Research Index

Catestatin Research Index

PSI surfaces 50 peer-reviewed studies on Catestatin, prioritized by evidence strength: human clinical research first, then animal studies. The full historical archive is linked below on PubMed.

Sort
Type
Condition

50 studies

A child with cobalamin C deficiency caused by complex heterozygous variation of c.567dupT and c.80A > G complicated with pulmonary arterial hypertension and hydrocephalus: A case report and literature review.

Cui X, Zhong Y, Yin C

Medicine (Baltimore)·2026·Human·PubMed →

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross-Sectional Study and Systematic Literature Review.

Cinelli G, Della Vecchia S, Bergonzini P et al.

Am J Med Genet A·2026·Human·PubMed →

A novel de novo frameshift variant in ZMYM2 expands the neuropsychiatric spectrum of NECRC syndrome: a case report.

Mammadova N, Hatipoglu N, Dundar M

Mol Biol Rep·2026·Human·PubMed →

Early-Remitting Neonatal Diabetes in a Growth-Restricted Preterm Infant Requiring Insulin: A Case Report.

Boulfouyoul A, Ettoini K, Oulmaati A

Cureus·2026·Human·PubMed →

Long-Term Follow-Up of a Patient with a Novel Homozygous ASTN1 Variant: A Case Report.

Kasap B, Uludağ Alkaya D, Güneş N et al.

Neurol Int·2026·Human·PubMed →

The efficacy and safety of transcranial direct current stimulation in patients with ADHD: a systematic review and meta-analysis.

Li J, Hou X, Fan Q et al.

Front Psychiatry·2026·Human·PubMed →

Seizure and Neurodevelopmental Regression in Inherited N-Acetyl Glutamate Synthase Deficiency (NAGSD): A Case Series From Neuroimaging to Genome Sequencing.

Kooshki A, Moosavian T, Hosseini M

J Child Neurol·2026·Human·PubMed →

Diagnostic Dilemma in an Infant With Sound-Triggered Motor Events: Reflex Epilepsy Versus Exaggerated Startle-A Case Report.

Pandit A, Koirala M, Shahi A et al.

Clin Case Rep·2026·Human·PubMed →

The Median Effective Concentration of Sevoflurane for I-Gel Laryngeal Mask Insertion in Unpremedicated Children Aged 1-10 Years: A Prospective Concentration-Finding Study.

Gan Z, Li S, Yang S et al.

Pediatr Discov·2026·Human·PubMed →

Vision Intervention for Seeing Impaired Babies: Learning through Enrichment (VISIBLE) - protocol of a feasibility pilot randomised controlled trial.

Guzzetta A, Bancale A, Bedoshvili A et al.

BMJ Open·2026·Human·PubMed →

Electrical Stimulation of the Nucleus Accumbens for Severe, Refractory Self-Injurious Behaviour in Children (EASE-SIB): protocol for a randomised double-blinded crossover trial.

Mithani K, Sauter S, Hagopian LP et al.

BMJ Open·2026·Human·PubMed →

Predictors of Developmental Delays and Therapy Resource Utilization in Craniosynostosis Patients.

Guadix SW, Zappi KE, Webster T et al.

J Craniofac Surg·2026·Human·PubMed →

Paroxysmal neurological spells in TANGO2 deficiency disorder: a case report and a scoping review.

Turco EC, Pisanò G, Carestiato S et al.

Front Pediatr·2026·Human·PubMed →

Prader-Willi Syndrome Presenting With Early Infantile Hypotonia: A Case Report.

Alsindi AM, Amer RG, Boustros LM et al.

Cureus·2026·Human·PubMed →

The effect of daily vitamin B(12) supplementation on the incidence of common childhood infections in Nepal: secondary outcomes from a double-blind randomized controlled trial.

Strand TA, Chandyo RK, McCann A et al.

J Nutr·2026·Human·PubMed →

Effect of Aquatic Training Versus Land Exercises on Motor Function in Children With Autism Spectrum Disorder: A Randomized Controlled Trial.

Albadry ES, Ibrahim NM, Othman AA et al.

Physiother Res Int·2026·Human·PubMed →

Transient neonatal diabetes mellitus as an early diagnostic clue to HNF1B-related disease - two case reports and a literature review.

Kołbuc M, Bednarek P, Motyka R et al.

Mol Cell Pediatr·2026·Human·PubMed →

Microcephaly, seizures and developmental delay caused by two novel mutations in the PNKP gene: a case report.

Liu M, Huang DP, Wang ML et al.

Transl Pediatr·2026·Human·PubMed →

Early differential impact of MeCP2 mutations on functional networks in Rett syndrome patient-derived human cortical organoids.

Osaki T, Delepine C, Osako Y et al.

Nat Commun·2026·Human·PubMed →

Sedation and General Anesthesia in Non-Cooperative Dental Patients: An Italian Clinical Experience.

Cirignaco G, Lo Giudice G, Caso AR et al.

J Clin Med·2026·Human·PubMed →

Endocrine and metabolic features of PTEN hamartoma tumor syndrome in childhood: a pediatric case series.

Özsoy NS, Baştürk A, Altay D et al.

J Pediatr Endocrinol Metab·2026·Human·PubMed →

Spastic Quadriplegia Resulting From a Pathogenic Variant in the SPAST Gene: A First Report.

Kostopoulou E, Lagadinou M, Karatza A et al.

Case Rep Neurol Med·2026·Animal·PubMed →

Gut microbiota dynamics and its impact on the efficacy of ACTH therapy in infantile epileptic spasms syndrome.

Zhang X, Hu X, Hao X et al.

Front Neurol·2026·Animal·PubMed →

Chest compression superimposed with sustained inflation - translating preclinical findings into a neonatal clinical trial.

Chen S, O'Reilly M, Lee TF et al.

Resusc Plus·2026·Animal·PubMed →

Faecal inflammatory protein markers in children with autism spectrum disorder are comparable to their healthy siblings.

Osredkar J, Finderle P, Godnov U et al.

Front Psychiatry·2026·Animal·PubMed →

Early diagnosis and developmental outcome prediction of agenesis of the corpus callosum via an interpretable deep multimodal fusion model.

Chen J, Zhang WH, Bai Y et al.

Front Neurosci·2026·Animal·PubMed →

Long-Read HiFi Genome Sequencing Resolves Retrotransposon-Mediated Deletions in TANGO2 Deficiency Disorder.

Sabbagh Q, Villa Tobón F, Kazemi Z et al.

Neurol Genet·2026·Animal·PubMed →

Biallelic loss-of-function variants in DSCAM cause a neurodevelopmental syndrome with nystagmus and retinal dysfunction.

Douzgou Houge S, Bredrup C, Wivestad Jansson R et al.

HGG Adv·2026·Animal·PubMed →

Predictors of adverse outcome in infants with hypoxic-ischemic encephalopathy treated with therapeutic hypothermia: a real-world cohort study.

Chen L, Xia S, Zhu H et al.

BMC Pediatr·2026·Animal·PubMed →

Neonatal encephalopathy and 3 year outcomes: a French population-based cohort.

Debillon T, Vilotitch A, Guellec I et al.

Pediatr Res·2026·Animal·PubMed →

Functional impact of genetic background on variable expressivity in neurodevelopmental disorders.

Sun J, Noss S, Smolen C et al.

Nat Commun·2026·Animal·PubMed →

Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries.

Huerta-Chagoya A, Kim J, Mandla R et al.

Lancet Diabetes Endocrinol·2026·Animal·PubMed →

Genetic activation of ERK2 recapitulates core neurodevelopmental features of Rasopathy syndromes in mice.

Grover KE, Cappel ZR, Volz A et al.

HGG Adv·2026·Animal·PubMed →

Causal subgroups and declining rates of cerebral palsy in Victoria, Australia.

Reid SM, Hinwood GL, Guzys AT et al.

Dev Med Child Neurol·2026·Animal·PubMed →

FGF12-Related Early-Onset Epileptic Encephalopathies: Therapeutic Response to Sodium Channel Blockers.

Aldurayhim F, Basit S, Bashir S et al.

Am J Med Genet A·2026·Animal·PubMed →

Inhibition of PTEN nuclear translocation by peptide Tat-K13 attenuates p-JUN-SESN2-AMPK-dependent autophagy and enhances neurological recovery after neonatal hypoxic-ischemic brain damage.

Dai C, Wu X, Li X et al.

Cell Biosci·2026·Animal·PubMed →

Comparison of early growth and development in very preterm children in the Netherlands between the 1980s and 2000s.

Sexty RE, van Dommelen P, Bos AF et al.

BMC Pediatr·2026·Animal·Weight Loss·PubMed →

[Sleep disorders in children and adolescents: Clinical assessment and principles of management].

Rolling J, Zanfonato T, Bioulac S et al.

Encephale·2026·Animal·PubMed →

Developmental follow-up, surveillance and support at the age of 4 years: a best practice guide from the British Association for Neonatal Neurodevelopmental Follow-Up.

Mckinnon K, Arasu A, Beckmann J et al.

Arch Dis Child Fetal Neonatal Ed·2026·Animal·PubMed →

Sleep disorders in children with Cri du Chat syndrome: A questionnaire-based study.

Ferretti A, Bellone G, Di Napoli A et al.

Sleep Med·2026·Animal·PubMed →

Paeoniflorin mitigates hyperoxia-induced cognitive deficits in neonatal mice by modulating p38/JNK signaling to reduce oxidative stress and neuroinflammation.

Huang C, Zhang X, Yu J et al.

Neuropharmacology·2026·Animal·PubMed →

The relationship between sonographically assessed volumetric brain development in VLBW preterm infants and neurodevelopmental outcome at 2 years of age-data from the NeoNEVS project.

Brickmann C, Lampe R, Sidorenko I et al.

Front Pediatr·2026·Animal·PubMed →

Choroid plexus and perivascular space abnormalities in CerTra syndrome: neuroimaging and histological findings.

Li C, Leitner D, Pang H et al.

Front Neurol·2026·Animal·PubMed →

Relationship between thyroid hormones and bronchopulmonary dysplasia in extremely and very preterm infants.

Ma Y, Liu G, Li H et al.

Front Physiol·2026·Animal·PubMed →

De Novo TRIO Missense Variants Disrupt Ras-GEF Domains and Cause Congenital Ventriculomegaly and Hydrocephalus.

Mehta NH, Dennis E, Allington G et al.

Hum Mutat·2026·Animal·PubMed →

Robotic Surgery in Pediatric Epilepsy : Current Evidence, Clinical Impact, and Future Directions.

Lee S

J Korean Neurosurg Soc·2026·Animal·PubMed →

Measures of neonatal glycemia from blood glucose concentrations and neurodevelopmental outcomes at 2 years.

May RW, Gamble GD, McKinlay CJD et al.

Pediatr Res·2026·Animal·PubMed →

Maternal pre-pregnancy BMI and neurodevelopmental outcomes in children aged 18-36 months: a nationwide cohort study in Korea.

Shin J, Kim TE, Park SH et al.

Sci Rep·2026·Animal·PubMed →

Development of a tic service model for children and young people in England: a Delphi study.

Hall SS, Rattu NR, Hall CL et al.

BMJ Open·2026·Animal·PubMed →

The Impact of 8p23 Copy Number Variations on Neurodevelopmental Aetiology: A Focus on Rare Deletions.

Güleç A, Gerik-Celebi HB

Int J Dev Neurosci·2026·Animal·PubMed →