Výsledky vyhledávání

Diagnostic Value of Serum Gamma Glutamyl Transpeptidase (GGT) for Early Diagnosis of Biliary Atresia

Autor: M A, Haque, M B, Karim, K, Sultana, M S, Hasan, F, Hussain, N, Musabbir, S A, Anwar

Publikováno v: Mymensingh medical journal : MMJ. 32(1)

Early differentiation of biliary atresia (BA) from idiopathic neonatal hepatitis (INH) is of important as outcome of Kasai portoenterostomy is directly related to the age of surgery. We need to have a simple and cheap biochemical test in resource poo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f6cc7f1f60145876b3bfa105f04ab7ad
https://pubmed.ncbi.nlm.nih.gov/36594320

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Efficacy of Different Diagnostic Test for Identifying Wilson's Disease

Autor: Z F, Sonia, M, Rukunuzzaman, M B, Karim, A, Yasmin, R, Alam

Publikováno v: Mymensingh medical journal : MMJ. 31(1)

Wilson disease is an autosomal recessive disorder in which copper pathologically accumulates primarily within the liver, brain and other tissues. It can presents clinically as liver disease, as a progressive neurological disorder or as psychiatric il

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::869e62efb5ad34f2047a4fa65ea4aa36
https://pubmed.ncbi.nlm.nih.gov/34999690

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Penicillamine challenge test in the diagnosis of Wilson's disease

Autor: M W, Mazumder, M B, Karim, M, Rukunuzzaman

Publikováno v: Mymensingh medical journal : MMJ. 23(3)

Wilson's disease (WD) is one of the most common metabolic liver diseases encountered in children. Early diagnosis of the disease is essential because specific treatment can be offered, that will prevent further hepatocellular injury and neurologic co

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fec47b454a7b18d4d1750844d74d44e8
https://pubmed.ncbi.nlm.nih.gov/25178601

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Wilson's disease in children with blindness: an atypical presentation

Autor: M, Rukunuzzaman, M B, Karim, M M, Rahman, M S, Islam, M W, Mazumder

Publikováno v: Mymensingh medical journal : MMJ. 22(1)

Wilson's disease (WD) is an autosomal recessive disease affecting copper metabolism causing copper induced organ damage. Common organs involved are liver and central nervous system. But RBC, eye, kidneys and bone may also be affected. In WD main defe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7685826db8f4ef497e6aa25e31fff4dc
https://pubmed.ncbi.nlm.nih.gov/23416828

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Wilson's disease with hepatic presentation in childhood

Autor: M B Karim, Mukhlesur Rahman, Mohammad Safiqul Islam

Publikováno v: Mymensingh medical journal : MMJ. 16(1)

Diagnosis of Wilson's disease with hepatic presentation in childhood using clinical and common laboratory parameters is still challenging and is often missed or delayed. The aim of the study was to document the clinical and laboratory parameters of h

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ebcc65a45e892ba3000d61b28c4101a
https://pubmed.ncbi.nlm.nih.gov/17344776

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