Анемии - Алексеева Н.А.
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// Eur. J. Haematol I win ' ¦ ( ¦ 1
P. 221.
Dokal I. A discusc ol |нмпиіпм н, ni|i '
1.Dokal II I am.I Mini Vo| ISK.
Suppl.—P. 27
Donato J. Human II lint • • ¦ li n 1 r icttc
cell cycle rcglllaloi і ........... I Ко,
J.Kutok II .1 ( Iln bn і • MMijj Vol.
109,—P. 51
Doitnai D. I he non «I¦ I....... и Ihalasscmia/mental гсіапінп..................nr further
suupport loi \ link i<i" D Donnai,
J.Clayton-.KiiiMli, It (пМіііііч ' .1 Med.
Genet.— 1991 Vnl I' 742.
Draptchinskaia N Iln г " i moiling ribosomal prolcin S19 і imitated in Dia-mond-Blacklan am............ N Draptchins-
kaia, P.Guntttvsmu. Il Andersson II Nat. Genet — 1999 Vnl .’I P. 169.
Dufourq-Lagelou.se N I inka^e of familial hemophagocytic lymplmhistiocytosis to
12 Uui Mi AUi
497
ЬИІІЛИОІРАФИЧЄСКИЙ список
І(кі21 -22 and evidence lor heterogeneity / R. D u fou rq - Lagclou se, N.Jabado,
F.Deist // Am. J. Hum. Genet.— 1999,— Vol (>4,—P. 172.
Dufourq-I.agelnuse H Genetic basis of he-mophtigoeytic lymphohisltocytosis syndrome / R Dufourq-Lagelouse, E.Pastural,
F.Barral // Ini. J. Mol. Med.— 1999.— Vol. 4,—P. 127.
Darken M. Improve outcome in haemopha-gocytic lymphohistioeytosis al'lcr bone marrow transplantation from related and unrelated donors: a single-centre experience of 12 patients / M.Durkcn, M.Kor-tsmann, P.Biciing // Br. J. Haematol.—
1999,— Vol. 106,—P. 1052.
D;ierzak E. A dynamic system / E.Dzierzak П Lancet.— 2001.— Vol. 358, Suppl.— P. 31.
Edgar A X-iinked sidcroblastic anaemia due to a mutation in ihe erythroid 5-amino-laevulinate synthase gene leading to an arginine11'1 to leucine substitution / A.Edgar, H.Vidyatilake, S.Wickramansin-ghe H Eur. J. Haematol.— 1998.— Vol. 61,—P. 55.
Edwards C. Screening lor hemochromatosis /
C.Edwards, J.Kushner // N. EngJ. J. Med.— 1993,— Vol. 328,—P. 1616.
El-Beshlawy A. Long-term cyclosporine therapy for severe acquired aplastic anemia in 144 Egyptian children. Factors influence response / A.EI-Besblawy, N.Kad-dah, M.EI-Tagi II Pediatr. Res.— 2001.— Vol. 49 —P. 874.
Ellervik C. Prevalence of hereditary haerooc-hromatosis in late-onset type 1 diabetes mellitus: a retrospective study / C.Ellervik, T.Mandrup-Poulsen, B.Nordestgaard // Lancel.—2000,—Vol. 358.—P. 1405.
Ешегаті M. Xerocytosis with concomitanl intrauterine ascites; first description and therapeutic approach / M.Emczami. R.Becker, H.Menssen II Blood.— 1996.— Vol. 87,—P. 5392.
Erickson K. Spectrum of perforin gene mutations in familial hemophagocytic lym-phohislocyiosis / K.Erickson, B.Fadeel, S.N ilsson-Ardnor II Am. }. Hum. Genet.—2001,—Vol. 68,—P. 590.
Faivre L. Association of complementation group and mutation type with clinical outcome in Faneoni anemia / L.Faivre, I’.Guardiola, C.Lewis II Blood.— 2000.— Vol. 96,—P. 4064.
Fargion S. Hereditary hemochromatosis in a patient with congenital dyserythropoietic ane-
mia / S.Fargion, L.Volenti, A.Fracanzani II Blood.—2000.—Vol. 96.— P. 3653.
Ferrara Л/. Hematological and molecular analysis of p-thalassemia and 11b Lepore m Campania, Italy I M.Ferrara, S.Maia-rese. M.Francese II Hemoglobin.— 2000.—Vol. 25,—P. 29,
Filipovich A. Expcricncc from the International bone marrow transplant registry and the National Marrow donor program with bone marrow transplantation of gcnctic diseases / A.Filipovich II Correction of genetic diseases by transplantation IV.— Cogent press.— Ruislip.— 1997.— P. 75.
Filzimons E. The anaemias of chronic disease. Remains hard to distinguish front iron deficiency anaemia in some cases I E.Filzimons, J.Brock // Brit. Med. J.— 2001.— Vol. 322.—P. 811.
Flegel W. Molecular genetics of RH / W.FIc-gel, F.Wagner II Vox Sang,— 2000.— Vol. 78, Suppf 2.—P. 109.
Flemming R. Fcrroportion mutation in autosomal dominant hemochromatosis: loss of function, gam in understanding / R.Flemming. W.Sly // J. Clin. Invest.— 2001—Vol. 108,—P. 521.
Fox /, Treatment of the Criglcr-Najjar syndrome type 1 with hepatocyte transplantation / l.Fox, J.Roy-Chowdhury. S.Ka-ufman // N. Engl. J. Med.— 1998,— Vol. 338.—P. 1422.
Freedman M. Risk of myelodysplasia and acute myeloid leukemia in Shwachman — Diamond syndrome I M.Freedman, Y.Dror II Pediatr. Res —2001,—Vol.
50.—P. 140.
Freedman M. Shwachman — Diamond syndrome is characterized by faulty marrow microenvironment, aberrant hematopoietic progenitors and abnormaly increased apoplosis mediated through the F AS pathway I M.Freedman, Y.Dror II Pediatr. Res.—2001.—Vol. 49 —P. 887.
Fugardi M- Kaposiform haemangioendotelio-ma (Нас) with Kasabach — Merritt syndrome in a in fa її I і successful treatment with alph-2A interferon I M Fugardi,
D.Termim, D.Russo // Med. Pediatr. Oncol.—2000,—Vol. 35 —P. 338.
