Orthostatic tremor and behavioral frontotemporal dementia: a case report with 7 years of follow-up

Rare Neurologic Diseases and Neurological Sciences: a report for the celebration of the 2020 Rare Diseases Day

“…Luo et al [28], Efficacy and safety of edaravone in treatment of amyotrophic lateral sclerosis-a systematic review and meta-analysis Sivaramakrishnan et al [29], Recumbent stepping aerobic exercise in amyotrophic lateral sclerosis: a pilot study Amin Lari et al [30], A review of electrophysiological studies of lower motor neuron involvement in amyotrophic lateral sclerosis Hancevic et al [31], Attenuation of ALS progression during pregnancylessons to be learned or just a coincidence? Verde et al [32], PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival Sprovieri et al [33], A novel S379A TARDBP mutation associated to late-onset sporadic ALS Yang et al [34], UNC13Avariant rs12608932 is associated with increased risk of amyotrophic lateral sclerosis and reduced patient survival: a meta-analysis Park et al [35], Under-recognized primary spontaneous pneumothorax in ALS: a multicenter retrospective study Corrado et al [36], Analysis of the GCG repeat length in NIPA1 gene in C9orf72-mediated ALS in a large Italian ALS cohort Santus et al [37], Orthostatic tremor and behavioral frontotemporal dementia: a case report with 7 years of follow-up. [38], Decreasing 123I-ioflupane SPECT accumulation and 123 I-MIBG myocardial scintigraphy uptake in a patient with a novel homozygous mutation in the ZFYVE26 gene Abdulkareem et al [39], A novel homozygous nonsense mutation in CCDC88A gene cause PEHO-like syndrome in consanguineous Saudi family Zhang et al [40], A novel missense mutation in the ABCD1 gene of a Chinese boy diagnosed with X-linked adrenoleukodystrophy: case report Genc et al [41], Methylation of cation-chloride cotransporters NKCC1 and KCC2 in patients with juvenile myoclonic epilepsy Kaur et al [42], L-type calcium channel blockers and a symptom complex mimicking de Melo-Souza's syndrome Oliva [43], A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient Du [44], A novel mutation in the CSF1R gene causes hereditary diffuse leukoencephalopathy with axonal spheroids Liu et al [45], G327E mutation in SCN9A gene causes idiopathic focal epilepsy with Rolandic spikes: a case report of twin sisters Catania et al [46], DNMT1-complex disorder caused by a novel mutation associated with an overlapping phenotype of autosomal-dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN) and hereditary sensory neuropathy with dementia and hearing loss (HSN1E) Ferrante et al [47], Identification of a novel NOTCH3 mutation in an Italian family affected by a mild form of CADASIL…”