Letter: Alpha-fetoprotein as predictor of fetal neural-tube defects

Medium chain acyl-CoA dehydrogenase deficiency human genome epidemiology review.

Genetics in medicine : official journal of the American College of Medical Genetics·2001

Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency.

Genetics in medicine : official journal of the American College of Medical Genetics·2001

Tocolytic magnesium sulfate exposure and risk of cerebral palsy among children with birth weights less than 1,750 grams.

American journal of epidemiology·2000

Monitoring the prevalence of congenital hypothyroidism for 20 years near the Savannah River site.

Journal of the Medical Association of Georgia·2000

Lymphedema as a postulated cause of cutis verticis gyrata in Turner syndrome.

Pediatric dermatology·1998

Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979-1992.

American journal of medical genetics·1997

Wildfire smoke and health: current evidence, mechanisms, and future challenges.

Lancet (London, England)·2026

Use of the bacterial lysate OM-85 for the primary prevention of wheezing lower respiratory illness in preschool children: a randomised, placebo-controlled trial.

Lancet (London, England)·2026

Wealth redistribution policies to mitigate the impact of development assistance defunding: a retrospective evaluation and forecasting analysis up to 2030.

Lancet (London, England)·2026

Induction and consolidation atezolizumab with stereotactic body radiation therapy versus radiation alone in high-risk, early-stage non-small-cell lung cancer (SWOG/NRG S1914): a multicentre, open-label, superiority, phase 3, randomised controlled trial.

Lancet (London, England)·2026

The changing therapeutic landscape of small-cell lung cancer.

Lancet (London, England)·2026

Natural history and clinical impact of epilepsy in adults with Down syndrome: a multicentre clinical study.

Lancet (London, England)·2026

Fetal Craniopharyngioma: A Rare Prenatal Diagnosis.

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society·2026

miR-197 Targets NLRP3 3' UTR and Correlates with NLRP3/Caspase-1/IL-18 Signaling in Hyperoxia-Stimulated Neonatal BPD Mouse Model.

Journal of visualized experiments : JoVE·2026

Fetal Hydronephrosis: A Narrative Review of Diagnostic Pathways, Prognostic Markers, and Management.

Cureus·2026

Pain Management During Neonatal Blood Sampling: An Overview of Systematic Reviews.

Paediatric & neonatal pain·2026

Clinical Presentation, Orthopedic Outcomes, and Microbiological Spectrum in Pediatric Septic Arthritis: A Prospective Study.

Journal of orthopaedic case reports·2026

Osteomyelitis Secondary to Infected Cephalhematoma in a Female Neonate: A Case Report and Clinical Insights.

Case reports in pediatrics·2026

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Letter: Alpha-fetoprotein as predictor of fetal neural-tube defects

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Medium chain acyl-CoA dehydrogenase deficiency human genome epidemiology review.

Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency.

Tocolytic magnesium sulfate exposure and risk of cerebral palsy among children with birth weights less than 1,750 grams.

Monitoring the prevalence of congenital hypothyroidism for 20 years near the Savannah River site.

Lymphedema as a postulated cause of cutis verticis gyrata in Turner syndrome.

Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979-1992.

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