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Three-dimensional stereophotogrammetry measurement of facial asymmetry in patients with congenital muscular torticollis: a non-invasive method.

International journal of oral and maxillofacial surgery·2020

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Genetic counseling (Geneva, Switzerland)·2016

Dilatative uropathy as a manifestation of neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin-neurophysin-II gene.

Klinische Padiatrie·2013

Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum.

Molecular syndromology·2010

Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly.

Clinical genetics·2008

Gut microbiota and blood biomarkers as correlating factors in patients with postoperative delirium: analysis of three prospective observational studies.

Molecular psychiatry·2026

Spatial lipidomics of the human brain: systematic review of current state and future perspectives.

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Iron dyshomeostasis and its neurobiological mechanisms in psychiatric disorders.

Molecular psychiatry·2026

CSF p-tau205: a biomarker of Alzheimer's disease progression and biological staging.

Molecular psychiatry·2026

Higher frequencies of CNV deletions in bipolar disorder among Chinese Population.

Molecular psychiatry·2026

Sexual dimorphism of midbrain catecholaminergic metabolism revealed by neuromelanin-sensitive MRI.

Molecular psychiatry·2026

Multiple congenital dermal sinus tracts: a case-based review involving a unique triple-tract configuration that challenges current embryological concepts.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery·2026

Astrocyte-Predominant Tau Pathology in a Patient With VCP R191Q Variant.

Neuropathology : official journal of the Japanese Society of Neuropathology·2026

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Neurology international·2026

Epidemiological investigation and risk factor analysis of acute kidney injury in non-intensive care unit hospitalized patients following neurosurgery.

Frontiers in neurology·2026

The origin of non-specific effects of vaccines and the role of randomised clinical trials.

Human vaccines & immunotherapeutics·2026

Non-alcoholic Wernicke-Korsakoff Syndrome: A Narrative Review.

Saudi journal of medicine & medical sciences·2026

Related Experiment Videos

Mutation screening of the KCNN3 gene reveals a rare frameshift mutation

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Exploring early intervention in psychosis (EIP) perspectives towards pharmacogenomics (PGx) implementation to support antipsychotic prescribing: a multi-method qualitative exploration.

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Dilatative uropathy as a manifestation of neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin-neurophysin-II gene.

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Mutation screening of the KCNN3 gene reveals a rare frameshift mutation

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