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Анемии - Алексеева Н.А.

Алексеева Н.А. Анемии — Спб.: Гипократ, 2004. — 512 c.
ISBN 5-8232-0243-1
Скачать (прямая ссылка): anemii2004.pdf
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Liu J. Fanconi anemia and novel strategies for therapy / J.Liu, M.Uuchwaid, С .Walsh II Blood.—1994.—Vol. 84.— P. 3995.
Louahed J. Interleukin 9 promotes influx and local maturation of eosinophils / J.Louahed, Y.Zhou, W.Maloy II Blood.—
2001,—Vol. 97 —P. 1035.
Luo H. Embryonic hemoglobins are expressed in definitive cells / II I no, L.Xi, C.Fryc II Blood.—1999.—Vol. 94,—P. 359.
Lyon M. X-chromosome inactivation: Pin pointing the centre / M.Lyon II Nature.—
1996.—Vol 379.—P. 116.
Macheta M. Prominent dyserythropoiesis in tour cases of haemophagocytic lympho-histiocytosis / M.Macheta, A.Will. J.Houghton II J. Clin. Pathol.— 2001. Vol. 54,—P. 961.
Mahadeva U. Haemophagocytic syndrome and histiocytic neerotising lymphadenitis (Kikuchi's disease) / U.Mahadeva, T.Allport, B.Bain II J. Clin. Pathol.— 2000.— Vol. 53 —P 636.
Maisels M. Neonatal jaundice and kern icterus / M.Maisels. R.Baltz, V.Bhutan! II Pediatrics.—2001,—Vol. 108.—P. 763.
Mari G. Non invasive diagnosis by Doppler ultrasonography of fetal anemia due to maternal rcd-ccll alloimmunisation I
G.Mari II N. Engl. J. Med.— 2000. Vol. 342.—P. 9.
Maroeska D. Detection of apoptosis in kidney biopsies of patients with D * hcmolylie uremic syndrome / D.Maroeska. I..Mon
502
I.HI,Im)l I'ЛФИЧЕСКИИ список
iicns, I van ilcn I lowi'l I: IVdiuli Kes. 20001. Vol. 49 P 41J
Marsh J, Treatment oi aplastic anaemia: first do not harm / J.Mursh // Lanecl.—
2000. Vol іУі I*. 1536.
Marlin M A point mutation in the bulge of the iron-responsive clement of the L-fcr-ritin gene in two families with hereditary hyperferritinemia-cataract syndrome / M.Marlin. S.Fargion, P.Brissot II Blood.— 1998.—Vol. 91,—P. 319.
M alhews-Roih M. Burst-forming units-eryth-roid from erythropoietic protoporphyria patients fluoresce under 405 nm light / M.Mathcws-Roth, R.Wise, B.Miller. I/ Blood —1996,—Vol. 87,—P. 4480.
Matles-Martin S. Successful stem cell transplantation following orthotopic liver transplantation from the same haploidentical family donor in a girl with hemophago-cytic lymphohistocytosis / S.Mattes-Mar-tin, C.Peters, A.Konigsrainer // Blood.—
2000.—Vol. 96 — P. 3997.
Me Carthy T. Hemolytic—uremic syndrome and Escherichia coli 0121 al a Lake in Connecticut, 1999 / Carthy T.Me, N.Barret, J.Hadlcr // Pediatrics.— 2001.— Vol. 108,— P. 991.
Me Mullin M. The molecular basis of red cell enzymes / Mullin M.Me // J. Clin, Pathol— 1999,—Vol. 52,—P. 241.
McMullin M. The molecular basis of disorders of the red cel membrane I M.McMullin // J. Clin Pathol.— 1999,— Vol. 52.— P. 245.
Means K. Progress in understanding (he pathogenesis of the anemia of chronic disease / R.Means. S.Krantz // Blood.— 1992.—Vol. 80,— P. 1639.
Mehta N. Haemophagocytic lymphohistiocy-tosis (HLH) on the intensive carc unit / N.Mehta, S.Nadel, M.Levin II Br. J. Anacsth.— 2000,— Vol. 84,—P. 687P.
Mentzer W. Stomalocytosis is absent in «stomatin» deficient murine red cells / W.Mentzer, C.Paszty, Y.Zhy I/ Blood.—
1998,— Vol. 92, Suppl. I, Pt. I.— P. 470.
Messer J, Early treatment of premature infants with recombinant human erythropoietin / J.Messer, J Haddad, L.L.Donato // Pedi-aria 1993 VoL 42 - P 519.
Miruglia del (Jiudice E. Clinical and molecular evaluation of non-dominant hereditary spherocytosis (IIS) / I-. Miraglia del (iiu-dicc, И Nohili, ti.D'Urzo // Bril. J. Haematol IW8 Vol 10.! »• .102
Malloy A. termolabile variant of 5,10-mclhy lenetetrahydrofolate reductase associated with low red-cell folates: implications Ini folate intake recommendations / A.Mol loy, S.Dalv, J.Mills II Lancet. 1997. Vol. 349,—P. 1591.
Monsen A.L. Determinants of calmlamin status in newborns / A.I.Monsen, P.Ueland, S.Vollsset II Pediatrics
2001.—Vol. 108.—P. 624.
Montosi G. Autosomal-dominant hcmocliro maiosis is associated with a mutation ш the ferroportin (SLCIIA3) gene I Ci Mon tosi, A.Donovan, A.Totaro II J Clin Invest —2001,—Vol. І0К. P. 619.
Mortt L. Ankyrin Bugey: a de novo deletional frameshift in exon 6 of the ankyrin gene associated with spherocytosis I L.Morld, M.Bozon. N.Alloisio II Am. J. HematoL
1997,— Vol. 54.—P. 242.
MoltuM. Neonatal occurrence of autoimmune hemolytic anemia and hypoparuthyroi dism / M.Motta, A.Cavazza, C.Migliori // Pediatr. Res.— 2001,— Vol. 50.
P. 150.
Mumford A. Hereditary hypertcrritinemiu-i ii taract syndrome in two novel mutations in the L-ferritin iron-responsive element /
A.Mumford, T.Vulliamy, J.Lindsay II Blood.—1998.—Vol. 91,—1». 367.
Mura C. HFE mutations analysis in 711 hemochromatosis probands: evidence lot S65C implication in mild form ofhcmoc hromatosis / C.Mura, O.Ragucncs,
C.Ferec II Blood—1999,—Vol 93.
P. 2502.
Murakami K. Organization of the gene lor both the erythroid —specific hcxokinusr isozyme, HKr and the ubiquitous iso/ушг HKi / K.Murakami, H.Xanno. S.Miwii II Blood.— 1998,—vol. 92, Suppl. I. Pt
2,—P. 154.
Murray K. Neonatal hemochromatosis K.Murray, K.Kowdlcy // Pediulms 2001—Vol. 108,—P. 960
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