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1
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0018851859
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The CHILD syndrome: Congenital hemidysplasia with ichthyosiform erythroderma and limb defects
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Happle R, Koch H, Lenz W. The CHILD syndrome: congenital hemidysplasia with ichthyosiform erythroderma and limb defects. Eur J Pediatr 1980;134:27-33.
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(1980)
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Happle, R.1
Koch, H.2
Lenz, W.3
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2
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0029161652
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The CHILD nevus: A distinct skin disorder
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Happle R, Mittag H, Küster W. The CHILD nevus: a distinct skin disorder. Dermatology 1995;191:210-6.
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(1995)
Dermatology
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Happle, R.1
Mittag, H.2
Küster, W.3
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3
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0033972847
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Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome
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König A, Happle R, Bornholdt D. Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome. Am J Med Genet 2000;90:339-46.
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Am J Med Genet
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König, A.1
Happle, R.2
Bornholdt, D.3
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4
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0025038684
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Ptychotropism as a cutaneous feature of the CHILD syndrome
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Happle R. Ptychotropism as a cutaneous feature of the CHILD syndrome. J Am Acad Dermatol 1990;23:763-6.
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(1990)
J Am Acad Dermatol
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Happle, R.1
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5
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0026016452
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CHILD naevus is not ILVEN
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Happle R. CHILD naevus is not ILVEN. J Med Genet 1991;28:214.
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(1991)
J Med Genet
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Happle, R.1
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8
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0031665988
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CHILD syndrome with linear eruptions, hypopigmented bands and verruciform xanthoma
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Hashimoto K, Prada S, López AP. CHILD syndrome with linear eruptions, hypopigmented bands and verruciform xanthoma. Pediatr Dermatol 1998;15:360-6.
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(1998)
Pediatr Dermatol
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Hashimoto, K.1
Prada, S.2
López, A.P.3
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9
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0027367118
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CHILD-Syndrom: Fallbericht einer seltenen Genodermatose
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Peter C, Meinecke P. CHILD-Syndrom: Fallbericht einer seltenen Genodermatose. Hautarzt 1993;44:590-3.
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(1993)
Hautarzt
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Peter, C.1
Meinecke, P.2
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11
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0030915561
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Systematized inflammatory epidermal nevus with symmetrical involvement: An unusual case of CHILD syndrome?
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Fink-Puches R, Soyer HP, Pierer G. Systematized inflammatory epidermal nevus with symmetrical involvement: an unusual case of CHILD syndrome? J Am Acad Dermatol 1997;36:823-6.
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(1997)
J Am Acad Dermatol
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Fink-Puches, R.1
Soyer, H.P.2
Pierer, G.3
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12
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0029035688
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CHILD syndrome: Analysis of abnormal keratinization and ultrastructure
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Hashimoto K, Topper S, Sharata H. CHILD syndrome: analysis of abnormal keratinization and ultrastructure. Pediatr Dermatol 1995;12:116-29.
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(1995)
Pediatr Dermatol
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Hashimoto, K.1
Topper, S.2
Sharata, H.3
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14
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0024395245
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CHILD syndrome: Phenotype dichotomy in eicosanoid metabolism and proliferative rates among cultured dermal fibroblasts
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Goldyne ME, Williams ML. CHILD syndrome: phenotype dichotomy in eicosanoid metabolism and proliferative rates among cultured dermal fibroblasts. J Clin Invest 1989;84:357-60.
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(1989)
J Clin Invest
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Goldyne, M.E.1
Williams, M.L.2
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15
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0026674614
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Peroxisomal abnormality in fibroblasts from involved skin of CHILD syndrome: Case study and review of peroxisomal disorders in relation to skin disease
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Emami S, Rizzo WB, Hanley KP. Peroxisomal abnormality in fibroblasts from involved skin of CHILD syndrome: case study and review of peroxisomal disorders in relation to skin disease. Arch Dermatol 1992;128:1213-22.
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(1992)
Arch Dermatol
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Emami, S.1
Rizzo, W.B.2
Hanley, K.P.3
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16
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0026605285
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CHILD syndrome: Lack of expression of epidermal differentiation markers in lesional ichthyotic skin
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Dale BA, Kimball JR, Fleckman P. CHILD syndrome: lack of expression of epidermal differentiation markers in lesional ichthyotic skin. J Invest Dermatol 1992; 98:442-9.
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(1992)
J Invest Dermatol
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Dale, B.A.1
Kimball, J.R.2
Fleckman, P.3
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17
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0034127976
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Surgical treatment of CHILD nevus
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Fink-Puches R, Soyer HP, Pierer G, Kerl H, Happle R. Surgical treatment of CHILD nevus. Eur J Dermatol 2000;10:262-4.
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(2000)
Eur J Dermatol
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Fink-Puches, R.1
Soyer, H.P.2
Pierer, G.3
Kerl, H.4
Happle, R.5
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