 14():11. PubMed ID: 24433566
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Two Novel Mutations in the
    Zhou J; Zhao Y; Qian X; Cheng Y; Cai H; Chen M; Zhou S
    Front Pediatr; 2021; 9():731716. PubMed ID: 34926337
    [No Abstract]   [Full Text] [Related]  

  • 25. Sucrase-Isomaltase Deficiency as a Potential Masquerader in Irritable Bowel Syndrome.
    Kim SB; Calmet FH; Garrido J; Garcia-Buitrago MT; Moshiree B
    Dig Dis Sci; 2020 Feb; 65(2):534-540. PubMed ID: 31493040
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Genetics of sucrose metabolism disorders in different population groups].
    Kozlov AI; Malyarchuk BA
    Vopr Pitan; 2024; 93(2):52-62. PubMed ID: 38809799
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hypomorphic SI genetic variants are associated with childhood chronic loose stools.
    Chumpitazi BP; Lewis J; Cooper D; D'Amato M; Lim J; Gupta S; Miranda A; Terry N; Mehta D; Scheimann A; O'Gorman M; Tipnis N; Davies Y; Friedlander J; Smith H; Punati J; Khlevner J; Setty M; Di Lorenzo C
    PLoS One; 2020; 15(5):e0231891. PubMed ID: 32433684
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Sucrase-Isomaltase Deficiency Causing Persistent Bloating and Diarrhea in an Adult Female.
    Chiruvella V; Cheema A; Arshad HMS; Chan JT; Yap JEL
    Cureus; 2021 Apr; 13(4):e14349. PubMed ID: 33972906
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The sucrose challenge symptoms test optimized for diagnosis of congenital sucrase isomaltase deficiency.
    Street K; Tao W; Cash B; Leung J; Hayes C; Cooper D; Peterson W
    PLoS One; 2024; 19(9):e0310705. PubMed ID: 39292728
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Congenital and putatively acquired forms of sucrase-isomaltase deficiency in infancy: effects of sacrosidase therapy.
    Lücke T; Keiser M; Illsinger S; Lentze MJ; Naim HY; Das AM
    J Pediatr Gastroenterol Nutr; 2009 Oct; 49(4):485-7. PubMed ID: 19680155
    [No Abstract]   [Full Text] [Related]  

  • 32. Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
    Belmont JW; Reid B; Taylor W; Baker SS; Moore WH; Morriss MC; Podrebarac SM; Glass N; Schwartz ID
    BMC Pediatr; 2002 Apr; 2():4. PubMed ID: 12014995
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum.
    Ritz V; Alfalah M; Zimmer KP; Schmitz J; Jacob R; Naim HY
    Gastroenterology; 2003 Dec; 125(6):1678-85. PubMed ID: 14724820
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Onset of sucrase-isomaltase deficiency in late adulthood.
    Muldoon C; Maguire P; Gleeson F
    Am J Gastroenterol; 1999 Aug; 94(8):2298-9. PubMed ID: 10445568
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Enzyme-substitution therapy with the yeast Saccharomyces cerevisiae in congenital sucrase-isomaltase deficiency.
    Harms HK; Bertele-Harms RM; Bruer-Kleis D
    N Engl J Med; 1987 May; 316(21):1306-9. PubMed ID: 3553946
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Altered folding, turnover, and polarized sorting act in concert to define a novel pathomechanism of congenital sucrase-isomaltase deficiency.
    Keiser M; Alfalah M; Pröpsting MJ; Castelletti D; Naim HY
    J Biol Chem; 2006 May; 281(20):14393-9. PubMed ID: 16543230
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Sucrase-isomaltase Gene Variants in Patients With Abnormal Sucrase Activity and Functional Gastrointestinal Disorders.
    Deb C; Campion S; Derrick V; Ruiz V; Abomoelak B; Avdella A; Zou B; Horvath K; Mehta DI
    J Pediatr Gastroenterol Nutr; 2021 Jan; 72(1):29-35. PubMed ID: 32732636
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The glucose-regulated protein GRP94 interacts avidly in the endoplasmic reticulum with sucrase-isomaltase isoforms that are associated with congenital sucrase-isomaltase deficiency.
    Hoter A; Naim HY
    Int J Biol Macromol; 2021 Sep; 186():237-243. PubMed ID: 34242650
    [TBL] [Abstract][Full Text] [Related]  

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

    [Previous]   [Next]    [New Search]
    of 7.