Multiplex ligation-dependent probe amplification versus fluorescent in situ hybridization for screening RB1 copy number variations in Egyptian patients with retinoblastoma.

Autor: Eid OM; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., El Zomor H; Pediatric Department, Children's Cancer Hospital, Cairo, Egypt.; Pediatric Oncology Department, National Cancer Institute, Cairo University, Cairo, Egypt., Mohamed AM; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., El-Bassyouni HT; Clinical Genetics Department, National Research Centre, Cairo, Egypt., Afifi HH; Clinical Genetics Department, National Research Centre, Cairo, Egypt., El-Ayadi M; Pediatric Department, Children's Cancer Hospital, Cairo, Egypt.; Pediatric Oncology Department, National Cancer Institute, Cairo University, Cairo, Egypt., Sadek SH; Ophthalmology Department, Children's Cancer Hospital, Egypt.; Ophthalmology Department, Fayoum University, Faiyum, Egypt., Hammad SA; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Salem SI; Clinical Pathology Department, Children's Cancer Hospital, Egypt.; Clinical Pathology Department, National Cancer Institute, Cairo University, Cairo, Egypt., Mahrous R; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Fadel IM; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Refaat K; Human Cytogenetics Department, National Research Centre, Cairo, Egypt., Afifi MA; Research Department, Children's Cancer Hospital, Egypt., Shelil AE; Ophthalmology Department, Children's Cancer Hospital, Egypt.; Ophthalmology Department, Al-Azhar University, Cairo, Egypt., Ziko OAO; Ophthalmology Department, Ain Shams University, Cairo, Egypt., Abdel Azeem AA; Ophthalmic Genetics Department, Research Institute of Ophthalmology, Cairo, Egypt., El-Haddad A; Pediatric Department, Children's Cancer Hospital, Cairo, Egypt.; Pediatric Oncology Department, National Cancer Institute, Cairo University, Cairo, Egypt.

Publikováno v: Ophthalmic genetics [Ophthalmic Genet] 2022 Dec; Vol. 43 (6), pp. 789-794. Date of Electronic Publication: 2022 Sep 13.

Quantitative shotgun proteomics distinguishes wound-healing biomarker signatures in common carp skin mucus in response to Ichthyophthirius multifiliis.

Autor: Saleh M; Clinical Division of Fish Medicine, University of Veterinary Medicine, Vienna, Austria. mona.saleh@vetmeduni.ac.at., Kumar G; Clinical Division of Fish Medicine, University of Veterinary Medicine, Vienna, Austria., Abdel-Baki AA; Zoology Department, College of Science, King Saud University, Riyadh, Saudi Arabia.; Zoology Department, Faculty of Science, Beni-Suef University, Beni Suef, Egypt., Dkhil MA; Zoology Department, College of Science, King Saud University, Riyadh, Saudi Arabia.; Department of Zoology and Entomology, Faculty of Science, Helwan University, Cairo, Egypt., El-Matbouli M; Clinical Division of Fish Medicine, University of Veterinary Medicine, Vienna, Austria., Al-Quraishy S; Zoology Department, College of Science, King Saud University, Riyadh, Saudi Arabia.

Publikováno v: Veterinary research [Vet Res] 2018 Apr 20; Vol. 49 (1), pp. 37. Date of Electronic Publication: 2018 Apr 20.

Antiprotozoal effects of metal nanoparticles against Ichthyophthirius multifiliis.

Autor: Saleh M; Clinical Division of Fish Medicine,University of Veterinary Medicine,Vienna,Austria., Abdel-Baki AA; Zoology Department,College of Science, KingSaudUniversity,Riyadh,Saudi Arabia., Dkhil MA; Zoology Department,College of Science, KingSaudUniversity,Riyadh,Saudi Arabia., El-Matbouli M; Clinical Division of Fish Medicine,University of Veterinary Medicine,Vienna,Austria., Al-Quraishy S; Zoology Department,College of Science, KingSaudUniversity,Riyadh,Saudi Arabia.

Publikováno v: Parasitology [Parasitology] 2017 Nov; Vol. 144 (13), pp. 1802-1810. Date of Electronic Publication: 2017 Jul 12.

Assessment of Vitamin D status in a group of Egyptian children with non alcoholic fatty liver disease (multicenter study).

Autor: Mohamed Ahmed A; Department of Biochemistry, National Hepatology and Tropical Medicine Institute, Cairo, Egypt., Abdel Ghany M; Pediatric Department, El Sahel teaching hospital, Cairo, Egypt., Abdel Hakeem GL; Pediatric Department, Minia University, El Minya, Egypt., Kamal A; Public health Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt., Khattab R; Microbiology and Immunology Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt., Abdalla A; Department of Clinical Nutrition, Faculty of Applied Medical Science, King Abdul-Aziz University, Jeddah, Kingdom of Saudi Arabia., Abou El Fotoh Lel M; Pediatric Department, Minia University, El Minya, Egypt., El Mazary AA; Pediatric Department, Minia University, El Minya, Egypt., Sayed MA; Pediatric Department, Minia University, El Minya, Egypt., Abdel Fadil AM; Pediatric Department, Minia University, El Minya, Egypt.

Publikováno v: Nutrition & metabolism [Nutr Metab (Lond)] 2016 Aug 19; Vol. 13, pp. 53. Date of Electronic Publication: 2016 Aug 19 (Print Publication: 2016).

Expanding the mutation and clinical spectrum of Roberts syndrome.

Autor: Afifi HH; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt., Abdel-Salam GM; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt., Eid MM; Human Cytogenetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt., Tosson AM; Pediatrics Department, Faculty of Medicine, Cairo University, Cairo, Egypt., Shousha WG; Chemistry Department, Biochemistry Unit, Faculty of Science, Helwan University, Cairo, Egypt., Abdel Azeem AA; Ophthalmic Genetics Department, Research Institute of Ophthalmology, Cairo, Egypt., Farag MK; Prenatal Diagnosis and Fetal Medicine Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt., Mehrez MI; Orodental Genetics Department, Oral and Dental Research Division, National Research Centre, Cairo, Egypt., Gaber KR; Prenatal Diagnosis and Fetal Medicine Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

Publikováno v: Congenital anomalies [Congenit Anom (Kyoto)] 2016 Jul; Vol. 56 (4), pp. 154-62.