• A Case Study of Intractable Diarrhea Due to Neonatal Microvillous Inclusion Disease
• A CRISPR screen in intestinal epithelial cells identifies novel factors for polarity and apical transport
• A Functional Relationship Between UNC45A and MYO5B Connects Two Rare Diseases With Shared Enteropathy
• A Novel Homozygous Mutation in the MYO5B Gene Associated With Normal-Gamma-Glutamyl Transferase Progressive Familial Intrahepatic Cholestasis
• A V0-ATPase-dependent apical trafficking pathway maintains the polarity of the intestinal absorptive membrane
• Abnormal Rab11-Rab8-vesicles cluster in enterocytes of patients with microvillus inclusion disease
• Acetylated sialic acid residues and blood group antigens localise within the epithelium in microvillous atrophy indicating internal accumulation of the glycocalyx
• Advanced Microscopy for Liver and Gut Ultrastructural Pathology in Patients with MVID and PFIC Caused by MYO5B Mutations
• Altered MYO5B Function Underlies Microvillus Inclusion Disease: Opportunities for Intervention at a Cellular Level
• An Intravenous Fish Oil-Based Lipid Emulsion Successfully Treats Intractable Pruritus and Cholestasis in a Patient with Microvillous Inclusion Disease
• Apical Membrane Alterations in Non-intestinal Organs in Microvillus Inclusion Disease
• Case Report: <em>MYO5B</em> Homozygous Variant c.2090+3A&gt;T Causes Intron Retention Related to Chronic Cholestasis and Diarrhea
• CD10 expression in a case of microvillous inclusion disease
• Cell differentiation is disrupted by MYO5B loss through Wnt/Notch imbalance
• Challenges of Microvillus Inclusion Disease in the NICU
• Clinical features and MYO5B mutations of a family affected by microvillus inclusion disease
• Clinicopathologic Features of IDEDNIK (MEDNIK) Syndrome in a Term Infant: Histopathologic Features of the Gastrointestinal Tract and Report of a Novel <em>AP1S1</em> Variant
• Complications during home parenteral nutrition in children affected by congenital microvillous atrophy
• Compound Heterozygous MYO5B Mutation, a Cause of Infantile Cholestasis: A Case Report
• Concise Review: The Potential Use of Intestinal Stem Cells to Treat Patients with Intestinal Failure
• Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations
• Congenital diarrhea in a newborn infant: A case report
• Congenital Fatal Diarrhea in Newborns
• Congenital microvillous atrophy
• Congenital microvillous atrophy: report of two cases
• Congenital microvillous atrophy: specific diagnostic features
• Congenital microvillus inclusion disease in a child
• Congenital Microvillus Inclusion Disease in the Differential Diagnosis of Intractable Metabolic Acidosis
• Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ-glutamyltransferase cholestasis
• Dihydropyrimidinase deficiency and congenital microvillous atrophy: coincidence or genetic relation?
• Disrupted apical exocytosis of cargo vesicles causes enteropathy in FHL5 patients with Munc18-2 mutations
• Dynamic Formation of Microvillus Inclusions During Enterocyte Differentiation in <em>Munc18-2</em>-Deficient Intestinal Organoids
• Editing Myosin VB Gene to Create Porcine Model of Microvillus Inclusion Disease, With Microvillus-Lined Inclusions and Alterations in Sodium Transporters
• Expanding the clinical spectrum in trichohepatoenteric syndrome
• Exploiting Alternative Brush Border Trafficking Routes to Treat Microvillous Inclusion Disease
• Extraintestinal manifestations in an infant with microvillus inclusion disease: complications or features of the disease?
• Familial microvillous atrophy: a clinicopathological survey of 23 cases
• Fetal Bowel Abnormalities Suspected by Ultrasonography in Microvillus Inclusion Disease: Prevalence and Clinical Significance
• Generation of induced pluripotent stem cells (iPSCs) from a microvillus inclusion disease patient with a homozygous missense mutation in UNC45A
• Glucocorticoids and myosin5b loss of function induce heightened PKA signaling in addition to membrane traffic defects
• Hyaline fibromatosis syndrome: Clinical update and phenotype-genotype correlations
• Hypophosphatemic rickets accompanying congenital microvillous atrophy
• Immunoreactive epidermal growth factor receptors are present in gastrointestinal epithelial cells of preterm infants with necrotising enterocolitis
• Intestinal epithelial cell polarity defects in disease: lessons from microvillus inclusion disease
• Intractable diarrhea of infancy with congenital intestinal mucosa abnormalities: outcome of four cases
• Intractable diarrhoea in infancy in the 1990s: a survey in Italy
• Intravenous epidermal growth factor/urogastrone increases small-intestinal cell proliferation in congenital microvillous atrophy
• Kinetic signatures of myosin-5B, the motor involved in microvillus inclusion disease
• Late Manifestation of Massive Jejunal and Cecal Varices Post Liver and Small Bowel Transplantation in a Patient With Microvillus Inclusion Disease
• Loss of MYO5B Leads to Reductions in Na⁺ Absorption With Maintenance of CFTR-Dependent Cl^- Secretion in Enterocytes
• Loss of myosin Vb promotes apical bulk endocytosis in neonatal enterocytes
• Loss of Serum Glucocorticoid-Inducible Kinase 1 SGK1 Worsens Malabsorption and Diarrhea in Microvillus Inclusion Disease (MVID)
• Lysophosphatidic Acid Increases Maturation of Brush Borders and SGLT1 Activity in MYO5B-deficient Mice, a Model of Microvillus Inclusion Disease
• Microvillous inclusion disease
• Microvillous inclusion disease (microvillous atrophy)
• Microvillous Inclusion Disease as a Cause of Protracted Diarrhea
• Microvillous inclusion disease as a cause of severe congenital diarrhea in a newborn
• Microvillous inclusion disease as a cause of severe congenital diarrhea. Case report
• Microvillous inclusion disease with abundant vermiform, electron-lucent vesicles
• Microvillous inclusion disease: a clinicopathologic study of 17 cases from the UK
• Microvillus Inclusion Disease Caused by <em>MYO5B</em>: Different Presentation and Phenotypes Despite Same Mutation
• Microvillus Inclusion Disease Variant in an Infant with Intractable Diarrhea
• Microvillus inclusion disease with novel MYO5B pathogenic variants
• Microvillus inclusion disease with prenatal ultrasound findings and postpartum confirmed
• Microvillus inclusion disease, a diagnosis to consider when abnormal stools and neurological impairments run together due to a rare syntaxin 3 gene mutation
• Microvillus Inclusion Disease: A Rare Mutation of STX3 in Exon 9 Causing Fatal Congenital Diarrheal Disease
• Monogenic mutations in four cases of neonatal-onset watery diarrhea and a mutation review in East Asia
• MYO5B Gene Mutations: A Not Negligible Cause of Intrahepatic Cholestasis of Infancy With Normal Gamma-Glutamyl Transferase Phenotype
• MYO5B mutations cause cholestasis with normal serum gamma-glutamyl transferase activity in children without microvillous inclusion disease
• MYO5B Pathogenic Variants Found to Cause Intestinal Symptoms Without Microvillus Inclusion Disease in a Child Who Previously Underwent Liver Transplantation for PFIC-like Cholestasis
• MYO5B-associated diseases: Novel liver-related variants and genotype-phenotype correlation
• MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update
• Neonatal congenital microvillus atrophy
• New Mouse Models for Microvillus Inclusion Disease (MVID): Where Do the Inclusions Come From and Are They Cause or Consequence?
• Nonobstructive Diffuse Dilated Bowel Loops: Prenatal Diagnosis, Fetal Characteristics and Neonatal Outcomes
• Not all enteropathies are coeliac disease! Report of an infant with microvillus inclusion disease
• Novel <em>MYO5B</em> mutation in microvillous inclusion disease of Syrian ancestry
• Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects
• Periodic acid-Schiff staining abnormality in microvillous atrophy: photometric and ultrastructural studies
• Pharmacological and Parenteral Nutrition-Based Interventions in Microvillus Inclusion Disease
• Phenotypic and genetic analysis of a family affected with microvillus inclusion disease
• Racecadotril May Reduce Diarrhoea in Microvillous Inclusion Disease
• Recent advances in understanding and managing malabsorption: focus on microvillus inclusion disease
• Recruitment of Polarity Complexes and Tight Junction Proteins to the Site of Apical Bulk Endocytosis
• Recurrent episodes of necrotizing enterocolitis complicating congenital microvillous atrophy
• Risk and Clinical Significance of Idiopathic Preterm Birth in Microvillus Inclusion Disease
• SNAREs and developmental disorders
• The challenge of personalized cell biology: The example of microvillus inclusion disease
• The Endosomal Protein Endotubin Is Required for Enterocyte Differentiation
• The Endosomal Recycling Pathway-At the Crossroads of the Cell
• The Rab11 effectors Fip5 and Fip1 regulate zebrafish intestinal development
• Therapy Development for Microvillus Inclusion Disease using Patient-derived Enteroids
• Trafficking Ion Transporters to the Apical Membrane of Polarized Intestinal Enterocytes
• Two cases of microvillus inclusion disease caused by MYO5B deficiency with prenatal abnormalities
• UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking
• Unequal Effects of Myosin 5B Mutations in Liver and Intestine Determine the Clinical Presentation of Low-Gamma-Glutamyltransferase Cholestasis
• Unusual feature of neonatal hypernatremic dehydration due to microvillus inclusion disease: a case report
• Urogastrone/epidermal growth factor in treatment of congenital microvillous atrophy
• Weibel-Palade Body Localized Syntaxin-3 Modulates Von Willebrand Factor Secretion From Endothelial Cells
• Weight loss and metabolic acidosis in a neonate: Answers