Paroxysmal nocturnal hemoglobinuria in a-17 year old (a case report) / (Record no. 3705)

MARC details
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fixed length control field 01127nam a22001697a 4500
003 - CONTROL NUMBER IDENTIFIER
control field DOH
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20210320151642.0
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100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Yu, Marie Emmeline B.
245 00 - TITLE STATEMENT
Title Paroxysmal nocturnal hemoglobinuria in a-17 year old (a case report) /
Statement of responsibility, etc. Marie Emmeline B. Yu
520 3# - SUMMARY, ETC.
Summary, etc. A rare disease merits general attention if it is associated with extraordinary clinical manifestations, unusual laboratory findings, or an instructive molecular defect. Paroxysmal nocturnal hemoglobinuria has all three. Its clinical hallmark, tea-colored urine in arising from sleep, is graphic testimony to intravascular hemolysis during the night. Even more peculiar is the hemolysis that occurs after blood from a patient with PNH is mixed with acidified serum or ordinary table sugar. The molecular abnormality in PNH not only inform us about this unusual disease but also points to a genetic lesion of widespread interest.
580 ## - LINKING ENTRY COMPLEXITY NOTE
Linking entry complexity note Cebu Doctors' Proceedings, 1995 11 (2) pages 73-77
650 #2 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Hemoglobinuria, Paroxysmal
650 #2 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Case Reports
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Journal Article
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Holdings
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    Dewey Decimal Classification     DOH Central Library DOH Central Library Electronic Resource Section 03/20/2021   J000255 D0001J000255 03/20/2021 03/20/2021 Journal Article