HOME

Crigler Najjar Syndrome (Bilirubin Uridinediphosphate Glucuronosylyltransferase Deficiency)

• Type I
• Treatment of Crigler-Najjar Syndrome
• Crigler-Najjar syndrome : sites francophones 
• CRIGLER
• crigler-najjar syndrome
• Lack of deafness in Crigler-Najjar syndrome type 1: a patient survey.
• Molecular analysis of patients of Sardinian descent with Crigler-Najjar syndrome type I.
• Oral calcium phosphate: a new therapy for Crigler-Najjar disease?
• Improvements in long term phototherapy for patients with Crigler-Najjar syndrome type I.
• Current therapy for Crigler-Najjar syndrome type 1: report of a world registry.
• Crigler-Najjar syndrome type II is inherited both as a dominant and as a recessive trait.
• Orthotopic liver transplantation for Crigler-Najjar type I disease in six children
• CRIGLER-NAJJAR SYNDROME, TYPE I
• Bilirubin uridinediphosphate glucuronosylyltransferase deficiency
• SINDROME DI CRIGLER-NAJJAR 
• Type II
• See Gilbert('s) Syndrome

---

HOME