All Stories

  1. Development of a novel reference nomogram for endotracheal intubation in neonatal emergency transport setting
  2. Evaluation of neonatal transport in a European country shows that regional provision is not cost-effective or sustainable and needs to be re-organised
  3. The impact of Italian regionalisation on transporting neonatal patients back from the neonatal intensive care unit to the referring level two unit
  4. Neonatal emergency transport has played a key role in the regionalisation of perinatal care in the Liguria Region of Italy
  5. Phototherapy in transport for neonates with unconjugated hyperbilirubinaemia
  6. Etiology of non-immune hydrops fetalis: An update
  7. Solving the Problem of the Transport of Twin Newborns
  8. God Was Born Prematurely
  9. Nonimmune Hydrops Fetalis and Lysosomal Storage Diseases
  10. Simultaneous Transport of Twin Newborns
  11. Clinical Disorders of Primary Malfunctioning of the Lymphatic System
  12. Clinical difficulties and forensic diagnosis: Histopathological pitfalls of villus mesenchymal dysplasia in the third trimester causing foetal death
  13. Non-immune hydrops fetalis: A short review of etiology and pathophysiology
  14. Cited or read?
  15. Nonimmune Hydrops Fetalis in the Stillborn
  16. Immunohistochemistry in non-immune hydrops fetalis: A single center experience in 79 fetuses
  17. Diagnostic assessment and therapeutic approach for immunodeficiency due to chylous dysplasia: A case report
  18. Microsurgery for lymphedema: Clinical research and long-term results
  19. S100B protein increases in human blood and urine during stressful activity
  20. A diagnostic flow chart for non-immune hydrops fetalis
  21. Etiology of nonimmune hydrops fetalis: A systematic review
  22. Nuchal translucency and lymphatic system maldevelopment
  23. An Historical Perspective of Early Italian Air Medical Transport
  24. Peroxisomal acyl‐CoA‐oxidase deficiency: Two new cases
  25. Slipped capital femoral epiphysis associated with Rubinstein-Taybi syndrome
  26. Lymphatic Dysplasias in Newborns and Children: The Role of Lymphoscintigraphy
  27. Reliability assessment of glucose measurement by HemoCue analyzer in a neonatal intensive care unit: reply to Dr. Joakim Hagvik
  28. A neonate with acute renal failure: answer
  29. A neonate with acute renal failure: question
  30. Pediatric lymphedema and correlated syndromes: Role of microsurgery
  31. Reliability assessment of glucose measurement by HemoCue analyser in a neonatal intensive care unit
  32. Microsurgery for treatment of peripheral lymphedema: Long-term outcome and future perspectives
  33. The lymphatics in the pathophysiology of thoracic and abdominal surgical pathology: Immunological consequences and the unexpected role of microsurgery
  34. The sanctity of life: A micropreemie twin transport
  35. Diagnosis and management of primary chylous ascites
  36. Congenital fibrous hamartoma of the knee
  37. Dwarfism in the ancient Mediterranean world
  38. Nonimmune idiopathic hydrops fetalis and congenital lymphatic dysplasia
  39. Pulmonary interstitial emphysema in preterm twins on continuous positive airway pressure
  40. Helicopter emergency medical service in Italy
  41. X-linked creatine transporter deficiency
  42. Aplasia cutis congenita, skull defect, brain heterotopia, and intestinal lymphangiectasia
  43. Spontaneous recovery in neonatal hemochromatosis
  44. Congenital right diaphragmatic hernia
  45. Erratum: Neurofibromatosis type 1 (NF1): Identification of eight unreported mutations in NF1 gene in Italian patients
  46. Neurofibromatosis eurofibromatosis type 1 (NF1): Identification of eight unreported mutations in NF1 gene in Italian patients
  47. Phenobarbital Enhances Sister Chromatid Exchanges In Vivo
  48. Hennekam syndrome presenting as nonimmune hydrops fetalis, congenital chylothorax, and congenital pulmonary lymphangiectasia
  49. Persistent left superior vena cava in a preterm newborn
  50. A Newborn with Rash and Chorioretinitis
  51. Ten novel mutations in the human neurofibromatosis type 1 (NF1) gene in Italian patients
  52. ?Apple-peel? intestinal atresia, ocular anomalies, and microcephaly syndrome: Brain magnetic resonance imaging study
  53. Lymphoscintigraphic Evaluation of Congenital Lymphedema of the Newborn
  54. Lymphedema-lymphangiectasia-mental retardation (Hennekam) syndrome: A review
  55. Radiological Case of the Month
  56. Branchio-oto-renal syndrome: A report on nine family groups
  57. Persistence of M�llerian derivatives and intestinal lymphangiectasis in two newborn brothers: Confirmation of the Urioste syndrome
  58. Partial agenesis of corpus callosum in LEOPARD syndrome
  59. ASYMPTOMATIC INTRACRANIAL HYPERTENSION ASSOCIATED WITH TETRACYCLINE USE
  60. Altered response to stimuli of the AP-1/DNA binding activity in a syndrome of precocious ageing (geroderma osteodysplastica hereditaria)
  61. Sebaceous nevus syndrome: Report of two cases
  62. Pseudolithiasis and Intractable Hiccups in a Boy Receiving Ceftriaxone
  63. Surgical vs. medical treatment of seizures in hemimegalencephaly
  64. Rubinstein-Taybi syndrome and pheochromocytoma
  65. Therapy for hereditary nephrogenic diabetes insipidus
  66. Insulin receptor gene expression is reduced in cells from a progeric patient
  67. Phenobarbital Enhances Sister Chromatid Exchanges In Vivo
  68. Unusual association: Dandy-Walker-like malformation in the Rubinstein-Taybi syndrome
  69. Inheritance of Rubinstein-Taybi syndrome