Nelly Alieldin

Dr. Nelly Alieldin


Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2016 in British Journal of Radiology
Verified
Journal Article
Closed access
RKRasha M Kamal
Rasha M Kamal
MHMaha H Helal
Maha H Helal
SMSahar Mansour
Sahar Mansour
MHMarwa A Haggag
Marwa A Haggag
ONOmniya M Nada
Omniya M Nada
NANelly Alieldin
Nelly Alieldin
Objective:To assess the feasibility of using the MRI breast imaging reporting and data system (BI-RADS) lexicon morphology descriptors to characterize enhancing breast lesions identified on contrast-enhanced spectral mammography (CESM).Methods:The study is a retrospective analysis of the morphology descriptors of 261 enhancing breast lesions identified on CESM in 239 patients. We presented the morphological categorization of the included lesions into focus, mass and non-mass. Further classifications included (1) the multiplicity for “focus” category, (2) the shape, margin and internal enhancement for “mass” category and (3) the distribution and internal enhancement for “non-mass” category. Each morphology descriptor was evaluated individually (irrespective of all other descriptors) by calculating its sensitivity, specificity, positive-predictive value (PPV) and negative-predictive value (NPV) and likelihood ratios (LRs).Results:The study included 68/261 (26.1%) benign lesions and 193/261 (73.9%) malignant...

1 June 2015 in European Journal of Radiology
Verified
Journal Article
Closed access
RKRasha Mohamed Kamal
Rasha Mohamed Kamal
MHMaha Hussien Helal
Maha Hussien Helal
RWRasha Wessam
Rasha Wessam
SMSahar Mansour
Sahar Mansour
IGIman Godda
Iman Godda
NANelly Alieldin
Nelly Alieldin

11 July 2018 in European journal of pain
Verified
Journal Article
Closed access
PDF file
SAS.A. Amr
S.A. Amr
RRR.M. Reyad
R.M. Reyad
AAAhmed Abdelmaksoud
Ahmed Abdelmaksoud
MMM.F. Mohamad
M.F. Mohamad
MMM.M. Mostafa
M.M. Mostafa
FHF.A. Hamed
F.A. Hamed

20 March 2016 in Hepatitis Monthly
Verified
Journal Article
Open access
PDF file
NENadia Mohamed El-Guendy
Nadia Mohamed El-Guendy
RHReham Helwa
Reham Helwa
MEMedhat Salah El-Halawany
Medhat Salah El-Halawany
SAShimaa Abdel Rahman Ali
Shimaa Abdel Rahman Ali
MTMarwa Tantawy
Marwa Tantawy
AAAbdel-Hady Ali Abdel-Wahab
Abdel-Hady Ali Abdel-Wahab
Background: MicroRNAs (miRNAs) have been repeatedly shown to play important roles in liver pathologies, including hepatitis, liver cirrhosis, and liver cancer. Egypt has the highest hepatitis C virus (HCV) infection rate worldwide, predominantly involving genotype-4. Objectives: In this study, we attempted to characterize the miRNA profile of the poorly studied genotype 4 of HCV in chronically infected Egyptian patients to obtain a better understanding of the disease and its complications and help in the design of better management protocols. Patients and Methods: We analyzed the expression levels of a selected panel of 94 miRNAs in fresh liver biopsies collected from 50 Egyptian patients diagnosed with chronic HCV infection using quantitative real-time polymerase chain reaction (PCR) assay. Non-parametric tests were used to analyze the expression level of each miRNA and association with the clinicopathological features of enrolled patients in this study. Results: Our results revealed differential expression levels of the analyzed miRNAs compared to the normal controls. Twenty-seven miRNAs (including miR-105, miR-147, miR-149-3p, and miR-196b) showed up-regulation, while 17 miRNAs (including miR-21, miR-122, miR-199a-3p, and miR-223) showed down-regulation. An inverse correlation was observed between levels of miR-95, miR-130a, and miR-142-5p with the blood albumin level. Increased expression levels of seven miRNAs (miR-29c, miR-30c, miR-126, miR-145, miR-199a, miR-199a-3p, and miR-222) were observed with severe chronic hepatic inflammation. Several deregulated miRNAs found in this study have been previously linked to chronic liver inflammation and the risk of hepatocellular carcinoma (HCC) development. Conclusions: The identified expression profiles of some examined miRNAs might offer important points to consider for the treatment of naive patients and the management of chronically infected HCV patients in Egypt and around the world. Keywords: Hepatitis C; MicroRNAs; Genotype-4; Real-Time Polymerase Chain Reaction; Liver Cirrhosis

24 September 2014
Verified
Journal Article
Closed access
SMSahar Mohamed
Sahar Mohamed
KFKhaled M Fares
Khaled M Fares
AMAshraf Amin Mohamed
Ashraf Amin Mohamed
NANelly Alieldin
Nelly Alieldin

1 March 2014 in Journal of the Egyptian National Cancer Institute
Verified
Journal Article
Open access
NANelly Alieldin
Nelly Alieldin
OAOmnia M. Abo-Elazm
Omnia M. Abo-Elazm
DBDalia Bilal
Dalia Bilal
SSSalem Eid Salem
Salem Eid Salem
EGEman Gouda
Eman Gouda
AIAmal S. Ibrahim
Amal S. Ibrahim
Objective: Primary objective was to verify whether breast cancer patients aged less than 40 years at diagnosis have poorer prognosis than older patients. Secondary to assess prognostic factors influencing disease free survival. Methods: 941 women were diagnosed with non-metastatic breast cancer at NCI, Cairo in 2003. Epidemiologic, clinico-pathological characteristics, treatment modalities and disease free survival were compared among the two age groups. Prognostic factors were evaluated for association with disease-free survival. Results: One hundred-eighty-one patients (19.2%) were younger than 40 years and 760 (80.8%) were older. Older women presented with higher rates of comorbidities and younger women presented with more hormone non-responsive tumors. Young women presented with larger tumors pT4 = 13.8% compared to 8.6% in older women, yet not significant. Young women were treated with more conservative surgery, more adjuvant chemotherapy and radiotherapy while older women with more radical mastectomies and more hormonal treatment. Recurrence rates were significantly higher among young women 44.2% compared to 34.5% in older women. Five year disease free survival in young women was 38.9% +/- 4.6% compared to 48.6% +/- 2.5% with adjusted hazard ratio of 1.22 95% CI (0.91-1.64), p = 0.19. Multivariate analyses identified positive axillary lymph nodes (pN2-pN3), larger tumor size (pT3-pT4), hypertension, lobular carcinoma type and lack of adjuvant systemic treatment as independent factors associated with poor DFS. Conclusion: Young women were not found to have poorer prognosis, yet they presented with more ER negative tumors. Most of women presented with advanced stage and young women had higher recurrence rates. (C) 2013 Production and hosting by Elsevier B.V. on behalf of National Cancer Institute, Cairo University.