Published in Arch Fr Pediatr on January 01, 1969
Clinical problems in hepatitis in childhood King's College Hospital experience 1970-73. Postgrad Med J (1974) 0.75
Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases. J Pediatr (1987) 3.50
Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur. J Pediatr (1975) 3.17
Occurrence of myeloproliferative disorder in patients with Noonan syndrome. J Pediatr (1997) 3.14
Idiopathic disseminated bacillus Calmette-Guérin infection: a French national retrospective study. Pediatrics (1996) 2.14
Autoimmune hepatitis with initial presentation as acute hepatic failure in young children. J Pediatr (1990) 1.61
Seroimmunologic classification of chronic hepatitis in 57 children. Hepatology (1983) 1.48
Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis. Blood (2001) 1.48
Erythroblastic and/or megakaryoblastic leukemia in Down syndrome: treatment with low-dose arabinosyl cytosine. J Pediatr Hematol Oncol (1996) 1.42
Incidence of cirrhosis in children with chronic hepatitis. J Pediatr (1990) 1.41
[Analgesics in pediatrics. Drugs for pain relief in children]. Presse Med (1997) 1.41
Portal obstruction in children. I. Clinical investigation and hemorrhage risk. J Pediatr (1983) 1.40
Alpha1-antitrypsin deficiency and liver disease in children: phenotypes, manifestations, and prognosis. Pediatrics (1976) 1.27
Portal obstruction in children. II. Results of surgical portosystemic shunts. J Pediatr (1983) 1.26
Congenital hepatic fibrosis in children. J Pediatr (1981) 1.24
Long-term outcome of idiopathic pulmonary hemosiderosis in children. Medicine (Baltimore) (2000) 1.20
Early assessment of evolution of liver disease associated with alpha 1-antitrypsin deficiency in childhood. J Pediatr (1983) 1.20
Liver disease associated with anti-liver-kidney microsome antibody in children. J Pediatr (1986) 1.19
Portal diversion for portal hypertension in children. The first ninety patients. Ann Surg (1980) 1.18
Collagen type III glomerulopathy: a new type of hereditary nephropathy. Pediatr Nephrol (1993) 1.15
Autoimmune hepatitis associated with anti-actin antibodies in children and adolescents. J Pediatr Gastroenterol Nutr (1993) 1.15
Hepatic porto-enterostomy or cholecystostomy in the treatment of extrahepatic biliary atresia. A study of 49 cases. J Pediatr (1976) 1.13
Bacterial cholangitis after surgery for biliary atresia. J Pediatr (1987) 1.10
Liver transplantation for ornithine transcarbamylase deficiency in a girl. J Pediatr (1989) 1.10
Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome). J Pediatr (1990) 1.08
Obstructive jaundice in children with histiocytosis X. Gastroenterology (1981) 1.07
Histological liver evaluation 5 years after surgery for extrahepatic biliary atresia: a study of 20 cases. J Pediatr Surg (1984) 1.07
Hereditary fructose intolerance in childhood. Diagnosis, management, and course in 55 patients. Am J Dis Child (1978) 1.07
Paediatric Castleman disease: report of seven cases and review of the literature. Eur J Pediatr (1999) 1.06
Long-term prognosis for infants with intrahepatic cholestasis and patent extrahepatic biliary tract. Arch Dis Child (1981) 1.05
Severe viral hepatitis type B in infancy;. Lancet (1975) 1.04
Initial assessment of the beneficial effect of partial splenectomy in hereditary spherocytosis. Blood (1993) 0.99
Mastoiditis, meningitis and venous sinus thrombosis caused by Fusobacterium necrophorum. Eur J Pediatr (1994) 0.98
Long-term outcome after surgery for biliary atresia. Study of 40 patients surviving for more than 10 years. Gastroenterology (1990) 0.98
Glomerular mesangiolipidosis in Alagille syndrome (arteriohepatic dysplasia). Pediatr Nephrol (1987) 0.98
Sequences involved in initiation of simian virus 40 late transcription in the absence of T antigen. Mol Cell Biol (1986) 0.97
Severe giant cell hepatitis with autoimmune hemolytic anemia in early childhood. J Pediatr (1981) 0.97
Pharmacokinetics and safety of a new solution of vitamin K1(20) in children with cholestasis. J Pediatr Gastroenterol Nutr (1992) 0.96
Chronic hepatitis in children. Acta Paediatr Scand (1973) 0.96
Berger's disease in children. Natural history and outcome. Medicine (Baltimore) (1985) 0.95
Normal serum gamma-glutamyl-transpeptidase activity identifies groups of infants with idiopathic cholestasis with poor prognosis. J Pediatr (1987) 0.94
Late cholangitis after successful surgical repair of biliary atresia. Am J Dis Child (1991) 0.94
Budd-Chiari syndrome in children: report of 22 cases. J Pediatr (1988) 0.92
Clinical aspects of neonatal hepatitis. Am J Dis Child (1972) 0.92
Hepatitis B in children. I. Analysis of 80 cases of acute and chronic hepatitis B. J Pediatr (1978) 0.92
Diagnostic value of serum gamma-glutamyl transpeptidase activity in liver diseases in children. J Pediatr Gastroenterol Nutr (1991) 0.92
Conversion through homologous recombination of the gene encoding Simian virus 40 115,000-molecular-weight super T antigen to a gene encoding a normal-size large T antigen variant. Mol Cell Biol (1984) 0.91
Effectiveness of partial splenectomy in hereditary spherocytosis. Curr Opin Hematol (1997) 0.90
[Congenital malaria. A case observed in twins born to an asymptomatic mother]. Presse Med (1994) 0.90
Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24. Blood (2000) 0.90
[Pre- and postoperative hepatic biopsy data in prolonged cholestasis in infants. Study of 128 cases]. Arch Fr Pediatr (1969) 0.90
Induction of apoptosis by transiently transfected metabolically stable wt p53 in transformed cell lines. Cell Death Differ (1994) 0.89
Long-term neuropsychological outcome in children undergoing portal-systemic shunts for portal vein obstruction without liver disease. J Pediatr Gastroenterol Nutr (1987) 0.89
Nervous and ocular disorders in children with cholestasis and vitamin A and E deficiencies. Hepatology (1983) 0.88
Synthesis and in vitro cytotoxic evaluation of N-substituted benzo[5,6]cycloheptal[b]indoles. Chem Pharm Bull (Tokyo) (2000) 0.86
A genetic syndrome associating dehydrated hereditary stomatocytosis, pseudohyperkalaemia and perinatal oedema. Br J Haematol (1998) 0.86
Cholestasis in the first three months of life. Prog Liver Dis (1979) 0.86
Diamond-blackfan anemia and growth status: the French registry. J Pediatr (2005) 0.86
Sclerosing cholangitis with neonatal onset. J Pediatr (1987) 0.85
Is there still a place for the Kasai procedure in the treatment of extrahepatic biliary atresia? J Pediatr Gastroenterol Nutr (1989) 0.85
Refractory anaemia and mitochondrial cytopathy in childhood. Br J Haematol (1994) 0.85
An ultrasound study of portal hypertension in children. Ann Radiol (Paris) (1981) 0.85
Management of paucity of interlobular bile ducts. J Hepatol (1985) 0.85
Renal granulomatous sarcoidosis in childhood: a report of 11 cases and a review of the literature. Eur J Pediatr (1999) 0.85
[Streptococcus group B tardive meningitis revealing chronic septic granulomatosis]. Ann Pediatr (Paris) (1989) 0.84
Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha-interferon therapy. Br J Haematol (2000) 0.84
Characterization of SV40 enhancer motifs involved in positive and negative regulation of the constitutive late promoter activity; effect of T-antigen. Virology (1991) 0.84
Intrahepatic bile duct damage in children with Kawasaki disease. J Pediatr (1992) 0.83
[Wiskott-Aldrich syndrome with prolonged survival (9 years). Fatal evolution caused by thymosarcoma]. Arch Fr Pediatr (1966) 0.83
Portal hypertension in children. Clin Gastroenterol (1985) 0.83
Detection of anti-endoplasmic reticulum antibody-positive autoimmune hepatitis in children, using an ELISA technique. J Pediatr Gastroenterol Nutr (1989) 0.83
Severe familial intrahepatic cholestasis. Arch Dis Child (1973) 0.83
Neonatal hemolytic anemia due to inherited harderoporphyria: clinical characteristics and molecular basis. Blood (1998) 0.83
Des-gamma-carboxyprothrombin and hepatoblastoma. J Clin Pathol (1988) 0.83
Experience with choledocal cyst. J Pediatr Surg (1975) 0.83
[How are personal child health records completed? A multicentric evaluation study]. Arch Pediatr (2003) 0.82
[Surgical attempts in atresia of the intrahepatic bile ducts with permeable extrahepatic bile duct. Study of 14 cases in children]. Arch Fr Pediatr (1969) 0.82
[Hypergammaglobulinemia D and familial urticaria in children]. Ann Dermatol Venereol (1996) 0.82
Necrotising leukoencephalopathy complicating treatment of childhood leukaemia. J Neurol Neurosurg Psychiatry (1984) 0.81
[A new bone syndrome with skin anomalies and neurologic disorders]. Arch Fr Pediatr (1968) 0.81
Biliary atresia and reovirus type 3 infection. N Engl J Med (1984) 0.81
[Association of left diaphragmatic hernia, lung agenesia and esophageal atresia (author's transl)]. Chir Pediatr (1979) 0.80
[Utilization of epsilon-amino-caproic acid in hemostasis in stomatology in hemophiliacs]. Rev Stomatol Chir Maxillofac (1965) 0.80
[Fibromatosis in children: regression with prolonged chemotherapy. Apropos of 2 cases]. Chir Pediatr (1988) 0.80
[Portal hypertension in children. Hemorrhagic risk and measures for prevention (author's transl)]. Chir Pediatr (1982) 0.80
[Angioma in infants: favorable effect of intravenous hydrocortisone]. Arch Fr Pediatr (1971) 0.80
[Serum DNA of hepatitis B virus in children with chronic infection]. An Esp Pediatr (1986) 0.80
[Portal obstructions in children]. Gastroenterol Clin Biol (1984) 0.80
Long-term therapy with 1alpha-hydroxyvitamin D3 in children with 'pseudo-deficiency' rickets. Clin Endocrinol (Oxf) (1977) 0.79
Severe hyporegenerative viral hepatitis in children. Proc R Soc Med (1977) 0.79
Simian virus 40 T antigen activates the late promoter by modulating the activity of negative regulatory elements. J Virol (1992) 0.79