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1. Advances in pediatrics in 2023: choices in allergy, analgesia, cardiology, endocrinology, gastroenterology, genetics, global health, hematology, infectious diseases, neonatology, neurology, pulmonology

2. First case of infant botulism in Sicily—case report

3. The awareness of sharenting in Italy: a pilot study

4. Group B streptococcus colonization in pregnancy and neonatal outcomes: a three-year monocentric retrospective study during and after the COVID-19 pandemic

5. Increased adherence to influenza vaccination among Palermo family pediatricians: a study on safety and compliance of qLAIV vaccination

6. A talented giant: a tribute to the memory of John M. Opitz

7. Enough with simplifying: 'eat less and move more': at what point are we with the treatment of excess weight in paediatrics?

8. Cardiovascular involvement in children with COVID-19 temporally related multisystem inflammatory syndrome (MIS-C): can cardiac magnetic resonance arrive to the heart of the problem?

9. Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcome

10. Adolescent gender dysphoria management: position paper from the Italian Academy of Pediatrics, the Italian Society of Pediatrics, the Italian Society for Pediatric Endocrinology and Diabetes, the Italian Society of Adolescent Medicine and the Italian Society of Child and Adolescent Neuropsychiatry

11. New and old criteria for diagnosing celiac disease: do they really differ? A retrospective observational study

12. Present and future are getting confused: are we equipped to face the technological revolution?

13. Use of complementary and alternative medicine in children affected by oncologic, neurologic and liver diseases: a narrative review

14. Year 2022: exploring COVID-19 pandemic in children

15. Report and follow-up on two new patients with congenital mesoblastic nephroma

16. Advances for pediatricians in 2022: allergy, anesthesiology, cardiology, dermatology, endocrinology, gastroenterology, genetics, global health, infectious diseases, metabolism, neonatology, neurology, oncology, pulmonology

17. Acute Respiratory Tract Infections (ARTIs) in Children after COVID-19-Related Social Distancing: An Epidemiological Study in a Single Center of Southern Italy

18. A pediatric case of Chlamydia psittaci caused severe Acute Respiratory Distress Syndrome (ARDS) in Italy

19. Ten-month follow-up of patients with covid-19 temporally related multi-system inflammatory syndrome in children: the experience of the children hospital of Palermo

20. New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception

21. UPDATE - 2022 Italian guidelines on the management of bronchiolitis in infants

22. Genetics and'democracy'

23. Congenital syphilis in a preterm newborn with gastrointestinal disorders and postnatal growth restriction

24. Intestinal malrotation in a female newborn affected by Osteopathia Striata with Cranial Sclerosis due to a de novo heterozygous nonsense mutation of the AMER1 gene

25. Febrile infection-related Epilepsy Syndrome (FIRES): a severe encephalopathy with status epilepticus. Literature review and presentation of two new cases

26. The awareness and acceptance of anti-COVID 19 vaccination in adolescence

27. Sensitivity of three commercial tests for SARS-CoV-2 serology in children: an Italian multicentre prospective study

29. New insights in pediatrics in 2021: choices in allergy and immunology, critical care, endocrinology, gastroenterology, genetics, haematology, infectious diseases, neonatology, neurology, nutrition, palliative care, respiratory tract illnesses and telemedicine

30. A novel NF1 mutation in a pediatric patient with renal artery aneurysm

31. The year 2021 in COVID-19 pandemic in children

32. Epstein-Barr virus-associated acute pancreatitis: a clinical report and review of literature

33. Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome

34. Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 gene

35. Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis

36. Distal Arthrogryposis type 5 in an Italian family due to an autosomal dominant gain-of-function mutation of the PIEZO2 gene

37. The pandemic within the pandemic: the surge of neuropsychological disorders in Italian children during the COVID-19 era

38. Novel de novo missense mutation in the interferon regulatory factor 6 gene in an Italian infant with IRF6-related disorder

39. Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2 K2 gene

40. Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profiles

41. Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report

42. Alternating Hemiplegia of Childhood: neurological comorbidities and intrafamilial variability

43. Safety and efficacy of a probiotic-containing infant formula supplemented with 2’-fucosyllactose: a double-blind randomized controlled trial

44. Developments in pediatrics in 2020: choices in allergy, autoinflammatory disorders, critical care, endocrinology, genetics, infectious diseases, microbiota, neonatology, neurology, nutrition, ortopedics, respiratory tract illnesses and rheumatology

45. The social role of pediatrics in the past and present times

46. Acute hemorrhagic edema of infancy (AHEI): Alarming cutaneous presentation of a benign and self‐limited disease

47. Necrotizing enterocolitis in the preterm: newborns medical and nutritional Management in a Single-Center Study

48. Analysis of risk and prognostic factors in a population of pediatric patients hospitalized for acute malnutrition at the Chiulo hospital, Angola

49. Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-up

50. Penile Length Assessment of Children Treated for Primary Buried Penis: Can Satisfying Penile Growth Always Be Achieved?

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