Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Mohammed SEM"'
Publikováno v:
Journal of Nutrition and Metabolism, Vol 2021 (2021)
Background. Child undernourishment is the disturbance of body function arising from a dietary imbalance between body demand and supply, which is the most serious public health problem in developing countries. Objective. This study aimed to assess the
Externí odkaz:
https://doaj.org/article/692192ee5e904d74819ac7c3ed0668e2
Publikováno v:
Bulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca: Agriculture, Vol 73, Iss 2, Pp 306-310 (2016)
Proline accumulation, as a marker of resistance to the abiotic constraints, was evaluated on seventeen genotypes of Durum wheat (Triticum Durum Desf) under water stress conditions. An experiment was implemented at INRAA research station located at Ba
Externí odkaz:
https://doaj.org/article/61c8f7c3d8824e5d9f7e8eeeb339b559
Autor:
Mohammed SEM; Department of Biomedical Sciences and Pathobiology, Centre of Biomedical Sciences, Institute of Physiology, Pathophysiology and Biophysics, Vetmeduni, Vienna, Austria., Nowikovsky K; Department of Biomedical Sciences and Pathobiology, Centre of Biomedical Sciences, Institute of Physiology, Pathophysiology and Biophysics, Vetmeduni, Vienna, Austria. Electronic address: Karin.nowikovsky@vetmeduni.ac.at.
Publikováno v:
Pharmacological research [Pharmacol Res] 2024 Oct 30; Vol. 210, pp. 107485. Date of Electronic Publication: 2024 Oct 30.
Autor:
Shokre ES; Department of Psychiatric Mental Health Nursing, Faculty of Nursing, Fayoum University, Fayoum, Egypt. ess03@fayoum.edu.eg., Mohammed SEM; Department of Medical-Surgical Nursing, Faculty of Nursing, Mansoura University, Mansoura, Egypt., Elhapashy HMM; Department of Medical-Surgical Nursing, Faculty of Nursing, Mansoura University, Mansoura, Egypt., Elsharkawy NB; College of Nursing, Jouf University, Sakaka, 72388, Saudi Arabia.; Department of Maternal and New-born Health Nursing, Faculty of Nursing, Cairo University, Cairo, 11562, Egypt., Ramadan OME; College of Nursing, Jouf University, Sakaka, 72388, Saudi Arabia.; Department of Paediatric Nursing, Faculty of Nursing, Cairo University, Cairo, 11562, Egypt., Abdelaziz EM; College of Nursing, Jouf University, Sakaka, 72388, Saudi Arabia.; Department of Psychiatric Mental Health Nursing, Faculty of Nursing, Cairo University, Cairo, 11562, Egypt.
Publikováno v:
BMC nursing [BMC Nurs] 2024 Jan 16; Vol. 23 (1), pp. 45. Date of Electronic Publication: 2024 Jan 16.
Autor:
Austin S; Department of Internal Medicine I and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria., Mekis R; Department of Internal Medicine I and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.; Department of Biomedical Sciences, Institute of Physiology, Pathophysiology and Biophysics, University of Veterinary Medicine Vienna, Vienna, Austria., Mohammed SEM; Department of Biomedical Sciences, Institute of Physiology, Pathophysiology and Biophysics, University of Veterinary Medicine Vienna, Vienna, Austria., Scalise M; Department DiBEST (Biologia, Ecologia, Scienze della Terra) Unit of Biochemistry and Molecular Biotechnology, University of Calabria, Arcavacata di Rende, Italy., Wang WA; Department of Cell Physiology & Metabolism, University of Geneva, Geneva, Switzerland., Galluccio M; Department DiBEST (Biologia, Ecologia, Scienze della Terra) Unit of Biochemistry and Molecular Biotechnology, University of Calabria, Arcavacata di Rende, Italy., Pfeiffer C; Department of Internal Medicine I and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria., Borovec T; Department of Internal Medicine I and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.; Department of Biomedical Sciences, Institute of Physiology, Pathophysiology and Biophysics, University of Veterinary Medicine Vienna, Vienna, Austria., Parapatics K; CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria., Vitko D; CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria., Dinhopl N; Department of Pathobiology, Institute of Pathology, University of Veterinary Medicine, Vienna, Austria., Demaurex N; Department of Cell Physiology & Metabolism, University of Geneva, Geneva, Switzerland., Bennett KL; CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria., Indiveri C; Department DiBEST (Biologia, Ecologia, Scienze della Terra) Unit of Biochemistry and Molecular Biotechnology, University of Calabria, Arcavacata di Rende, Italy.; CNR Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies (IBIOM), Bari, Italy., Nowikovsky K; Department of Internal Medicine I and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.; Department of Biomedical Sciences, Institute of Physiology, Pathophysiology and Biophysics, University of Veterinary Medicine Vienna, Vienna, Austria.
Publikováno v:
EMBO reports [EMBO Rep] 2022 Dec 06; Vol. 23 (12), pp. e54978. Date of Electronic Publication: 2022 Nov 02.
Autor:
Kaiyrzhanov R; Department of Neuromuscular Diseases, University College London, Queen Square, Institute of Neurology, London WC1N 3BG, UK., Mohammed SEM; Department of Biomedical Sciences, Institute of Physiology, Pathophysiology and Biophysics, University of Veterinary Medicine Vienna, Vienna 1210, Austria., Maroofian R; Department of Neuromuscular Diseases, University College London, Queen Square, Institute of Neurology, London WC1N 3BG, UK., Husain RA; Department of Neuropediatrics, Jena University Hospital, Jena 07747, Germany; Center for Rare Diseases, Jena University Hospital, Jena 07747, Germany., Catania A; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan 20126, Italy., Torraco A; Unit of Muscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, IRCCS, Rome 00146, Italy., Alahmad A; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne NE2 4HH, UK; Kuwait Medical Genetics Centre, Al-Sabah Medical Area 80901, Kuwait., Dutra-Clarke M; Division of Medical Genetics, Department of Pediatrics, David Geffen School of Medicine, the University of California at Los Angeles, Los Angeles, CA 90095, USA., Grønborg S; Center for Rare Diseases, Department of Pediatrics and Department of Genetics, Copenhagen University Hospital Rigshospitalet, Blegdamsvej 9, Copenhagen 2100, Denmark., Sudarsanam A; West Midlands Regional Genetics Service, Birmingham Women's and Children's Hospital, Birmingham B15 2TG, UK., Vogt J; West Midlands Regional Genetics Service, Birmingham Women's and Children's Hospital, Birmingham B15 2TG, UK., Arrigoni F; Paediatric Radiology and Neuroradiology Department, V. Buzzi Children's Hospital, Milan 20154, Italy., Baptista J; Peninsula Medical School, Faculty of Health, University of Plymouth, Plymouth PL4 8AA, UK., Haider S; Paediatrics Wah Medical College NUMS, Wah Cantonment, Punjab 44000, Pakistan., Feichtinger RG; University Children's Hospital, Salzburger Landeskliniken (SALK) and Paracelsus Medical University (PMU), Salzburg 5020, Austria., Bernardi P; Department of Biomedical Sciences, University of Padova, Via Ugo Bassi 58/B, Padova 35131, Italy., Zulian A; Department of Biomedical Sciences, University of Padova, Via Ugo Bassi 58/B, Padova 35131, Italy., Gusic M; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany; DZHK (German Centre for Cardiovascular Research), Partner Site Munich Heart Alliance, Munich 81675, Germany; Institute of Human Genetics, Technical University of Munich, Munich 81675, Germany., Efthymiou S; Department of Neuromuscular Diseases, University College London, Queen Square, Institute of Neurology, London WC1N 3BG, UK., Bai R; GeneDx Inc, Gaithersburg, MD 20877, USA., Bibi F; Institute of Biochemistry and Biotechnology, Pir Mehar Ali Shah Arid Agriculture University, Rawalpindi 44000, Pakistan., Horga A; Department of Neuromuscular Diseases, University College London, Queen Square, Institute of Neurology, London WC1N 3BG, UK; Neuromuscular Diseases Unit, Department of Neurology, Hospital Clinico San Carlos and San Carlos Health Research Institute (IdISSC), Madrid 28040, Spain., Martinez-Agosto JA; Department of Human Genetics, Division of Medical Genetics, Department of Pediatrics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA., Lam A; Neurometabolic Unit, National Hospital for Neurology and Neurosurgery, London, UK; Department of Chemical Pathology, Great Ormond Street Hospital, WC1N 3BG London, UK., Manole A; Department of Neuromuscular Diseases, University College London, Queen Square, Institute of Neurology, London WC1N 3BG, UK., Rodriguez DP; Department of Clinical Movement Neurosciences, Royal Free Campus, University College of London, Queen Square Institute of Neurology, London WC1N 3BG, UK., Durigon R; Department of Clinical Movement Neurosciences, Royal Free Campus, University College of London, Queen Square Institute of Neurology, London WC1N 3BG, UK., Pyle A; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne NE2 4HH, UK., Albash B; Kuwait Medical Genetics Centre, Al-Sabah Medical Area 80901, Kuwait., Dionisi-Vici C; Division of Metabolism, Bambino Gesù Children's Hospital, IRCCS, Rome 00146, Italy., Murphy D; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK., Martinelli D; Division of Metabolism, Bambino Gesù Children's Hospital, IRCCS, Rome 00146, Italy., Bugiardini E; Department of Neuromuscular Diseases, University College London, Queen Square, Institute of Neurology, London WC1N 3BG, UK., Allis K; GeneDx Inc, Gaithersburg, MD 20877, USA., Lamperti C; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan 20126, Italy., Reipert S; Core Facility of Cell Imaging and Ultrastructure Research, University of Vienna, Djerassiplatz 1, 1030 Wien, Austria., Risom L; Department of Genetics, Copenhagen University Hospital Rigshospitalet Blegdamsvej, Copenhagen 2100, Denmark., Laugwitz L; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, 72076 Tübingen, Germany; Department of Neuropediatrics, Developmental Neurology and Social Pediatrics, University of Tübingen, Tübingen 72076, Germany., Di Nottia M; Unit of Muscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, IRCCS, Rome 00146, Italy., McFarland R; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne NE2 4HH, UK; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne NE1 4LP, UK., Vilarinho L; Unit of Neonatal Screening, Metabolism and Genetics, Department of Human Genetics, National Institute of Health Dr Ricardo Jorge, Porto 4000-055, Portugal., Hanna M; Department of Neuromuscular Diseases, University College London, Queen Square, Institute of Neurology, London WC1N 3BG, UK., Prokisch H; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany; Institute of Human Genetics, Technical University of Munich, Munich 81675, Germany., Mayr JA; University Children's Hospital, Salzburger Landeskliniken (SALK) and Paracelsus Medical University (PMU), Salzburg 5020, Austria., Bertini ES; Unit of Muscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, IRCCS, Rome 00146, Italy., Ghezzi D; Unit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan 20126, Italy; Department of Pathophysiology and Transplantation, University of Milan, Milan 20122, Italy., Østergaard E; Department of Genetics, Copenhagen University Hospital Rigshospitalet Blegdamsvej, Copenhagen 2100, Denmark; Institute for Clinical Medicine, University of Copenhagen, Copenhagen 2200, Denmark., Wortmann SB; University Children's Hospital, Salzburger Landeskliniken (SALK) and Paracelsus Medical University (PMU), Salzburg 5020, Austria; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg 85764, Germany; Institute of Human Genetics, Technical University of Munich, Munich 81675, Germany; Radboud Center for Mitochondrial Medicine, Department of Pediatrics, Amalia Children's Hospital, Radboudumc, Nijmegen 6525 EZ, the Netherlands., Carrozzo R; Unit of Muscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, IRCCS, Rome 00146, Italy., Haack TB; Department of Neuropediatrics, Developmental Neurology and Social Pediatrics, University of Tübingen, Tübingen 72076, Germany; Centre for Rare Diseases, University of Tuebingen, Tübingen 72076, Germany., Taylor RW; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne NE2 4HH, UK; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne NE1 4LP, UK., Spinazzola A; Department of Clinical Movement Neurosciences, Royal Free Campus, University College of London, Queen Square Institute of Neurology, London WC1N 3BG, UK., Nowikovsky K; Department of Biomedical Sciences, Institute of Physiology, Pathophysiology and Biophysics, University of Veterinary Medicine Vienna, Vienna 1210, Austria; Department of Internal Medicine I, ASCTR and Comprehensive Cancer Center, Medical University of Vienna, Vienna 1090, Austria. Electronic address: karin.nowikovsky@vetmeduni.ac.at., Houlden H; Department of Neuromuscular Diseases, University College London, Queen Square, Institute of Neurology, London WC1N 3BG, UK. Electronic address: h.houlden@ucl.ac.uk.
Publikováno v:
American journal of human genetics [Am J Hum Genet] 2022 Sep 01; Vol. 109 (9), pp. 1692-1712.
Autor:
Mehdar KM; Department of Anatomy, Faculty of Medicine, Najran University, Najran, Kingdom of Saudi Arabia. khlood.mehdar02@gmail.com., Alsareii SA; Department of Surgery, Faculty of Medicine, Najran University, Najran, Kingdom of Saudi Arabia, Najran, Saudi Arabia., Alshafie SEM; Department of Anatomy, Faculty of Medicine, Najran University, Najran, Kingdom of Saudi Arabia., Al-Rafiah AR; Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdul Aziz University, Kingdom of Saudi Arabia, Jeddah, Saudi Arabia., Alamri AM; Department of Surgery, Faculty of Medicine, Najran University, Najran, Kingdom of Saudi Arabia, Najran, Saudi Arabia.
Publikováno v:
Folia histochemica et cytobiologica [Folia Histochem Cytobiol] 2020; Vol. 58 (4), pp. 235-246. Date of Electronic Publication: 2020 Dec 18.