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Andreea Ilinca

Showing results (1-10 of 22) with videos related to

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BMJ Case Reports|December 11, 2023
Varicella-zoster virus vasculopathy in a patient with multiple sclerosis receiving natalizumabAnna Elmståhl, Fredrik Buchwald, Andreea Ilinca
Parkinsonism & Related Disorders|January 25, 2022
A relatively common hypomorphic variant in WARS2 causes monogenic diseaseAndreea Ilinca, Efthymia Kafantari, Andreas Puschmann
Journal of Neurology|September 14, 2025
Genetic background of neurological disorders with basal ganglia calcificationMaha Yektay Farahmand, Joel Wallenius, Johan Wasselius, et al.
Parkinsonism & Related Disorders|April 11, 2020
New generation genetic testing entering the clinicSorina Gorcenco, Andreea Ilinca, Wejdan Almasoudi, et al.
European Journal of Human Genetics : EJHG|October 26, 2018
A stroke gene panel for whole-exome sequencingAndreea Ilinca, Sofie Samuelsson, Paul Piccinelli, et al.
Neurologia I Neurochirurgia Polska|December 29, 2023
Small vessel disease in primary familial brain calcification with novel truncating PDGFB variantsMaha Yektay Farahmand, Johan Wasselius, Elisabet Englund, et al.
Movement Disorders Clinical Practice|May 13, 2021
Throat-Clearing Vocalizations in Primary Brain Calcification SyndromesEoin Mulroy, Andreea Ilinca, Cristina Gonzalez-Robles, et al.
Stroke|November 5, 2024
Diagnosing Monogenic Stroke at Younger AgeAndreea Ilinca, Efthymia Kafantari, Joel Wallenius, et al.
Acta Neuropathologica|November 25, 2024
Lipid storage myopathy associated with sertraline treatment is an acquired mitochondrial disorder with respiratory chain deficiencyCarola Hedberg-Oldfors, Ulrika Lindgren, Kittichate Visuttijai, et al.
European Journal of Human Genetics : EJHG|October 17, 2022
Updated Stroke Gene Panels: Rapid evolution of knowledge on monogenic causes of strokeAndreea Ilinca, Andreas Puschmann, Jukka Putaala, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
BMJ Case Reports|December 11, 2023
Varicella-zoster virus vasculopathy in a patient with multiple sclerosis receiving natalizumabAnna Elmståhl, Fredrik Buchwald, Andreea Ilinca
Parkinsonism & Related Disorders|January 25, 2022
A relatively common hypomorphic variant in WARS2 causes monogenic diseaseAndreea Ilinca, Efthymia Kafantari, Andreas Puschmann
Journal of Neurology|September 14, 2025
Genetic background of neurological disorders with basal ganglia calcificationMaha Yektay Farahmand, Joel Wallenius, Johan Wasselius, et al.
Parkinsonism & Related Disorders|April 11, 2020
New generation genetic testing entering the clinicSorina Gorcenco, Andreea Ilinca, Wejdan Almasoudi, et al.
European Journal of Human Genetics : EJHG|October 26, 2018
A stroke gene panel for whole-exome sequencingAndreea Ilinca, Sofie Samuelsson, Paul Piccinelli, et al.
Neurologia I Neurochirurgia Polska|December 29, 2023
Small vessel disease in primary familial brain calcification with novel truncating PDGFB variantsMaha Yektay Farahmand, Johan Wasselius, Elisabet Englund, et al.
Movement Disorders Clinical Practice|May 13, 2021
Throat-Clearing Vocalizations in Primary Brain Calcification SyndromesEoin Mulroy, Andreea Ilinca, Cristina Gonzalez-Robles, et al.
Stroke|November 5, 2024
Diagnosing Monogenic Stroke at Younger AgeAndreea Ilinca, Efthymia Kafantari, Joel Wallenius, et al.
Acta Neuropathologica|November 25, 2024
Lipid storage myopathy associated with sertraline treatment is an acquired mitochondrial disorder with respiratory chain deficiencyCarola Hedberg-Oldfors, Ulrika Lindgren, Kittichate Visuttijai, et al.
European Journal of Human Genetics : EJHG|October 17, 2022
Updated Stroke Gene Panels: Rapid evolution of knowledge on monogenic causes of strokeAndreea Ilinca, Andreas Puschmann, Jukka Putaala, et al.
Pageof 3