The Turkish Journal of Pediatrics
Smilar Issues: 17 Record Found
Byler's disease and anesthetic consideration Abstract Similar Articles Mail to Editor Clinical and pathological aspects of ARC (arthrogryposis, renal dysfunction and cholestasis) syndrome in two siblings Abstract Similar Articles Mail to Editor Anaplastic large cell lymphoma in a child presenting with cutaneous nodules and blisters Abstract Similar Articles Mail to Editor Progressive familial intrahepatic cholestasis with normal GGT level appearing with lichenification and enlargement of hands and feet Abstract Similar Articles Mail to Editor Cholestatic hepatitis as a result of severe cortisol deficiency in early infancy: report of two cases and review of literature Abstract Similar Articles Mail to Editor Erythropoietic Protoporphyria and Early Onset of Cholestasis Abstract Similar Articles Mail to Editor Bullous Skin Lesions in a Jaundiced Infant after Phototherapy: A Case of Congenital Erythropoietic Porphyria Abstract Similar Articles Mail to Editor Cholestasis in infants with immune hydrops fetalis Abstract Similar Articles Mail to Editor Composition of Parenteral Nutrition Solution Affects the Time of Occurrence But Not the Incidence of Cholestasis in Surgical Infants Abstract Similar Articles Mail to Editor Cytomegalovirus hepatitis and ganciclovir treatment in immunocompetent children Abstract Similar Articles Mail to Editor Two cases of Kawasaki disease presented with acute febrile jaundice Abstract Similar Articles Mail to Editor ARC syndrome Abstract Similar Articles Mail to Editor Chelation therapy for secondary neonatal iron over load: Lessons learned from rhesus hemolytic disease Abstract Similar Articles Mail to Editor The effectiveness of serum amyloid A for prediction of neonatal cholestasis associated with parenteral nutrition in premature infants Abstract Similar Articles Mail to Editor Childhood sclerosing cholangitis associations in a Tunisian tertiary care hospital: a many-faceted disease Abstract Similar Articles Mail to Editor Serum alpha-fetoprotein levels in neonatal cholestasis Abstract Similar Articles Mail to Editor A novel homozygous mutation in the USP53 gene as the cause of benign recurrent intrahepatic cholestasis in children: a case report Abstract Similar Articles Mail to Editor
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