The clinical use of intravenous immunoglobulin in pediatrics

[Interdisciplinary AWMF guideline for the treatment of primary antibody deficiencies].

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Hereditary angioedema (HAE) in children and adolescents--a consensus on therapeutic strategies.

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Efficacy and safety of Hizentra(®) in patients with primary immunodeficiency after a dose-equivalent switch from intravenous or subcutaneous replacement therapy.

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Hyperbilirubinemia and rapid fatal hepatic failure in severe combined immunodeficiency caused by adenosine deaminase deficiency (ADA-SCID).

Klinische Padiatrie·2011

Delayed onset of (severe) combined immunodeficiency (S)CID (T-B+NK+): complete IL-7 receptor deficiency in a 22 months old girl.

Klinische Padiatrie·2009

Adolescent Obesity: A Stepwise Clinical Approach.

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Evaluation of Systemic Inflammation in Pediatric Rheumatic Diseases Using a Composite Systemic Inflammation Score.

Indian journal of pediatrics·2026

Impella Versus Intra-aortic Balloon Pump in Cardiogenic Shock: Arrhythmias, Bleeding Complications, and In-Hospital Outcomes in a Propensity-Matched Analysis of the National Inpatient Sample.

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Unsupervised Machine Learning of Intrapancreatic Fat Deposition Reveals Distinct Clinical Phenotypes: A CT Study.

Diabetes, metabolic syndrome and obesity : targets and therapy·2026

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Layered immune biomarker monitoring in IgA nephropathy: from mucosal IgA dysregulation to precision therapeutic response assessment.

Frontiers in medicine·2026

Gastrointestinal Histoplasmosis Mimicking Intestinal Tuberculosis and Crohn's Disease: Ileocecal Involvement in an Immunocompetent Host.

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Peripheral immune phenotyping identifies an immunosuppressed sepsis endotype with potential relevance for immune stratification.

Frontiers in immunology·2026

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The clinical use of intravenous immunoglobulin in pediatrics

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[Interdisciplinary AWMF guideline for the treatment of primary antibody deficiencies].

[Diagnostics and exclusion of hereditary angioedema : a standarized approach for the practice].

Hereditary angioedema (HAE) in children and adolescents--a consensus on therapeutic strategies.

Efficacy and safety of Hizentra(®) in patients with primary immunodeficiency after a dose-equivalent switch from intravenous or subcutaneous replacement therapy.

Hyperbilirubinemia and rapid fatal hepatic failure in severe combined immunodeficiency caused by adenosine deaminase deficiency (ADA-SCID).

Delayed onset of (severe) combined immunodeficiency (S)CID (T-B+NK+): complete IL-7 receptor deficiency in a 22 months old girl.

Adolescent Obesity: A Stepwise Clinical Approach.

Evaluation of Systemic Inflammation in Pediatric Rheumatic Diseases Using a Composite Systemic Inflammation Score.

Impella Versus Intra-aortic Balloon Pump in Cardiogenic Shock: Arrhythmias, Bleeding Complications, and In-Hospital Outcomes in a Propensity-Matched Analysis of the National Inpatient Sample.

Unsupervised Machine Learning of Intrapancreatic Fat Deposition Reveals Distinct Clinical Phenotypes: A CT Study.

Predictive value of stress-induced hyperglycemia for 28-day all-cause mortality in ICU patients with sepsis: a MIMIC-IV-based retrospective cohort study.

Layered immune biomarker monitoring in IgA nephropathy: from mucosal IgA dysregulation to precision therapeutic response assessment.

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