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Publications by Lara Gibellini
Core-Rod Myopathy Due to a Novel Mutation in BTB/POZ Domain of KBTBD13 Manifesting as Late Onset LGMD
Acta neuropathologica communications
Forensic Medicine
Molecular Neuroscience
Pathology
Neurology
Cellular
Mitochondrial Changes During D-Drug-Containing Once-Daily Therapy in HIV-positive Treatment-Naive Patients
Antiviral Therapy
Infectious Diseases
Pharmacology
Related publications
Backbone Resonance Assignment of the BCL6-BTB/POZ Domain
Biomolecular NMR Assignments
Biochemistry
Structural Biology
Novel BTB/POZ Domain Zinc-Finger Protein, LRF, Is a Potential Target of the LAZ-3/BCL-6 Oncogene
Oncogene
Cancer Research
Genetics
Molecular Biology
Juvenile Onset Autoinflammatory Disease Due to a Novel Mutation in TNFAIP3 (A20)
Arthritis Research & Therapy
A Novel Mutation of the Arylsulfatase a Gene in Late-Onset Metachromatic Leukodystrophy
Journal of Clinical Psychiatry
Medicine
Psychiatry
Mental Health
Slow‐channel Myasthenia Due to Novel Mutation in M2 Domain of AChR Delta Subunit
Annals of Clinical and Translational Neurology
Neuroscience
Neurology
A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy
American Journal of Human Genetics
Genetics
GNE Myopathy in Turkish Sisters With a Novel Homozygous Mutation
Case Reports in Neurological Medicine
Late Adult-Onset of X-Linked Myopathy With Excessive Autophagy
Muscle and Nerve
Molecular Neuroscience
Neurology
Physiology
Cellular
Identification of a Novel Nonsense Mutation in the Rod Domain of GFAP That Is Associated With Alexander Disease
European Journal of Human Genetics
Genetics