Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Gebril Oh"'
Publikováno v:
Journal of Neurology, Neurological Science and Disorders. 3:028-032
Megalocornea is a defi ning feature of megalocornea-mental retardation (MMR) syndromealso calledNeuhauser syndrome, a rare condition of unknown etiology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfb8e9c19f469ff3c624f1bd0cd9fce4
https://doi.org/10.17352/jnnsd.000017
https://doi.org/10.17352/jnnsd.000017
Autor:
Gebril, OH
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 15, No 1 (2014); 91-94
Background: Allgrove or AAA (Triple A) syndrome is a rare autosomal recessive disease characterized by achalasia, alacrima, adrenocorticotrophic insufficiency and some neurologic abnormalities.Case report: Here we report two brothers 13 and 15 years
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=78975075580c::22cae567eb0d49a5505f166b9efb9a7f
https://www.ajol.info/index.php/ejhg/article/view/100853
https://www.ajol.info/index.php/ejhg/article/view/100853
Autor:
Elhadidy ME; Children with Special Needs Research Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt., Kilany A; Children with Special Needs Research Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.; Pediatric Neurology Research Field, Medical Research Centre of Excellence, National Research Centre, Cairo, Egypt., Gebril OH; Children with Special Needs Research Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt., Nashaat NH; Children with Special Needs Research Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt. dr.neveennashaat@gmail.com.; Learning Disability and Neurorehabilitation Research Field, Medical Research Centre of Excellence, National Research Centre, Cairo, Egypt. dr.neveennashaat@gmail.com., Zeidan HM; Children with Special Needs Research Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt., Elsaied A; Children with Special Needs Research Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.; Learning Disability and Neurorehabilitation Research Field, Medical Research Centre of Excellence, National Research Centre, Cairo, Egypt., Hashish AF; Children with Special Needs Research Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt., Abdelraouf ER; Children with Special Needs Research Department, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.; Learning Disability and Neurorehabilitation Research Field, Medical Research Centre of Excellence, National Research Centre, Cairo, Egypt.
Publikováno v:
Journal of molecular neuroscience : MN [J Mol Neurosci] 2023 Jan; Vol. 73 (1), pp. 39-46. Date of Electronic Publication: 2022 Dec 23.
Autor:
Meguid NA; Department of Research on Children with Special Needs, National Research Centre, Giza, Egypt.; CONEM Egypt Child Brain Research Group, National Research Center, Giza, Egypt., Bjørklund G; Council for Nutritional and Environmental Medicine (CONEM), Toften 24, 8610, Mo I Rana, Norway. bjorklund@conem.org., Gebril OH; Department of Research on Children with Special Needs, National Research Centre, Giza, Egypt., Doşa MD; Department of Pharmacology, Faculty of Medicine, Ovidius University, Constanţa, Romania., Anwar M; Department of Research on Children with Special Needs, National Research Centre, Giza, Egypt.; Department of Basic Sciences and Biomechanics, Faculty of Physical Therapy, Heliopolis University, Cairo, Egypt., Elsaeid A; Department of Research on Children with Special Needs, National Research Centre, Giza, Egypt., Gaber A; Department of Research on Children with Special Needs, National Research Centre, Giza, Egypt., Chirumbolo S; Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.; CONEM Scientific Secretary, Verona, Italy.
Publikováno v:
Acta neurologica Belgica [Acta Neurol Belg] 2019 Dec; Vol. 119 (4), pp. 577-583. Date of Electronic Publication: 2019 Jul 13.
Autor:
Abdelraouf ER; 1Research on Children with Special Needs Department, Medical Research division, National Research Centre, Elbuhouth Street, 12622, Dokki, Cairo, Egypt.; 2Learning Disability Research Clinic, Medical Research Centre of Excellence, National Research Centre, Cairo, Egypt., Kilany A; 1Research on Children with Special Needs Department, Medical Research division, National Research Centre, Elbuhouth Street, 12622, Dokki, Cairo, Egypt.; 3Pediatric Neurology Research Clinic, Medical Research Centre of Excellence, National Research Centre, Cairo, Egypt., Hashish AF; 1Research on Children with Special Needs Department, Medical Research division, National Research Centre, Elbuhouth Street, 12622, Dokki, Cairo, Egypt., Gebril OH; 1Research on Children with Special Needs Department, Medical Research division, National Research Centre, Elbuhouth Street, 12622, Dokki, Cairo, Egypt., Helal SI; 1Research on Children with Special Needs Department, Medical Research division, National Research Centre, Elbuhouth Street, 12622, Dokki, Cairo, Egypt.; 4Neurology Research Clinic, Medical Research Centre of Excellence, National Research Centre, Cairo, Egypt., Hasan HM; 1Research on Children with Special Needs Department, Medical Research division, National Research Centre, Elbuhouth Street, 12622, Dokki, Cairo, Egypt.; 5Neuropsychiatry Department, Faculty of Medicine, Helwan University, Cairo, Egypt., Nashaat NH; 1Research on Children with Special Needs Department, Medical Research division, National Research Centre, Elbuhouth Street, 12622, Dokki, Cairo, Egypt.; 2Learning Disability Research Clinic, Medical Research Centre of Excellence, National Research Centre, Cairo, Egypt.; 6Phoniatric Research Clinic, Medical Research Centre of Excellence, National Research Centre, Cairo, Egypt.
Publikováno v:
The Egyptian journal of neurology, psychiatry and neurosurgery [Egypt J Neurol Psychiatr Neurosurg] 2018; Vol. 54 (1), pp. 39. Date of Electronic Publication: 2018 Nov 27.
Autor:
Boycott KM; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON K1H 8L1, Canada. Electronic address: kboycott@cheo.on.ca., Beaulieu CL; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON K1H 8L1, Canada., Kernohan KD; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON K1H 8L1, Canada., Gebril OH; National Research Centre, El Bohoth Street, Dokki, Giza 12622, Egypt., Mhanni A; Section of Genetics and Metabolism, Children's Hospital and the Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, MB R3A 1S1, Canada., Chudley AE; Section of Genetics and Metabolism, Children's Hospital and the Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, MB R3A 1S1, Canada., Redl D; Department of Medical Genetics, University of Calgary, Calgary, AB T2N 4N1, Canada., Qin W; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON K1H 8L1, Canada., Hampson S; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON K1H 8L1, Canada., Küry S; Department of Medical Genetics, CHU Nantes, Nantes 44093, France., Tetreault M; Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada., Puffenberger EG; Clinic for Special Children, Strasburg, PA 17579, USA., Scott JN; Department of Radiology, Foothills Hospital, Calgary, AB T2N 2T9, Canada., Bezieau S; Department of Medical Genetics, CHU Nantes, Nantes 44093, France., Reis A; Institute of Human Genetics, FAU Erlangen-Nürnberg, Erlangen 91054, Germany., Uebe S; Institute of Human Genetics, FAU Erlangen-Nürnberg, Erlangen 91054, Germany., Schumacher J; Institute of Human Genetics, University of Bonn, Bonn 53012, Germany., Hegele RA; Robarts Research Institute and University of Western Ontario, London, ON N6A 5B7, Canada., McLeod DR; Department of Medical Genetics, University of Calgary, Calgary, AB T2N 4N1, Canada., Gálvez-Peralta M; Department of Environmental Health, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA., Majewski J; Department of Human Genetics, McGill University, Montreal, QC H3A 1B1, Canada., Ramaekers VT; Department of Paediatric Neurology, Centre Hospitalier Universitaire, Liege 4032, Belgium., Nebert DW; Department of Environmental Health, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA; Department of Pediatrics & Molecular Developmental Biology, Division of Human Genetics, Cincinnati Children's Hospital, Cincinnati, OH 45229, USA., Innes AM; Department of Medical Genetics, University of Calgary, Calgary, AB T2N 4N1, Canada., Parboosingh JS; Department of Medical Genetics, University of Calgary, Calgary, AB T2N 4N1, Canada., Abou Jamra R; Institute of Human Genetics, FAU Erlangen-Nürnberg, Erlangen 91054, Germany. Electronic address: rami.aboujamra@medizin.uni-leipzig.de.
Publikováno v:
American journal of human genetics [Am J Hum Genet] 2015 Dec 03; Vol. 97 (6), pp. 886-93.
Autor:
Meguid NA; Department of Research on Children with Special Needs, Medical Division National Research Centre, Cairo, Egypt., Gebril OH; Department of Research on Children with Special Needs, Medical Division National Research Centre, Cairo, Egypt., Khalil RO; Department of Research on Children with Special Needs, Medical Division National Research Centre, Cairo, Egypt.
Publikováno v:
Advanced biomedical research [Adv Biomed Res] 2015 May 11; Vol. 4, pp. 94. Date of Electronic Publication: 2015 May 11 (Print Publication: 2015).
Autor:
Abdel-Meguid N; Department of Children with Special Needs, Medical Division, National Research Centre, Cairo, Egypt., Gebril OH; Department of Children with Special Needs, Medical Division, National Research Centre, Cairo, Egypt., Abdelraouf ER; Department of Children with Special Needs, Medical Division, National Research Centre, Cairo, Egypt., Shafie MA; Department of Children with Special Needs, Medical Division, National Research Centre, Cairo, Egypt., Bahgat M; Department of Ear Nose and Throat, Faculty of Medicine, Cairo University, Cairo, Egypt.
Publikováno v:
Journal of family medicine and primary care [J Family Med Prim Care] 2014 Jul; Vol. 3 (3), pp. 275-8.
Autor:
Janaway BM; Sheffield Institute for Translational Neuroscience, University of Sheffield, Sheffield, UK., Simpson JE, Hoggard N, Highley JR, Forster G, Drew D, Gebril OH, Matthews FE, Brayne C, Wharton SB, Ince PG
Publikováno v:
Neuropathology and applied neurobiology [Neuropathol Appl Neurobiol] 2014 Apr; Vol. 40 (3), pp. 258-69.
Autor:
Gebril OH; Human Genetics Department, Medical Division, National Research Centre, Dokki, Cairo, Egypt. olahossny@hotmail.com, Simpson JE, Kirby J, Brayne C, Ince PG
Publikováno v:
Neuromolecular medicine [Neuromolecular Med] 2011 Dec; Vol. 13 (4), pp. 289-99. Date of Electronic Publication: 2011 Oct 07.