Familial Haemophagocytic Reticulosis

Abt A. F. Denenholz E. J. (1936). Letterer-Siwe's disease. Amer. J. Dis. Child., 51, 499

Aherne W. A. (1957). The ‘burr’ red cell and azotaemia. J. clin. Path., 10, 252

Azzopardi J. G. (1965). A case of sickle-cell anaemia with pneumococcal meningitis. (Clinico-pathological conference at Postgraduate Medical School of London—postmortem findings). Brit. med. J., 1, 1049

Batson R. Shapiro J. Christie A. Riley H. D. Jr. (1955). Acute non-lipid disseminated reticuloendo-theliosis. Amer. J. Dis. Child., 90, 323

Brain M. C. Dacie J. V. Hourihane D. O'B. (1962). Microangiopathic haemolytic anaemia: The possible role of vascular lesions in pathogenesis. Brit. J. Haemat., 8, 358

Campbell W. A. B. Macafee A. L. Wade W. G. (1962). Familial neonatal leukaemia. Arch. Dis. Child., 37, 93

Chédiak M. M. (1952). Nouvelle anomalie leucocytaire de caractere constitutionele et familiale. Rev. Hémat., 7, 362

Dacie J. V. (1962). The bone marrow in auto-immune haemolytic anaemia. In The haemolytic anaemias, congenital and acquired. Part 2. The auto-immune anaemias. 2nd edition, p. 380. London: Churchill

Desai R. G. Creger W. P. (1963). Maternofetal passage of leucocytes and platelets in man. Blood, 21, 665

Doan C. A. Wright C.-S. (1946). Primary congenital and secondary acquired splenic panhematopenia. Blood, 1, 10

Donohue W. L. Bain H. W. (1957). Chédiak-Higashi syndrome, a lethal familial disease with anomalous inclusions in the leucocytes and constitutional stigmata: Report of a case with necropsy. Pediatrics, 20, 416

Falk W. Gellei B. (1957). The familial occurrence of Letterer-Siwe disease. Acta Paediat., 46, 471

Farquhar J. W. Claireaux A. E. (1952). Familial haemophagocytic reticulosis. Arch. Dis. Child., 27, 519

Farquhar J. W. MacGregor Agnes R. Richmond J. (1958). Familial haemophagocytic reticulosis. Brit, med. J., 2, 1561

Higashi O. (1954). Congenital gigantism of peroxidase granules. Tohoku J. exp. Med., 59, 315

Humble J. G. Jayne W. H. W. Pulvertaft R. J. V. (1956). Biological interaction between lymphocytes and other cells. Brit. J. Haemat., 2, 283

Kaplan H. S. Smithers D. W. (1959). Autoimmunity in man and homologous disease in mice in relation to the malignant lymphomas. Lancet, 2, 1

Letterer E. (1924). Aleukämische retikulose. Ein Beiträg zu den proliferativen Erkrankungen des Reticuloendothelialapparates. Frankfurt. Z. Path., 30, 377

MacMahon H. E. Bedizel M. Ellis C. A. (1963). Familial erythrophagocytic lymphohistiocytosis. Pediatrics, 32, 868

Marrian Valerie J. Sanerkin N. G. (1963). Familial histiocytic reticulosis (familial haemophagocytic reticulosis). J. clin. Path., 16, 65

Marshall A. H. E. (1956). Histiocytic medullary reticulosis. J. Path. Bact., 71, 61

Nelson P. Santamaria A. Olson R. L. Nayak N. C. (1961). Generalised lymphohistiocytic infiltration: A familial disease not previously described and different from Letterer-Siwe disease and the Chédiak-Higashi syndrome. Pediatrics, 27, 931

Reese A. J. M. Levy E. (1951). Familial incidence of non-lipoid reticulo-endotheliosis. Arch. Dis. Child., 26, 578

Saltzstein S. L. Ackerman L. V. (1959). Lympha-denopathy induced by anticonvulsant drugs and mimicking clinically and pathologically malignant lymphoma. Cancer, 12, 164

Sato A. (1955). Chédiak and Higashi's disease: Probable identity of a ‘new leucocytal anomaly (Chédiak)’ and ‘congenital gigantism of peroxidase granules (Higashi)’. Tohoku J. exp. Med., 61, 201

Schoeck V. W. Peterson R. D. Good R. A. (1963). Familial occurrence of Letterer-Siwe disease. Pediatrics, 32, 1055

Scott R. B. Robb-Smith A. H. T. , (1939). Histiocytic medullary reticulosis. Lancet, 2, 194

Shelton E. Dalton A. J. (1959). Electron microscopy of emperipolesis. J. biophys. biochem. Cytol., 6, 513

Siwe S. A. (1933). Die Reticuloendotheliose—ein neues Krankheitsbild under den Hepatosplenomegalien. Z. Kinderheilk., 55, 212

Varadi S. Gordon R. R. Abbott D. (1963). Haemophagocytic reticulosis diagnosed by sternal puncture during life. Proceedings of the 71st General Meeting of the Association of Clinical Pathologists

Varadi S. Gordon R. R. Abbot D. (1964). Haemophagocytic reticulosis diagnosed by sternal puncture during life. Acta haemat., 31, 349

Williams G. Whittaker J. S. (1965). Diagnostic problems in biliary duct lymph nodes. J. clin. Path., 18, 43

Wiseman B. K. Doan C. A. (1942). Primary splenic neutropenia; a newly recognised syndrome closely related to congential hemolytic icterus and essential thrombocytopenic purpura. Ann. intern. Med., 16, 1097

Zinkham W. H. Diamond L. K. (1952). In vitro erythrophagocytosis in acquired hemolytic anaemia Blood, 7, 592