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Distribution of rotavirus genotypes in three Croatian regions among children ≤5 years of age (2012–2014)

International journal of infectious diseases, 2019-12, Vol.89, p.3-9

2019

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Pleuroparenchymal Fibroelastosis as a Late-Onset Pulmonary Toxicity after Treatment with Anticancer Chemotherapy for High-Risk Neuroblastoma

Case reports in pediatrics, 2024, Vol.2024 (1), p.4352032

2024

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Beyond Infantile Hemangiomas: A Glimpse into Overlapping Rare Syndromes Emphasizing the Vigilant Screening for PHACE and LUMBAR Syndromes

Case reports in pediatrics, 2024, Vol.2024 (1), p.7501793

2024

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Helmet Ventilation in a Child with COVID-19 and Acute Respiratory Distress Syndrome

Case reports in pediatrics, 2024, Vol.2024 (1), p.5519254

2024

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Cytokine Storm Syndrome Responsive to IL-1 Inhibition in Trisomy 21

Case reports in pediatrics, 2024, Vol.2024 (1), p.9946401

2024

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SARS-CoV-2-Triggered Hemophagocytic Lymphohistiocytosis with Complications of Posterior Reversible Encephalopathy Syndrome

Case reports in pediatrics, 2024, Vol.2024 (1), p.8829060

2024

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Asymptomatic Esophageal Eosinophilia in an 11-Year-Old with Severe Persistent Asthma

Case reports in pediatrics, 2023-10, Vol.2023, p.1-3

2023

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Effect of Recombinant Human Growth Hormone Treatment in a Patient with Short Stature Associated with the Ring Chromosome 17 Syndrome

Case reports in pediatrics, 2023-09, Vol.2023, p.1-4

2023

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The Use of Amantadine in Treating Extrapyramidal Symptoms in Organophosphates Poisoning in a Child

Case reports in pediatrics, 2023-09, Vol.2023, p.1-3

2023

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Enzyme Replacement Therapy (ERT) on Heart Function Changes the Outcome in Patients with Infantile-Onset Pompe Disease: A Familial History

Case reports in pediatrics, 2023-02, Vol.2023, p.8470341-5

2023

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Ectopia Cordis as a Lethal Neonatal Condition: A Case Report from Bahrain and a Literature Review

Case reports in pediatrics, 2022-08, Vol.2022, p.1-5

2022

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Identification of a New Variant of the MBTPS1 Gene of the Kondo-Fu Type of Spondyloepiphyseal Dysplasia (SEDKF) in a Saudi Patient

Case reports in pediatrics, 2022-10, Vol.2022, p.1-5

2022

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Congenital Tufting Enteropathy, a Rare Cause of Diarrhea and Malnourishment in Arab Child with Genetic and Histopathology Investigations

Case reports in pediatrics, 2023, Vol.2023, p.6301065-3

2023

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Acute Rhabdomyolysis in a Child with Multiple Suspicious Gene Variants

Case reports in pediatrics, 2022-09, Vol.2022, p.1-5

2022

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Diplopia and Optic Disc Edema as the Ocular Manifestations of COVID-19 in a Seven-Year-Old Child

Case reports in pediatrics, 2022-06, Vol.2022, p.1-3

2022

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Intrauterine Limb Ischemia in Patient Heterozygous for the 677C>T) RS1801133 (Polymorphism of Methylenetetrahydrofolate Reductase MTHR Gene

Case reports in pediatrics, 2022-10, Vol.2022, p.1-6

2022

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Late-Onset Hypertrophic Pyloric Stenosis in a 14-Weeks-Old Full Term Male Infant

Acta medica Lékarskí fakulty Univerzity Karlovy v Hradci Králove, 2019, Vol.62 (2), p.82-84

2019

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Concomitant MPZ and MFN2 Gene Variants and Charcot Marie Tooth Disease in a Boy: Clinical and Genetic Analysis—Literature Review

Case reports in pediatrics, 2022-04, Vol.2022, p.3793226-6

2022

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Juvenile Hemochromatosis due to a Homozygous Variant in the HJV Gene

Case reports in pediatrics, 2022-04, Vol.2022, p.7743748-4

2022

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Cardiac Calcified Amorphous Tumor in the Neonatal Period

Case reports in pediatrics, 2022-01, Vol.2022, p.9087597-3

2022

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A Case Report and Literature Review of Pseudo-TORCH Syndrome Type 2 (PTORCH2)

Case reports in pediatrics, 2022, Vol.2022 (1), p.3555532

2022

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Successful Treatment with Antibiotics Alone for Infant Rib Osteomyelitis

Case reports in pediatrics, 2022-01, Vol.2022, p.1-5

2022

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Obstructive Sleep Apnea with Paradoxical Vocal Cord Movement in Children during Sleep Endoscopy: Case Series

Case reports in pediatrics, 2020, Vol.2020 (2020), p.1-4

2020

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Congenital Cytomegalovirus Infection Presenting with Hyperbilirubinemia and Splenomegaly in a Term Infant with Trisomy 21

Case reports in pediatrics, 2020, Vol.2020 (2020), p.1-4

2020

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Successful Liposteroid Therapy for a Recurrent Idiopathic Pulmonary Hemosiderosis with Down Syndrome

Case reports in pediatrics, 2020, Vol.2020 (2020), p.1-5

2020

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Distribution of rotavirus genotypes in three Croatian regions among children ≤5 years of age (2012–2014)

Pleuroparenchymal Fibroelastosis as a Late-Onset Pulmonary Toxicity after Treatment with Anticancer Chemotherapy for High-Risk Neuroblastoma

Beyond Infantile Hemangiomas: A Glimpse into Overlapping Rare Syndromes Emphasizing the Vigilant Screening for PHACE and LUMBAR Syndromes

Helmet Ventilation in a Child with COVID-19 and Acute Respiratory Distress Syndrome

Cytokine Storm Syndrome Responsive to IL-1 Inhibition in Trisomy 21

SARS-CoV-2-Triggered Hemophagocytic Lymphohistiocytosis with Complications of Posterior Reversible Encephalopathy Syndrome

Asymptomatic Esophageal Eosinophilia in an 11-Year-Old with Severe Persistent Asthma

Effect of Recombinant Human Growth Hormone Treatment in a Patient with Short Stature Associated with the Ring Chromosome 17 Syndrome

The Use of Amantadine in Treating Extrapyramidal Symptoms in Organophosphates Poisoning in a Child

Enzyme Replacement Therapy (ERT) on Heart Function Changes the Outcome in Patients with Infantile-Onset Pompe Disease: A Familial History

Ectopia Cordis as a Lethal Neonatal Condition: A Case Report from Bahrain and a Literature Review

Identification of a New Variant of the MBTPS1 Gene of the Kondo-Fu Type of Spondyloepiphyseal Dysplasia (SEDKF) in a Saudi Patient

Congenital Tufting Enteropathy, a Rare Cause of Diarrhea and Malnourishment in Arab Child with Genetic and Histopathology Investigations

Acute Rhabdomyolysis in a Child with Multiple Suspicious Gene Variants

Diplopia and Optic Disc Edema as the Ocular Manifestations of COVID-19 in a Seven-Year-Old Child

Intrauterine Limb Ischemia in Patient Heterozygous for the 677C>T) RS1801133 (Polymorphism of Methylenetetrahydrofolate Reductase MTHR Gene

Late-Onset Hypertrophic Pyloric Stenosis in a 14-Weeks-Old Full Term Male Infant

Concomitant MPZ and MFN2 Gene Variants and Charcot Marie Tooth Disease in a Boy: Clinical and Genetic Analysis—Literature Review

Juvenile Hemochromatosis due to a Homozygous Variant in the HJV Gene

Cardiac Calcified Amorphous Tumor in the Neonatal Period

A Case Report and Literature Review of Pseudo-TORCH Syndrome Type 2 (PTORCH2)

Successful Treatment with Antibiotics Alone for Infant Rib Osteomyelitis

Obstructive Sleep Apnea with Paradoxical Vocal Cord Movement in Children during Sleep Endoscopy: Case Series

Congenital Cytomegalovirus Infection Presenting with Hyperbilirubinemia and Splenomegaly in a Term Infant with Trisomy 21

Successful Liposteroid Therapy for a Recurrent Idiopathic Pulmonary Hemosiderosis with Down Syndrome

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