Radioulnar synostosis and craniosynostosis in one family

Insulin in human milk and the prevention of type 1 diabetes.

Pediatric diabetes·2004

Reversal of cardiac complications in thalassemia major by long-term intermittent daily intensive iron chelation.

European journal of haematology·2003

A novel thermoregulatory system maintains perioperative normothermia in children undergoing elective surgery.

Paediatric anaesthesia·2001

Prolidase deficiency among an Israeli population: prenatal diagnosis in a genetic disorder with uncertain prognosis.

Prenatal diagnosis·2000

[1000 cardiac catheterizations in congenital heart disease].

Harefuah·2000

[Percutaneous closure of patent arterial ducts with occluding spring coils].

Harefuah·2000

School-Based Health and Healthcare Utilization Among Rural Youth: Evidence from a School-Based Health Center Opening.

The Journal of pediatrics·2026

Associations Between Saliva-Based Biomarkers and Pediatric Concussion Subtypes.

The Journal of pediatrics·2026

Outpatient Respiratory Outcomes in Infants Who Survive Hospitalization for Extreme Prematurity.

The Journal of pediatrics·2026

Relationship Between Bronchopulmonary Dysplasia, Corpus Callosum Microstructure at Term-Equivalent Age, and Neurodevelopment at Age 2 Years in Infants Born Preterm.

The Journal of pediatrics·2026

Magnetic Resonance Imaging During Therapeutic Hypothermia Accurately Reflects the Degree of Brain Injury in Neonates with Hypoxic-Ischemic Encephalopathy.

The Journal of pediatrics·2026

Acute Emotional Symptoms Predict Emotional Functioning Up to 6 Months After Pediatric Concussion: An A-CAP Study.

The Journal of pediatrics·2026

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Research (Washington, D.C.)·2026

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Clinical case reports·2026

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Journal of human genetics·2026

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

Nature genetics·2026

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Psychiatric genetics·2026

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Frontiers in genetics·2026

Related Experiment Videos

Radioulnar synostosis and craniosynostosis in one family

Related Concept Videos

Insulin in human milk and the prevention of type 1 diabetes.

Reversal of cardiac complications in thalassemia major by long-term intermittent daily intensive iron chelation.

A novel thermoregulatory system maintains perioperative normothermia in children undergoing elective surgery.

Prolidase deficiency among an Israeli population: prenatal diagnosis in a genetic disorder with uncertain prognosis.

[1000 cardiac catheterizations in congenital heart disease].

[Percutaneous closure of patent arterial ducts with occluding spring coils].

School-Based Health and Healthcare Utilization Among Rural Youth: Evidence from a School-Based Health Center Opening.

Associations Between Saliva-Based Biomarkers and Pediatric Concussion Subtypes.

Outpatient Respiratory Outcomes in Infants Who Survive Hospitalization for Extreme Prematurity.

Relationship Between Bronchopulmonary Dysplasia, Corpus Callosum Microstructure at Term-Equivalent Age, and Neurodevelopment at Age 2 Years in Infants Born Preterm.

Magnetic Resonance Imaging During Therapeutic Hypothermia Accurately Reflects the Degree of Brain Injury in Neonates with Hypoxic-Ischemic Encephalopathy.

Acute Emotional Symptoms Predict Emotional Functioning Up to 6 Months After Pediatric Concussion: An A-CAP Study.

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Related Experiment Videos

Radioulnar synostosis and craniosynostosis in one family

Related Concept Videos

Related Articles