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Genotype phenotype relationship in gaucher's disease / (Record no. 78901)

MARC details
000 -LEADER
fixed length control field 020760000a22003250004500
003 - CONTROL NUMBER IDENTIFIER
control field EG-GICUC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250223032634.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 070326s2006 ua a f m 000 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency EG-GICUC
Language of cataloging eng
Transcribing agency EG-GICUC
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title Eng
049 ## - LOCAL HOLDINGS (OCLC)
Holding library Deposite
097 ## - Thesis Degree
Thesis Level M.Sc
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
Classification number Cai01.11.07.M.Sc.2006.Mo.G
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Mostafa Ahmed Ezzat
245 10 - TITLE STATEMENT
Title Genotype phenotype relationship in gaucher's disease /
Statement of responsibility, etc. Mostafa Ahmed Ezzat ; Supervised Somaya Elgawhary , Manal Niazi Elsaeed , Aamal Ibrahim Elbeshlawy
246 15 - VARYING FORM OF TITLE
Title proper/short title العلاقة بين الطفرات الجينية و الانواع الاكلينيكية فى مرض جوشر
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Cairo :
Name of publisher, distributor, etc. Mostafa Ahmed Ezzat ,
Date of publication, distribution, etc. 2006
300 ## - PHYSICAL DESCRIPTION
Extent 106P :
Other physical details ill ;
Dimensions 25cm
502 ## - DISSERTATION NOTE
Dissertation note Thesis (M.Sc.) - Cairo University - Faculty Of Medicine - Department Of Clinical and Chemical Pathology
520 ## - SUMMARY, ETC.
Summary, etc. Gaucher's disease is the most prevalent of the genetic lysosomal storage disorderIt is an autosomal recessive disease which was described by the French Physician Philippe Gaucher in 1882It is caused by a severe deficiency of glucocerebrosidase enzymatic activity with resultant accumulation of large quantities of glycolipid , glucocerebrosidase within the lysosomes of the phagocytic cells of the monocyte - macrophage systemGaucher's disease is classified to three conventional types ; Type I : chronic non - neuropathic form which usually found in adults especially in Jewish population , Type II : infantile neuropathic form which always appears by 6 months of age by rapidly progressive neurological affection , and Type III : juvenile sub - acute neuropathic with slowly progressive neurological disease that begins at childhood or adolescence
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Additional physical form available note Issued also as CD
653 #4 - INDEX TERM--UNCONTROLLED
Uncontrolled term Gaucher's disease
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Amal Ibrahim Elbeshlawy ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Manal Niazi Elsaeed ,
Relator term
700 0# - ADDED ENTRY--PERSONAL NAME
Personal name Somaya Elgawhary ,
Relator term
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="http://172.23.153.220/th.pdf">http://172.23.153.220/th.pdf</a>
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN)
Cataloger Aml
Reviser Cataloger
905 ## - LOCAL DATA ELEMENT E, LDE (RLIN)
Cataloger Esam
Reviser Revisor
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Thesis
Holdings
Source of classification or shelving scheme Not for loan Home library Current library Date acquired Full call number Barcode Date last seen Koha item type Copy number
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة قاعة الرسائل الجامعية - الدور الاول 11.02.2024 Cai01.11.07.M.Sc.2006.Mo.G 01010110046825000 22.09.2023 Thesis  
Dewey Decimal Classification   المكتبة المركزبة الجديدة - جامعة القاهرة مخـــزن الرســائل الجـــامعية - البدروم 11.02.2024 Cai01.11.07.M.Sc.2006.Mo.G 01020110046825000 22.09.2023 CD - Rom 46825.CD