Literature DB >> 1173174

Serum alkaline phosphatase isoenzymes in sickle cell anemia.

J I Brody, W N Ryan, M A Haidar.   

Abstract

Alkaline phosphatase isoenzymes in sera from patients with sickle cell anemia were separated by electrophoresis on starch gel. Physical and biochemical criteria identified bone alkaline phosphatase as the principal, although not necessarily the sole, enzyme fraction that increases during symptomatic sickle cell crises. Moreover, there appeared to be concordance between crisis severity, serum levels of alkaline phosphatase, and isoenzyme patterns; electrophoretic and biochemical abnormalities could be detected even when the patients were asymptomatic. The present data suggest that the serum alkaline phosphatase level may be an additional indicator of the degree, frequency, and persistence of tissue injuries that occur in sickle cell anemia.

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Year:  1975        PMID: 1173174

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


  6 in total

1.  Acute hepatic sequestration in sickle cell disease.

Authors:  William E Norris
Journal:  J Natl Med Assoc       Date:  2004-09       Impact factor: 1.798

Review 2.  Acute liver function decompensation in a patient with sickle cell disease managed with exchange transfusion and endoscopic retrograde cholangiography.

Authors:  Haris Papafragkakis; Mel A Ona; Kinesh Changela; Swayamprabha Sadanandan; Abraham Jelin; Sury Anand; Sushil Duddempudi
Journal:  Therap Adv Gastroenterol       Date:  2014-09       Impact factor: 4.409

Review 3.  Clinical management of sickle cell liver disease in children and young adults.

Authors:  Eirini Kyrana; David Rees; Florence Lacaille; Emer Fitzpatrick; Mark Davenport; Nigel Heaton; Sue Height; Marianne Samyn; Fulvio Mavilio; Valentine Brousse; Abid Suddle; Subarna Chakravorty; Anita Verma; Girish Gupte; Marki Velangi; Baba Inusa; Emma Drasar; Nedim Hadzic; Tassos Grammatikopoulos; Jonathan Hind; Maesha Deheragoda; Maria Sellars; Anil Dhawan
Journal:  Arch Dis Child       Date:  2020-11-11       Impact factor: 3.791

4.  Exacerbation of sickle cell disease itself as a cause of abnormal liver chemistry tests.

Authors:  Carmen M Stanca; Maria Isabel Fiel; Thomas D Schiano
Journal:  Dig Dis Sci       Date:  2006-12-15       Impact factor: 3.487

Review 5.  Sickle Hepatopathy.

Authors:  Dibya L Praharaj; Anil C Anand
Journal:  J Clin Exp Hepatol       Date:  2020-08-09

6.  Hepatic manifestations in hematological disorders.

Authors:  Jun Murakami; Yukihiro Shimizu
Journal:  Int J Hepatol       Date:  2013-03-31
  6 in total

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