Published in Pediatr Dermatol on October 02, 2003
Harlequin ichthyosis and juvenile idiopathic arthritis: a rare combination. Clin Rheumatol (2006) 0.75
Deficiency of PORCN, a regulator of Wnt signaling, is associated with focal dermal hypoplasia. Nat Genet (2007) 2.75
LOH-pitfalls of an ambiguous abbreviation. Aging Male (2008) 2.01
Linear atrophoderma of Moulin: postulation of mosaicism for a predisposing gene. J Am Acad Dermatol (2003) 1.80
Naevus lentiginosus linearis: A distinct skin disorder. Acta Derm Venereol (2010) 1.80
Pronounced linear calcinosis in a boy with mild dermatomyositis. A further possible example of superimposed segmental manifestation of a polygenic disorder. Dermatology (2009) 1.49
Familial cutis tricolor: a possible example of paradominant inheritance. Eur J Dermatol (2003) 1.44
Phacomatosis pigmentovasculosebacea: an unusual case of phacomatosis multiplex. Eur J Dermatol (2003) 1.39
The pattern and profile of alopecia areata in Singapore--a study of 219 Asians. Int J Dermatol (2002) 1.33
Tufted angioma: a report of five cases. Pediatr Dermatol (2002) 1.25
Phacomatosis melanorosea with heterochromia of scalp hair. Eur J Dermatol (2011) 1.13
IFAP syndrome is caused by deficiency in MBTPS2, an intramembrane zinc metalloprotease essential for cholesterol homeostasis and ER stress response. Am J Hum Genet (2009) 1.09
Monozygotic twins discordant for Proteus syndrome. Am J Med Genet A (2008) 1.09
Extensive speckled lentiginous nevus associated with giant congenital melanocytic nevus: an unusual example of twin spotting? Eur J Dermatol (2004) 1.08
Aggressive subcutaneous panniculitis-like T-cell lymphoma with hemophagocytosis in two children (subcutaneous panniculitis-like T-cell lymphoma). J Am Acad Dermatol (2009) 1.07
Sturge-Weber-Klippel-Trenaunay syndrome: what's in a name? Eur J Dermatol (2003) 1.07
Segmental lesions are not always agminated. Arch Dermatol (2002) 1.02
PORCN mutations in focal dermal hypoplasia: coping with lethality. Hum Mutat (2009) 1.02
Inverse Klippel-Trenaunay syndrome: review of cases showing deficient growth. Dermatology (2007) 1.01
Alopecia areata: treatment of today and tomorrow. J Investig Dermatol Symp Proc (2003) 1.00
Treatment of Kimura's disease with cyclosporine. J Dermatolog Treat (2005) 1.00
CHILD syndrome in 3 generations: the importance of mild or minimal skin lesions. Arch Dermatol (2006) 0.99
Becker's nevus syndrome revisited. J Am Acad Dermatol (2004) 0.97
A hairy paradox: congenital triangular alopecia with a central hair tuft. Dermatology (2010) 0.97
Staging of necrotizing fasciitis based on the evolving cutaneous features. Int J Dermatol (2007) 0.97
Allelic loss underlies type 2 segmental Hailey-Hailey disease, providing molecular confirmation of a novel genetic concept. J Clin Invest (2004) 0.96
Porokeratotic eccrine nevus may be caused by somatic connexin26 mutations. J Invest Dermatol (2012) 0.95
Papular eruption on a tattoo: a case of primary inoculation tuberculosis. Australas J Dermatol (2005) 0.95
Diphencyprone for the treatment of alopecia areata: more data and new aspects. Arch Dermatol (2002) 0.94
Nevoid hypertrichosis and hypomelanosis. Eur J Dermatol (2002) 0.93
An epidermal nevus syndrome with cerebral involvement caused by a mosaic FGFR3 mutation. Am J Med Genet A (2008) 0.93
Retrospective analysis of drug-induced hypersensitivity syndrome: a study of 27 patients. J Am Acad Dermatol (2010) 0.92
Stevens-Johnson syndrome and toxic epidermal necrolysis in Asian children. J Am Acad Dermatol (2009) 0.91
Linear psoriasis and ILVEN: is lumping or splitting appropriate? Dermatology (2006) 0.91
Fatal Lucio's phenomenon in 2 patients with previously undiagnosed leprosy. J Am Acad Dermatol (2003) 0.90
Nevus psiloliparus and aplasia cutis: a further possible example of didymosis. Pediatr Dermatol (2005) 0.89
Presumed dapsone-induced drug hypersensitivity syndrome causing reversible hypersensitivity myocarditis and thyrotoxicosis. Ann Acad Med Singapore (2006) 0.88
Angioma serpiginosum arranged in a systematized segmental pattern suggesting mosaicism. Dermatology (2006) 0.88
Folliculocystic and collagen hamartoma of tuberous sclerosis complex. J Am Acad Dermatol (2011) 0.88
Multiple familial trichoepithelioma caused by mutations in the cylindromatosis tumor suppressor gene. Cancer Res (2004) 0.88
Trichorrhizophagia. Eur J Dermatol (2004) 0.88
Multiple eruptive dermatofibromas: a review of the literature. Acta Derm Venereol (2002) 0.87
Two distinct types of speckled lentiginous nevi characterized by macular versus papular speckles. Dermatology (2006) 0.87
Cryptic splicing at a non-consensus splice-donor in a patient with a novel mutation in the plakophilin-1 gene. J Invest Dermatol (2004) 0.86
Genotype-phenotype correlations emerging from the identification of missense mutations in MBTPS2. Hum Mutat (2013) 0.85
Targeting epidermal lipids for treatment of Mendelian disorders of cornification. Orphanet J Rare Dis (2014) 0.85
Interleukin-10-deficient mice are less susceptible to the induction of alopecia areata. J Invest Dermatol (2002) 0.85
Evidence for a new fumarate hydratase gene mutation in a unilateral type 2 segmental leiomyomatosis. Dermatology (2010) 0.85
Revertant mosaicism in a human skin fragility disorder results from slipped mispairing and mitotic recombination. J Clin Invest (2012) 0.85
Profile and pattern of Stevens-Johnson syndrome and toxic epidermal necrolysis in a general hospital in Singapore: treatment outcomes. Acta Derm Venereol (2012) 0.85
Speckled lentiginous nevus syndrome: report of a further case. Dermatology (2004) 0.85
Squamous cell carcinoma and Bowen's disease of the skin in Singapore. Ann Acad Med Singapore (2007) 0.85
Familial disseminated comedones without dyskeratosis: report of an affected family and review of the literature. Dermatology (2014) 0.85
Delineation of the various shapes and patterns of nevi. Eur J Dermatol (2005) 0.85
A novel missense mutation of NSDHL in an unusual case of CHILD syndrome showing bilateral, almost symmetric involvement. J Am Acad Dermatol (2002) 0.85
Donor dominance cures CHILD nevus. Dermatology (2010) 0.84
Phacomatosis cesioflammea with unilateral lipohypoplasia. Am J Med Genet A (2008) 0.84
Partial unilateral lentiginosis with ipsilateral Lisch nodules and axillary freckling. Dermatology (2004) 0.84
Papular epidermal nevus with "skyline" basal cell layer (PENS). J Am Acad Dermatol (2011) 0.84
A clinical study of childhood alopecia areata in Singapore. Pediatr Dermatol (2002) 0.83
Mucocutaneous telangiectases of the head and neck in individuals with hereditary hemorrhagic telangiectasia -- analysis of distribution and symptoms. Eur J Dermatol (2004) 0.82
Type 1 segmental Galli-Galli disease resulting from a previously unreported keratin 5 mutation. J Invest Dermatol (2012) 0.82
Infantile myofibromatosis: a case report and review of the literature. Cutis (2004) 0.82
Oculoectodermal syndrome: report of a new case with a broad clinical spectrum. Am J Med Genet A (2014) 0.82
Superimposed segmental dermatomyositis: an emerging new paradigm. Eur J Dermatol (2010) 0.82
Cutaneous melioidosis. J Eur Acad Dermatol Venereol (2006) 0.81
Cutaneous Langerhans cell histiocytosis: study of Asian children shows good overall prognosis. Acta Paediatr (2013) 0.81
The South African "bathing suit ichthyosis" is a form of lamellar ichthyosis caused by a homozygous missense mutation, p.R315L, in transglutaminase 1. J Invest Dermatol (2006) 0.81
Large congenital melanocytic nevi may reflect paradominant inheritance implying allelic loss. Eur J Dermatol (2003) 0.81
Cutis tricolor parvimaculata: a distinct neurocutaneous syndrome? Dermatology (2005) 0.80
Melorheostosis with ipsilateral nevus sebaceus (didymosis melorheosebacea). Eur J Dermatol (2003) 0.80
Eccrine angiomatous hamartoma associated with spontaneous regression. Pediatr Dermatol (2006) 0.80
Darier disease with paired segmental manifestation of either excessive or absent involvement: a further step in the concept of twin spotting. Dermatology (2002) 0.80
Cutis tricolor coexistent with cutis marmorata telangiectatica congenita: "phacomatosis achromico-melano-marmorata". Eur J Dermatol (2008) 0.80
Autologous in vitro reconstituted epidermis in the treatment of a large nevus depigmentosus. J Am Acad Dermatol (2006) 0.80
Whorled scarring alopecia: a rare phenomenon in incontinentia pigmenti? J Am Acad Dermatol (2003) 0.79
Revertant mosaicism and retrotransposons: another explanation of "natural gene therapy". Am J Med Genet A (2005) 0.79
Giant melanocytic nevus may be explained as a superimposed patchy manifestation of a polygenic trait. Dermatology (2010) 0.79
Lepromatous leprosy in erythema nodosum leprosum reaction mimicking Sweet's syndrome. Int J Dermatol (2011) 0.79
Angioma serpiginosum is not caused by PORCN mutations. Eur J Hum Genet (2009) 0.79
An update on Stevens-Johnson syndrome and toxic epidermal necrolysis in children. Curr Opin Pediatr (2009) 0.79
Giant café-au-lait macule in neurofibromatosis 1: a type 2 segmental manifestation of neurofibromatosis 1? J Am Acad Dermatol (2008) 0.79
Hematological abnormalities and the use of granulocyte-colony-stimulating factor in patients with Stevens-Johnson syndrome and toxic epidermal necrolysis. Int J Dermatol (2011) 0.79
[Alopecia areata in animal models--new insights into pathogenesis and treatment of a T cell-mediated autoimmune disorder]. J Dtsch Dermatol Ges (2004) 0.79
Angiokeratoma circumscriptum arranged in a systematized band-like pattern suggesting mosaicism. J Dermatol (2006) 0.79
Understanding the biology of X-linked diseases. Acta Paediatr Suppl (2006) 0.79
Speckled lentiginous nevi: no longer one single disorder. Arch Dermatol (2010) 0.79
Linear intraoral lesions in the sebaceous nevus syndrome. J Am Acad Dermatol (2005) 0.78
Morphological approach to hair disorders. J Investig Dermatol Symp Proc (2003) 0.78
Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entity. Arch Dermatol (2009) 0.78
Stevens-Johnson syndrome due to strontium ranelate. Ann Acad Med Singapore (2011) 0.78
Intronic mutations affecting splicing of MBTPS2 cause ichthyosis follicularis, alopecia and photophobia (IFAP) syndrome. Exp Dermatol (2011) 0.78
Fas-deficient C3.MRL-Tnfrsf6(lpr) mice and Fas ligand-deficient C3H/HeJ-Tnfsf6(gld) mice are relatively resistant to the induction of alopecia areata by grafting of alopecia areata-affected skin from C3H/HeJ mice. J Investig Dermatol Symp Proc (2003) 0.78
Two cases of cephalic Becker nevus with asymmetrical growth of beard or scalp hair. Dermatology (2003) 0.78
A study on the knowledge, attitudes and practices of Southeast Asian dermatologists in the management of atopic dermatitis. Ann Acad Med Singapore (2006) 0.78
Paradominant inheritance of twin spotting: phacomatosis pigmentovascularis as a further possible example. Eur J Dermatol (2004) 0.78
Diphencyprone immunotherapy alters anti-hair follicle antibody status in patients with alopecia areata. Eur J Dermatol (2002) 0.78
Cutaneous focal mucinosis: a case report. Pediatr Dermatol (2002) 0.78
Left-sided CHILD syndrome caused by a nonsense mutation in exon 7 of the NSDHL gene. Eur J Dermatol (2010) 0.77