[Pediatric neurology in the works of Veszprémi, Csapó and Rozén Rosenstein]

[Temporary bone defect following cranial contusion in infants].

Orvosi hetilap·1996

Ultrasound control of progressive hydrocephalus in infancy.

Child's brain·1984

Prognosis of benign cerebellar astrocytomas in children.

Child's brain·1983

Epilepsy and brain abscess.

Acta paediatrica Academiae Scientiarum Hungaricae·1979

Benign intracranial hypertension of uncertain origin.

Acta paediatrica Academiae Scientiarum Hungaricae·1979

[Spinal tumors in infancy and childhood].

Zentralblatt fur Neurochirurgie·1977

[Disordered eating behaviors and eating disorders among athletes II.]

Orvosi hetilap·2026

[Acute psychological stress and endometriosis-related pain].

Orvosi hetilap·2026

[Thoracic trauma in Hungary today: heritage, current challenges and future directions].

Orvosi hetilap·2026

[Integrated use of ketamine in emergency care].

Orvosi hetilap·2026

[Principles of treating patients with chronic obstructive pulmonary disease].

Orvosi hetilap·2026

[The gut-muscle axis and the role of Roseburia inulinivorans in age-related muscle loss: a narrative review].

Orvosi hetilap·2026

Mixed Presentation of Hyperglycemic Hyperosmolar State and Diabetic Ketoacidosis in a Pediatric Patient: a Case Report and Literature Review.

Journal of clinical research in pediatric endocrinology·2026

Renin-Aldosterone Activation and Enhanced Urinary Potassium Excretion in Asphyxiated Newborns Treated with Therapeutic Hypothermia: A Prospective Study.

Therapeutic hypothermia and temperature management·2026

Population pharmacokinetics of levetiracetam in term neonates with hypoxic-ischemic encephalopathy and therapeutic hypothermia: The LEVNEONAT-1 study.

British journal of clinical pharmacology·2026

Intubation videoendoscopy in a preterm infant with congenital tracheal stenosis and laryngotracheoesophageal cleft: a case report.

BMC pediatrics·2026

Incidence and predictors of early neonatal mortality among neonates admitted to neonatal intensive care units in public general hospitals in Northwest Ethiopia: a multicenter prospective cohort study.

BMC pediatrics·2026

Loss of protein function resulting in severe phenotypes of X-linked myotubular myopathy caused by novel synonymous and splice-site variants in the MTM1 gene.

Pediatrics and neonatology·2026

Related Experiment Videos

[Pediatric neurology in the works of Veszprémi, Csapó and Rozén Rosenstein]

Related Concept Videos

[Temporary bone defect following cranial contusion in infants].

Ultrasound control of progressive hydrocephalus in infancy.

Prognosis of benign cerebellar astrocytomas in children.

Epilepsy and brain abscess.

Benign intracranial hypertension of uncertain origin.

[Spinal tumors in infancy and childhood].

[Disordered eating behaviors and eating disorders among athletes II.]

[Acute psychological stress and endometriosis-related pain].

[Thoracic trauma in Hungary today: heritage, current challenges and future directions].

[Integrated use of ketamine in emergency care].

[Principles of treating patients with chronic obstructive pulmonary disease].

[The gut-muscle axis and the role of Roseburia inulinivorans in age-related muscle loss: a narrative review].

Mixed Presentation of Hyperglycemic Hyperosmolar State and Diabetic Ketoacidosis in a Pediatric Patient: a Case Report and Literature Review.

Renin-Aldosterone Activation and Enhanced Urinary Potassium Excretion in Asphyxiated Newborns Treated with Therapeutic Hypothermia: A Prospective Study.

Population pharmacokinetics of levetiracetam in term neonates with hypoxic-ischemic encephalopathy and therapeutic hypothermia: The LEVNEONAT-1 study.

Intubation videoendoscopy in a preterm infant with congenital tracheal stenosis and laryngotracheoesophageal cleft: a case report.

Incidence and predictors of early neonatal mortality among neonates admitted to neonatal intensive care units in public general hospitals in Northwest Ethiopia: a multicenter prospective cohort study.

Loss of protein function resulting in severe phenotypes of X-linked myotubular myopathy caused by novel synonymous and splice-site variants in the MTM1 gene.

Related Experiment Videos

[Pediatric neurology in the works of Veszprémi, Csapó and Rozén Rosenstein]

Related Concept Videos

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