BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 38105403)

  • 1. Approach to Congenital Diarrhea and Enteropathies (CODEs).
    Kijmassuwan T; Balouch F
    Indian J Pediatr; 2024 Jun; 91(6):598-605. PubMed ID: 38105403
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital Diarrhea and Enteropathies in Infants: Approach to Diagnosis.
    Mantoo MR; Malik R; Das P; Yadav R; Nakra T; Chouhan P
    Indian J Pediatr; 2021 Nov; 88(11):1135-1138. PubMed ID: 34292522
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Case Study of Intractable Diarrhea Due to Neonatal Microvillous Inclusion Disease.
    Bulut O; Ahishali B; Gulluoglu M; Arslanoglu S
    Fetal Pediatr Pathol; 2017 Aug; 36(4):340-343. PubMed ID: 28707991
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Challenges of Microvillus Inclusion Disease in the NICU.
    Badawy A; Elfadul M; Aziabi M; Ageel HI; Aqeel A
    Neoreviews; 2020 Sep; 21(9):e600-e604. PubMed ID: 32873653
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Microvillus inclusion disease, a diagnosis to consider when abnormal stools and neurological impairments run together due to a rare syntaxin 3 gene mutation.
    Julia J; Shui V; Mittal N; Heim-Hall J; Blanco CL
    J Neonatal Perinatal Med; 2019; 12(3):313-319. PubMed ID: 30909251
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Congenital diarrhoea].
    Buda P; Friedman-Gruszczyńska J; Książyk J
    Med Wieku Rozwoj; 2011; 15(4):477-86. PubMed ID: 22516705
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Microvillous inclusion disease as a cause of severe congenital diarrhea. Case report].
    Schoen K; Puchi A; González I; Torres MT; Espinosa R; González R
    Rev Chil Pediatr; 2017; 88(5):662-667. PubMed ID: 29546954
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evaluation of intestinal biopsies for pediatric enteropathy: a proposed immunohistochemical panel approach.
    Martin BA; Kerner JA; Hazard FK; Longacre TA
    Am J Surg Pathol; 2014 Oct; 38(10):1387-95. PubMed ID: 25188866
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic Enteropathies Linked to Epithelial Structural Abnormalities and Enteroendocrine Deficiency: A Systematic Review.
    Caralli M; Roman C; Coste ME; Roquelaure B; Buffat C; Bourgeois P; Badens C; Fabre A
    J Pediatr Gastroenterol Nutr; 2021 Jun; 72(6):826-832. PubMed ID: 33976085
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Microvillous atrophy: atypical presentations.
    Perry A; Bensallah H; Martinez-Vinson C; Berrebi D; Arbeille B; Salomon J; Goulet O; Marinier E; Drunat S; Samson-Bouma ME; Gérard B; Hugot JP
    J Pediatr Gastroenterol Nutr; 2014 Dec; 59(6):779-85. PubMed ID: 25111220
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microvillous inclusion disease (microvillous atrophy).
    Ruemmele FM; Schmitz J; Goulet O
    Orphanet J Rare Dis; 2006 Jun; 1():22. PubMed ID: 16800870
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form.
    Salomon J; Goulet O; Canioni D; Brousse N; Lemale J; Tounian P; Coulomb A; Marinier E; Hugot JP; Ruemmele F; Dufier JL; Roche O; Bodemer C; Colomb V; Talbotec C; Lacaille F; Campeotto F; Cerf-Bensussan N; Janecke AR; Mueller T; Koletzko S; Bonnefont JP; Lyonnet S; Munnich A; Poirier F; Smahi A
    Hum Genet; 2014 Mar; 133(3):299-310. PubMed ID: 24142340
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Microvillous Inclusion Disease as a Cause of Protracted Diarrhea.
    Phulware RH; Gahlot GPS; Malik R; Gupta SD; Das P
    Indian J Pediatr; 2019 Sep; 86(9):854-856. PubMed ID: 31049800
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital Fatal Diarrhea in Newborns.
    Lingaldinna S; Sundaram MB; Kamalarathnam CN; Bavanandam S
    Indian J Pediatr; 2017 Dec; 84(12):953-954. PubMed ID: 28842815
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Clinical features and MYO5B mutations of a family affected by microvillus inclusion disease].
    Cheng Y; Liang H; Cai NL; Guo L; Huang YG; Song YZ
    Zhongguo Dang Dai Er Ke Za Zhi; 2017 Sep; 19(9):968-974. PubMed ID: 28899465
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Severe hypernatremic dehydration and metabolic acidosis due to neonatal intestinal microvillus inclusion disease.
    Shahid S; Fraser DD; Driman DK; Bax KC
    Neonatology; 2012; 101(2):154-8. PubMed ID: 21968248
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Microvillus inclusion disease: loss of Myosin vb disrupts intracellular traffic and cell polarity.
    Thoeni CE; Vogel GF; Tancevski I; Geley S; Lechner S; Pfaller K; Hess MW; Müller T; Janecke AR; Avitzur Y; Muise A; Cutz E; Huber LA
    Traffic; 2014 Jan; 15(1):22-42. PubMed ID: 24138727
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Features of gastric and colonic mucosa in congenital enteropathies: a study in histology and immunohistochemistry.
    Treetipsatit J; Hazard FK
    Am J Surg Pathol; 2014 Dec; 38(12):1697-706. PubMed ID: 25007148
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical studies of pediatric malabsorption syndromes].
    Hosoyamada T
    Fukuoka Igaku Zasshi; 2006 Nov; 97(11):322-50. PubMed ID: 17228786
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A rare cause of congenital diarrhea in a Turkish newborn: tufting enteropathy.
    Kahvecioğlu D; Yıldız D; Kılıç A; İnce-Alkan B; Erdeve Ö; Kuloğlu Z; Atasay B; Ensari A; Yılmaz R; Arsan S
    Turk J Pediatr; 2014; 56(4):440-3. PubMed ID: 25818968
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.