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Association of CTRP and chemokine ligand-2 in Egyptian diabetic women with or without CAD / (Record no. 12946)

MARC details
000 -LEADER
fixed length control field 04168ntm a2200337 i 4500
001 - CONTROL NUMBER
control field 12102116
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20211025113041.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 150118s2019 ua a f bm 000 0 eng |
040 ## - CATALOGING SOURCE
Original cataloging agency EG-EULC
Transcribing agency EG-EULC
Description conventions rda
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title eng
Language code of summary or abstract/overprinted title or subtitle ara
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 572
Item number A.F.S
Edition number 22
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Ahmed, Sara Faisal Abdel Aal,
9 (RLIN) 33876
Relator term author
245 10 - TITLE STATEMENT
Title Association of CTRP and chemokine ligand-2 in Egyptian diabetic women with or without CAD /
Statement of responsibility, etc Sara Faisal Abdel Aal Ahmed, (Biochemistry teaching assistant, Faculty of Pharmaceutical Sciences and Pharmaceutical Industries, Future University in Egypt, B. Ph. Sci., Assuit University); Supervisors Prof. Dr. Hala Osman El- Mesallamy, (Professor of Biochemistry, Head of Biochemistry Department, Faculty of Pharmacy, Ain Shams University.), Prof. Dr. Mohamed Hesham El-Hefnawy, (Professor of Pediatric Endocrinology, Dean of the National Institute of Diabetes and Endocrinology.), Ass. Prof. Dr. Marwa Ismail Shabayek, (Assistant Professor of Biochemistry, Faculty of Pharmaceutical Sciences and Pharmaceutical Industries, Future University in Egypt.)<br/>
246 15 - VARYING FORM OF TITLE
Title proper/short title ارتباط معدلات CTRP وكيموكاين ليجند - 2 في السيدات المصريات المصابات بداء السكري في وجود أو عدم وجود أمراض الشريان التاجي
264 #1 - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Date of publication, distribution, etc 2019
300 ## - PHYSICAL DESCRIPTION
Extent 133 pages, 4 pages :
Other physical details illustrations (black and white) ;
Dimensions 24 cm
336 ## - CONTENT TYPE
Source rdacontent
Content type term text
337 ## - MEDIA TYPE
Source rdamedia
Media type term unmediated
338 ## - CARRIER TYPE
Source rdacarrier
Carrier type term volume
500 ## - GENERAL NOTE
General note Supervisors Prof. Dr. Hala Osman El- Mesallamy, (Professor of Biochemistry, Head of Biochemistry Department, Faculty of Pharmacy, Ain Shams University.), Prof. Dr. Mohamed Hesham El-Hefnawy, (Professor of Pediatric Endocrinology, Dean of the National Institute of Diabetes and Endocrinology.), Ass. Prof. Dr. Marwa Ismail Shabayek, (Assistant Professor of Biochemistry, Faculty of Pharmaceutical Sciences and Pharmaceutical Industries, Future University in Egypt.)
502 ## - DISSERTATION NOTE
Dissertation note Thesis (M.Sc.)-Ain Shams university, Faculty of pharmacy, Department of Biochemistry, 2019.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references.
520 3# - SUMMARY, ETC.
Summary, etc Renal allograft survival requires multiple immunosuppressive drugs. This strategy<br/>may lead to gastric complications that necessitate gastro-protective medications,<br/>notably, proton pump inhibitors (PPI). This study aimed to compare the influence<br/>of pantoprazole and esomeprazole on serum cyclosporine trough levels (C0) in<br/>renal transplant recipients (RTR). A prospective, parallel, open-label trial was<br/>conducted on 47 adult RTR receiving cyclosporine doses adjusted to attain trough<br/>concentrations of 100 to 150 μg/L, mycophenolate mofetil (MMF) 750 mg<br/>q12 hour and prednisolone at 5 mg daily at Nasser Institute, Cairo, Egypt from<br/>January to September 2016. Patients were randomized into the esomeprazole<br/>group (25) or pantoprazole group (22) receiving the same dose (40 mg once daily).<br/>The study outcomes included clinical signs of rejection and renal function<br/>decline, assessed by elevations in serum creatinine, caused by cyclosporine level<br/>variations in either of the two study groups. Renal function, C0 and CBC measurements were measured at baseline and monthly for 6 months. The mean C0<br/>values were higher in the pantoprazole group than in the esomeprazole group in<br/>the sixth month only (P = .007). Serum creatinine level was lower in the sixth<br/>month than at baseline in the esomeprazole group (P = .004). There were no<br/>signs of rejection biochemical or clinical in any of the study groups. In conclusion,<br/>PPIs should be used with caution and doses should be titrated to reach the C0 targets in RTR, which is of more importance in pantoprazole than esomeprazole to<br/>avoid C0 level elevation or decline affecting the allograft function
546 ## - LANGUAGE NOTE
Language note Text in English, abstracts in English and Arabic.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Biochemistry
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Diabetes
General subdivision Complications
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Coronary heart disease
856 40 - ELECTRONIC LOCATION AND ACCESS
Materials specified DSpace electronic resource
Uniform Resource Identifier <a href="http://repository.fue.edu.eg/xmlui/handle/123456789/5783">http://repository.fue.edu.eg/xmlui/handle/123456789/5783</a>
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Thesis
Source of classification or shelving scheme Dewey Decimal Classification
Holdings
Lost status Source of classification or shelving scheme Damaged status Not for loan Collection code Home library Current library Shelving location Date acquired Acquisition method Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
  Dewey Decimal Classification     Pharmacy ( Pharmacology ) Main library Main library C3 THESIES 04/04/2021 Donation 2021   572 A.F.S 00016498 19/02/2025 04/04/2021 Thesis