Published in Pediatr Dermatol on October 11, 2013
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A randomized, controlled trial of oral propranolol in infantile hemangioma. N Engl J Med (2015) 4.05
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Phacomatosis pigmentokeratotica is caused by a postzygotic HRAS mutation in a multipotent progenitor cell. J Invest Dermatol (2013) 2.31
Childhood bullous pemphigoid: clinical and immunological findings in a series of 4 cases. Arch Dermatol (2007) 2.10
Infantile transient smooth muscle contraction of the skin. J Am Acad Dermatol (2013) 1.95
Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity. Arthritis Rheum (2012) 1.87
One-step detection of c-kit point mutations using peptide nucleic acid-mediated polymerase chain reaction clamping and hybridization probes. Am J Pathol (2003) 1.72
Prevalence study of nevi in children from Barcelona. Dermoscopy, constitutional and environmental factors. Dermatology (2008) 1.46
Cutaneous and mucosal mucormycosis mimicking pancreatic panniculitis and gouty panniculitis. J Am Acad Dermatol (2011) 1.44
Keratinocytic epidermal nevi are associated with mosaic RAS mutations. J Med Genet (2012) 1.40
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Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome. J Am Acad Dermatol (2010) 1.25
Hobnail hemangioma reclassified as superficial lymphatic malformation: a study of 52 cases. J Am Acad Dermatol (2011) 1.22
Transitional cell carcinoma of the bladder in children and adolescents: six-case series and review of the literature. J Pediatr Urol (2010) 1.18
Phacomatosis melanovascularis: a new example of non-allelic twin spotting. Eur J Dermatol (2011) 1.15
Propranolol for infantile hemangiomas. Pediatr Dermatol (2011) 1.11
An immunohistochemical study of verrucous hemangiomas. J Cutan Pathol (2013) 1.06
Expression of the neuron-specific protein CHD5 is an independent marker of outcome in neuroblastoma. Mol Cancer (2010) 1.03
A three-gene expression signature model for risk stratification of patients with neuroblastoma. Clin Cancer Res (2012) 1.02
Median raphe cysts of the perineum in children. Urology (2008) 1.00
DNA hypomethylation affects cancer-related biological functions and genes relevant in neuroblastoma pathogenesis. PLoS One (2012) 0.95
Brain stem tumors in children and adolescents: single institutional experience. Childs Nerv Syst (2013) 0.94
Eosinophilic pustular folliculitis of infancy: a series of 15 cases and review of the literature. J Am Acad Dermatol (2012) 0.94
Effect of ABCB1 and ABCC3 polymorphisms on osteosarcoma survival after chemotherapy: a pharmacogenetic study. PLoS One (2011) 0.94
Fatal hepatic failure secondary to acute herpes simplex virus infection. J Pediatr Hematol Oncol (2004) 0.94
Pyoderma gangrenosum in an infant. Pediatr Dermatol (2006) 0.93
Nevoid hypertrichosis and hypomelanosis. Eur J Dermatol (2002) 0.93
Wilms tumor 1 expression in vascular neoplasms and vascular malformations. Am J Dermatopathol (2011) 0.92
Infantile acne treated with oral isotretinoin. Pediatr Dermatol (2012) 0.91
Persistent agmination of lymphomatoid papulosis. Pediatr Dermatol (2010) 0.91
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production. J Clin Invest (2015) 0.90
Primary Ewing sarcoma of the tentorium presenting with intracranial hemorrhage in a child. J Neurosurg (2007) 0.90
Recurrence of infantile hemangiomas treated with propranolol. Pediatr Dermatol (2011) 0.90
Nevus psiloliparus and aplasia cutis: a further possible example of didymosis. Pediatr Dermatol (2005) 0.89
Systemic juvenile xanthogranuloma with fatal outcome. Pediatr Dermatol (2010) 0.88
Neonatal functional intestinal obstruction and the presence of severely immature ganglion cells on rectal biopsy: 6 year experience. Pediatr Surg Int (2011) 0.88
Hereditary mucoepithelial dysplasia: report of two sporadic cases. Pediatr Dermatol (2011) 0.88
Folliculocystic and collagen hamartoma of tuberous sclerosis complex. J Am Acad Dermatol (2011) 0.88
Pediatric dermatofibrosarcoma protuberans in Madrid, Spain: multi-institutional outcomes. Pediatr Dermatol (2014) 0.88
Prevalence of autosomal recessive congenital ichthyosis: a population-based study using the capture-recapture method in Spain. J Am Acad Dermatol (2011) 0.88
Deep morphea after vaccination in two young children. Pediatr Dermatol (2006) 0.87
Disseminated congenital comedones. Pediatr Dermatol (2011) 0.87
Emperipolesis: an additional common histopathologic finding in H syndrome and Rosai-Dorfman disease. Am J Dermatopathol (2012) 0.85
Familial nonmembranous aplasia cutis of the scalp. Pediatr Dermatol (2005) 0.85
Bone environment is essential for osteosarcoma development from transformed mesenchymal stem cells. Stem Cells (2014) 0.84
Papular epidermal nevus with "skyline" basal cell layer (PENS). J Am Acad Dermatol (2011) 0.84
Papular epidermal nevus with "skyline" basal cell layer (PENS) with extracutaneous findings. Pediatr Dermatol (2012) 0.84
Aplasia cutis congenita and other anomalies associated with methimazole exposure during pregnancy. Pediatr Dermatol (2011) 0.83
Intra-arterial chemotherapy for retinoblastoma. Challenges of a prospective study. Acta Ophthalmol (2014) 0.82
The calcium-sensing receptor and parathyroid hormone-related protein are expressed in differentiated, favorable neuroblastic tumors. Cancer (2009) 0.82
Prioritization of therapy uncertainties in Dystrophic Epidermolysis Bullosa: where should research direct to? an example of priority setting partnership in very rare disorders. Orphanet J Rare Dis (2013) 0.82
Dermatomyofibromas presenting in pediatric patients: clinicopathologic characteristics and differential diagnosis. J Cutan Pathol (2011) 0.81
Exercise benefits in chronic graft versus host disease: a murine model study. Med Sci Sports Exerc (2013) 0.81
Malignant atrophic papulosis: a case report with severe visual and neurological impairment. Pediatr Dermatol (2010) 0.81
Epidermolysis bullosa simplex with mottled pigmentation: a family report and review. Pediatr Dermatol (2012) 0.81
Cutaneous aspergillosis mimicking pancreatic and gouty panniculitis. J Am Acad Dermatol (2012) 0.81
Therapeutic patient education in children with atopic dermatitis: position paper on objectives and recommendations. Pediatr Dermatol (2013) 0.80
From Severe Combined Immunodeficiency to Omenn syndrome after hematopoietic stem cell transplantation in a RAG1 deficient family. Pediatr Allergy Immunol (2012) 0.80
Facial capillary malformation and Dyke-Davidoff-Masson syndrome. Pediatr Neurol (2010) 0.80
Treatment of Ewing sarcoma family of tumors with a modified P6 protocol in children and adolescents. Pediatr Blood Cancer (2011) 0.79
Recalcitrant pustular psoriasis successfully treated with adalimumab. Pediatr Dermatol (2011) 0.79
An unusual congenital presentation of infantile digital fibromatosis. J Paediatr Child Health (2007) 0.79
Beau's lines and multiple periungueal pyogenic granulomas after long stay in an intensive care unit. Pediatr Dermatol (2008) 0.79
Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entity. Arch Dermatol (2009) 0.78
Reduced efficacy of mesenchymal stromal cells in preventing graft-versus-host disease in an in vivo model of haploidentical bone marrow transplant with leukemia. Cell Transplant (2012) 0.78
Extensive acantholysis as the major histological feature of a severe case of Dowling Meara-epidermolysis bullosa simplex: a reappraisal of acantholysis in the newborn. Eur J Dermatol (2012) 0.78
Rituximab in lymphomatoid granulomatosis. J Pediatr Hematol Oncol (2014) 0.78
The H syndrome: two novel mutations affecting the same amino acid residue of hENT3. J Dermatol Sci (2009) 0.78
Histologic and Immunohistochemical Features of the Skin Lesions in CANDLE Syndrome. Am J Dermatopathol (2015) 0.77
A novel heterozygous point mutation in the p63 gene in a patient with ectodermal dysplasia associated with B-cell leukemia. Pediatr Dermatol (2011) 0.77
Multiple lichenoid juvenile xanthogranuloma. Pediatr Dermatol (2009) 0.77
cblE-Type Homocystinuria Presenting with Features of Haemolytic-Uremic Syndrome in the Newborn Period. JIMD Rep (2012) 0.77
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production. J Clin Invest (2016) 0.77
Nuclear factor-kappaB inducing kinase is required for graft-versus-host disease. Haematologica (2010) 0.77
Effects of exercise interventions in graft-versus-host disease models. Cell Transplant (2012) 0.77
[Focal epithelial hyperplasia]. Actas Dermosifiliogr (2005) 0.77
Primary cutaneous anaplastic large cell lymphoma of the nasal tip in a child. Pediatr Dermatol (2010) 0.77
High-risk alpha-human papillomavirus types: detection in HIV-infected children with acquired epidermodysplasia verruciformis. J Am Acad Dermatol (2013) 0.77
Invasive lymphatic malformation (gorham-stout) of the pelvis with prominent skin involvement. Pediatr Dermatol (2012) 0.77
X-linked reticulate pigmentary disorder: report of a new family. Eur J Dermatol (2007) 0.77