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Current and emerging therapeutic options for the management of functional dyspepsia.

Expert opinion on pharmacotherapy·2020

Molecular Diagnostic Testing in Charcot-Marie-Tooth Disease and Related Disorders: Approaches and Results.

Annals of the New York Academy of Sciences·2017

Distal Hereditary Motor Neuropathy Type II (Distal HMN Type II): Phenotype and Molecular Genetics.

Annals of the New York Academy of Sciences·2017

Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family.

Pflugers Archiv : European journal of physiology·2017

[A Pair of Siblings with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis and a Novel Thr462Lysfs Mutation in the TBK1 Gene].

Fortschritte der Neurologie-Psychiatrie·2016

Validation of the Leuven Postprandial Distress Scale, a questionnaire for symptom assessment in the functional dyspepsia/postprandial distress syndrome.

Alimentary pharmacology & therapeutics·2016

Efficacy and safety of tradipitant in motion sickness: a systematic review and meta-analysis.

Acta neurologica Belgica·2026

Cervical artery dissection after upper respiratory infection: clinical features and prognosis.

Acta neurologica Belgica·2026

Recurrent ischemic strokes with normal inflammatory markers: when tests mislead.

Acta neurologica Belgica·2026

Outcomes of neuromuscular retraining and adjunctive electrical stimulation in Bell's palsy: a single-centre observational cohort study.

Acta neurologica Belgica·2026

Kinetic and inhibitory profiling of serum MMP-9 in acute spinal cord injury: neurochemical links to injury severity and neuroinflammation.

Acta neurologica Belgica·2026

Reliability and convergent validity of the 6-minute pegboard and ring test in people with Parkinson's disease: a cross-sectional study.

Acta neurologica Belgica·2026

Hyperexcitability in hippocampal CA1 pyramidal cells OF Fmr1 knockout mice emerges during late postnatal development.

Neuroscience·2026

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

American journal of medical genetics. Part A·2026

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

International journal of molecular sciences·2026

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

International journal of molecular sciences·2026

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

Cells·2026

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

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Current and emerging therapeutic options for the management of functional dyspepsia.

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