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52. Skin manifestations of COVID‐19 in children: Part 3.

53. Skin manifestations of COVID‐19 in children: Part 2.

54. Skin manifestations of COVID‐19 in children: Part 1.

55. A position paper on the management of itch and pain in atopic dermatitis from the International Society of Atopic Dermatitis (ISAD)/Oriented Patient‐Education Network in Dermatology (OPENED) task force.

56. Kawasaki disease: guidelines of the Italian Society of Pediatrics, part I - definition, epidemiology, etiopathogenesis, clinical expression and management of the acute phase

57. Kawasaki disease: guidelines of the Italian Society of Pediatrics, part II - treatment of resistant forms and cardiovascular complications, follow-up, lifestyle and prevention of cardiovascular risks

58. Are SARS‐CoV‐2 IgA antibodies in paediatric patients with chilblain‐like lesions indicative of COVID‐19 asymptomatic or paucisymptomatic infection?

59. Giant congenital exophytic strawberry‐like mass in a newborn.

60. Linee Guida SICVE: 11. Anomalie vascolari

61. Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa.

62. PSS2 - VALIDATION STUDY OF AN INFANTILE HEMANGIOMA (IH) SCORING TOOL FOR PRIMARY CLINICIANS TO IDENTIFY PATIENTS REQUIRING REFERRAL TO EXPERT CENTERS

68. Consensus Conference Italiana 'La gestione clinica della dermatite atopica in età pediatrica'

69. Management of congenital ichthyoses: European guidelines of care, part two.

70. Management of congenital ichthyoses: European guidelines of care, part one.

71. Cushing’s Syndrome in a 6-month-old Boy: A Rare Side-effect due to Inadequate use of Topical Corticosteroids

73. Linee guida. Diagnosi delle epidermolisi bollose ereditarie

76. Preemptive liver transplantation in a child with familial hypercholesterolemia

78. The Italian Registry of Hereditary Epidermolysis Bullosa

79. Facial comedonal acne in orofaciodigital syndrome type 1 caused by a novel frameshift variant in OFD1.

82. Epidermolysis bullosa simplex withPLECmutations: new phenotypes and new mutations

88. Association of Intermediate Osteopetrosis with Poikiloderma

92. Acral skin atrophy in an infant: an early clue to Kindler syndrome diagnosis.

94. Autosomal recessive epidermolysis bullosa simplex due to <italic>KRT14</italic> mutation: two large Palestinian families and literature review.

95. Novel <italic>PNPLA1</italic> mutations in two Italian siblings with autosomal recessive congenital ichthyosis.

99. Antiinflammatory therapy with canakinumab for atherosclerotic disease

100. Chapter Patient-generated evidence in Epidermolysis Bullosa (EB): Development of a questionnaire to assess the Quality of Life

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