Morphology, Damage Symptoms and Biology of Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae) Strains in Egypt.

Authors: EL-Lebody, Kreema A.¹ weqaytfcorp@gmail.com, Allam, Rabab D. A.¹, Rashad, Amira M.¹

Source: Egyptian Academic Journal of Biological Sciences. A, Entomology. Dec2024, Vol. 17 Issue 4, p17-26. 10p.

Subject Terms: *FALL armyworm, *LIFE cycles (Biology), *CASTOR oil, *FIELD crops, *PADDY fields

Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease

Authors: Imtiaz, Faiqa, Al-Mostafa, Abeer, Allam, Rabab, Ramzan, Khushnooda, Al-Tassan, Nada, Tahir, Asma I., Al-Numair, Nouf S., Al-Hamed, Mohamed H., Al-Hassnan, Zuhair, Al-Owain, Mohammad, Al-Zaidan, Hamad, Al-Amoudi, Mohammad, Qari, Alya, Balobaid, Ameera, Al-Sayed, Moeenaldeen

Source: In Molecular Genetics and Metabolism Reports June 2017 11:17-23

Detoxifying Enzymatic Activity and Insecticide-Resistance Gene Expression in Field Populations of Pink Bollworm, (Pectinophora gossypiella (Saund.)).

Authors: Allam Rabab, A. D.¹ rbaballam22@gmail.com, A. K., Sobeiha², A. A., Khidr¹, Al-Senosy, Neima K.³

Source: Arab Universities Journal of Agricultural Sciences. Dec2021, Vol. 29 Issue 3, p925-931. 7p.

Subject Terms: *PINK bollworm, *INSECTICIDE resistance, *GENE expression, *INSECTICIDES, *SPODOPTERA littoralis

Variable expression pattern in Donnai-Barrow syndrome: Report of two novel LRP2 mutations and review of the literature

Authors: Khalifa, Ola, Al-Sahlawi, Zahra, Imtiaz, Faiqa, Ramzan, Khushnooda, Allam, Rabab, Al-Mostafa, Abeer, Abdel-Fattah, Maaly, Abuharb, Gheid, Nester, Michael, Verloes, Alain, Al-Zaidan, Hamad

Source: In European Journal of Medical Genetics May 2015 58(5):293-299

Clinical, Endocrine, and Molecular Genetic Analysis of a Large Cohort of Saudi Arabian Patients with Laron Syndrome

Authors: Al-Ashwal, Abdullah A., Al-Sagheir, Afaf, Ramzan, Khushnooda, Al-Owain, Mohammed, Allam, Rabab, Qari, Alya, Al-Numair, Nouf S., Imtiaz, Faiqa

Source: Hormone research in pædiatrics. 88(2):119-126

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100084696881.0x000001&indx=1&recIds=ETOCvdc_100084696881.0x000001

Two novel LHX3 mutations in patients with combined pituitary hormone deficiency including cervical rigidity and sensorineural hearing loss

Authors: Ramzan, Khushnooda, Bin-Abbas, Bassam, Al-Jomaa, Lolwa, Allam, Rabab, Al-Owain, Mohammed, Imtiaz, Faiqa

Source: BMC endocrine disorders. 17(1):1-10

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100112258165.0x000001&indx=1&recIds=ETOCvdc_100112258165.0x000001

SLC5A1 Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption

Authors: Al-Suyufi, Yasir, ALSaleem, Khalid, Al-Mehaidib, Ali, Banemai, Mohammed, Aldekhail, Wajeeh M., Al-Muhandes, Abdulhakim, Mohammed, Manal, Allam, Rabab, Jambi, Amani, Ramzan, Khushnooda, Imtiaz, Faiqa

Source: Journal of pediatric gastroenterology and nutrition. 66(2):250-252

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100055294397.0x000001&indx=1&recIds=ETOCvdc_100055294397.0x000001

Prefilled Saline Syringes versus Those Prepared at Bedside for Flushing Central Venous Catheters in Neonatal ICU.

Authors: Imam, Safaa Shafik, Ismaiel Elkomy, Shereen Atef, Allam, Rabab

Source: QJM: An International Journal of Medicine; 2024 Supplement, Vol. 117, pii369-ii370, 2p

Subject Terms: CENTRAL line-associated bloodstream infections, CENTRAL venous catheters, CATHETER-related thrombosis, NOSOCOMIAL infections, LAMINAR flow

Effect of Oral N-Acetyl Cysteine in Prevention of Necrotizing Enterocolitis in Preterm Neonates with Feeding Intolerance.

Authors: Naguib Youssef, Ekram El-Hassan, EL-Ganzoury, Mona Mostafa, EL-Farash, Rania Ali, Allam, Rabab Gameel

Source: QJM: An International Journal of Medicine; 2024 Supplement, Vol. 117, pii329-ii330, 2p

Subject Terms: NEONATAL intensive care units, ACETYLCYSTEINE, DISTILLED water, RANDOMIZED controlled trials, ENTEROCOLITIS

A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population

Authors: Al-Shaikh Abdulmoneem H, Sogaty Sameera, Al-Mostafa Abeer, Allam Rabab, Trabzuni Daniah, Al-Mubarak Bashayer, Kennedy Shelley, Bin-Khamis Ghada, Ramzan Khushnooda, Taibah Khalid, Imtiaz Faiqa, Bamukhayyar Saeed S, Meyer Brian F, Al-Owain Mohammed

Source: BMC Medical Genetics, Vol 12, Iss 1, p 91 (2011)

Subject Terms: Internal medicine, RC31-1245, Genetics, QH426-470

File Description: electronic resource

Relation: http://www.biomedcentral.com/1471-2350/12/91; https://doaj.org/toc/1471-2350

Access URL: https://doaj.org/article/7cc7b30f3f204eda8d3a587f734759c3

Alterations in the Plasma Proteome Induced by SARS-CoV-2 and MERS-CoV Reveal Biomarkers for Disease Outcomes for COVID-19 Patients.

Authors: Alaiya, Ayodele, Alshukairi, Abeer, Shinwari, Zakia, AL-Fares, Mariam, Alotaibi, Jawaher, AlOmaim, Waleed, Alsharif, Ibtihaj, Bakheet, Razan, Alharbi, Layla, Allam, Rabab, Asiri, Ayed, Memish, Ziad, Alromaih, Khaldoun, Al-Mozaini, Maha

Source: Journal of Inflammation Research; Sep2021, Vol. 14, p4313-4328, 16p

Subject Terms: COVID-19, MERS coronavirus, SARS-CoV-2, TREATMENT effectiveness, RETINOID X receptors

Geographic Terms: RIYADH (Saudi Arabia)

Variation in DNAH1 may contribute to primary ciliary dyskinesia.

Authors: Imtiaz, Faiqa¹ fahmad@kfshrc.edu.sa, Allam, Rabab¹, Ramzan, Khushnooda¹, Al-Sayed, Moeenaldeen²

Source: BMC Medical Genetics. 2015, Vol. 16 Issue 1, p1-6. 6p.

Subject Terms: *CILIARY motility disorders, *CILIOPATHY, *CELLULAR pathology, *DISABILITY identification, *GENITAL diseases

Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin

Authors: Imtiaz, Faiqa, Rashed, Mohamed S., Al-Mubarak, Bashayer, Allam, Rabab, El-Karaksy, Hanaa, Al-Hassnan, Zuhair, Al-Owain, Mohammed, Al-Zaidan, Hamad, Rahbeeni, Zuhair, Qari, Alya, Meyer, Brian F., Al-Sayed, Moeen

Source: In Molecular Genetics and Metabolism December 2011 104(4):688-690

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Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia.

Authors: Imtiaz, Faiqa, Al-Mubarak, Bashayer M., Al-Mostafa, Abeer, Al-Hamed, Mohamed, Allam, Rabab, Al-Hassnan, Zuhair, Al-Owain, Mohammed, Al-Zaidan, Hamad, Rahbeeni, Zuhair, Qari, Alya, Faqeih, Eissa Ali, Alasmari, Ali, Al-Mutairi, Fuad, Alfadhel, Majid, Eyaid, Wafaa M., Rashed, Mohamed S., Al-Sayed, Moeenaldeen

Source: JIMD Reports, Volume 29; 2016, p39-46, 8p

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A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population.

Authors: Imtiaz, Faiqa, Taibah, Khalid, Ramzan, Khushnooda, Bin-Khamis, Ghada, Kennedy, Shelley, Al-Mubarak, Bashayer, Trabzuni, Daniah, Allam, Rabab, Al-Mostafa, Abeer, Sogaty, Sameera, Al-Shaikh, Abdulmoneem H., Bamukhayyar, Saeed S., Meyer, Brian F., Al-Owain, Mohammed

Source: BMC Medical Genetics; 2011, Vol. 12 Issue 1, p91-96, 6p

Subject Terms: GENETIC mutation, HEARING disorders, LOCUS (Genetics)

Geographic Terms: SAUDI Arabia

SLC5A1Mutations in Saudi Arabian Patients With Congenital Glucose-Galactose Malabsorption

Authors: Al-Suyufi, Yasir, ALSaleem, Khalid, Al-Mehaidib, Ali, Banemai, Mohammed, Aldekhail, Wajeeh M., Al-Muhandes, Abdulhakim, Mohammed, Manal, Allam, Rabab, Jambi, Amani, Ramzan, Khushnooda, Imtiaz, Faiqa

Source: Journal of Pediatric Gastroenterology & Nutrition; February 2018, Vol. 66 Issue: 2 p250-252, 3p

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