Subclinical hypothyroidism in the neonate: not to treat

Mutational analysis of the PHEX gene: novel point mutations and detection of large deletions by MLPA in patients with X-linked hypophosphatemic rickets.

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Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997.

European journal of pediatrics·1999

Newborn screening for hyperphenylalaninemia on day 5: is 240 mumol/liter the most appropriate cut-off level?

Preventive medicine·1990

[The phenylalanine stress test in the classification of patients with phenylketonuria].

Klinische Padiatrie·1989

Comprehensive Geriatric Assessment in Older Adults with Rheumatoid Arthritis: A Pilot Cross-Sectional Study.

The American journal of the medical sciences·2026

The evolving burden of hepatitis B and C: Past trends and future projections from the global burden of disease study 2021.

The American journal of the medical sciences·2026

Associations of biological aging and biological age acceleration with mortality in patients with cardiorenal syndrome: A prospective cohort study.

The American journal of the medical sciences·2026

Comparative Effectiveness and Outcomes of Direct Oral Anticoagulants vs. Vitamin K Antagonists (VKA) in Atrial Arrhythmias Patients with Isolated Lupus Anticoagulant Without Antiphospholipid Syndrome: A Real-World Cohort Analysis.

The American journal of the medical sciences·2026

Beyond monotherapy: The evolving role of CTLA-4 in combination immunotherapy for gastrointestinal cancers.

The American journal of the medical sciences·2026

Acidemia, Lactate, and Anemia Are Associated With Clinically Meaningful SpO2-SaO2 Discordance in Critically Ill Adults.

The American journal of the medical sciences·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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Subclinical hypothyroidism in the neonate: not to treat

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Mutational analysis of the PHEX gene: novel point mutations and detection of large deletions by MLPA in patients with X-linked hypophosphatemic rickets.

Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997.

Newborn screening for hyperphenylalaninemia on day 5: is 240 mumol/liter the most appropriate cut-off level?

[The phenylalanine stress test in the classification of patients with phenylketonuria].

Comprehensive Geriatric Assessment in Older Adults with Rheumatoid Arthritis: A Pilot Cross-Sectional Study.

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Subclinical hypothyroidism in the neonate: not to treat

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