Inherited bone marrow failure: The men behind the empty space

British Journal of Haematology

Volumn 107, Issue 2, 1999, Pages 242-246

  Smith, Owen P ^a,b   Cox, John ^c,d  

^a Consultant Paediatric Haematologist ^*  (Ireland)

^b ST JAMES S HOSPITAL   (Ireland)

^c Department of Haematology   (Ireland)

^d UNIVERSITY COLLEGE CORK   (Ireland)

Author keywords

Blackfan; Diamond; Fanconi; Kostmann; Schwachmann

Indexed keywords

ART; ARTICLE; BONE MARROW DISEASE; FINLAND; GENETICS; HEMATOLOGY; HISTORY; HUMAN; PEDIATRICS; SWITZERLAND; UNITED STATES;

BONE MARROW DISEASES; FINLAND; HEMATOLOGY; HISTORY, 20TH CENTURY; HUMANS; PEDIATRICS; PORTRAITS; SWITZERLAND; UNITED STATES;

EID: 0033220566     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1999.01720.x     Document Type: Article

References (15)

1. Bernheim, M., Monnet, P. & Germain, D. (1963) La thrombopenie hypoplastique amegàcaryocytic congénitale. Pédiatrie, 28, 367-371.
2. Blackfan, K.D. & Diamond, L.K. (1944) Atlas of the Blood in Children. The Commonwealth Fund, New York.
3. Diamond, L.K. & Blackfan, K.D. (1938) Hypoplastic anémia. American Journal of Diseases of Childhood, 56, 464-467.
4. Ehrlich, P. (1888) lieber einem Fall von Anaemie mit Bemerkungen über regenerative Veränderungen des Knochenmarks. Chariteannalen, 13, 301-309.
5. Engman M.F., Jr (1935) Congenital atrophy of the skin, with reticular pigmentation. Journal of the American Medical Association, 105, 1252.
6. Fanconi, G. (1927) Familaare infantile perniziosaartige Anämie (perniziones Blutbild und Konstitution). Jahrbuch für Kindreh, 117, 257-281.
7. Farber, S., Diamond, L.K., Mercer, R.D., Sylvester R.F., Jr & Wolff, J.A. (1948) Temporary remissions in acute leukemia in children produced by folie antagonist, 4-aminopteroylgIutamic acid (aminopterin). New England Journal of Medicine, 238, 787-793.
8. Gross, H., Groh, H. & U'eippl, G. (1956) Kongenitale hypoplastiche Thrombopenie mit Radiusaplasie: ein Syndrom multipler Abartungen. Neue Oesterriche zur Kinderheilkunde, l, 574-579.
9. Josephs. H.W. (1936) Anemia of infancy and early childhood. Medicine. 15, 307-309.
10. Kostmann, R. (1956) Infantile genetic agranulocytosis (agranulocytosis infantilis hereditaria): a new recessive lethal disease in man. Acta Paediatrica, 45, 1-7.
11. Kznelson, P. (1922) Zur Entstehung der Blutplattchen. Vem Dtsch Ges Inn Ned. 34, 557-558.
12. Levine, P.. Katzin, E.M. & Burnham. L. (1941) Isoimmunisation in pregnancy: its possible bearing on the etiology of erythroblastosis foetalis. Journal 0}the American Medical Association, 116, 825-827.
13. O'Gorman Hughes, D.W. (1966) The varied pattern of aplastic anaemia in childhood. Australian Paediatric Journal, 2, 228-234.
14. Shwachmann, IL, Diamond, L.K., Oski, F.A. & Khaw Kon-T (1964) The syndrome of pancreatic insufficiency and bone marrow dysfunction. Journal of Pediatrics, 65, 645-663.
15. Zinsser, F. (1910) Atrophia cutis reticularis cum pigmentatione, dystrophia unguium et leukoplakia oris (poikilodermia atrophicans vascularis Jacobi). Ikonogr Dennatolog Kioto. 5, 219-221.