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Volumn 196, Issue 4, 1998, Pages 463-466

The Schopf-Schulz-Passarge syndrome

Author keywords

Genodermatosis; Poroma with follicular differentiation; Schopf Schulz Passarge syndrome; Tumor of the follicular infundibulum

Indexed keywords

ACTINIC KERATOSIS; ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; DISEASE ASSOCIATION; EPITHELIUM TUMOR; EYELID; GENODERMATOSIS; HIDRADENOMA; HUMAN; HYPODONTIA; HYPOTRICHOSIS; KERATOSIS PALMOPLANTARIS; MALE; NAIL HYPOPLASIA; PRIORITY JOURNAL; SCHOPF SCHULZ PASSARGE SYNDROME; TUMOR DIFFERENTIATION; EYELID DISEASE; MIDDLE AGED; NAIL DISEASE; PATHOLOGY; SKIN TUMOR; SYNDROME;

EID: 0031595154     PISSN: 10188665     EISSN: None     Source Type: Journal    
DOI: 10.1159/000017951     Document Type: Article
Times cited : (27)

References (10)
  • 1
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    • Syndrome of cystic eyelids, palmoplantar keratosis, hypodontia and hypotrichosis as a possible autosomal recessive trait
    • Schöpf E, Schulz HJ, Passarge E: Syndrome of cystic eyelids, palmoplantar keratosis, hypodontia and hypotrichosis as a possible autosomal recessive trait. Birth Defects 1971;8: 219-221.
    • (1971) Birth Defects , vol.8 , pp. 219-221
    • Schöpf, E.1    Schulz, H.J.2    Passarge, E.3
  • 2
    • 0026610619 scopus 로고
    • Schöpf-SchulzPassarge syndrome
    • Monk B, Pieris S, Soni V: Schöpf-SchulzPassarge syndrome. Br J Dermatol 1992;127:33-35.
    • (1992) Br J Dermatol , vol.127 , pp. 33-35
    • Monk, B.1    Pieris, S.2    Soni, V.3
  • 3
    • 0008150013 scopus 로고
    • Schöpf syndrome
    • Perret C: Schöpf syndrome. Br J Dermatol 1989;120:131-132.
    • (1989) Br J Dermatol , vol.120 , pp. 131-132
    • Perret, C.1
  • 6
    • 0000253318 scopus 로고
    • A tumor of the follicular infundibulum
    • Mehregan AH, Butler JD: A tumor of the follicular infundibulum. Arch Dermatol 1961;83: 924-927.
    • (1961) Arch Dermatol , vol.83 , pp. 924-927
    • Mehregan, A.H.1    Butler, J.D.2
  • 8
    • 0019993284 scopus 로고
    • Aspects of heredity, syndromic associations, and course of conditions in which cutaneous lesions occur solitarily or in multiplicity
    • Jelinek JE: Aspects of heredity, syndromic associations, and course of conditions in which cutaneous lesions occur solitarily or in multiplicity. J Am Acad Dermatol 1982;7:526-540.
    • (1982) J Am Acad Dermatol , vol.7 , pp. 526-540
    • Jelinek, J.E.1
  • 9
    • 0023685640 scopus 로고
    • Familial occurrence of eccrine tumours in a family with ectodermal dysplasia
    • Nordin H, Mansson T, Svensson A: Familial occurrence of eccrine tumours in a family with ectodermal dysplasia. Acta Derm Venereol 1988;68:523-550.
    • (1988) Acta Derm Venereol , vol.68 , pp. 523-550
    • Nordin, H.1    Mansson, T.2    Svensson, A.3
  • 10
    • 0030981933 scopus 로고    scopus 로고
    • Eccrine syringofibroadenoma: Multiple lesions representing a new cutaneous marker in the Schöpf syndrome, and solitary nonhereditary tumors
    • Starink TM: Eccrine syringofibroadenoma: Multiple lesions representing a new cutaneous marker in the Schöpf syndrome, and solitary nonhereditary tumors. J Am Acad Dermatol 1997;36:569-576.
    • (1997) J Am Acad Dermatol , vol.36 , pp. 569-576
    • Starink, T.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.