<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
<title>المجلد الاول العدد 2 2022</title>
<link href="http://dspace-su.server.ly:8080/xmlui/handle/123456789/2697" rel="alternate"/>
<subtitle/>
<id>http://dspace-su.server.ly:8080/xmlui/handle/123456789/2697</id>
<updated>2026-05-03T11:59:35Z</updated>
<dc:date>2026-05-03T11:59:35Z</dc:date>
<entry>
<title>Mesenteric Cyst Lymphangiomas in 6 years Old Boy (A Case Report)</title>
<link href="http://dspace-su.server.ly:8080/xmlui/handle/123456789/2711" rel="alternate"/>
<author>
<name>Gharib, Khalid y.</name>
</author>
<author>
<name>Ali, Maryam M</name>
</author>
<author>
<name>hafad, Jamal</name>
</author>
<author>
<name>Athiallah, Jamal M</name>
</author>
<id>http://dspace-su.server.ly:8080/xmlui/handle/123456789/2711</id>
<updated>2025-02-02T10:23:39Z</updated>
<published>2022-12-30T00:00:00Z</published>
<summary type="text">Mesenteric Cyst Lymphangiomas in 6 years Old Boy (A Case Report)
Gharib, Khalid y.; Ali, Maryam M; hafad, Jamal; Athiallah, Jamal M
mesenteric cyst lymphangioma is a rare benign intra-abdominal tumour, It is located in the mesentery of the gastrointestinal tract and may extend from the base of the mesentery into the retroperitoneum. chylous ascites is an uncommon form of ascites due to leakage of lipid-rich lymph into the peritoneal cavity, it is diagnosed by the presence of milky-appearing ascites fluid and white triglyceride content &gt;200mg/dl. We report 6-year-old boy presented progressive Vega abdominal pain over one month associated lately with abdominal distention and vomiting, abdominal ultrasound and NON-CONTRAST computed tomography (CT) revealed a large cystic abdominal lesion demonstrating multiple septations involving the retroperitoneal region. The intra-operative finding was a large yellowish septate mesenteric cyst arising from both mesenteric borders of jejunal loop extending retroperitoneal with white mesentery and multiple reactionary lymph node and chylous acites.
</summary>
<dc:date>2022-12-30T00:00:00Z</dc:date>
</entry>
<entry>
<title>Pulsed radiofrequency applied to the suprascapular nerve before rotator cuff tear arthroscopic repair: A prospective randomized clinical trial</title>
<link href="http://dspace-su.server.ly:8080/xmlui/handle/123456789/2710" rel="alternate"/>
<author>
<name>Almabsoot, Abdalmenam Abdalftahe</name>
</author>
<author>
<name>Mamdouh, Ayman Ahmed</name>
</author>
<author>
<name>M.Amaigil, Hussain</name>
</author>
<id>http://dspace-su.server.ly:8080/xmlui/handle/123456789/2710</id>
<updated>2025-02-02T10:20:47Z</updated>
<published>2022-12-30T00:00:00Z</published>
<summary type="text">Pulsed radiofrequency applied to the suprascapular nerve before rotator cuff tear arthroscopic repair: A prospective randomized clinical trial
Almabsoot, Abdalmenam Abdalftahe; Mamdouh, Ayman Ahmed; M.Amaigil, Hussain
Background: clinical studies have demonstrated the efficacy of pulsed radiofrequency (PRF) in treating many pain syndromes. PRF energy is delivered via a percutaneous needle under an image guide to reach the suprascapular nerve as it supplies more than 70% of the shoulder sensation. PRF was introduced as a non-destructive minimally invasive procedure in comparison with arthroscopic management of rotator cuff injury. However, there is a controversy regarding both measures in treating shoulder pain in rotator cuff injuries as standard methods.&#13;
&#13;
Objective: to evaluate the ability of PRF to produce shoulder pain relief by applying of PRF to the suprascapular nerve and measure the pain relief by VAS score at various time intervals prior to arthroscopic repair for rotator cuff injuries. The study should be in comparison with control group undergo arthroscopic repair without attacking of the suprascapular nerve by PRF.&#13;
&#13;
Methods: a prospective randomised controlled trial study including 40 patients divided as PRF or (P) group and control group (C) group equally. Each patient in our study whom their history and examination were fulfilled quietly including pain assessment by Visual Assessment Score (VAS). In The (P) group, a needle is inserted through a well-known point in the shoulder leading directly to the suprascapular notch (where the nerve is hooked above it) under image guidance. Radiofrequency waves at 2Hz of 20 milliseconds and 42 C in the pattern of three cycles each one lasting for 120 seconds. VAS score was assessed postoperatively for 7 time intervals starting from immediate postoperative (after arthroscopic repair) up to 3 months.&#13;
&#13;
Result: Pulsed radiofrequency produced dramatic progressive pain relief throughout our study time. In the 1st 48 hours, the VAS score dropped about 30% in (P) group with comparison to 22% in control group. At 3 months interval the VAS score was reduced by 45% from the preoperative period in comparison to 23% of the control group (P=0.000)&#13;
&#13;
Conclusion&#13;
&#13;
PRF is the safest, optimally invasive method to treat shoulder joint pain in rotator cuff injuries especially in unfitted patients for surgeries.
</summary>
<dc:date>2022-12-30T00:00:00Z</dc:date>
</entry>
<entry>
<title>Various technique of cell culture and slide preparation for human chromosome</title>
<link href="http://dspace-su.server.ly:8080/xmlui/handle/123456789/2709" rel="alternate"/>
<author>
<name>Mohamed, Faraj Saad Faraj</name>
</author>
<id>http://dspace-su.server.ly:8080/xmlui/handle/123456789/2709</id>
<updated>2025-02-02T10:03:33Z</updated>
<published>2022-12-30T00:00:00Z</published>
<summary type="text">Various technique of cell culture and slide preparation for human chromosome
Mohamed, Faraj Saad Faraj
The cell culture and slide preparation method of human chromosome is the mechanism that is a corresponding change in DNA content. In this research we used various techniques of cell culture and slide preparation for human chromosome and examined for 2 days, 3 days and 4 days cell culture because these are average days for approximately the good results and the treatment will still be good also the result has minimum bias.&#13;
&#13;
The research objectives were to determine the appropriate length of cell culture needed for human chromosome with different lengths and to determine the appropriate method for staining the slide for human chromosome with different lengths.&#13;
&#13;
Based on the data analysis, the result of this research shows that the appropriate length of cell culture needed for human chromosome with different lengths is 2 days of incubation. Although there were no significant differences between 2,3 and 4 days length based on statistical analysis, still there is little difference between them and the best is 2 days rather than 3 and 4 days based on the graph analysis. The appropriate method for staining the slide for human chromosome with different lengths is hot plate rather than another technique
</summary>
<dc:date>2022-12-30T00:00:00Z</dc:date>
</entry>
<entry>
<title>Method Validation for Determination of Paracetamol in Tablet Dosage Form Using UV-Visible Spectrophotometer</title>
<link href="http://dspace-su.server.ly:8080/xmlui/handle/123456789/2706" rel="alternate"/>
<author>
<name>Ben-Hander, Gazala Mohamed</name>
</author>
<author>
<name>Gaeth, Mohammed Eshtewi</name>
</author>
<author>
<name>Otmaan, Nasser Ali</name>
</author>
<id>http://dspace-su.server.ly:8080/xmlui/handle/123456789/2706</id>
<updated>2025-02-02T10:16:59Z</updated>
<published>2022-12-30T00:00:00Z</published>
<summary type="text">Method Validation for Determination of Paracetamol in Tablet Dosage Form Using UV-Visible Spectrophotometer
Ben-Hander, Gazala Mohamed; Gaeth, Mohammed Eshtewi; Otmaan, Nasser Ali
A simple, accurate, and cost-effective UV-spectrophotometric method for determining Paracetamol in tablet pharmaceutical formulations has been developed. The method was designed and validated in accordance with the criteria of the International Conference on Harmonization (ICH). The developed method was validated statistically concerning linearity range, precision, accuracy, the limit of detection and the limit of quantitation. The study used ethanol-water as a solvent, and λmax was found to be 243 nm. In the range of 2.0–16.0 µg mL-1, a pure drug concentration was prepared, and linear regression analysis revealed a good linear connection with an R2 value of 0.999. The detection and quantification limits were determined to be 0.5 and 1.5 µg mL-1, respectively. The recoveries ranged between 103 and 109%, and the relative standard deviation was less than 2%, indicating that this method was developed for the potential determination of Paracetamol in tablet dosage formulations.
</summary>
<dc:date>2022-12-30T00:00:00Z</dc:date>
</entry>
</feed>
