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Showing 1 to 12 of 850 entries
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Concurrent adrenal neuroblastoma and kawasaki disease: a report of a rare case.

Case reports in pediatrics

Alavi S, Fahimzad A, Jadali F, Ghazizadeh F, Rashidi A.
PMID: 23476867
Case Rep Pediatr. 2013;2013:931703. doi: 10.1155/2013/931703. Epub 2013 Feb 06.

Kawasaki disease (KD) is a systemic vasculitis of unknown etiology and a leading cause of acquired heart disease. It is assumed that there is an activation of the immune system by an infectious trigger in a genetically susceptible host....

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Alavi S, Fahimzad A, Jadali F, et al. Concurrent adrenal neuroblastoma and kawasaki disease: a report of a rare case. Case Rep Pediatr. 2013;2013:931703doi: 10.1155/2013/931703.
Alavi, S., Fahimzad, A., Jadali, F., Ghazizadeh, F., & Rashidi, A. (2013). Concurrent adrenal neuroblastoma and kawasaki disease: a report of a rare case. Case reports in pediatrics, 2013931703. https://doi.org/10.1155/2013/931703
Alavi, Samin, et al. "Concurrent adrenal neuroblastoma and kawasaki disease: a report of a rare case." Case reports in pediatrics vol. 2013 (2013): 931703. doi: https://doi.org/10.1155/2013/931703
Alavi S, Fahimzad A, Jadali F, Ghazizadeh F, Rashidi A. Concurrent adrenal neuroblastoma and kawasaki disease: a report of a rare case. Case Rep Pediatr. 2013;2013:931703. doi: 10.1155/2013/931703. Epub 2013 Feb 06. PMID: 23476867; PMCID: PMC3580901.
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An unusual case of rapidly progressive hyperbilirubinemia.

Case reports in pediatrics

Thornton KM, Nyp MF, Music Aplenc L, Jones GL, Carpenter SL, Guest EM, Shapiro SM, Manimtim WM.
PMID: 24288641
Case Rep Pediatr. 2013;2013:284029. doi: 10.1155/2013/284029. Epub 2013 Oct 29.

We present an unusual case of hyperbilirubinemia with rapid early progression leading to bilirubin encephalopathy in a term neonate. Despite early recognition and intervention, the total serum bilirubin reached a maximum level of 39 mg/dL at 32 hours of...

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Thornton KM, Nyp MF, Music Aplenc L, et al. An unusual case of rapidly progressive hyperbilirubinemia. Case Rep Pediatr. 2013;2013:284029doi: 10.1155/2013/284029.
Thornton, K. M., Nyp, M. F., Music Aplenc, L., Jones, G. L., Carpenter, S. L., Guest, E. M., Shapiro, S. M., & Manimtim, W. M. (2013). An unusual case of rapidly progressive hyperbilirubinemia. Case reports in pediatrics, 2013284029. https://doi.org/10.1155/2013/284029
Thornton, Kimberly M, et al. "An unusual case of rapidly progressive hyperbilirubinemia." Case reports in pediatrics vol. 2013 (2013): 284029. doi: https://doi.org/10.1155/2013/284029
Thornton KM, Nyp MF, Music Aplenc L, Jones GL, Carpenter SL, Guest EM, Shapiro SM, Manimtim WM. An unusual case of rapidly progressive hyperbilirubinemia. Case Rep Pediatr. 2013;2013:284029. doi: 10.1155/2013/284029. Epub 2013 Oct 29. PMID: 24288641; PMCID: PMC3830790.
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Corrigendum to "Multiple Congenital Colonic Stenosis: A Rare Gastrointestinal Malformation".

Case reports in pediatrics

Zambaiti E, Chiaramonte C, Salerno S, Li Voti G, Siracusa F.
PMID: 27525146
Case Rep Pediatr. 2016;2016:5353012. doi: 10.1155/2016/5353012. Epub 2016 Jul 25.

[This corrects the article DOI: 10.1155/2016/6329793.].

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Zambaiti E, Chiaramonte C, Salerno S, et al. Corrigendum to "Multiple Congenital Colonic Stenosis: A Rare Gastrointestinal Malformation". Case Rep Pediatr. 2016;2016:5353012doi: 10.1155/2016/5353012.
Zambaiti, E., Chiaramonte, C., Salerno, S., Li Voti, G., & Siracusa, F. (2016). Corrigendum to "Multiple Congenital Colonic Stenosis: A Rare Gastrointestinal Malformation". Case reports in pediatrics, 20165353012. https://doi.org/10.1155/2016/5353012
Zambaiti, Elisa, et al. "Corrigendum to "Multiple Congenital Colonic Stenosis: A Rare Gastrointestinal Malformation"." Case reports in pediatrics vol. 2016 (2016): 5353012. doi: https://doi.org/10.1155/2016/5353012
Zambaiti E, Chiaramonte C, Salerno S, Li Voti G, Siracusa F. Corrigendum to "Multiple Congenital Colonic Stenosis: A Rare Gastrointestinal Malformation". Case Rep Pediatr. 2016;2016:5353012. doi: 10.1155/2016/5353012. Epub 2016 Jul 25. PMID: 27525146; PMCID: PMC4976166.
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Thermal Esophageal Injury following Ingestion of Boiling Mushroom Water.

Case reports in pediatrics

Prevost A, Talley A, Klepper E, McDonough E.
PMID: 28484658
Case Rep Pediatr. 2017;2017:1859352. doi: 10.1155/2017/1859352. Epub 2017 Apr 18.

Thermal esophageal and gastric damage from ingestion of hot liquids is poorly studied in pediatrics. Limited case reports exist in the literature. Many cases presented with chest pain, dysphagia, and odynophagia. Variable histologic findings were reported. No definitive management...

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Prevost A, Talley A, Klepper E, et al. Thermal Esophageal Injury following Ingestion of Boiling Mushroom Water. Case Rep Pediatr. 2017;2017:1859352doi: 10.1155/2017/1859352.
Prevost, A., Talley, A., Klepper, E., & McDonough, E. (2017). Thermal Esophageal Injury following Ingestion of Boiling Mushroom Water. Case reports in pediatrics, 20171859352. https://doi.org/10.1155/2017/1859352
Prevost, Allison, et al. "Thermal Esophageal Injury following Ingestion of Boiling Mushroom Water." Case reports in pediatrics vol. 2017 (2017): 1859352. doi: https://doi.org/10.1155/2017/1859352
Prevost A, Talley A, Klepper E, McDonough E. Thermal Esophageal Injury following Ingestion of Boiling Mushroom Water. Case Rep Pediatr. 2017;2017:1859352. doi: 10.1155/2017/1859352. Epub 2017 Apr 18. PMID: 28484658; PMCID: PMC5412167.
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Apparent Life-Threatening Event following Maternal Use of Temazepam during Labour.

Case reports in pediatrics

Damen L, Visser DH, Sie SD, van Weissenbruch MM.
PMID: 25024861
Case Rep Pediatr. 2014;2014:650605. doi: 10.1155/2014/650605. Epub 2014 Jun 15.

Benzodiazepines are one of the most frequently prescribed psychotropic drugs during pregnancy. Despite the fact that these drugs have been in use for a long time, there is still debate about the safety for the developing fetus and neonate....

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Damen L, Visser DH, Sie SD, et al. Apparent Life-Threatening Event following Maternal Use of Temazepam during Labour. Case Rep Pediatr. 2014;2014:650605doi: 10.1155/2014/650605.
Damen, L., Visser, D. H., Sie, S. D., & van Weissenbruch, M. M. (2014). Apparent Life-Threatening Event following Maternal Use of Temazepam during Labour. Case reports in pediatrics, 2014650605. https://doi.org/10.1155/2014/650605
Damen, L, et al. "Apparent Life-Threatening Event following Maternal Use of Temazepam during Labour." Case reports in pediatrics vol. 2014 (2014): 650605. doi: https://doi.org/10.1155/2014/650605
Damen L, Visser DH, Sie SD, van Weissenbruch MM. Apparent Life-Threatening Event following Maternal Use of Temazepam during Labour. Case Rep Pediatr. 2014;2014:650605. doi: 10.1155/2014/650605. Epub 2014 Jun 15. PMID: 25024861; PMCID: PMC4082877.
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Two mutations in surfactant protein C gene associated with neonatal respiratory distress.

Case reports in pediatrics

Tarocco A, Ballardini E, Contiero MR, Garani G, Fanaro S.
PMID: 26000190
Case Rep Pediatr. 2015;2015:591783. doi: 10.1155/2015/591783. Epub 2015 Apr 27.

Multiple mutations of surfactant genes causing surfactant dysfunction have been described. Surfactant protein C (SP-C) deficiency is associated with variable clinical manifestations ranging from neonatal respiratory distress syndrome to lethal lung disease. We present an extremely low birth weight...

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Tarocco A, Ballardini E, Contiero MR, et al. Two mutations in surfactant protein C gene associated with neonatal respiratory distress. Case Rep Pediatr. 2015;2015:591783doi: 10.1155/2015/591783.
Tarocco, A., Ballardini, E., Contiero, M. R., Garani, G., & Fanaro, S. (2015). Two mutations in surfactant protein C gene associated with neonatal respiratory distress. Case reports in pediatrics, 2015591783. https://doi.org/10.1155/2015/591783
Tarocco, Anna, et al. "Two mutations in surfactant protein C gene associated with neonatal respiratory distress." Case reports in pediatrics vol. 2015 (2015): 591783. doi: https://doi.org/10.1155/2015/591783
Tarocco A, Ballardini E, Contiero MR, Garani G, Fanaro S. Two mutations in surfactant protein C gene associated with neonatal respiratory distress. Case Rep Pediatr. 2015;2015:591783. doi: 10.1155/2015/591783. Epub 2015 Apr 27. PMID: 26000190; PMCID: PMC4426665.
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Costello syndrome with severe nodulocystic acne: unexpected significant improvement of acanthosis nigricans after oral isotretinoin treatment.

Case reports in pediatrics

Sriboonnark L, Arora H, Falto-Aizpurua L, Choudhary S, Connelly EA.
PMID: 25815234
Case Rep Pediatr. 2015;2015:934865. doi: 10.1155/2015/934865. Epub 2015 Feb 28.

We report the case of 17-year-old female diagnosed with Costello syndrome. Genetic testing provided a proof with G12S mutation in the HRAS gene since 3 years of age with a presentation of severe nodulocystic acne on her face. After...

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Sriboonnark L, Arora H, Falto-Aizpurua L, et al. Costello syndrome with severe nodulocystic acne: unexpected significant improvement of acanthosis nigricans after oral isotretinoin treatment. Case Rep Pediatr. 2015;2015:934865doi: 10.1155/2015/934865.
Sriboonnark, L., Arora, H., Falto-Aizpurua, L., Choudhary, S., & Connelly, E. A. (2015). Costello syndrome with severe nodulocystic acne: unexpected significant improvement of acanthosis nigricans after oral isotretinoin treatment. Case reports in pediatrics, 2015934865. https://doi.org/10.1155/2015/934865
Sriboonnark, Leelawadee, et al. "Costello syndrome with severe nodulocystic acne: unexpected significant improvement of acanthosis nigricans after oral isotretinoin treatment." Case reports in pediatrics vol. 2015 (2015): 934865. doi: https://doi.org/10.1155/2015/934865
Sriboonnark L, Arora H, Falto-Aizpurua L, Choudhary S, Connelly EA. Costello syndrome with severe nodulocystic acne: unexpected significant improvement of acanthosis nigricans after oral isotretinoin treatment. Case Rep Pediatr. 2015;2015:934865. doi: 10.1155/2015/934865. Epub 2015 Feb 28. PMID: 25815234; PMCID: PMC4359863.
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17-Year-Old Boy with Renal Failure and the Highest Reported Creatinine in Pediatric Literature.

Case reports in pediatrics

Master Sankar Raj V, Garcia J, Gordillo R.
PMID: 26199780
Case Rep Pediatr. 2015;2015:703960. doi: 10.1155/2015/703960. Epub 2015 Jun 14.

The prevalence of chronic kidney disease (CKD) is on the rise and constitutes a major health burden across the world. Clinical presentations in early CKD are usually subtle. Awareness of the risk factors for CKD is important for early...

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Master Sankar Raj V, Garcia J, Gordillo R. 17-Year-Old Boy with Renal Failure and the Highest Reported Creatinine in Pediatric Literature. Case Rep Pediatr. 2015;2015:703960doi: 10.1155/2015/703960.
Master Sankar Raj, V., Garcia, J., & Gordillo, R. (2015). 17-Year-Old Boy with Renal Failure and the Highest Reported Creatinine in Pediatric Literature. Case reports in pediatrics, 2015703960. https://doi.org/10.1155/2015/703960
Master Sankar Raj, Vimal, et al. "17-Year-Old Boy with Renal Failure and the Highest Reported Creatinine in Pediatric Literature." Case reports in pediatrics vol. 2015 (2015): 703960. doi: https://doi.org/10.1155/2015/703960
Master Sankar Raj V, Garcia J, Gordillo R. 17-Year-Old Boy with Renal Failure and the Highest Reported Creatinine in Pediatric Literature. Case Rep Pediatr. 2015;2015:703960. doi: 10.1155/2015/703960. Epub 2015 Jun 14. PMID: 26199780; PMCID: PMC4496647.
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The Combination of Gastroschisis, Jejunal Atresia, and Colonic Atresia in a Newborn.

Case reports in pediatrics

Bauman Z, Nanagas V.
PMID: 26180651
Case Rep Pediatr. 2015;2015:129098. doi: 10.1155/2015/129098. Epub 2015 Jun 09.

We encountered a rare case of gastroschisis associated with jejunal atresia and colonic atresia. In our case, the jejunal atresia was not discovered for 27 days after the initial abdominal wall closure. The colonic atresia was not discovered for...

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Bauman Z, Nanagas V. The Combination of Gastroschisis, Jejunal Atresia, and Colonic Atresia in a Newborn. Case Rep Pediatr. 2015;2015:129098doi: 10.1155/2015/129098.
Bauman, Z., & Nanagas, V. (2015). The Combination of Gastroschisis, Jejunal Atresia, and Colonic Atresia in a Newborn. Case reports in pediatrics, 2015129098. https://doi.org/10.1155/2015/129098
Bauman, Zachary, and Nanagas, Victor. "The Combination of Gastroschisis, Jejunal Atresia, and Colonic Atresia in a Newborn." Case reports in pediatrics vol. 2015 (2015): 129098. doi: https://doi.org/10.1155/2015/129098
Bauman Z, Nanagas V. The Combination of Gastroschisis, Jejunal Atresia, and Colonic Atresia in a Newborn. Case Rep Pediatr. 2015;2015:129098. doi: 10.1155/2015/129098. Epub 2015 Jun 09. PMID: 26180651; PMCID: PMC4477220.
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A 14-Year-Old Boy with Unusual Presentation of Respiratory Distress.

Case reports in pediatrics

Powell AW, Hanke S, Tweddell JS, Madsen N.
PMID: 28044119
Case Rep Pediatr. 2016;2016:7313942. doi: 10.1155/2016/7313942. Epub 2016 Dec 01.

There are multiple cardiac etiologies for wheezing and respiratory distress which require a high degree of suspicion for the pediatrician to diagnose. We present a case of a patient with a history of long-standing mild persistent asthma with minimal...

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Powell AW, Hanke S, Tweddell JS, et al. A 14-Year-Old Boy with Unusual Presentation of Respiratory Distress. Case Rep Pediatr. 2016;2016:7313942doi: 10.1155/2016/7313942.
Powell, A. W., Hanke, S., Tweddell, J. S., & Madsen, N. (2016). A 14-Year-Old Boy with Unusual Presentation of Respiratory Distress. Case reports in pediatrics, 20167313942. https://doi.org/10.1155/2016/7313942
Powell, Adam W, et al. "A 14-Year-Old Boy with Unusual Presentation of Respiratory Distress." Case reports in pediatrics vol. 2016 (2016): 7313942. doi: https://doi.org/10.1155/2016/7313942
Powell AW, Hanke S, Tweddell JS, Madsen N. A 14-Year-Old Boy with Unusual Presentation of Respiratory Distress. Case Rep Pediatr. 2016;2016:7313942. doi: 10.1155/2016/7313942. Epub 2016 Dec 01. PMID: 28044119; PMCID: PMC5156805.
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Neonatal Hyperglycemia due to Transient Neonatal Diabetes Mellitus in Puerto Rico.

Case reports in pediatrics

Fargas-Berríos N, García-Fragoso L, García-García I, Valcárcel M.
PMID: 26576310
Case Rep Pediatr. 2015;2015:984214. doi: 10.1155/2015/984214. Epub 2015 Oct 20.

Neonatal hyperglycemia is a metabolic disorder found in the neonatal intensive care units. Neonatal diabetes mellitus (NDM) is a very uncommon cause of hyperglycemia in the newborn, occurring in 1 in every 400,000 births. There are two subtypes of...

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Fargas-Berríos N, García-Fragoso L, García-García I, et al. Neonatal Hyperglycemia due to Transient Neonatal Diabetes Mellitus in Puerto Rico. Case Rep Pediatr. 2015;2015:984214doi: 10.1155/2015/984214.
Fargas-Berríos, N., García-Fragoso, L., García-García, I., & Valcárcel, M. (2015). Neonatal Hyperglycemia due to Transient Neonatal Diabetes Mellitus in Puerto Rico. Case reports in pediatrics, 2015984214. https://doi.org/10.1155/2015/984214
Fargas-Berríos, N, et al. "Neonatal Hyperglycemia due to Transient Neonatal Diabetes Mellitus in Puerto Rico." Case reports in pediatrics vol. 2015 (2015): 984214. doi: https://doi.org/10.1155/2015/984214
Fargas-Berríos N, García-Fragoso L, García-García I, Valcárcel M. Neonatal Hyperglycemia due to Transient Neonatal Diabetes Mellitus in Puerto Rico. Case Rep Pediatr. 2015;2015:984214. doi: 10.1155/2015/984214. Epub 2015 Oct 20. PMID: 26576310; PMCID: PMC4630382.
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Transient Ischemic Attack and Ischemic Stroke in Danon Disease with Formation of Left Ventricular Apical Thrombus despite Normal Systolic Function.

Case reports in pediatrics

Tsuda T, Shillingford AJ, Vetter J, Kandula V, Jain B, Temple J.
PMID: 29085695
Case Rep Pediatr. 2017;2017:6576382. doi: 10.1155/2017/6576382. Epub 2017 Sep 20.

Danon disease is a rare X-linked dominant skeletal and cardiac muscle disorder presenting with hypertrophic cardiomyopathy, Wolf-Parkinson-White syndrome, skeletal myopathy, and mild intellectual disability. Early morbidity and mortality due to heart failure or sudden death are known in Danon...

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Tsuda T, Shillingford AJ, Vetter J, et al. Transient Ischemic Attack and Ischemic Stroke in Danon Disease with Formation of Left Ventricular Apical Thrombus despite Normal Systolic Function. Case Rep Pediatr. 2017;2017:6576382doi: 10.1155/2017/6576382.
Tsuda, T., Shillingford, A. J., Vetter, J., Kandula, V., Jain, B., & Temple, J. (2017). Transient Ischemic Attack and Ischemic Stroke in Danon Disease with Formation of Left Ventricular Apical Thrombus despite Normal Systolic Function. Case reports in pediatrics, 20176576382. https://doi.org/10.1155/2017/6576382
Tsuda, Takeshi, et al. "Transient Ischemic Attack and Ischemic Stroke in Danon Disease with Formation of Left Ventricular Apical Thrombus despite Normal Systolic Function." Case reports in pediatrics vol. 2017 (2017): 6576382. doi: https://doi.org/10.1155/2017/6576382
Tsuda T, Shillingford AJ, Vetter J, Kandula V, Jain B, Temple J. Transient Ischemic Attack and Ischemic Stroke in Danon Disease with Formation of Left Ventricular Apical Thrombus despite Normal Systolic Function. Case Rep Pediatr. 2017;2017:6576382. doi: 10.1155/2017/6576382. Epub 2017 Sep 20. PMID: 29085695; PMCID: PMC5632496.
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Showing 1 to 12 of 850 entries