Published in Int Surg on January 27, 1998
The relationship of Mirizzi syndrome and cholecystoenteric fistula: validation of a modified classification. World J Surg (2008) 3.09
Cholecystoenteric fistula (CF) is not a contraindication for laparoscopic surgery. Surg Endosc (2001) 1.87
Laparoscopic management of gallstone ileus. JSLS (2001) 1.33
Pneumobilia, chronic diarrhea, vitamin K malabsorption: a pathognomonic triad for cholecystocolonic fistulas. World J Gastroenterol (2009) 1.21
Internal biliary fistula due to cholelithiasis: a single-centre experience. World J Gastroenterol (2007) 0.94
Enterolithiasis. World J Gastroenterol (2014) 0.94
Management of gall bladder perforation evaluation on ultrasonography: report of six rare cases with review of literature. J Med Life (2011) 0.85
Double Incomplete Internal Biliary Fistula: Coexisting Cholecystogastric and Cholecystoduodenal Fistula. Case Rep Surg (2016) 0.79
Gallbladder-duodenal fistula presenting with liver abscess and upper gastrointestinal bleeding. HPB (Oxford) (2006) 0.78
Glucagon-like peptide-1 inhibits gastric emptying via vagal afferent-mediated central mechanisms. Am J Physiol (1997) 1.67
Bile duct varices or "pseudo-cholangiocarcinoma sign" in portal hypertension due to cavernous transformation of the portal vein. Am J Gastroenterol (1992) 1.30
High dose intravenous glucocorticoid in the treatment of childhood acquired aplastic anaemia. Scand J Haematol (1984) 1.25
A case of Pearson syndrome associated with multiple renal cysts. Pediatr Nephrol (1996) 1.10
Intestinal Behçet's disease: surgical experience in seven cases. Hepatogastroenterology (1991) 1.04
Novel splice, missense, and nonsense mutations in the fumarylacetoacetase gene causing tyrosinemia type 1. Am J Hum Genet (1994) 1.02
Mutation analysis in Turkish phenylketonuria patients. J Med Genet (1993) 1.02
Two missense mutations causing tyrosinemia type 1 with presence and absence of immunoreactive fumarylacetoacetase. Hum Genet (1994) 0.97
Anaesthetic management in maple syrup urine disease. Anaesthesia (1996) 0.96
Neurological crisis mimicking acute pancreatitis in tyrosinemia type I. Turk J Pediatr (2000) 0.94
Sodium chloride deficiency in cystic fibrosis patients. Eur J Pediatr (1994) 0.89
Endothelin-1-induced PMN infiltration and mucosal dysfunction in the rat small intestine. Am J Physiol Gastrointest Liver Physiol (2000) 0.87
Identification of mutations and evaluation of cardiomyopathy in Turkish patients with primary carnitine deficiency. JIMD Rep (2011) 0.87
Glucagon-like peptide (GLP-1) is involved in the central modulation of fecal output in rats. Am J Physiol Gastrointest Liver Physiol (2000) 0.86
Newborn PKU screening in Turkey: at present and organization for future. Turk J Pediatr (2001) 0.85
The major presenting symptom in a biotinidase-deficient patient: laryngeal stridor. J Inherit Metab Dis (1992) 0.84
Study of 12 mutations in Turkish cystic fibrosis patients. Hum Hered (1995) 0.84
Anaemia and thrombocytopenia due to haemophagocytosis in a 7-month-old boy with galactosialidosis. J Inherit Metab Dis (1998) 0.84
Recurrent meningitis associated with congenital paravertebral dermal sinus tract. Turk J Pediatr (1998) 0.84
Role of neutrophils in indomethacin-induced gastric mucosal lesions in rats. Inflamm Res (1995) 0.83
Isovaleric acidemia. Clinical presentation of 6 cases. Turk J Pediatr (1998) 0.83
Factors affecting postoperative mortality in abdominal trauma. Int Surg (1992) 0.82
Nutritional assessment of children on haemodialysis: value of IGF-I, TNF-alpha and IL-1beta. Nephrol Dial Transplant (1998) 0.82
Indicators of nutritional status in Turkish preschool children: results of Turkish Demographic and Health Survey 1993. J Trop Pediatr (1996) 0.82
The effect of thermal injury on gastric emptying in rats. Burns (1995) 0.82
Xanthoma disseminatum: a child with respiratory system involvement and bronchiectasis. Pediatr Pulmonol (2005) 0.81
Inhibitory effects of gastrin releasing peptide on gastric emptying in rats. Regul Pept (1996) 0.81
Capsaicin-sensitive vagal fibres and 5-HT3-, gastrin releasing peptide- and cholecystokinin A-receptors are involved in distension-induced inhibition of gastric emptying in the rat. Regul Pept (1999) 0.81
Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE). Hum Genet (2000) 0.81
Maple syrup urine disease: mutation analysis in Turkish patients. J Inherit Metab Dis (2002) 0.81
Audiologic findings in children with biotinidase deficiency in Turkey. Int J Pediatr Otorhinolaryngol (2006) 0.79
Rehydration of moderately dehydrated children with transient glucose intolerance using rice oral rehydration solution. Acta Paediatr (1999) 0.79
Factor V Leiden mutation in Turkish patients with homozygous cystathionine beta-synthase deficiency. J Inherit Metab Dis (2001) 0.79
Type I glycogenosis with renal tubular dysfunction (presentation of two cases). Turk J Pediatr (1994) 0.79
Fifteen years' experience with 212 hyperammonaemic cases at a metabolic unit. J Inherit Metab Dis (1991) 0.78
Evaluation of a fetus at risk for dihydropteridine reductase deficiency by direct mutation analysis using denaturing gradient gel electrophoresis. Prenat Diagn (2001) 0.78
Citrullinemia. Clinical experience with 23 cases. Turk J Pediatr (1998) 0.77
Molecular genetic analyses of cystinuria type 1 in 24 Turkish patients. Turk J Pediatr (2001) 0.77
The effect of nitric oxide synthase blockade and indomethacin on gastric emptying and gastric contractility. Pharmacology (1997) 0.77
Inflammatory response to cold injury in remote organs is reduced by corticotropin-releasing factor. Regul Pept (2001) 0.77
Portomesenteric gas due to intestinal obstruction: a case report. Acta Chir Belg (2002) 0.77
Effect of hydrogen peroxide on permeability of the main pancreatic duct and morphology of the pancreas. Am J Surg (1998) 0.77
Mutation spectrum of fumarylacetoacetase gene and clinical aspects of tyrosinemia type I disease. JIMD Rep (2011) 0.77
Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients. J Inherit Metab Dis (1994) 0.76
Low serum carnitine concentrations in healthy children with iron deficiency anemia. Pediatr Hematol Oncol (2001) 0.76
Mutation analysis in Turkish patients with hereditary fructose intolerance. J Inherit Metab Dis (2001) 0.76
I-cell disease. A case report and review of the literature. Turk J Pediatr (1994) 0.76
Biotinidase deficiency with neurological features resembling multiple sclerosis. J Inherit Metab Dis (1997) 0.75
Intussusception due to ectopic pancreatic tissue in a nine-month-old child. Turk J Pediatr (1993) 0.75
Hypophosphatemic vitamin-D resistant rickets associated with epidermal nevus syndrome. A case report. Turk J Pediatr (1997) 0.75
The effect of aqueous garlic extract on the levels of arachidonic acid metabolites (leukotriene C4 and prostaglandin E2) in rat forebrain after ischemia-reperfusion injury. Prostaglandins Leukot Essent Fatty Acids (1996) 0.75
Valproate-induced lethal hyperammonaemic coma in a carrier of ornithine carbamoyltransferase deficiency. J Inherit Metab Dis (1991) 0.75
Effects of alpha-tocopherol on reperfusion injury in the canine small bowel autotransplantation model. Transplant Proc (1998) 0.75
Analysis of delta F508 mutation in cystic fibrosis pathology specimens. Pediatr Pathol (1994) 0.75
Hypophosphatasia in a newborn infant. Turk J Pediatr (1995) 0.75
Classical phenylketonuria associated with Goldenhar's syndrome. A case report. Turk J Pediatr (1994) 0.75
Aase-Smith syndrome: report of a new case with unusual features. Turk J Pediatr (1994) 0.75
Molecular basis of mild hyperphenylalaninaemia in Turkey. J Inherit Metab Dis (2000) 0.75
Leprechaunism in two Turkish patients. Turk J Pediatr (1997) 0.75
Allele frequencies of Mp6D-9 and GATT markers in 32 Turkish cystic fibrosis families. Clin Genet (1994) 0.75
3-Hydroxy-3-methylglutaryl coenzyme A lyase deficiency. J Inherit Metab Dis (1993) 0.75
Nonketotic hyperglycinemia in a newborn infant. Turk J Pediatr (1995) 0.75
Is L-carnitine protective in hypoxic cerebral edema in newborn mice? Turk J Pediatr (1994) 0.75
Hypouricemia and molybdenum-cofactor deficiency. J Pediatr (1997) 0.75
Effect of encapsulation of chloramphenicol in albumin microspheres on its in vitro transfer across the human placenta. J Microencapsul (1995) 0.75
Cerebrospinal fluid amino acid levels in newborn infants with intracranial hemorrhage. Acta Paediatr Jpn (1995) 0.75
Phenylketonuria and cystic fibrosis in the same patient. Pediatr Int (2000) 0.75
The effect of oral L-carnitine supplementation on the lipid profiles of hyperlipidaemic children. Acta Paediatr (2005) 0.75
Alpha-mannosidosis: the first Turkish case. Acta Paediatr Jpn (1995) 0.75
Cardiovascular effects of centrally active cholinomimetics in conscious and anesthetized rats: the role of amygdala. Brain Res Bull (1995) 0.75
Cerebrospinal fluid glutamine level in the differential diagnosis of a "bloody tap" in newborn infants. Brain Dev (1992) 0.75
Combined saccular aneurysm and proximal interruption of the inferior vena cava associated with Budd-Chiari syndrome. AJR Am J Roentgenol (1992) 0.75
Prenatal diagnosis of cystic fibrosis in a Turkish family. Turk J Pediatr (1993) 0.75
Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patients. Turk J Pediatr (1993) 0.75
Sodium nitroprusside treatment in erythromelalgia. Eur J Pediatr (1984) 0.75
Beta-ketothiolase deficiency. A case report. Turk J Pediatr (1992) 0.75
Blood uric acid as a pointer to the diagnosis of molybdenum cofactor deficiency. Acta Paediatr (1998) 0.75
Decrease in the placental transfer of chloramphenicol when administered in albumin microspheres into rats. J Microencapsul (1993) 0.75
Superior mesenteric artery syndrome. A case report. Turk J Pediatr (1996) 0.75
Genetic and neurological evaluation of untreated and late-treated patients with phenylketonuria. J Inherit Metab Dis (1994) 0.75
The effect of live measles vaccines on serum vitamin A levels in healthy children. Acta Paediatr Jpn (1998) 0.75
Neuroleptic malignant syndrome in a patient with citrullinaemia. J Inherit Metab Dis (2000) 0.75
Carnitinuria in rickets due to vitamin D deficiency. Turk J Pediatr (2001) 0.75