[Delayed puberty and hypogonadism in boys]

Growth hormone therapy with three dosage regimens in children with idiopathic short stature. European Study Group Participating Investigators.

The Journal of pediatrics·1998

Pituitary dwarfism in the R271W Pit-1 gene mutation.

European journal of pediatrics·1997

Increased neutrophil insulin-like growth factor-I (IGF-I) receptor expression and IGF-I-induced functional capacity in patients with untreated Laron syndrome.

European journal of endocrinology·1997

Final height after long-term growth hormone treatment in Turner syndrome. European Study Group.

The Journal of pediatrics·1995

Expression of leukocyte differentiation antigens during the differentiation of HL-60 cells induced by 1,25-dihydroxyvitamin D3: comparison with the maturation of normal monocytic and granulocytic bone marrow cells.

Journal of leukocyte biology·1995

Priming of human polymorphonuclear neutrophilic leukocytes by insulin-like growth factor I: increased phagocytic capacity, complement receptor expression, degranulation, and oxidative burst.

The Journal of clinical endocrinology and metabolism·1995

A woman in her 70s with chest pain and elevated troponin T levels.

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·2026

Ductus arteriosus aneurysm in a neonate with inspiratory stridor.

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·2026

Confined to a lunatic asylum for eleven years: the case of Haaken Bergh.

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·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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[Delayed puberty and hypogonadism in boys]

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Growth hormone therapy with three dosage regimens in children with idiopathic short stature. European Study Group Participating Investigators.

Pituitary dwarfism in the R271W Pit-1 gene mutation.

Increased neutrophil insulin-like growth factor-I (IGF-I) receptor expression and IGF-I-induced functional capacity in patients with untreated Laron syndrome.

Final height after long-term growth hormone treatment in Turner syndrome. European Study Group.

Expression of leukocyte differentiation antigens during the differentiation of HL-60 cells induced by 1,25-dihydroxyvitamin D3: comparison with the maturation of normal monocytic and granulocytic bone marrow cells.

Priming of human polymorphonuclear neutrophilic leukocytes by insulin-like growth factor I: increased phagocytic capacity, complement receptor expression, degranulation, and oxidative burst.

A woman in her 70s with chest pain and elevated troponin T levels.

Ductus arteriosus aneurysm in a neonate with inspiratory stridor.

Confined to a lunatic asylum for eleven years: the case of Haaken Bergh.

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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