Acute and chronic hepatobiliary manifestations of sickle cell disease: A review.

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Hemosiderosis causing liver cirrhosis in a patient with Hb S/beta thalassemia and no other known causes of hepatic disease.

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P2860

Acute and chronic hepatobiliary manifestations of sickle cell disease: A review.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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2017年论文

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2017年论文

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name

Acute and chronic hepatobiliary manifestations of sickle cell disease: A review.

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Acute and chronic hepatobiliary manifestations of sickle cell disease: A review.

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Acute and chronic hepatobiliary manifestations of sickle cell disease: A review.

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P1476

Acute and chronic hepatobiliary manifestations of sickle cell disease: A review

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Cesar Taborda

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Rushikesh Shah

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P2860

Gall stones in sickle cell disease in the United Kingdom.

Iron overload in sickle cell disease.

Sickle cell hepatopathy.

Gastrointestinal and hepatic complications of sickle cell disease.

Hepatic sequestration in sickle cell anaemia.

Endoscopic and gastric acid studies in homozygous sickle cell disease and upper abdominal pain.

Global epidemiology of sickle haemoglobin in neonates: a contemporary geostatistical model-based map and population estimates.

Reverse sequestration in a case of sickle crisis.

Sickle cell cholangiopathy: an endoscopic retrograde cholangiopancreatography evaluation.

Serum ferritin level changes in children with sickle cell disease on chronic blood transfusion are nonlinear and are associated with iron load and liver injury.

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108-116

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scholarly article

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10.4291/WJGP.V8.I3.108

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Saurabh Chawla

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2017-08-01T00:00:00Z

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28868180

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sickle-cell disease

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5561431

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Acute and chronic hepatobiliary manifestations of sickle cell disease: A review.

about

P2860

P2860

Acute and chronic hepatobiliary manifestations of sickle cell disease: A review.

description

name

type

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P1433

P1476

P2093

P2860

P304

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P356

P433

P478

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P698

P921

P932

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P1433

P1476

P2093

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P356

P433

P478

P50

P577

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P921

P932