Published in J Pediatr Gastroenterol Nutr on April 01, 2010
The epigenetic effects of butyrate: potential therapeutic implications for clinical practice. Clin Epigenetics (2012) 1.26
DGAT1 mutation is linked to a congenital diarrheal disorder. J Clin Invest (2012) 1.07
Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea. Hum Mol Genet (2015) 0.99
Congenital proprotein convertase 1/3 deficiency causes malabsorptive diarrhea and other endocrinopathies in a pediatric cohort. Gastroenterology (2013) 0.99
Syndromic diarrhea/Tricho-hepato-enteric syndrome. Orphanet J Rare Dis (2013) 0.98
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Congenital secretory diarrhoea caused by activating germline mutations in GUCY2C. Gut (2015) 0.96
Congenital diarrhoeal disorders: advances in this evolving web of inherited enteropathies. Nat Rev Gastroenterol Hepatol (2015) 0.83
Congenital protein losing enteropathy: an inborn error of lipid metabolism due to DGAT1 mutations. Eur J Hum Genet (2016) 0.83
Genotype-dependency of butyrate efficacy in children with congenital chloride diarrhea. Orphanet J Rare Dis (2013) 0.82
Extensive molecular analysis suggested the strong genetic heterogeneity of idiopathic chronic pancreatitis. Mol Med (2016) 0.76
A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge. Pediatr Rep (2014) 0.75
Microvillus inclusion disease associated with necrotizing enterocolitis in a premature infant. AJP Rep (2014) 0.75
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Formula selection for management of children with cow's milk allergy influences the rate of acquisition of tolerance: a prospective multicenter study. J Pediatr (2013) 2.08
Efficacy of a new hypotonic oral rehydration solution containing zinc and prebiotics in the treatment of childhood acute diarrhea: a randomized controlled trial. J Pediatr (2010) 2.03
Effect of Lactobacillus GG on tolerance acquisition in infants with cow's milk allergy: a randomized trial. J Allergy Clin Immunol (2011) 1.97
Genetic modifiers of liver disease in cystic fibrosis. JAMA (2009) 1.88
Therapy with gastric acidity inhibitors increases the risk of acute gastroenteritis and community-acquired pneumonia in children. Pediatrics (2006) 1.51
Increased BDNF promoter methylation in the Wernicke area of suicide subjects. Arch Gen Psychiatry (2010) 1.49
Adherence to recommendations for primary prevention of atopic disease in neonatology clinical practice. Pediatr Allergy Immunol (2010) 1.39
Neurotrophin and neurotrophin receptor protein expression in the human lung. Am J Respir Cell Mol Biol (2003) 1.38
Genotype-phenotype correlation in cystic fibrosis: the role of modifier genes. Am J Med Genet (2002) 1.28
Surgical repair of post-traumatic lung hernia using a video-assisted open technique. Interact Cardiovasc Thorac Surg (2008) 1.25
Combined use of noninvasive tests is useful in the initial diagnostic approach to a child with suspected inflammatory bowel disease. J Pediatr Gastroenterol Nutr (2006) 1.20
Novel synthetic, salt-resistant analogs of human beta-defensins 1 and 3 endowed with enhanced antimicrobial activity. Antimicrob Agents Chemother (2010) 1.14
Intracranial pressure in unresponsive chronic migraine. J Neurol (2014) 1.14
Early stage non-small-cell lung cancer: surgical implications of the new adenocarcinoma classification. J Thorac Oncol (2013) 1.10
The efficacy and safety of telaprevir - a new protease inhibitor against hepatitis C virus. Expert Opin Investig Drugs (2010) 1.10
Pediatric portal vein thrombosis: more on thrombophilic risk factors. J Pediatr Gastroenterol Nutr (2013) 1.10
Molecular genotyping of the Italian cohort of patients with hemophilia B. Haematologica (2005) 1.08
Malignant solitary fibrous tumors of the pleura: retrospective review of a multicenter series. J Thorac Oncol (2012) 1.07
Neonatal onset intestinal failure: an Italian Multicenter Study. J Pediatr (2008) 1.02
Butyrate as an effective treatment of congenital chloride diarrhea. Gastroenterology (2004) 0.98
Large cell neuroendocrine carcinoma of the lung: a retrospective analysis of 144 surgical cases. Lung Cancer (2006) 0.96
Congenital diarrheal disorders: an updated diagnostic approach. Int J Mol Sci (2012) 0.96
Limbal stem cell deficiency and ocular phenotype in ectrodactyly-ectodermal dysplasia-clefting syndrome caused by p63 mutations. Ophthalmology (2011) 0.96
A novel de novo missense mutation in TP63 underlying germline mosaicism in AEC syndrome: implications for recurrence risk and prenatal diagnosis. Am J Med Genet A (2012) 0.95
A rare case of primary pulmonary epithelioid angiosarcoma detected by (18)F-FDG PET/CT. Clin Nucl Med (2014) 0.95
Ledipasvir : a novel synthetic antiviral for the treatment of HCV infection. Expert Opin Investig Drugs (2014) 0.95
Multicenter comparison of 18F-FDG and 68Ga-DOTA-peptide PET/CT for pulmonary carcinoid. Clin Nucl Med (2015) 0.94
Recent progress in congenital diarrheal disorders. Curr Gastroenterol Rep (2011) 0.93
Early and late outcome after surgical treatment of acquired non-malignant tracheo-oesophageal fistulae. Eur J Cardiothorac Surg (2013) 0.93
Extensive molecular analysis of patients bearing CFTR-related disorders. J Mol Diagn (2011) 0.91
Chromatin and DNA methylation dynamics of Helicobacter pylori-induced COX-2 activation. Int J Med Microbiol (2010) 0.91
The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype. Haematologica (2008) 0.91
Molecular diagnosis of cystic fibrosis: comparison of four analytical procedures. Clin Chem Lab Med (2003) 0.89
Distribution of human beta-defensin polymorphisms in various control and cystic fibrosis populations. Genomics (2005) 0.89
The Potential Therapeutic Efficacy of Lactobacillus GG in Children with Food Allergies. Pharmaceuticals (Basel) (2012) 0.89
Identification of EGFR mutations in lung sarcomatoid carcinoma. Int J Cancer (2011) 0.88
The Italian External Quality Control Programme for cystic fibrosis molecular diagnosis: 4 years of activity. Clin Chem Lab Med (2007) 0.88
Recurrent pregnancy loss and thrombophilia. Clin Lab (2007) 0.88
MK-5172 : a second-generation protease inhibitor for the treatment of hepatitis C virus infection. Expert Opin Investig Drugs (2014) 0.88
Gene mutation in microRNA target sites of CFTR gene: a novel pathogenetic mechanism in cystic fibrosis? PLoS One (2013) 0.87
Three novel CFTR polymorphic repeats improve segregation analysis for cystic fibrosis. Clin Chem (2009) 0.87
Enhanced frequency of CFTR gene variants in couples who are candidates for assisted reproductive technology treatment. Clin Chem Lab Med (2011) 0.87
High prevalence of bilateral transverse sinus stenosis-associated IIHWOP in unresponsive chronic headache sufferers: pathogenetic implications in primary headache progression. Cephalalgia (2011) 0.87
Molecular diagnostics: between chips and customized medicine. Clin Chem Lab Med (2010) 0.86
A mannose-binding lectin-defective haplotype is a risk factor for gastric cancer. Clin Chem (2006) 0.86
TrkB gene expression and DNA methylation state in Wernicke area does not associate with suicidal behavior. J Affect Disord (2011) 0.86
Gastric acidity inhibitors and the risk of intestinal infections. Curr Opin Gastroenterol (2010) 0.86
Surgical treatment of stage III thymic tumors: a multi-institutional review from four Italian centers. Eur J Cardiothorac Surg (2010) 0.86
ABT-450: a novel protease inhibitor for the treatment of hepatitis C virus infection. Curr Med Chem (2014) 0.85
Functional and structural characterization of novel mutations and genotype-phenotype correlation in 51 phenylalanine hydroxylase deficient families from Southern Italy. FEBS J (2009) 0.85
Effects of disease activity on anti-Saccharomyces cerevisiae antibodies: implications for diagnosis and follow-up of children with Crohn's disease. Inflamm Bowel Dis (2004) 0.85
Safety and effectiveness of a new fibrin pleural air leak sealant: a multicenter, controlled, prospective, parallel-group, randomized clinical trial. Ann Thorac Surg (2011) 0.85
Pre-analytical stability of the plasma proteomes based on the storage temperature. Proteome Sci (2013) 0.84
Neurotrophin system expression in human pulmonary carcinoid tumors. Growth Factors (2005) 0.84
Quality assessment in cytogenetic and molecular genetic testing: the experience of the Italian Project on Standardisation and Quality Assurance. Clin Chem Lab Med (2004) 0.83
Crenotherapy modulates the expression of proinflammatory cytokines and immunoregulatory peptides in nasal secretions of children with chronic rhinosinusitis. Am J Rhinol Allergy (2012) 0.83
Molecular analysis of cluster headache. Clin J Pain (2015) 0.83
Nitric oxide production in rectal dialysate is a marker of disease activity and location in children with inflammatory bowel disease. Am J Gastroenterol (2002) 0.83
Genotype-dependency of butyrate efficacy in children with congenital chloride diarrhea. Orphanet J Rare Dis (2013) 0.82
The nutritional modulation of the evolving intestine. J Clin Gastroenterol (2008) 0.82
Haplogroup T is an obesity risk factor: mitochondrial DNA haplotyping in a morbid obese population from southern Italy. Biomed Res Int (2013) 0.81
Phenotypic expression of genotype-phenotype correlation in cystic fibrosis patients carrying the 852del22 mutation. Am J Med Genet A (2005) 0.80
Diarrhea in neonatal intensive care unit. World J Gastroenterol (2010) 0.80
An update on laboratory diagnosis of liver inherited diseases. Biomed Res Int (2013) 0.80
Long-term disease-free survival of a patient with synchronous bilateral lung adenocarcinoma displaying different EGFR and C-MYC molecular characteristics. Chest (2011) 0.80
A polymorphism in the 5' UTR of the DEFB1 gene is associated with the lung phenotype in F508del homozygous Italian cystic fibrosis patients. Clin Chem Lab Med (2010) 0.80
Efficacy and Safety of Sofosbuvir in the Treatment of Chronic Hepatitis C: The Dawn of a New Era. Rev Recent Clin Trials (2014) 0.79
Prothrombotic gene variants as risk factors of acute myocardial infarction in young women. J Transl Med (2012) 0.79
S100 A8/A9 protein as a marker for early diagnosis of necrotising enterocolitis in neonates. Arch Dis Child (2012) 0.79
Molecular and functional analysis of the large 5' promoter region of CFTR gene revealed pathogenic mutations in CF and CFTR-related disorders. J Mol Diagn (2013) 0.79
The effects of dietary counseling on children with food allergy: a prospective, multicenter intervention study. J Acad Nutr Diet (2014) 0.79
Catechol-O-methyltransferase (COMT) gene polymorphisms as risk factor in temporomandibular disorders patients from Southern Italy. Clin J Pain (2014) 0.78
Activity of mannose-binding lectin in centenarians. Aging Cell (2012) 0.78
Different outcome of six homozygotes for prothrombin A20210A gene variant. J Transl Med (2008) 0.78
Five human phenylalanine hydroxylase proteins identified in mild hyperphenylalaninemia patients are disease-causing variants. Biochim Biophys Acta (2008) 0.78
Fetuin-A serum levels are not correlated to kidney function in long-lived subjects. Clin Biochem (2012) 0.78
A cluster headache family with possible autosomal recessive inheritance. Neurology (2003) 0.78
Prenatal diagnosis of inherited diseases: 20 years' experience of an Italian Regional Reference Centre. Clin Chem Lab Med (2013) 0.77
Prenatal diagnosis of cystic fibrosis: an experience of 181 cases. Clin Chem Lab Med (2013) 0.77
Cystic fibrosis presenting as metabolic alkalosis in a boy with the rare D579G mutation. J Cyst Fibros (2004) 0.77