Summary
Dr Kinali is a Honorary Senior Lecturer in Paediatric Neurology at Imperial College.
She is also a Consultant Paediatric Neurologist at Chelsea and Westminster Hospital, BUPA Cromwell Hospital and The Portland Hospital.
Publications
Journals
Sewani S, Azamian MS, Mendelsohn BA, et al., 2024, Neurodevelopmental and other phenotypes recurrently associated with heterozygous BAZ2B loss-of-function variants., Am J Med Genet A, Vol:194
Stafki SA, Turner J, Littel HR, et al., 2023, The Spectrum of MORC2-Related Disorders: A Potential Link to Cockayne Syndrome, Pediatric Neurology, Vol:141, ISSN:0887-8994, Pages:79-86
Frasca A, Pavlidou E, Bizzotto M, et al., 2022, Not Just Loss-of-Function Variations Identification of a Hypermorphic Variant in a Patient With a CDKL5 Missense Substitution, Neurology-genetics, Vol:8, ISSN:2376-7839
Zimmels S, Balfour-Lynn IM, Christodoulou L, et al., 2022, Isolated bulbar palsy and dysphagia in children with respiratory symptoms, Developmental Medicine and Child Neurology, Vol:64, ISSN:0012-1622, Pages:518-522
Fernandez-Garcia MA, Stettner GM, Kinali M, et al., 2021, Genetic neuropathies presenting with CIDP-like features in childhood, Neuromuscular Disorders, Vol:31, ISSN:0960-8966, Pages:113-122