[Genetic causes of mental retardation]

A Novel Prognostication System for Spinal Metastasis Patients Based on Network Science and Correlation Analysis.

Clinical oncology (Royal College of Radiologists (Great Britain))·2022

A population-based epidemiological study of neuromyelitis optica spectrum disorder in Hungary.

European journal of neurology·2019

First Report of Phytophthora Root and Collar Rot of Alder in Hungary.

Plant disease·2019

Structure of photodissociation fronts in star-forming regions revealed by observations of high-J CO emission lines with Herschel.

Astronomy and astrophysics·2018

XPC is an RNA polymerase II cofactor recruiting ATAC to promoters by interacting with E2F1.

Nature communications·2018

Developing the combined magnetic, electric and air flow (KLME) separator for RMSW processing.

Waste management & research : the journal of the International Solid Wastes and Public Cleansing Association, ISWA·2018

[Clinical and preprocedural factors influencing in vitro fertilization outcomes: a machine learning-based analysis].

Orvosi hetilap·2026

[Focus on testicular torsion: differential diagnosis of acute scrotum].

Orvosi hetilap·2026

[Energy drinks: composition, physiological effects and health risks].

Orvosi hetilap·2026

[Vision saved: the first four years of the pediatric ophthalmology screening program of the Hungarian Charity Service of the Order of Malta - Part II.]

Orvosi hetilap·2026

[Angina-induced marked, positive U-waves in leads V1-3].

Orvosi hetilap·2026

[Albuminuria for detection of chronic kidney disease: biomarker and therapeutic target].

Orvosi hetilap·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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[Genetic causes of mental retardation]

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A Novel Prognostication System for Spinal Metastasis Patients Based on Network Science and Correlation Analysis.

A population-based epidemiological study of neuromyelitis optica spectrum disorder in Hungary.

First Report of Phytophthora Root and Collar Rot of Alder in Hungary.

Structure of photodissociation fronts in star-forming regions revealed by observations of high-J CO emission lines with Herschel.

XPC is an RNA polymerase II cofactor recruiting ATAC to promoters by interacting with E2F1.

Developing the combined magnetic, electric and air flow (KLME) separator for RMSW processing.

[Clinical and preprocedural factors influencing in vitro fertilization outcomes: a machine learning-based analysis].

[Focus on testicular torsion: differential diagnosis of acute scrotum].

[Energy drinks: composition, physiological effects and health risks].

[Vision saved: the first four years of the pediatric ophthalmology screening program of the Hungarian Charity Service of the Order of Malta - Part II.]

[Angina-induced marked, positive U-waves in leads V1-3].

[Albuminuria for detection of chronic kidney disease: biomarker and therapeutic target].

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

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

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

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

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

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

Related Experiment Videos

[Genetic causes of mental retardation]

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