Published in J Pediatr on July 01, 1983
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Response of deep tufted angioma to interferon alfa. J Am Acad Dermatol (1995) 1.39
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Drug-induced hypersensitivity syndrome in pediatric patients. Pediatrics (2001) 1.29
Intracranial gliomas in neurofibromatosis type 1. Am J Med Genet (1999) 1.29
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Localized facial flushing in infancy. Auriculotemporal nerve (Frey) syndrome. Arch Dermatol (1997) 1.22
Optic pathway tumors in children: the effect of neurofibromatosis type 1 on clinical manifestations and natural history. J Pediatr (1995) 1.20
Pyoderma gangrenosum in infants and children. Pediatr Dermatol (1994) 1.19
Increased skin permeability in preterm infants. J Pediatr (1971) 1.18
Late-onset optic pathway tumors in children with neurofibromatosis 1. Neurology (2004) 1.17
'Membranous aplasia cutis' with hair collars. Congenital absence of skin or neuroectodermal defect? Arch Dermatol (1995) 1.17
The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: implications for mutation detection and first case of prenatal diagnosis. J Invest Dermatol (2001) 1.16
Cutaneous changes associated with inflammatory bowel disease. Pediatr Dermatol (1986) 1.16
A novel KIT mutation results in piebaldism with progressive depigmentation. J Am Acad Dermatol (2001) 1.13
Report of an infant with GM1 gangliosidosis type I and extensive and unusual mongolian spots. Br J Dermatol (1981) 1.11
Hydroa vacciniforme. Diagnosis by repetitive ultraviolet-A phototesting. Arch Dermatol (1986) 1.10
Tissue expansion in a patient with extensive nevus comedonicus. Ann Plast Surg (1992) 1.10
Black clouds. Work load, sleep, and resident reputation. Am J Dis Child (1993) 1.10
Rat bite fever in a pet lover. J Am Acad Dermatol (1998) 1.09
Aquagenic palmoplantar keratoderma. J Am Acad Dermatol (2001) 1.09
Biochemical abnormalities in rhizomelic chondrodysplasia punctata. J Pediatr (1988) 1.08
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Disseminated BCG in twin boys with presumed chronic granulomatous disease of childhood. Pediatrics (1971) 1.07
Molecular analysis of an extended family with type IA (tyrosinase-negative) oculocutaneous albinism. J Invest Dermatol (1991) 1.06
The relationship of transferrin and iron to serum inhibition of Candida albicans. J Invest Dermatol (1967) 1.06
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Chondrodysplasia punctata. Conradi-Hünermann syndrome. Arch Dermatol (1977) 1.06
The treatment of pyoderma in children. JAMA (1970) 1.04
Epidermal growth factor receptor glycosylation is required for ganglioside GM3 binding and GM3-mediated suppression [correction of suppresion] of activation. Glycobiology (2001) 1.02
Ichthyosis follicularis with alopecia and photophobia. Arch Dermatol (1985) 1.02
Primary generalized and localized hypertrichosis in children. Arch Dermatol (2001) 1.01
Mongolian spots and GM1 type 1 gangliosidosis. J Am Acad Dermatol (1990) 1.00
Histiocytosis X: a seven-year experience at a children's hospital. J Am Acad Dermatol (1985) 0.99
Full-thickness surgical excision for the treatment of inflammatory linear verrucous epidermal nevus. Ann Plast Surg (2001) 0.99
Pupillotonia, hyporeflexia, and segmental hypohidrosis: autonomic dysfunction in a child. J Pediatr (1968) 0.99
Sacral hemangiomas and multiple congenital abnormalities. Arch Dermatol (1986) 0.99
Management of Stevens-Johnson syndrome and toxic epidermal necrolysis in children. J Pediatr (1989) 0.99
Cutaneous polyarteritis nodosa of childhood. J Am Acad Dermatol (1994) 0.98
Nevoid basal cell carcinoma syndrome: bilateral ovarian fibromas in a 3 1/2-year-old girl. J Am Acad Dermatol (1986) 0.98
A mouse monoclonal antibody against a newly discovered basement membrane component, the epidermolysis bullosa acquisita antigen. J Invest Dermatol (1985) 0.98
Childhood rosacea. Pediatr Dermatol (1992) 0.98
Localization of the alpha 3 (V) chain of type V collagen in human skin. J Invest Dermatol (1987) 0.97
Fatal cardiovascular disease and cutis laxa following acute febrile neutrophilic dermatosis. J Pediatr (1983) 0.96
Prenatal diagnosis of harlequin ichthyosis. Clin Genet (1980) 0.96
Factitial cheilitis in an adolescent. Pediatr Dermatol (1999) 0.96
Duplication 3p syndrome: report of a new case and review of the literature. Am J Med Genet (1981) 0.96
Neurofibromatosis type 1 in childhood. J Pediatr (1990) 0.96
Consequences of seven novel mutations on the expression and structure of keratinocyte transglutaminase. J Biol Chem (1997) 0.96
Dental abnormalities in Schimke immuno-osseous dysplasia. J Dent Res (2012) 0.95
Acne: current concepts. Pediatrics (1978) 0.95
Pustulosis palmaris et plantaris: its association with chronic recurrent multifocal osteomyelitis. J Am Acad Dermatol (1985) 0.94
Knuckle pads in children. Am J Dis Child (1986) 0.94
A systematic review of the safety of topical therapies for atopic dermatitis. Br J Dermatol (2007) 0.93
Disseminated Fusarium solani infection with cutaneous nodules in a bone marrow transplant patient. Int J Dermatol (1988) 0.92
Langerhans cell histiocytosis presenting in the neonatal period: a retrospective case series. Arch Pediatr Adolesc Med (2001) 0.92
What syndrome is this? Ankyloblepharon-ectodermal defects--cleft lip and palate (Hay-Wells) syndrome. Pediatr Dermatol (1998) 0.92
Early surgical intervention in a patient with Kasabach-Merritt phenomenon. J Pediatr (2001) 0.92
Hodgkin's disease manifesting as prurigo nodularis. Pediatr Dermatol (1990) 0.91
Genetic mutations in the K1 and K10 genes of patients with epidermolytic hyperkeratosis. Correlation between location and disease severity. J Clin Invest (1994) 0.91