{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,4]],"date-time":"2022-04-04T12:46:41Z","timestamp":1649076401202},"reference-count":9,"publisher":"BMJ","issue":"10","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Archives of Disease in Childhood"],"published-print":{"date-parts":[[1973,10,1]]},"DOI":"10.1136\/adc.48.10.816","type":"journal-article","created":{"date-parts":[[2008,12,22]],"date-time":"2008-12-22T21:05:14Z","timestamp":1229979914000},"page":"816-818","source":"Crossref","is-referenced-by-count":0,"title":["Hydatid disease of interatrial septum."],"prefix":"10.1136","volume":"48","author":[{"given":"H V","family":"Price","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"222","DOI":"10.1002\/bjs.18004016106","article-title":"Pulmonary hydatid disease","volume":"40","author":"Barrett, N.R.; Thomas, D.","year":"1952","unstructured":"Barrett, N. R., and Thomas, D. (1952). Pulmonary hydatid disease. British Journal of Surgery, 40, 222.","journal-title":"British Journal of Surgery"},{"key":"ref_2","first-page":"514","article-title":"La rupture iterative des kystes hydatiques du coeur. Comptes Rendus des Seances de la Sociiet de Biologie et de ses","volume":"79","author":"Deve, F.","year":"1916","unstructured":"Deve, F. (1916). La rupture iterative des kystes hydatiques du coeur. Comptes Rendus des Seances de la Sociiet de Biologie et de ses Filiales, 79, 514.","journal-title":"Filiales"},{"key":"ref_3","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1016\/0002-9149(72)90076-8","article-title":"Echinococcus of the heart","volume":"30","author":"Dodek, A.; DeMots, H.; Antonovic, J.A.; Hodam, R.P.","year":"1972","unstructured":"Dodek, A., DeMots, H., Antonovic, J. A., and Hodam, R. P. (1972). Echinococcus of the heart. American Journal of Cardiology, 30, 293.","journal-title":"American Journal of Cardiology"},{"key":"ref_4","article-title":"Cardiac hydatid cysts","volume-title":"Hydatid disease","author":"Gibson, D.S.","year":"1964","unstructured":"Gibson, D. S. (1964). Cardiac hydatid cysts. Thorax, 19, 151. Public Health Laboratory Service (1972). Hydatid disease."},{"key":"ref_5","first-page":"679","article-title":"British Medical","volume":"4","unstructured":"British Medical Journal, 4, 679.","journal-title":"Journal"},{"key":"ref_6","article-title":"The Wiskott-Aldrich syndrome is an X-linked recessive disorder characterized by thrombocytopenia, purpura, eczema, and recurrent infections","volume-title":"Infantile cortical hyperostosis is a well-recognized clinical and radiological entity of unknown cause which usually resolves spontaneously (Caffey and Silverman, 1945). We report briefly the details of two unrelated male infants with the WiskottAldrich syndrome who developed cortical hyperostoSiS","author":"Aldrich, Steinberg; Campbell","year":"1937","unstructured":"The Wiskott-Aldrich syndrome is an X-linked recessive disorder characterized by thrombocytopenia, purpura, eczema, and recurrent infections (Wiskott, 1937; Aldrich, Steinberg, and Campbell, 1954). Infantile cortical hyperostosis is a well-recognized clinical and radiological entity of unknown cause which usually resolves spontaneously (Caffey and Silverman, 1945). We report briefly the details of two unrelated male infants with the WiskottAldrich syndrome who developed cortical hyperostoSiS."},{"key":"ref_7","article-title":"Case reports Case 1. A male born","volume-title":"is the only child of his mother's second marriage. By her first marriage she had two children, one of whom, a boy died at the age of one year from bronchopneumonia having suffered from thrombocytopenia, purpura, eczema, and recurrent infections since early infancy","year":"1967","unstructured":"Case reports Case 1. A male born 15 September 1967 is the only child of his mother's second marriage. By her first marriage she had two children, one of whom, a boy died at the age of one year from bronchopneumonia having suffered from thrombocytopenia, purpura, eczema, and recurrent infections since early infancy."},{"issue":"100","key":"ref_8","article-title":"Our patient developed purpura and a low platelet count within a few days of birth, and later had fresh blood in the stools. and eczema. On the ninth day of life the serum immunoglobulins were IgG 1050 mg\/100 ml","volume":"248","unstructured":"Our patient developed purpura and a low platelet count within a few days of birth, and later had fresh blood in the stools. and eczema. On the ninth day of life the serum immunoglobulins were IgG 1050 mg\/100 ml, IgA 248 mg\/100 ml (greatly raised, Stiehm and Fudenberg, 1966), IgM none detected. Marrow aspiration from a tibia at the age of 4 weeks was normal apart from defective budding of megakaryocytes. He continued to have thrombocytopenia (platelets usually < 10,000\/mm3), anaemia, and occasional epistaxes. In early life he had several infections, notably gastroenteritis (Esch. coli 055), otitis extema, skin sepsis, bronchitis, and lobar pneumonia.","journal-title":"IgA; ml (greatly raised, Stiehm and Fudenberg, 1966), IgM none detected. Marrow aspiration from a tibia at the age of 4 weeks was normal apart from defective budding of megakaryocytes. He continued to have thrombocytopenia (platelets usually < 10,000\/mm3), anaemia, and occasional epistaxes. In early life he had several infections, notably gastroenteritis (Esch. coli 055), otitis extema, skin sepsis, bronchitis, and lobar pneumonia"},{"issue":"100","key":"ref_9","article-title":"Case 2. A male bom","volume":"370","year":"1970","unstructured":"Case 2. A male bom 20 May 1970. On the first day of life this infant, an only child of unrelated parents, had a petechial rash and a platelet count of less than 10,000\/ mm3. The thrombocytopenia persisted and, at the age of 2 months serum immunoglobulins were IgG 370 mg\/100 ml, IgA 88 mg\/100 ml, IgM 14 mgf100 ml, indicating a raised IgA level with IgM at the lower limit of normal.","journal-title":"IgG; On the first day of life this infant, an only child of unrelated parents, had a petechial rash and a platelet count of less than 10,000\/ mm3. The thrombocytopenia persisted and, at the age of 2 months serum immunoglobulins were"}],"container-title":["Archives of Disease in Childhood"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/adc.48.10.816","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,9,26]],"date-time":"2020-09-26T08:58:39Z","timestamp":1601110719000},"score":1,"resource":{"primary":{"URL":"https:\/\/adc.bmj.com\/lookup\/doi\/10.1136\/adc.48.10.816"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1973,10,1]]},"references-count":9,"journal-issue":{"issue":"10","published-print":{"date-parts":[[1973,10,1]]}},"URL":"https:\/\/doi.org\/10.1136\/adc.48.10.816","relation":{},"ISSN":["0003-9888","1468-2044"],"issn-type":[{"value":"0003-9888","type":"print"},{"value":"1468-2044","type":"electronic"}],"subject":[],"published":{"date-parts":[[1973,10,1]]}}}