메뉴 건너뛰기




Volumn 10, Issue 1, 1984, Pages 1-16

Primary disorders of hyperpigmentation

(1)  Fulk, Charles Samuel a  

a NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DIAGNOSIS; DYSKERATOSIS CONGENITA; GENETICS; HEREDITY; HUMAN; HYPERPIGMENTATION; INCONTINENTIA PIGMENTI; INHERITANCE; REVIEW; XERODERMA PIGMENTOSUM;

EID: 0021360140     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0190-9622(84)80032-8     Document Type: Article
Times cited : (53)

References (141)
  • 17
    • 0041577935 scopus 로고
    • Keratosis, cancer, and the sign of Leser-Trelat
    • (1965) Cancer , vol.18 , pp. 1003-1006
    • Ronchese, F1
  • 21
    • 0000621108 scopus 로고
    • Concurrent melanosis and hypertrichosis in the distribution of nevus unius lateris
    • (1949) Arch Dermatol , vol.70 , pp. 155-160
    • Becker, SW1
  • 31
    • 0015707338 scopus 로고
    • Partial unilateral lentiginosis with associated developmental abnormalities
    • (1973) Guys Hosp Rep , vol.122 , pp. 361-370
    • Pickering, JG1
  • 36
    • 34347127724 scopus 로고
    • Über drei Generationer vererbte, auf Frauenbeschränkte Keratosis follicularis mit Alopecie, Hyphidrose, u abortiven Palmar-Plantar Keratosen in ihren Beziehungen zur Hypotrichosis congenita hereditaria
    • (1960) Arch Klin Exp Dermatol , vol.210 , pp. 123-140
    • Greither, A1
  • 44
    • 0008468980 scopus 로고
    • Gastrointestinal polyposis with mucocutaneous pigmentation
    • (1957) N Engt J Med , vol.256 , pp. 1093-1103
    • Dormandy, TL1
  • 45
    • 70449142956 scopus 로고
    • Gastrointestinal polyposis with mucocutaneous pigmentation
    • (1957) N Engt J Med , vol.256 , pp. 1141-1146
    • Dormandy, TL1
  • 46
    • 70449155523 scopus 로고
    • Gastrointestinal polyposis with mucocutaneous pigmentation
    • (1957) N Engt J Med , vol.256 , pp. 1186-1190
    • Dormandy, TL1
  • 48
    • 0000997544 scopus 로고
    • Hemangiomas of the small intestine associated with mucocutaneous pigmentation
    • (1960) Gastroenterology , vol.38 , pp. 641-645
    • Bandler, M1
  • 60
    • 0001698792 scopus 로고
    • Axillary freckling as a diagnostic aid in neurofibromatosis
    • (1964) Ann Intern Med , vol.61 , pp. 1142-1143
    • Crowe, FW1
  • 62
    • 0013922148 scopus 로고
    • Fibrosing alveolitis. Its occurrence, roentgenographic, and pathologic features in von Recklinghausen's neurofibromatosis
    • (1966) Am Rev Respir Dis , vol.93 , pp. 934-942
    • Massare, D1    Katz, S2
  • 65
    • 84995853510 scopus 로고
    • Syndrome characterized by osteitis fibrosa disseminata, areas of pigmentation, and a gonadal dysfunction
    • (1938) Endocrinology , vol.22 , pp. 411-426
    • Albright, F1
  • 72
    • 0014094718 scopus 로고
    • Pulmonary stenosis, cafe au lait spots, and dull intelligence
    • (1967) Arch Dis Child , vol.42 , pp. 303-307
    • Watson, GH1
  • 79
    • 79551520027 scopus 로고
    • A hitherto undescribed generalized pigmentation of the skin appearing in infancy in a brother and sister
    • (1919) J Cutan Dis , vol.37 , pp. 685-701
    • Wende, GW1    Bauckus, HH2
  • 85
    • 0008551081 scopus 로고
    • Akropigmentation symmetrica Dohi mit ängeborenem fundisveranderungen bei mutter and toch-ter
    • (1952) Dermatol Wchnschr , vol.23 , pp. 534-535
    • Gertler, W1
  • 95
    • 85025516814 scopus 로고
    • A case of possible transitional syndrome between incontinentia pigmenti and Naegeli syndrome
    • (1972) Arch Dermatol , vol.105 , pp. 286
    • Gross, DA1
  • 98
    • 8244235847 scopus 로고
    • Dermatopathia pigmentosa reticularis
    • (1960) Hautarzt , vol.6 , pp. 262-265
    • Flegel, H1
  • 107
    • 0000309721 scopus 로고
    • Genetical studies on skin diseases. VII. Dyschromatosis universalis hereditaria in 5 generations
    • (1952) Tohoku J Exp Med , vol.55 , pp. 373-376
    • Suenaga, M1
  • 110
    • 16444385545 scopus 로고
    • Congenital generalized melanoleukoderma associated with hypodontia, hypotrichosis, stunted growth, and mental retardation occurring in 2 brothers and 2 sisters
    • (1961) Dermatologica , vol.123 , pp. 227-243
    • Berlin, C1
  • 123
    • 3242804840 scopus 로고
    • Rothmund-Thomson syndrome. Congenital poikiloderma with or without juvenile cataract: A review of the literature, report of a case, and discussion of the relationship of the two syndromes
    • (1957) Arch Dermatol , vol.75 , pp. 236-244
    • Taylor, WB1
  • 127
    • 0000058407 scopus 로고
    • Dyskeratosis congenita. First report of its occurrence in a female and a review of the literature
    • (1963) Arch Dermatol , vol.88 , pp. 340-347
    • Sorrow, JM1    Hitch, JM2
  • 132
    • 0001306494 scopus 로고
    • Familiäre infantile perniziösaartige Anämie (perniziöses Blütblid und Konstitution)
    • (1927) Jahrb Kin-derheilk , vol.117 , pp. 257-280
    • Fanconi, G1
  • 134
    • 0014986159 scopus 로고
    • Spontaneous chromosomal breakage and high incidence of leukemia in inherited disease
    • (1971) Blood , vol.37 , pp. 91-112
    • Schroder, TM1    Kurth, R2
  • 136
    • 0002634144 scopus 로고
    • Xeroderm pigmentosum
    • DJ Demis, RL Dobson, J McGuire, Harper & Row, Publishers Inc., Philadelphia, unit 19-7
    • (1982) Clinical dermatology , vol.4 , pp. 1-33
    • Kraemer, KH1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.