Zobrazeno 1 - 10 of 308 pro vyhledávání: '"Mavraki, E"'
2
Editorial & Opinion
Spinal cord ischemia complicating BNT162b2 mRNA COVID-19 vaccination.
Autor: Fotiadou A; Neurology Department, Democritus University of Thrace, 68100, Alexandroupolis, Greece., Tsiptsios D; Neurology Department, Democritus University of Thrace, 68100, Alexandroupolis, Greece. tsiptsios.dimitrios@yahoo.gr., Kitmeridou S; Neurology Department, Democritus University of Thrace, 68100, Alexandroupolis, Greece., Mavraki E; Neurology Department, Democritus University of Thrace, 68100, Alexandroupolis, Greece., Iliopoulos I; Neurology Department, Democritus University of Thrace, 68100, Alexandroupolis, Greece.
Publikováno v: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2023 Feb; Vol. 44 (2), pp. 457-459. Date of Electronic Publication: 2022 Nov 03.
Zobrazit plný text záznamu
3
Akademický článek
Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines.
Autor: Mavraki E; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK., Labrum R; Neurogenetics Unit, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK., Sergeant K; Oxford Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust, Oxford, UK., Alston CL; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK., Woodward C; Neurogenetics Unit, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK., Smith C; Oxford Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust, Oxford, UK., Knowles CVY; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK., Patel Y; Neurogenetics Unit, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK., Hodsdon P; Oxford Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust, Oxford, UK., Baines JP; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK., Blakely EL; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK., Polke J; Neurogenetics Unit, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK., Taylor RW; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK., Fratter C; Oxford Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust, Oxford, UK. Carl.Fratter@ouh.nhs.uk.
Publikováno v: European journal of human genetics : EJHG [Eur J Hum Genet] 2023 Feb; Vol. 31 (2), pp. 148-163. Date of Electronic Publication: 2022 Dec 13.
Zobrazit plný text záznamu
4
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
5
Akademický článek
Computed tomographic appearance of transcaval ureter in two dogs and three cats: A novel CVC congenital malformation.
Autor: Spediacci C; Department of Veterinary Medicine and Animal Science (DIVAS), University of Milan, Lodi, LO, Italy., Longo M; Department of Veterinary Medicine and Animal Science (DIVAS), University of Milan, Lodi, LO, Italy.; Diagnostic Imaging Department C.T.O. Veterinary, via C. Festa Arenzano (Genova), Genova, Italy.; Antech Imaging Services, Irvine, CA, United States., Specchi S; Antech Imaging Services, Irvine, CA, United States.; Ospedale Veterinario I Portoni Rossi, Bologna, Italy., Pey P; Antech Imaging Services, Irvine, CA, United States.; Ospedale Veterinario I Portoni Rossi, Bologna, Italy.; Service d'Imagerie Médicale, Centre Hospitalier Universitaire Vétérinaire d'Alfort, Ecole Nationale Vétérinaire d'Alfort, Maisons-Alfort, France., Rabba S; Department of Diagnostic Imaging, Istituto Veterinario di Novara, Granozzo con Monticello, NO, Italy., Mavraki E; Vets4life Veterinary Clinic, Pikermi, Athens, Greece., Di Giancamillo M; Department of Veterinary Medicine and Animal Science (DIVAS), University of Milan, Lodi, LO, Italy., Panopoulos I; Alphavet Veterinary Diagnostic Imaging, Kifisia, Athens, Greece.
Publikováno v: Frontiers in veterinary science [Front Vet Sci] 2022 Sep 08; Vol. 9, pp. 965185. Date of Electronic Publication: 2022 Sep 08 (Print Publication: 2022).
Zobrazit plný text záznamu
6
Editorial & Opinion
Cerebral venous thrombosis: an unexpected Brissaud-Sicard syndrome mimicker.
Autor: Fotiadou A; Neurology Department, Democritus University of Thrace, 68100, Alexandroupolis, Greece., Tsiptsios D; Neurology Department, Democritus University of Thrace, 68100, Alexandroupolis, Greece. tsiptsios.dimitrios@yahoo.gr., Mavraki E; Neurology Department, Democritus University of Thrace, 68100, Alexandroupolis, Greece., Psatha EA; Radiology Department, Democritus University of Thrace, Alexandroupolis, Greece., Iliopoulos I; Neurology Department, Democritus University of Thrace, 68100, Alexandroupolis, Greece.
Publikováno v: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2022 May; Vol. 43 (5), pp. 3439-3441. Date of Electronic Publication: 2022 Mar 14.
Zobrazit plný text záznamu
7
Akademický článek
"Sleeping Beauty Syndrome" and Psychosis as Precursory Symptoms of Multiple Sclerosis: A Rare Case and Literature Review.
Autor: Evagorou O; Department of Psychiatry, Medical School, Democritus University of Thrace., Arvaniti A, Angelopoulou C; Neurology, University General Hospital of Alexandroupolis, Alexandroupolis, Greece., Mavraki E; Neurology, University General Hospital of Alexandroupolis, Alexandroupolis, Greece., Mikellides G, Samakouri M
Publikováno v: The Journal of nervous and mental disease [J Nerv Ment Dis] 2021 Dec 01; Vol. 209 (12), pp. 933-935.
Zobrazit plný text záznamu
8
Akademický článek
Multiple sclerosis in a patient with cryopyrin-associated autoinflammatory syndrome: Evidence that autoinflammation is the common link.
Autor: Papagoras C; First Department of Internal Medicine, University Hospital of Alexandroupolis, Democritus University of Thrace, Alexandroupolis, Greece; Laboratory of Molecular Hematology, Democritus University of Thrace, Alexandroupolis, Greece., Lampropoulou V; First Department of Internal Medicine, University Hospital of Alexandroupolis, Democritus University of Thrace, Alexandroupolis, Greece., Mavraki E; Department of Neurology, University Hospital of Alexandroupolis, Alexandroupolis, Greece., Chrysanthopoulou A; Laboratory of Molecular Hematology, Democritus University of Thrace, Alexandroupolis, Greece., Deftereos S; Department of Radiology, University Hospital of Alexandroupolis, Democritus University of Thrace, Alexandroupolis, Greece., Aróstegui JI; Department of Immunology, Hospital Clinic, Barcelona, Spain; Institut d' Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Barcelona, Spain., Skendros P; First Department of Internal Medicine, University Hospital of Alexandroupolis, Democritus University of Thrace, Alexandroupolis, Greece; Laboratory of Molecular Hematology, Democritus University of Thrace, Alexandroupolis, Greece., Ritis K; First Department of Internal Medicine, University Hospital of Alexandroupolis, Democritus University of Thrace, Alexandroupolis, Greece; Laboratory of Molecular Hematology, Democritus University of Thrace, Alexandroupolis, Greece. Electronic address: kritis@med.duth.gr.
Publikováno v: Clinical immunology (Orlando, Fla.) [Clin Immunol] 2021 Jun; Vol. 227, pp. 108750. Date of Electronic Publication: 2021 May 01.
Zobrazit plný text záznamu
9
Akademický článek
Genetic landscape of primary mitochondrial diseases in children and adults using molecular genetics and genomic investigations of mitochondrial and nuclear genome.
Autor: Ambrose, Anastasia1 (AUTHOR), Bahl, Shalini2,3 (AUTHOR), Sharma, Saloni1 (AUTHOR), Zhang, Dan1 (AUTHOR), Hung, Clara1 (AUTHOR), Jain-Ghai, Shailly1 (AUTHOR), Chan, Alicia1 (AUTHOR), Mercimek-Andrews, Saadet1,4,5,6 (AUTHOR) saadet@ualberta.ca
Publikováno v: Orphanet Journal of Rare Diseases. 11/12/2024, Vol. 19 Issue 1, p1-13. 13p.
Zobrazit plný text záznamu
10
Akademický článek
The quality and detection limits of mitochondrial heteroplasmy by long read nanopore sequencing.
Autor: Slapnik, Barbara1,2 (AUTHOR), Šket, Robert1,2 (AUTHOR), Črepinšek, Klementina1,2 (AUTHOR), Tesovnik, Tine1,2 (AUTHOR), Bizjan, Barbara Jenko1,2 (AUTHOR), Kovač, Jernej1,2 (AUTHOR) jernej.kovac@kclj.si
Publikováno v: Scientific Reports. 11/5/2024, Vol. 14 Issue 1, p1-12. 12p.
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje