1
|
Proteolytic activation cascade of the Netherton syndrome-defective protein, LEKTI, in the epidermis: implications for skin homeostasis.
|
J Invest Dermatol
|
2011
|
1.51
|
2
|
Laminin-5 mutational analysis in an Italian cohort of patients with junctional epidermolysis bullosa.
|
J Invest Dermatol
|
2004
|
1.42
|
3
|
The 420K LEKTI variant alters LEKTI proteolytic activation and results in protease deregulation: implications for atopic dermatitis.
|
Hum Mol Genet
|
2012
|
0.92
|
4
|
Melanoma in a 5-year-old child with a giant congenital melanocytic naevus.
|
Acta Derm Venereol
|
2012
|
0.84
|
5
|
Necrosis of the tongue as first symptom of Polyarteritis Nodosa (PAN): unusual presentation of a rare disease in children.
|
Rheumatol Int
|
2010
|
0.81
|
6
|
Early immunopathological diagnosis of ichthyosis with confetti in two sporadic cases with new mutations in keratin 10.
|
Acta Derm Venereol
|
2014
|
0.80
|
7
|
Therapeutic patient education in children with atopic dermatitis: position paper on objectives and recommendations.
|
Pediatr Dermatol
|
2013
|
0.80
|
8
|
Understanding probiotics' role in allergic children: the clue of gut microbiota profiling.
|
Curr Opin Allergy Clin Immunol
|
2015
|
0.77
|
9
|
Esophageal stenosis in epidermolysis bullosum: a challenge for the endoscopist.
|
J Pediatr Surg
|
2011
|
0.77
|
10
|
A waterborn zoonotic helminthiase in an Italian diver: a case report of a cutaneous Sparganum infection and a review of European cases.
|
Pathog Glob Health
|
2016
|
0.75
|
11
|
Prospective multicenter survey on the clinical management of pediatric contact dermatitis.
|
Minerva Pediatr
|
2016
|
0.75
|
12
|
A rare case of segmental neurofibromatosis with multiple blue-red pseudoatrophic plaques.
|
Cutis
|
2014
|
0.75
|
13
|
Heart transplant and 2-year follow up in a child with generalized arterial calcification of infancy.
|
Eur J Pediatr
|
2014
|
0.75
|
14
|
Naevoid basal cell carcinoma syndrome in a 22-month-old child presenting with multiple basal cell carcinomas and a fetal rhabdomyoma.
|
Acta Derm Venereol
|
2015
|
0.75
|
15
|
Long-term follow-up of a spontaneously improving patient with junctional epidermolysis bullosa associated with ITGB4 c.3977-19T>A splicing mutation.
|
Acta Derm Venereol
|
2013
|
0.75
|
16
|
T-lymphocytes are directly involved in the clinical expression of migratory circinate erythema in epidermolysis bullosa simplex patients.
|
Acta Derm Venereol
|
2014
|
0.75
|
17
|
Lethal Netherton syndrome due to homozygous p.Arg371X mutation in SPINK5.
|
Pediatr Dermatol
|
2013
|
0.75
|
18
|
A case of neonatal linear IgA bullous dermatosis with severe eye involvement.
|
Acta Derm Venereol
|
2015
|
0.75
|
19
|
Impressive pseudotumoral proliferative nodules in a giant congenital nevus of a newborn.
|
Pediatr Dermatol
|
2012
|
0.75
|
20
|
Glomerulocystic kidney disease in hypomelanosis of Ito.
|
Pediatr Nephrol
|
2008
|
0.75
|