Barth syndrome: mechanisms and management by Finsterer J

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Ketogenic diet in ATAD3A mutation carriers may not improve cerebellar atrophy but some clinical features [Letter] by Finsterer J

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Neurological Side Effects of SARS-CoV-2 Vaccinations are Not Uncommon but Frequently Ignored [Letter] by Finsterer J, Scorza FA

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Mitochondrial multiorgan disorder syndrome score generated from definite mitochondrial disorders by Finsterer J, Zarrouk-Mahjoub S

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Detection of the mutation may guide treatment of heart and muscle in Duchenne muscular dystrophy by Finsterer J, Zarrouk-Mahjoub S

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Psychological morbidity in Leber’s hereditary optic neuropathy depends on phenotypic, social, economic, and genetic factors by Finsterer J, Zarrouk-Mahjoub S

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Lymphangiopathy in neurofibromatosis 1 manifesting with chylothorax, pericardial effusion, and leg edema by Finsterer J, Stollberger C, Stubenberger E, Tschakoschian S

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Erratum to: Genetic Counselling for maternally inherited mitochondrial disorders. by Poulton, J, Finsterer, J, Yu-Wai-Man, P

Genetic counselling for maternally inherited mitochondrial disorders. by Poulton, J, Finsterer, J, Yu-Wai-Man, P

Lift the quilt in case of atrial fibrillation and disc prolapse by Bastovansky A, Ziegler K, Stöllberger C, Finsterer J

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Myotonic dystrophy-2: Unusual phenotype due to a small CCTG-expansion by Finsterer J, Stöllberger C, Reining-Festa A, Loewe-Grgurin M, Gencik M

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Female and male carriers of TAZ mutations need to be thoroughly investigated by Finsterer J, Stollberger C, Bakšienė M, Benušienė E, Morkūnienė A, Ambrozaitytė L, Utkus A, Kučinskas V

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