32 results on '"Siekmeyer, Manuela"'
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2. Intensive care drug therapy and its potential adverse effects on blood pressure and heart rate in critically ill children
3. Unusual mechanical failures of intrathecal baclofen pump systems: symptoms, signs, and trouble shooting
4. Drowning and Nonfatal Drowning in Children and Adolescents: A Subsequent Retrospective Data Analysis.
5. A rare combination of hydronephrosis, megaureter, and hyperphosphatasia
6. Choroid plexus coagulation in trisomy 9 mosaic–related hydrocephalus—a case report
7. In-Depth Analysis of the Re-Emergence of Respiratory Syncytial Virus at a Tertiary Care Hospital in Germany in the Summer of 2021 after the Alleviation of Non-Pharmaceutical Interventions Due to the SARS-CoV-2 Pandemic
8. Epidemiological Analysis of the Emergency Vascular Access in Pediatric Trauma Patients: Single-Center Experience of Intravenous, Intraosseous, Central Venous, and Arterial Line Placements
9. Possible pulmonary Rhizopus oryzae infection in a previously healthy child after a near-drowning incident
10. Endoscopic lavage and application of rTPA in multiloculated hydrocephalus: a mono-center experience
11. A Case Report: First Long-Term Treatment With Burosumab in a Patient With Cutaneous-Skeletal Hypophosphatemia Syndrome
12. Got a Pen for Allergen Immunotherapy? Lessons from Near-Fatal Anaphylaxis with Pulmonary Edema
13. Umbilical Cord Teratoma Presenting as Ruptured Omphalocele
14. Tracheal Tube Misplacement after Emergency Intubation in Pediatric Trauma Patients: A Retrospective, Exploratory Study
15. Retrospektive Analyse von 44 Ertrinkungsunfällen von Kindern und Jugendlichen
16. Combined heterotopic liver–pancreas transplantation as a curative treatment for liver cirrhosis and diabetes mellitus in cystic fibrosis
17. Treatment of Ruptured Giant Omphalocele and Gastroschisis with Liver Herniation using a Wound Retractor as a Novel Approach
18. VP-shunt dysfunction caused by malaria CNS infection
19. Combined Partial Trisomy 11q and Partial Monosomy 10p in a 19-Year-Old Female Patient: Phenotypic and Genotypic Findings
20. Acute cerebral infarction and extra pontine myelinolysis in children with new onset type 1 diabetes mellitus
21. Genotype–phenotype correlation at codon 1740 ofSETD2
22. Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder.
23. Glans Ischemia after Circumcision in a 16-Year-Old Boy: Full Recovery after Angiography with Local Spasmolysis, Systemic Vasodilatation, and Anticoagulation
24. A Fulminant Case of Haemophilus influenzae Serotype F Meningitis in an Immunocompetent 3-Year-Old Boy
25. A 33-year-old male patient with paternal derived duplication of 14q11.2–14q22.1~22.3: clinical course, phenotypic and genotypic findings
26. VP-shunt dysfunction caused by malaria CNS infection
27. Possible pulmonary Rhizopus oryzae infection in a previously healthy child after a near-drowning incident
28. Combined heterotopic liver–pancreas transplantation as a curative treatment for liver cirrhosis and diabetes mellitus in cystic fibrosis
29. Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435C
30. Citric acid as the last therapeutic approach in an acute life-threatening metabolic decompensation of propionic acidaemia
31. Fulminant and Fatal Course of Acute Lymphoblastic Leukemia Due to Lactic Acidosis and Suspected Abdominal Compartment Syndrome
32. Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder.
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