User profiles for Bareqa Salah

Bareqa Salah

University of Jordan
Verified email at ju.edu.jo
Cited by 180

Skin cancer recognition by using a neuro-fuzzy system

B Salah, M Alshraideh, R Beidas… - Cancer …, 2011 - journals.sagepub.com
Skin cancer is the most prevalent cancer in the light-skinned population and it is generally
caused by exposure to ultraviolet light. Early detection of skin cancer has the potential to …

An insight into the whole transcriptome profile of four tissue-specific human mesenchymal stem cells

…, S Adwan, R Rahmeh, O Samarah, B Salah… - Regenerative …, 2019 - Future Medicine
Aim: Variations in the clinical outcomes using mesenchymal stem cells (MSCs) treatments
exist, reflecting different origins and niches. To date, there is no consensus on the best source …

Breast reconstruction by local flaps after conserving surgery for breast cancer: an added asset to oncoplastic techniques

JK Almasad, B Salah - The Breast Journal, 2008 - Wiley Online Library
This study describes and evaluates the results of a proposed simple technique of volume
replacement by local flaps to reconstruct the breast after conserving surgery for breast cancer. …

[HTML][HTML] Congenital midline sinus of the upper lip: A case report and review of literature

BI Salah, B Al-Rawashdeh, ZR Al-Ali… - International journal of …, 2018 - Elsevier
Introduction Congenital pits of the lip are uncommon and may be associated with conditions
such as Van der Woude syndrome. Isolated lip pits are extremely rare developmental …

[HTML][HTML] Complete primary pachydermoperiostosis: A case report from Jordan and review of literature

BI Salah, KI Husari, Z Al‐Ali, B Rawashdeh - Clinical case reports, 2019 - ncbi.nlm.nih.gov
Pachydermoperiostosis (PDP), also known as primary hypertrophic osteoarthropathy or
Touraine‐Solente‐Gole syndrome, is a rare genetic disease with primary clinical features of …

[HTML][HTML] Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents

…, D Ali, B Al-Kurdi, M Sallam, AM Alzibdeh, B Salah… - Plos one, 2020 - journals.plos.org
Background Ataxia with oculomotor apraxia type 1 (AOA1) is a rare autosomal recessive
cerebellar ataxia, caused by mutations in the APTX gene. The disease is characterized by early-…

[HTML][HTML] Giant perianal Seborrheic keratosis: A case report

B Salah, M Mahseeri, Z Al-Ali, A Gaith, T Aldwan… - International journal of …, 2018 - Elsevier
Introduction Seborrheic keratosis is one of the most common benign epidermal cutaneous
lesions encountered by dermatologists and plastic surgeons in their daily practice. …

[PDF][PDF] Automated detection of breast cancer using artificial neural networks and fuzzy logic

EA AL-Dreabi, MM Otoom, B Salah, ZM Hawamdeh… - IJSBAR, 2017 - researchgate.net
Our aim was to develop a diagnostic system that could classify breast tumors as either
malignant or benign to provide a faster and more reliable method for patients. In order to …

Impact of Parental Consanguinity on the Frequency of Orofacial Clefts in Jordan

S Jabaiti, B Salah, M Al-Lawama… - Journal of …, 2022 - journals.lww.com
Orofacial clefts (OFCs) are the most common craniofacial congenital anomalies, and its
prevalence is highest among Asian populations. The aim of this retrospective case-control study …

[HTML][HTML] Establishment of a human induced pluripotent stem cell (iPSC) line (JUCTCi010-A) from a healthy Jordanian female skin dermal fibroblasts

…, B Al-Kurdi, D Ali, D Abuarqoub, R Barham, B Salah… - Stem Cell Research, 2020 - Elsevier
Human integration-free induced pluripotent pluripotent stem cells (hiPSCs) were generated
from skin fibroblasts obtained from a 27-year-old healthy Jordanian female. The resulting …