Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Mohamoud HS"'
Autor:
Bibi F; Special Infectious Agents Unit, King Fahd Medical Research Centre, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia., Ali I; Centre for Computational Intelligence (CCI), Faculty of Technology, De Montfort University, United Kingdom., Naseer MI; Center of Excellence in Genomic Medicine Research (CEGMR), King Abdulaziz University, Jeddah, Saudi Arabia., Ali Mohamoud HS; Department of Clinical Genetics, St George's University Hospitals NHS Foundation Trust, Cranmer Terrace London, United Kingdom., Yasir M; Special Infectious Agents Unit, King Fahd Medical Research Centre, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia., Alvi SA; Special Infectious Agents Unit, King Fahd Medical Research Centre, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia., Jiman-Fatani AA; Department of Medical Microbiology and Parasitology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Sawan A; Department of Anatomical Pathology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Azhar EI; Special Infectious Agents Unit, King Fahd Medical Research Centre, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.; Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Publikováno v:
PloS one [PLoS One] 2018 Sep 13; Vol. 13 (9), pp. e0202576. Date of Electronic Publication: 2018 Sep 13 (Print Publication: 2018).
Autor:
Mohamoud HS; St. George's University Hospitals, London, UK., Ahmed S; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Genetic Medicine, King Abdulaziz University Hospital, Jeddah, Saudi Arabia., Jelani M; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Genetic Medicine, King Abdulaziz University Hospital, Jeddah, Saudi Arabia., Alrayes N; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Childs K; Institute of Infection & Immunity, St. George's University of London, London, UK., Vadgama N; Institute of Neurology, University College London, London, UK., Almramhi MM; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Genetic Medicine, King Abdulaziz University Hospital, Jeddah, Saudi Arabia., Al-Aama JY; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Department of Genetic Medicine, King Abdulaziz University Hospital, Jeddah, Saudi Arabia., Goodbourn S; Institute of Infection & Immunity, St. George's University of London, London, UK., Nasir J; Genetics Unit, Cell Biology and Genetics Research Centre, Molecular & Clinical Sciences Research Institute, St. George's University of London, London, UK. jnasir1@uclan.ac.uk.; School of Medicine, UCLAN, Preston, UK. jnasir1@uclan.ac.uk.
Publikováno v:
Scientific reports [Sci Rep] 2018 Feb 01; Vol. 8 (1), pp. 2053. Date of Electronic Publication: 2018 Feb 01.
Autor:
Dursun F, Mohamoud HS, Karim N, Naeem M, Jelani M, Kırmızıbekmez H; Ümraniye Training and Research Hospital, Clinic of Pediatric Endocrinology, İstanbul, Turkey, Phone: +90 216 632 18 18 E-mail: heveskirmizibekmez@yahoo.com.
Publikováno v:
Journal of clinical research in pediatric endocrinology [J Clin Res Pediatr Endocrinol] 2016 Dec 01; Vol. 8 (4), pp. 472-477. Date of Electronic Publication: 2016 Apr 18.
Autor:
Alkhiary YM; Oral and Maxillofacial Prosthodontics Department, Faculty of Dentistry, King Abdulaziz University, Jeddah, Saudi Arabia., Jelani M; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Medical Genetics and Molecular Biology Unit, Biochemistry Department, Institute of Basic Medical Sciences, Khyber Medical University, Peshawar, Pakistan., Almramhi MM; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Mohamoud HS; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Human Genetics Research Centre, Division of Biomedical Sciences (BMS), St. George's University of London (SGUL), London SW17 0RE, United Kingdom., Al-Rehaili R; Oral and Maxillofacial Prosthodontics Department, Faculty of Dentistry, King Abdulaziz University, Jeddah, Saudi Arabia., Al-Zahrani HS; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Serafi R; Department of Dermatology, King Abdulaziz University Hospital, Jeddah, Saudi Arabia., Yang H; Oral and Maxillofacial Prosthodontics Department, Faculty of Dentistry, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Al-Aama JY; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; BGI-Shenzhen, Shenzhen 518083, China.
Publikováno v:
Saudi journal of biological sciences [Saudi J Biol Sci] 2016 Sep; Vol. 23 (5), pp. 571-6. Date of Electronic Publication: 2015 Jun 16.
Autor:
Jelani M; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Medical Genetics and Molecular Biology Unit, Biochemistry Department, Institute of Basic Medical Sciences, Khyber Medical University, Peshawar, Pakistan. Electronic address: mjelani@kau.edu.sa., Kang C; Department of Biology and Institute of Basic Sciences, Sungshin Women's University, Seoul, Republic of Korea, Republic of Korea., Mohamoud HS; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Human Genetics Research Centre, Division of Biomedical Sciences (BMS), St. George's University of London (SGUL), London SW17 0RE, United Kingdom, UK., Al-Rehaili R; Oral and Maxillofacial Prosthodontics Department, Faculty of Dentistry, King Abdulaziz University, Jeddah, Saudi Arabia., Almramhi MM; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Serafi R; Department of Dermatology, King Abdulaziz University Hospital, Jeddah, Saudi Arabia., Yang H; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; BGI-Shenzhen, Shenzhen, China., Al-Aama JY; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Naeem M; Medical Genetics Research Laboratory, Department of Biotechnology, Quaid-i-Azam University, Islamabad, Pakistan., Alkhiary YM; Oral and Maxillofacial Prosthodontics Department, Faculty of Dentistry, King Abdulaziz University, Jeddah, Saudi Arabia. Electronic address: yalkhiary@kau.edu.sa.
Publikováno v:
Archives of oral biology [Arch Oral Biol] 2016 Jul; Vol. 67, pp. 28-33. Date of Electronic Publication: 2016 Mar 23.
Autor:
Alrayes N; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Cell Sciences and Genetics Research Centre, St. George's University of London (SGUL), London SW17 0RE, United Kingdom., Mohamoud HS; Cell Sciences and Genetics Research Centre, St. George's University of London (SGUL), London SW17 0RE, United Kingdom., Ahmed S; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Genetic Medicine, King Abdulaziz University Hospital, Jeddah, Saudi Arabia., Almramhi MM; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Shuaib TM; Department of Paediatrics, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Wang J; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; BGI-Shenzhen, Shenzhen 518083, China., Al-Aama JY; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Everett K; Cell Sciences and Genetics Research Centre, St. George's University of London (SGUL), London SW17 0RE, United Kingdom., Nasir J; Cell Sciences and Genetics Research Centre, St. George's University of London (SGUL), London SW17 0RE, United Kingdom., Jelani M; Princess Al-Jawhara Albrahim Centre of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia; Medical Genetics and Molecular Biology Unit, Biochemistry Department, Institute of Basic Medical Sciences, Khyber Medical University, Peshawar, Pakistan. Electronic address: mjelani@kau.edu.sa.
Publikováno v:
Journal of the neurological sciences [J Neurol Sci] 2016 Apr 15; Vol. 363, pp. 240-4. Date of Electronic Publication: 2016 Mar 02.
Autor:
Gaboon NE; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.; Medical Genetic Center, Faculty of Medicine, Ain Shams University, Cairo, Egypt., Jelani M; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Medical Genetics and Molecular Biology Unit, Biochemistry Department, Institute of Basic Medical Sciences, Khyber Medical University, Peshawar, Pakistan., Almramhi MM; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia., Mohamoud HS; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.; Human Genetics Research Centre, Division of Biomedical Sciences (BMS), St George's University of London, London, UK., Al-Aama JY; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, Saudi Arabia.
Publikováno v:
The Journal of dermatology [J Dermatol] 2015 Jul; Vol. 42 (7), pp. 706-9. Date of Electronic Publication: 2015 Apr 09.
Autor:
Hussain MR; Faculty of Genetic Medicine, King Abdulaziz University, Jeddah, Saudi Arabia ; CAS-Institute of microbiology, University of Chinese Academy of Sciences, Beijing, China., Baig M; Faculty of Medicine, King Abdulaziz University, Rabigh Branch, Saudi Arabia., Mohamoud HS; Human Genetics Research Centre, Division of Biomedical Sciences (BMS), St. George's University of London (SGUL), London, UK., Ulhaq Z; Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi 75270, Pakistan., Hoessli DC; Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi 75270, Pakistan., Khogeer GS; Department of Biology, Genomics and Biotechnology Section, King Abdulaziz University, Jeddah, Saudi Arabia., Al-Sayed RR; Department of Biology, Genomics and Biotechnology Section, King Abdulaziz University, Jeddah, Saudi Arabia., Al-Aama JY; Faculty of Genetic Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Publikováno v:
Saudi journal of biological sciences [Saudi J Biol Sci] 2015 Jul; Vol. 22 (4), pp. 359-73. Date of Electronic Publication: 2014 Oct 23.
Autor:
Alrayes N; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, 80205, Kingdom of Saudi Arabia. nuharayes@gmail.com.; Division of Biomedical Sciences (BMS), Human Genetics Research Center, St. George's University of London (SGUL), London, SW17 0RE, UK. nuharayes@gmail.com., Mohamoud HS; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, 80205, Kingdom of Saudi Arabia. husseinsheekh@yahoo.co.uk.; Division of Biomedical Sciences (BMS), Human Genetics Research Center, St. George's University of London (SGUL), London, SW17 0RE, UK. husseinsheekh@yahoo.co.uk., Jelani M; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, 80205, Kingdom of Saudi Arabia. musharraf_jelani@yahoo.com.; Medical Genetics and Molecular Biology Unit, Biochemistry Department, Institute of Basic Medical Sciences, Khyber Medical University, Peshawar, 25000, Pakistan. musharraf_jelani@yahoo.com., Ahmad S; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia. sahmad@yahoo.com., Vadgama N; Division of Biomedical Sciences (BMS), Human Genetics Research Center, St. George's University of London (SGUL), London, SW17 0RE, UK. nvadgama@sgul.ac.uk., Bakur K; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, 80205, Kingdom of Saudi Arabia. kbakur@yahoo.com., Simpson M; Genetics and Molecular Medicine, King's College London, Guy's Hospital, London, SE1 9RT, UK. michael.simpson@kcl.ac.uk., Al-Aama JY; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah, 80205, Kingdom of Saudi Arabia. al-aama@yahoo.com.; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia. al-aama@yahoo.com., Nasir J; Division of Biomedical Sciences (BMS), Human Genetics Research Center, St. George's University of London (SGUL), London, SW17 0RE, UK. p1106394@sgul.ac.uk.
Publikováno v:
BMC research notes [BMC Res Notes] 2015 Jun 27; Vol. 8, pp. 271. Date of Electronic Publication: 2015 Jun 27.
Autor:
Jelani M; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah 21589, Saudi Arabia; Medical Genetics and Molecular Biology Unit, Biochemistry Department, Institute of Basic Medical Sciences, Khyber Medical University, Peshawar 25000, Pakistan. Electronic address: mjelani@kau.edu.sa., Ahmed S; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah 21589, Saudi Arabia; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Almramhi MM; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah 21589, Saudi Arabia., Mohamoud HS; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah 21589, Saudi Arabia; Human Genetics Research Centre, Division of Biomedical Sciences (BMS), St. George's, University of London (SGUL), London SW17 0RE, United Kingdom., Bakur K; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah 21589, Saudi Arabia., Anshasi W; Department of Pediatrics, King Abdulaziz University Hospital, Jeddah, Saudi Arabia., Wang J; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah 21589, Saudi Arabia; BGI-Shenzhen, Shenzhen 518083, China., Al-Aama JY; Princess Al-Jawhara Albrahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University, Jeddah 21589, Saudi Arabia; Department of Genetic Medicine, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Publikováno v:
European journal of medical genetics [Eur J Med Genet] 2015 Apr; Vol. 58 (4), pp. 216-21. Date of Electronic Publication: 2015 Feb 23.