{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,22]],"date-time":"2025-10-22T02:55:24Z","timestamp":1761101724756},"reference-count":30,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[1990,5,1]],"date-time":"1990-05-01T00:00:00Z","timestamp":641520000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Vichows Archiv A Pathol Anat"],"published-print":{"date-parts":[[1990,5]]},"DOI":"10.1007\/bf01600141","type":"journal-article","created":{"date-parts":[[2005,4,29]],"date-time":"2005-04-29T04:49:48Z","timestamp":1114750188000},"page":"247-253","source":"Crossref","is-referenced-by-count":14,"title":["Dyskeratosis congenita (Zinsser-Cole-Engman syndrome)"],"prefix":"10.1007","volume":"417","author":[{"given":"Kenji","family":"Kawaguchi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hisashi","family":"Sakamaki","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yasusuke","family":"Onozawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Morio","family":"Koike","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"100","DOI":"10.1111\/j.1365-2230.1988.tb00668.x","volume":"13","author":"A Aguilar-Martinez","year":"1988","unstructured":"Aguilar-Martinez A, Lautre-Ecenarro MJ, Urbina-Gonzalez F, Cristobal-Gil MC, Guerra-Rodriguez P, Garcia-Perez A (1988) Cytogenetic abnormalities in dyskeratosis congenita \u2014 report of five cases. Clin Exp Dermatol 13:100\u2013104","journal-title":"Clin Exp Dermatol"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1001\/jama.1965.03080160023005","volume":"192","author":"HG Bryan","year":"1965","unstructured":"Bryan HG, Nixon RK (1965) Dyskeratosis congenita and familial pancytopenia. JAMA 192:203\u2013208","journal-title":"JAMA"},{"key":"CR3","doi-asserted-by":"crossref","first-page":"71","DOI":"10.1001\/archderm.1930.01440070079008","volume":"21","author":"HN Cole","year":"1930","unstructured":"Cole HN, Rauschkolb J, Toomey J (1930) Dyskeratosis congenita with pigmentation, dystrophia unguium, and leukokeratosis oris. Arch Dermatol Syphilol 21:71\u201395","journal-title":"Arch Dermatol Syphilol"},{"key":"CR4","doi-asserted-by":"crossref","first-page":"451","DOI":"10.1001\/archderm.1955.01540280027005","volume":"71","author":"HN Cole","year":"1954","unstructured":"Cole HN, Rauschkolb J, Toomey J (1954) Dyskeratosis congenita with pigmentation, dystrophia unguium, and leucokeratosis oris. Arch Dermatol 71:451\u2013456","journal-title":"Arch Dermatol"},{"key":"CR5","doi-asserted-by":"crossref","first-page":"712","DOI":"10.1001\/archderm.1957.01550240030006","volume":"76","author":"HN Cole","year":"1957","unstructured":"Cole HN, Cole HN Jr, Lasheid WP (1957) Dyskeratosis congenita. Arch Dermatol 76:712\u2013719","journal-title":"Arch Dermatol"},{"key":"CR6","doi-asserted-by":"crossref","first-page":"513","DOI":"10.1111\/j.1365-2141.1984.tb03981.x","volume":"56","author":"BT Colvin","year":"1984","unstructured":"Colvin BT, Baker H, Hibbin JA, Gordon-Smith EC, Gordon MY (1984) Haemopoietic progenitor cells in dyskeratosis congenita. Br J Haematol 56:513\u2013517","journal-title":"Br J Haematol"},{"key":"CR7","doi-asserted-by":"crossref","first-page":"321","DOI":"10.1111\/j.1365-2133.1981.tb01292.x","volume":"105","author":"JM Connor","year":"1981","unstructured":"Connor JM, Teague RH (1981) Dyskeratosis congenita: report of a large kindred. Br J Dermatol 105:321\u2013325","journal-title":"Br J Dermatol"},{"key":"CR8","doi-asserted-by":"crossref","first-page":"348","DOI":"10.1007\/BF00290963","volume":"72","author":"JM Connor","year":"1986","unstructured":"Connor JM, Gatherer D, Gray FC, Pirrit LA, Affara NA (1986) Assignment of the gene for dyskeratosis congenita to Xq28. Hum Genet 72:348\u2013351","journal-title":"Hum Genet"},{"key":"CR9","doi-asserted-by":"crossref","first-page":"123","DOI":"10.1001\/archderm.1956.01550020023004","volume":"73","author":"MJ Costello","year":"1955","unstructured":"Costello MJ, Buncke CM (1955) Dyskeratosis congenita. Arch Dermatol 73:123\u2013132","journal-title":"Arch Dermatol"},{"key":"CR10","doi-asserted-by":"crossref","first-page":"843","DOI":"10.1136\/jmg.25.12.843","volume":"25","author":"HR Davidson","year":"1988","unstructured":"Davidson HR, Connor JM (1988) Dyskeratosis congenita. J Med Genet 25:843\u2013846","journal-title":"J Med Genet"},{"key":"CR11","doi-asserted-by":"crossref","first-page":"685","DOI":"10.1001\/archderm.1926.02370170087012","volume":"13","author":"MFSr Engman","year":"1926","unstructured":"Engman MFSr (1926) A unique case of reticular pigmentation of the skin with atrophy. Society Transactions, Arch Dermatol Syphilol 13:685\u2013687","journal-title":"Arch Dermatol Syphilol"},{"key":"CR12","doi-asserted-by":"crossref","first-page":"231","DOI":"10.1159\/000212345","volume":"25","author":"HH Fudenberg","year":"1979","unstructured":"Fudenberg HH, Goust JM, Vesole DH, Salinas CF (1979) Active and suppressor T cells: diminution in a patient with dyskeratosis congenita and in first-degree relatives. Gerontology 25:231\u2013237","journal-title":"Gerontology"},{"key":"CR13","doi-asserted-by":"crossref","first-page":"704","DOI":"10.1001\/archderm.1958.01560060070012","volume":"77","author":"J Garb","year":"1958","unstructured":"Garb J (1958) Dyskeratosis congenita with pigmentation, dystrophia unguium, and leukoplakia oris. Arch Dermatol 77:704\u2013712","journal-title":"Arch Dermatol"},{"key":"CR14","doi-asserted-by":"crossref","first-page":"36","DOI":"10.1111\/j.1440-0960.1965.tb01368.x","volume":"8","author":"K Georgouras","year":"1965","unstructured":"Georgouras K (1965) Dyskeratosis congenita. Australas J Dermatol 8:36\u201343","journal-title":"Australas J Dermatol"},{"key":"CR15","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1159\/000250482","volume":"160","author":"A Giannetti","year":"1980","unstructured":"Giannetti A, Seidenari S (1980) Deficit of cell-mediated immunity, chromosomal alterations and defective DNA repair in a case of dyskeratosis congenita. Dermatologica 160:113\u2013117","journal-title":"Dermatologica"},{"key":"CR16","doi-asserted-by":"crossref","first-page":"1667","DOI":"10.1001\/archderm.1978.01640230041011","volume":"114","author":"A Gutman","year":"1978","unstructured":"Gutman A, Frumkin A, Adam A, Bloch-Shtacher N, Rozenszajn LA (1978) X-linked dyskeratosis congenita with pancytopenia. Arch Dermatol 114:1667\u20131671","journal-title":"Arch Dermatol"},{"key":"CR17","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1001\/archpedi.1973.02110190337020","volume":"126","author":"S Inoue","year":"1973","unstructured":"Inoue S, Mekanik G, Mahallati M, Zuelzer WW (1973) Dyskeratosis congenita with pancytopenia: another constitutional anemia. Am J Dis Child 126:389\u2013396","journal-title":"Am J Dis Child"},{"key":"CR18","doi-asserted-by":"crossref","first-page":"461","DOI":"10.1111\/j.1600-0609.1984.tb02186.x","volume":"32","author":"P Jacobs","year":"1984","unstructured":"Jacobs P, Saxe N, Gordon W, Nelson M (1984) Dyskeratosis congenita; haematologic, cytogenetic, and dermatologic studies. Scand J Haematol 32:461\u2013468","journal-title":"Scand J Haematol"},{"key":"CR19","doi-asserted-by":"crossref","first-page":"306","DOI":"10.1111\/j.1600-0609.1987.tb00774.x","volume":"39","author":"HS Juneja","year":"1987","unstructured":"Juneja HS, Elder FFB, Gardner FH (1987) Abnormality of platelet size and T-lymphocyte proliferation in an autosomal recessive form of dyskeratosis congenita. Eur J Haematol 39:306\u2013310","journal-title":"Eur J Haematol"},{"key":"CR20","doi-asserted-by":"crossref","first-page":"1424","DOI":"10.1001\/archderm.1985.01660110072019","volume":"121","author":"NS Ling","year":"1985","unstructured":"Ling NS, Fenske NA, Julius RL, Espinoza CG, Drake LA (1985) Dyskeratosis congenita in a girl simulating chronic graft-vs-host disease. Arch Dermatol 121:1424\u20131428","journal-title":"Arch Dermatol"},{"key":"CR21","doi-asserted-by":"crossref","first-page":"345","DOI":"10.1001\/archderm.1964.01590270031007","volume":"89","author":"H Milgrom","year":"1964","unstructured":"Milgrom H, Stoll HL Jr, Crissey JT (1964) Dyskeratosis congenita; a case with new features. Arch Dermatol 89:345\u2013349","journal-title":"Arch Dermatol"},{"key":"CR22","doi-asserted-by":"crossref","first-page":"1437","DOI":"10.1001\/archderm.1979.04010120035015","volume":"115","author":"SE Mills","year":"1979","unstructured":"Mills SE, Cooper PH, Beacham BE, Greer KE (1979) Intracranial calcifications and dyskeratosis congenita. Arch Dermatol 115:1437\u20131439","journal-title":"Arch Dermatol"},{"key":"CR23","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1002\/ajmg.1320320114","volume":"32","author":"GS Pai","year":"1989","unstructured":"Pai GS, Morgan S, Whetsell C (1989) Etiologic heterogeneity in dyskeratosis congenita. Am J Med Genet 32:63\u201366","journal-title":"Am J Med Genet"},{"key":"CR24","doi-asserted-by":"crossref","first-page":"339","DOI":"10.1136\/jmg.12.4.339","volume":"12","author":"C Sirinavin","year":"1975","unstructured":"Sirinavin C, Trowbridge AA (1975) Dyskeratosis congenita: clinical features and genetic aspects; report of a family and review of the literature. J Med Genet 12:339\u2013354","journal-title":"J Med Genet"},{"key":"CR25","doi-asserted-by":"crossref","first-page":"340","DOI":"10.1001\/archderm.1963.01590210098015","volume":"88","author":"JM Sorrow Jr","year":"1963","unstructured":"Sorrow JM Jr, Hitch JM (1963) Dyskeratosis congenita; first report of its occurrence in a female and a review of the literature. Arch Dermatol 88:340\u2013347","journal-title":"Arch Dermatol"},{"key":"CR26","doi-asserted-by":"crossref","first-page":"510","DOI":"10.1182\/blood.V39.4.510.510","volume":"39","author":"W Steier","year":"1972","unstructured":"Steier W, Van Voolen GA, Selmanowitz VJ (1972) Dyskeratosis congenita: relationship to Fanconi's anemia. Blood 39:510\u2013521","journal-title":"Blood"},{"key":"CR27","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1002\/ajh.2830030205","volume":"3","author":"AA Trowbridge","year":"1977","unstructured":"Trowbridge AA, Sirinavin C, Linman JW (1977) Dyskeratosis congenita: hematologic evaluation of a sibship and review of the literature. Am J Hematol 3:143\u2013152","journal-title":"Am J Hematol"},{"key":"CR28","doi-asserted-by":"crossref","first-page":"397","DOI":"10.1001\/archinte.1984.00350140227031","volume":"144","author":"HP Wiedemann","year":"1984","unstructured":"Wiedemann HP, McGuire J, Dwyer JM, Sabetta J, Gee JML, Smith GJW, Loke J (1984) Progressive immune failure in dyskeratosis congenita; report of an adult in whomPneumocystitis carinii and fatal disseminated candidiasis developed. Arch Intern Med 144:397\u2013399","journal-title":"Arch Intern Med"},{"key":"CR29","doi-asserted-by":"crossref","first-page":"603","DOI":"10.1542\/peds.71.4.603","volume":"71","author":"R Womer","year":"1983","unstructured":"Womer R, Clark JE, Wood P, Sabio H, Kelly TE (1983) Dyskeratosis congenita: two examples of this multisystem disorder. Pediatrics 71:603\u2013609","journal-title":"Pediatrics"},{"key":"CR30","first-page":"219","volume":"5","author":"F Zinsser","year":"1906","unstructured":"Zinsser F (1906) Atrophia cutis reticularis cum pigmentatione, dystrophia unguium et leukoplakia oris. Ikonogr Dermatol (Kyoto) 5:219\u2013223","journal-title":"Ikonogr Dermatol (Kyoto)"}],"container-title":["Virchows Archiv A Pathological Anatomy and Histopathology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF01600141.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF01600141\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF01600141","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,3]],"date-time":"2023-05-03T03:10:24Z","timestamp":1683083424000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF01600141"}},"subtitle":["An autopsy case presenting with rectal carcinoma, non-cirrhotic portal hypertension, andPneumocystis carinii pneumonia"],"short-title":[],"issued":{"date-parts":[[1990,5]]},"references-count":30,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1990,5]]}},"alternative-id":["BF01600141"],"URL":"https:\/\/doi.org\/10.1007\/bf01600141","relation":{},"ISSN":["0174-7398","1432-2307"],"issn-type":[{"value":"0174-7398","type":"print"},{"value":"1432-2307","type":"electronic"}],"subject":[],"published":{"date-parts":[[1990,5]]}}}