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المؤلفون: Alisa Mo, Afshin Saffari, Melanie Kellner, Marion Döbler‐Neumann, Catherine Jordan, Siddharth Srivastava, Bo Zhang, Mustafa Sahin, John K. Fink, Linsley Smith, Jennifer E. Posey, Katharine E. Alter, Camilo Toro, Craig Blackstone, Ariane G. Soldatos, Michelle Christie, Rebecca Schüle, Darius Ebrahimi‐Fakhari
المصدر: Movement disorders 37(12), 2440-2446 (2022). doi:10.1002/mds.29225
Mov Disordمصطلحات موضوعية: Adult, cerebral palsy, Spastin, Adolescent, Spastic Paraplegia, Hereditary, childhood-onset movement disorders, Article, diagnosis [Spastic Paraplegia, Hereditary], Young Adult, Cross-Sectional Studies, Phenotype, Neurology, Muscle Spasticity, Child, Preschool, genetics [Spastic Paraplegia, Hereditary], Mutation, Humans, genetics [Spastin], SPAST, Neurology (clinical), ddc:610, hereditary spastic paraplegia, Child, neurogenetics
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb27dd83920485e0a4b88794a230e52cTest
https://pub.dzne.de/record/165247Test -
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المؤلفون: Darius, Ebrahimi-Fakhari, Julian E, Alecu, Marvin, Ziegler, Gregory, Geisel, Catherine, Jordan, Angelica, D'Amore, Rebecca C, Yeh, Shyam K, Akula, Afshin, Saffari, Sanjay P, Prabhu, Mustafa, Sahin, Edward, Yang, Conny M A, van Ravenswaaij-Arts
المصدر: Neurology
مصطلحات موضوعية: Pathology, medicine.medical_specialty, Hereditary spastic paraplegia, business.industry, Spastic Paraplegia, Hereditary, Adaptor Protein Complex 4, Splenium, Anterior commissure, Neuroimaging, Status epilepticus, medicine.disease, Corpus callosum, Magnetic Resonance Imaging, Cerebral palsy, Corpus Callosum, White matter, medicine.anatomical_structure, medicine, Polymicrogyria, Humans, Neurology (clinical), medicine.symptom, business, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcfcacb2aaf18a724159e2e69ac27c77Test
https://pubmed.ncbi.nlm.nih.gov/34544818Test -
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المؤلفون: Miriam Wimmer, Darius Ebrahimi-Fakhari, Robert Behne, Julian Teinert
المصدر: Journal of Inherited Metabolic Disease. 43:51-62
مصطلحات موضوعية: Movement disorders, Hereditary spastic paraplegia, Developmental Disabilities, Central nervous system, Biology, Cataract, Epilepsy, Autophagy, Genetics, medicine, Humans, Vici syndrome, Cognitive decline, Child, Genetics (clinical), Spastic Paraplegia, Hereditary, Neurodegeneration, Brain, Proteins, Neurodegenerative Diseases, medicine.disease, Magnetic Resonance Imaging, medicine.anatomical_structure, Agenesis of Corpus Callosum, medicine.symptom, Neuroscience
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f055a16d7adad06b9e527cedfd0cd9d2Test
https://doi.org/10.1002/jimd.12084Test -
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المؤلفون: James T. Bennett, Elisabeth Rosser, Kira A. Dies, Darius Ebrahimi-Fakhari, Danielle B. Pier, Conor S. Ryan, Jennifer Hirst, Chi Cheng, Amelia Diplock, Brendan C. Lanpher, Wendy K. Chung, Basil T. Darras, CureSPG, Mustafa Sahin
المصدر: American Journal of Medical Genetics Part A. 176:311-318
مصطلحات موضوعية: Diagnostic Imaging, Male, 0301 basic medicine, Microcephaly, Genotype, Hereditary spastic paraplegia, Adaptor Protein Complex 4, Compound heterozygosity, Bioinformatics, Corpus callosum, Cerebral palsy, 03 medical and health sciences, Genetics, medicine, Spastic, Humans, Genetic Predisposition to Disease, Spasticity, Child, Alleles, Genetic Association Studies, Genetics (clinical), Spastic Paraplegia, Hereditary, business.industry, Brain, Facies, medicine.disease, Magnetic Resonance Imaging, nervous system diseases, Phenotype, 030104 developmental biology, Child, Preschool, Mutation, Progressive spasticity, Female, Symptom Assessment, medicine.symptom, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb3bcead0fe03591f8e7fd8367c569b2Test
https://doi.org/10.1002/ajmg.a.38561Test -
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المؤلفون: Darius Ebrahimi-Fakhari, Mustafa Sahin, Julian Teinert, Sean Dwyer, Ivy Pin-Fang Chen, Miriam Wimmer, Teresa Chen, Robert Behne, Angelica D'Amore, Elizabeth D. Buttermore
المصدر: Stem Cell Res
Stem Cell Research, Vol 53, Iss, Pp 102335-(2021)مصطلحات موضوعية: Heterozygote, QH301-705.5, Hereditary spastic paraplegia, Adaptor Protein Complex 4, Cellular differentiation, Induced Pluripotent Stem Cells, Embryoid body, Article, medicine, Humans, Biology (General), Allele, Child, Induced pluripotent stem cell, biology, Spastic Paraplegia, Hereditary, Cerebral Palsy, Heterozygote advantage, Cell Biology, General Medicine, biology.organism_classification, medicine.disease, Sendai virus, Cancer research, Reprogramming, Developmental Biology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c72333093b660b2cfa64e687c7f291aTest
https://doi.org/10.1016/j.scr.2021.102335Test -
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المؤلفون: Yoshihisa Takiyama, Stefanie Brock, Jennifer Hirst, Niklas Dahl, Radka Kremlikova Pourova, Andrea Martinuzzi, Seth Perlman, Helene Verhelst, Omnia Fathy El-Rashidy, Nour Elkhateeb, Sarah I. Sheikh, Jamal Ghoumid, Erin Carmody, Georgia Xiromerisiou, Diego Miguel, James T. Bennett, Barbara Brechmann, William O. Walker, David Dacruz-Álvarez, Mathieu Anheim, Dana M. Jensen, Stefan Kölker, Uzma Shamshad, Darius Ebrahimi-Fakhari, Grace Yoon, Katharina Vill, David Bearden, Adel A. Mahmoud, Sheela Nampoothiri, Devorah Segal, Antje Wiesener, Shenela Lakhani, Joseph G. Gleeson, Chirag Patel, Angelica D'Amore, Abdelrahim Abdrabou Sadek, Marvin Ziegler, Mustafa Sahin, Toni S. Pearson, Julian Teinert, Kira A. Dies, Christopher J. Yuskaitis, Catherine L. Salussolia, Lubov Blumkin, Jonathan Baets, Laura Robelin, Daniel Ebrahimi-Fakhari, Parham Habibzadeh, Anju Shukla, Peter O. Bauer, Saskia Bulk, Afshin Saffari, Elizabeth Lim-Melia, Michael C. Kruer, Christian Beetz, Andreas Ziegler, Pankaj B. Agrawal, Thomas Bourinaris, Filippo M. Santorelli, Mireille Guillot, Abdullah Alamri, Mohammad Ali Faghihi, Kathrin Eberhardt, Thomas Smol, Henry Houlden, Nur Aydinli, Constanze Heine, Soroor Inaloo, Anaita Udwadia-Hegde, Alejandro Brea-Fernández, Yasemin Alanay, Rachana Dubey Gupta, Ayse Aksoy, Agathe Roubertie, Jens Volkmann, Basil T. Darras, Hendrik Langen, Mauricio R. Delgado, Jan Ulrich Schlump, Gregory Geisel, Anna Jansen, Somayeh Bakhtiari, Steven P. Miller, Miriam Wimmer, Maha S. Zaki, Premsai Nagabhyrava, Robert Behne, Hossein Darvish
المساهمون: Acibadem University Dspace
المصدر: Brain
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, SPG47, Microcephaly, Pediatrics, medicine.medical_specialty, Adolescent, Hereditary spastic paraplegia, Adaptor Protein Complex 4, Cerebral palsy, Corpus Callosum, Cohort Studies, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Spastic diplegia, medicine, SPG51, Humans, SPG50, Registries, SPG52, Child, Tetraplegia, business.industry, Spastic Paraplegia, Hereditary, neurodegeneration, Infant, Middle Aged, medicine.disease, Magnetic Resonance Imaging, Corrigenda, Hypotonia, 030104 developmental biology, Cross-Sectional Studies, Child, Preschool, Speech delay, Female, Neurology (clinical), Human medicine, medicine.symptom, business, 030217 neurology & neurosurgery, Ventriculomegaly
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e16bcaf88226cde8fedce925b8e3ea36Test
https://pubmed.ncbi.nlm.nih.gov/33294911Test -
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المؤلفون: Jenny Lu, Mustafa Sahin, Georg F. Hoffmann, Afshin Saffari, Lara Wahlster, Heinz Jungbluth, Susan Byrne, Darius Ebrahimi-Fakhari
المصدر: Ebrahimi-Fakhari, D, Saffari, A, Wahlster, L, Lu, J, Byrne, S, Hoffmann, G F, Jungbluth, H & Sahin, M 2016, ' Congenital disorders of autophagy : an emerging novel class of inborn errors of neuro-metabolism ', Brain : a journal of neurology, vol. 139, no. 2, pp. 317-337 . https://doi.org/10.1093/brain/awv371Test
مصطلحات موضوعية: 0301 basic medicine, Lysosomal Storage Diseases, Nervous System, Movement disorders, Hereditary spastic paraplegia, Disease, Review, Biology, Cataract, 03 medical and health sciences, WDR45, Intellectual disability, medicine, Autophagy, Humans, Vici syndrome, Spastic Paraplegia, Hereditary, Neurodegeneration, Brain Diseases, Metabolic, Inborn, medicine.disease, 030104 developmental biology, Neurology (clinical), medicine.symptom, Agenesis of Corpus Callosum, Lysosomes, Neuroscience
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d16b2898e78a66dbfee34328462c50ddTest
https://kclpure.kcl.ac.uk/ws/files/88791081/Congenital_Disorders_Of_Autophagy_EBRAHIMI_FAKHARI_Firstonline26December2015_GREEN_AAM.pdfTest