المؤلفون: Sofia Leka-Emiri, Adamantios Katerelos, Konstantinos A. Voudris, Artemis Doulgeraki, Emmanouil Manolakos, Anastasia Korona, Ioannis Papoulidis, Sotiria Mastroyanni, Athina Ververi, Stella Mouskou, Georgios Vartzelis

المصدر: Molecular Syndromology. 12:194-200

مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, biology, business.industry, medicine.disease, Hypotonia, Epilepsy, Spermine synthase, Intellectual disability, Genetics, medicine, biology.protein, Missense mutation, medicine.symptom, business, Kyphoscoliosis, Gene, Genetics (clinical), Snyder-Robinson syndrome

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::a7b594aa4c2171b710c2960dd9fd05afTest
https://doi.org/10.1159/000514122Test

المؤلفون: Manju A. Kurian, Dora Steel, Francesco Muntoni, Sniya Sudhakar, Richard H Scott, Lucinda Carr, Kshitij Mankad, Alison Male, Tarishi Nemani, Marios Kaliakatsos, Athina Ververi, Spas Getov, Mary M. Reilly, Pinki Munot, Catherine DeVile

المصدر: Journal of the Peripheral Nervous System. 25:117-124

مصطلحات موضوعية: Adult, Male, Nervous system, Pediatrics, medicine.medical_specialty, Sensory axonal neuropathy, Kinesins, Primary Dysautonomias, Young Adult, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Atrophy, Central Nervous System Diseases, medicine, Humans, Spasticity, Child, Retrospective Studies, Dystonia, Spastic Paraplegia, Hereditary, business.industry, General Neuroscience, Infant, Peripheral Nervous System Diseases, Dysautonomia, medicine.disease, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Peripheral nervous system, Female, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c80a3a29fdcf4ef73726251090fa2a5Test
https://doi.org/10.1111/jns.12368Test

المؤلفون: Athina Ververi

مصطلحات موضوعية: medicine.medical_specialty, education.field_of_study, Sensory processing, business.industry, medicine.medical_treatment, Population, Audiology, medicine.disease, Lateralization of brain function, Peripheral, Correlation, Somatosensory evoked potential, medicine, Childhood Autism Rating Scale, Autism, business, education

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::2834f154fa16b37cd60be2601aef04b3Test
https://doi.org/10.12681/eadd/34645Test

المؤلفون: John Dean, Ddd Study, A Ververi, Miranda Splitt, Angela F. Brady

المصدر: Clinical Genetics. 93:286-292

مصطلحات موضوعية: 0301 basic medicine, Genetics, biology, Inflammation, medicine.disease, Phenotype, QRICH1, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Speech delay, medicine, biology.protein, Autism, Creatine kinase, medicine.symptom, Gene, 030217 neurology & neurosurgery, Genetics (clinical), Exome sequencing

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::a977e09c4016dc1a5216313b14007302Test
https://doi.org/10.1111/cge.13096Test

المؤلفون: Athina Ververi, Beverley Bewes, Louise Busby, Natalie Canham, Lily Islam, Caroline Sullivan

المصدر: Cytogenetic and Genome Research. 152:132-136

مصطلحات موضوعية: 0301 basic medicine, Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Microcephaly, Ataxia, Genetic counseling, 030105 genetics & heredity, Biology, medicine.disease, 03 medical and health sciences, Angelman syndrome, UBE3A, medicine, Multiplex ligation-dependent probe amplification, medicine.symptom, Allele, Molecular Biology, Genetics (clinical), Aunt

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::3ea744a8cb9d4be50ab864760673744fTest
https://doi.org/10.1159/000480030Test

المؤلفون: A. Ververi, Eletherios Kontopoulos, Nikolaos Kozeis, Dimitrios I. Zafeiriou, Ethymia Vargiami, Ioannis Mavromatis, Ioannis G. Tsikoulas

المصدر: Scopus-Elsevier

مصطلحات موضوعية: medicine.medical_specialty, Periventricular leukomalacia, Visual acuity, genetic structures, medicine.diagnostic_test, business.industry, Magnetic resonance imaging, Audiology, medicine.disease, nervous system diseases, Cerebral palsy, Epilepsy, Ophthalmology, Pediatrics, Perinatology and Child Health, Spastic, medicine, Neurology (clinical), medicine.symptom, Evoked potential, business, Spastic tetraplegia

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f6e9bee1027dc8aa128dc93e25094ccTest
https://doi.org/10.1055/s-0035-1557489Test

المؤلفون: Euthymia Vargiami, A. Ververi, Dimitrios I. Zafeiriou

المصدر: Current Neuropharmacology

مصطلحات موضوعية: Autism, serotonergic, Stimulation, Developmental arrest, Serotonergic, 5-hydroxytryptophan, Article, Pathogenesis, chemistry.chemical_compound, Neuroplasticity, Medicine, Pharmacology (medical), Pharmacology, developmental intervention, business.industry, General Medicine, medicine.disease, serotonin, Psychiatry and Mental health, Neurology, chemistry, plasticity, Neurology (clinical), Serotonin, 5-Hydroxytryptophan, business, Neuroscience

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c970ebe6a0dfe7345f573b22f220937Test
https://doi.org/10.2174/157015909788848848Test

المؤلفون: Petra J. W. Pouwels, F. Athanasiadou-Piperopoulou, Richard J. Rodenburg, Hans Scheffer, A. Ververi, M.S. van der Knaap, Dimitrios I. Zafeiriou, L.P.W.J. van den Heuvel

المساهمون: Physics and medical technology, Pediatric surgery, Neuroscience Campus Amsterdam 2008, Other departments

المصدر: Neuropediatrics, 39(3), 172-175. Hippokrates Verlag GmbH
Neuropediatrics, 39, 3, pp. 172-5
Zafeiriou, D I, Rodenburg, R J T, Scheffer, H, van den Heuvel, L P, Pouwels, P J W, Ververi, A & van der Knaap, M S 2008, ' MR spectroscopy and serial magnetic resonance imaging in a patient with mitochondrial cystic leukoencephalopathy due to complex I deficiency and NDUFV1 mutations and mild clinical course ', Neuropediatrics, vol. 39, no. 3, pp. 172-175 . https://doi.org/10.1055/s-0028-1093336Test
Neuropediatrics, 39, 172-5

مصطلحات موضوعية: In vivo magnetic resonance spectroscopy, Heterozygote, Pathology, medicine.medical_specialty, Magnetic Resonance Spectroscopy, Mitochondrial Diseases, Energy and redox metabolism [NCMLS 4], NDUFV1, Corpus callosum, Compound heterozygosity, Genomic disorders and inherited multi-system disorders [IGMD 3], Leukoencephalopathy, White matter, SDG 3 - Good Health and Well-being, Translational research [ONCOL 3], Spastic diplegia, medicine, Humans, Child, Electron Transport Complex I, medicine.diagnostic_test, Brain Diseases, Metabolic, business.industry, NADH Dehydrogenase, Magnetic resonance imaging, General Medicine, medicine.disease, Magnetic Resonance Imaging, Mitochondrial medicine [IGMD 8], medicine.anatomical_structure, Genetic defects of metabolism [UMCN 5.1], Mutation, Pediatrics, Perinatology and Child Health, Female, Neurology (clinical), Cellular energy metabolism [UMCN 5.3], business, Functional Neurogenomics [DCN 2]

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1479a1952fbb560cfc49bfb87f016fc5Test
https://doi.org/10.1055/s-0028-1093336Test

المؤلفون: Nikoleta Printza, Fotios Papachristou, A. Ververi, Maria Bandouraki, Euthymia Vargiami, Dimos Gidaris

المصدر: Urologia Internationalis. 88:238-240

مصطلحات موضوعية: Male, medicine.medical_specialty, Time Factors, Urology, medicine.medical_treatment, Urinary system, Iatrogenic Disease, Urinary Bladder, Wounds, Penetrating, Urinary catheterization, Ascites, medicine, Humans, Intensive care medicine, Rupture, Wound Healing, Urinary bladder, business.industry, Infant, Newborn, Acute kidney injury, Bladder Perforation, Acute Kidney Injury, Abdominal distension, medicine.disease, Surgery, Radiography, Treatment Outcome, medicine.anatomical_structure, medicine.symptom, Urinary Catheterization, Hyponatremia, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71fd7c11d870684ef5bbc79739738403Test
https://doi.org/10.1159/000331495Test

المؤلفون: Dimitrios I. Zafeiriou, Michèl A.A.P. Willemsen, Marcel M. Verbeek, A. Ververi, Euthymia Vargiami, Ron A. Wevers

المصدر: Molecular Genetics and Metabolism, 97, 1, pp. 18-20
Molecular Genetics and Metabolism, 97, 18-20

مصطلحات موضوعية: Male, medicine.medical_specialty, Pyramidal Tract Dysfunction, Tyrosine 3-Monooxygenase, Energy and redox metabolism [NCMLS 4], Endocrinology, Diabetes and Metabolism, Biochemistry, Genomic disorders and inherited multi-system disorders [IGMD 3], Catecholamines, Endocrinology, Hypokinesia, Internal medicine, Perception and Action [DCN 1], Genetics, medicine, Humans, Missense mutation, Child, Molecular Biology, Dystonia, Tyrosine hydroxylase, business.industry, Parkinsonism, Selegiline, Infant, Glycostation disorders [IGMD 4], medicine.disease, Hypotonia, nervous system diseases, Case-Control Studies, Child, Preschool, medicine.symptom, business, Functional Neurogenomics [DCN 2], medicine.drug

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbe199040d1aad2ec984c2db1a0d0849Test
https://doi.org/10.1016/j.ymgme.2009.02.001Test