Published in Oman Med J on November 01, 2012
MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. Nat Genet (2008) 2.24
Microvillous inclusion disease: how to improve the prognosis of a severe congenital enterocyte disorder. J Pediatr Gastroenterol Nutr (2011) 2.20
Microvillous inclusion disease. The importance of electron microscopy for diagnosis. Am J Surg Pathol (1991) 1.51
Microvillous inclusion disease (microvillous atrophy). Orphanet J Rare Dis (2006) 1.32
Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model. Hum Mutat (2010) 1.20
Congenital diarrheal disorders: improved understanding of gene defects is leading to advances in intestinal physiology and clinical management. J Pediatr Gastroenterol Nutr (2010) 1.16
Periodic acid-Schiff staining abnormality in microvillous atrophy: photometric and ultrastructural studies. J Pediatr Gastroenterol Nutr (2000) 0.94
Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease. J Pediatr Gastroenterol Nutr (2011) 0.93
Recent progress in congenital diarrheal disorders. Curr Gastroenterol Rep (2011) 0.93
New perspectives for children with microvillous inclusion disease: early small bowel transplantation. Transplantation (2004) 0.92
Long-term outcome of children receiving home parenteral nutrition: a 20-year single-center experience in 302 patients. J Pediatr Gastroenterol Nutr (2007) 0.91
Serious renal impairment is associated with long-term parenteral nutrition. JPEN J Parenter Enteral Nutr (1994) 0.88
Prenatal diagnosis of microvillus inclusion disease. Taiwan J Obstet Gynecol (2011) 0.85
[CD10 expression in a case of microvillous inclusion disease]. Ann Pathol (2004) 0.84
Long-term outcome, growth and digestive function in children 2 to 18 years after intestinal transplantation. Gut (2007) 0.83
Microvillous inclusion disease: an evolving condition. J Pediatr Gastroenterol Nutr (2000) 0.82
Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea. Taiwan J Obstet Gynecol (2010) 0.80
Microvillous inclusion disease: a clinicopathologic study of 17 cases from the UK. Ultrastruct Pathol (2010) 0.78
Microvillous inclusion disease diagnosed by gastric biopsy. Indian Pediatr (2012) 0.78
Prevalence of celiac disease in omani children with type 1 diabetes mellitus: a cross sectional study. Oman Med J (2013) 1.18
Idiopathic Granulomatous Mastitis: Diagnostic strategy and therapeutic implications in Omani patients. Sultan Qaboos Univ Med J (2013) 0.92
Neuroprotective effects of a variety of pomegranate juice extracts against MPTP-induced cytotoxicity and oxidative stress in human primary neurons. Oxid Med Cell Longev (2013) 0.90
Geographical Clustering of Juvenile Onset Systemic Lupus Erythematosus within the Sultanate of Oman. Oman Med J (2013) 0.81
Multiple Enteric Duplication Cysts in a Twin Fetus: Diagnosis and management. Sultan Qaboos Univ Med J (2013) 0.78
Twist of taste: gastronomic allusions in medicine. Med Humanit (2014) 0.75
Gleason’s Grading of Prostatic Adenocarcinoma: Inter-Observer Variation Among Seven Pathologists at a Tertiary Care Center in Oman Asian Pac J Cancer Prev (2016) 0.75