[CONSIDERATIONS ON CONGENITAL CHONDROSTERNAL DEPRESSION. CASE CONTRIBUTION]

Effects of dexmedetomidine on kidney and brain tissue microcirculation and histology in ovine cardiopulmonary bypass: a randomised controlled trial.

Anaesthesia·2023

Congenital heart defects in the recurrent 2q13 deletion syndrome.

European journal of medical genetics·2021

Arbovirus serosurvey (Orthobunyavirus, Flavivirus, and Alphavirus) in a draft horse population from Santa Fe, Argentina (2013-2016).

Archives of virology·2021

Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehog.

Clinical genetics·2018

Renal haemodynamics and oxygenation during and after cardiac surgery and cardiopulmonary bypass.

Acta physiologica (Oxford, England)·2017

Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.

Clinical genetics·2017

Tumor-induced osteomalacia: a 2026 update.

Minerva medica·2026

How to become a centenarian in four weeks?. Myths and limits of longevity recipes: a critical review.

Minerva medica·2026

Comparative efficacy and safety between intravenous recombinant human prourokinase and alteplase in acute ischemic stroke treatment: a meta-analysis of randomized controlled trials.

Minerva medica·2026

Efficacy and safety of oral tapentadol for cancer-related pain: an updated systematic review and meta-analysis.

Minerva medica·2026

Use of the neurostimulator in thyroidectomy procedures: comparison between vagal and recurrent laryngeal nerve stimulation.

Minerva medica·2026

Iron deficiency and risk of acute kidney injury after TAVI: a machine learning analysis.

Minerva medica·2026

Diagnostic performance of adult-based ultrasound ACR-TIRADS and C-TIRADS in adolescent thyroid nodules.

Frontiers in endocrinology·2026

Photo-based deep learning for detection of pediatric adenoid hypertrophy.

Digital health·2026

Associations of alexithymia, psychological problems, and emotion regulation difficulties with disordered eating behaviors in adolescents with type 1 diabetes.

Dusunen adam : Bakirkoy Ruh ve Sinir Hastaliklari Hastanesi yayin organi·2026

Pediatric thyroid cancer: a retrospective analysis of 42 cases.

Frontiers in oncology·2026

Novel Homozygous Mitochondrial Calcium Uptake Protein 1 Variant (c.38T>C, p.Leu13Pro) in a 7-year-old Girl with Congenital Ptosis and Proximal Myopathy: Expanding the Phenotypic Spectrum.

Annals of African medicine·2026

Child Opportunity Index and Suicide Risk Screening Positivity in Pediatric Emergency and Urgent Care Patients Presenting Without Behavioral Health Complaints.

Pediatric emergency care·2026

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[CONSIDERATIONS ON CONGENITAL CHONDROSTERNAL DEPRESSION. CASE CONTRIBUTION]

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Effects of dexmedetomidine on kidney and brain tissue microcirculation and histology in ovine cardiopulmonary bypass: a randomised controlled trial.

Congenital heart defects in the recurrent 2q13 deletion syndrome.

Arbovirus serosurvey (Orthobunyavirus, Flavivirus, and Alphavirus) in a draft horse population from Santa Fe, Argentina (2013-2016).

Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehog.

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Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.

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How to become a centenarian in four weeks?. Myths and limits of longevity recipes: a critical review.

Comparative efficacy and safety between intravenous recombinant human prourokinase and alteplase in acute ischemic stroke treatment: a meta-analysis of randomized controlled trials.

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Use of the neurostimulator in thyroidectomy procedures: comparison between vagal and recurrent laryngeal nerve stimulation.

Iron deficiency and risk of acute kidney injury after TAVI: a machine learning analysis.

Diagnostic performance of adult-based ultrasound ACR-TIRADS and C-TIRADS in adolescent thyroid nodules.

Photo-based deep learning for detection of pediatric adenoid hypertrophy.

Associations of alexithymia, psychological problems, and emotion regulation difficulties with disordered eating behaviors in adolescents with type 1 diabetes.

Pediatric thyroid cancer: a retrospective analysis of 42 cases.

Novel Homozygous Mitochondrial Calcium Uptake Protein 1 Variant (c.38T>C, p.Leu13Pro) in a 7-year-old Girl with Congenital Ptosis and Proximal Myopathy: Expanding the Phenotypic Spectrum.

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