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Rotor syndrome
Porphyria
Neonatal Hyperbilirubinemia
Inherited Disorders of Bilirubin Clearance N
Dubin-Johnson Syndrome with Some Unusual Features in a Chinese Family
ACG Clinical Guideline: Evaluation of Abnormal Liver Chemistries
Wilson Disease Α1-Anti Antitrypsin Deficiency Hereditary Hyperbilirubinemia
The First Turkish Family with Rotor Syndrome Diagnosed at the Molecular Level Moleküler Düzeyde Tanısı Konulmuş Olan Ilk Türk Rotor Sendromlu Aile
APPROACH to ABNORMAL LIVER TESTS Mitchell L Shiffman, MD
A Rare Case Report of Crigler Najjar Syndrome Type II
Porphyrin Metabolism and Haem Biosynthesis in Gilbert's Syndrome
Dubin-Johnson Syndrome Aziz-Un-Nisa and Zubair Ahmad
Scintigraphicaspect of Rotor's Disease with Technetium-99M-.Mebrofemn
Rotor-Syndrome.Pdf
Clinical Chemistry Trainee Council Pearls of Laboratory Medicine
Liver Function Test
' T' Refer to Tables
Hereditary Conjugated Hyperbilirubinaemia: 37 Years Later
Interpretive Guide
Top View
Intermediary Metabolism
Crigler Najjar Syndrome Type I, a Rare but Severe Cause of Unconjugated Hyperbilirubinemia in Children
Metabolske Sykdommer V02
Marketing Fragment 8.5 X 12.T65
Dubin-Johnson Syndrome with Varied Manifestations
Cholescintigraphy in the Diagnosis of Rotor Syndrome
The Porphyrin Handbook
Ofhereditary, Chronic, Non-Haemolytic Hyperbilirubinaemias
Complete OATP1B1 and OATP1B3 Deficiency Causes Human Rotor Syndrome by Interrupting Conjugated Bilirubin Reuptake Into the Liver
Inherited Disorders of Bilirubin Clearance
Prevalence and Incidence of Rare Diseases
A Case of Dubin-Johnson Syndrome in Pregnancy
Rotor Syndrome: an Important Diagnosis to Make