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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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2000. Vol. 96,—P. 2613.
Kalu J. A mutation in the iron-responsive element of II ferritin inRNA, causing autosomal dominant iron overload / J.Kato, K.Fujikawa, M.Kanda II Am. J. Hum Genet 2001. Vol. 69 P. I‘»l.
Кіш/тчп /). I pideiniologiciil assessment of drug-induced disease I I) Kaufman,
S.Shapiro II Lancct. 2000. Vol. 356.
P 1339.
Knit P. The Fanconi anemia group C gone product modulates apoptotic responses to tumor necrosis factor-cc and I as ligand but does not suppress expression ol receptors of the turnor necrosis lacloi receptor superfamily / I’ К oh, G.Hughes,
G.Faulkner // bxp. Ilcmatol. 1994 Vol. 27,—P I.
Konrad P. Y-Glutamylcystcinc synthetase dc ficicncy: a new case of hereditary liemo lytic anemia / P.Konrad, F Richards, W.Valentine II Blood. 1971. Vol. 38,—P. 808
Koshy M. 2-dcoxy 5-azacytidinc and lct.il hemoglobin induction in sickle cell ane rnia I M,Koshy, I.Dorn, L.Brcsslcr II Blood.—2000,—Vol. 96 — P. 2379.
Koury M. Apoptosis in megaloblastic anemia occurs during DNA synthesis by a p53-indcpcndent, nuclco.sidc-revemblc mechanism / M.Koury, J.Price, G link'. // Blood —2000 —Vol. 96. P. 3249
Kozyraki R. The human intrinsic laclor-vita tnin B|2 receptor, cubilin: moleeuliit characterization and chromosomal шир ping of the gene to Hip within the autosomal recessive megaloblastic anemia (MGAI) region / R Kozyraki. M Kiimi anscn, A.Silahtarolu II Blood. I*>'>K Vol. 91,—P. 3593.
Kruyi F. The Fanconi anemia proteins Г ЛЛ and FAC function in different cellulai compartments to protect against cions linking agent cytotoxicity I F.Kruyt,
H.Youssoufian // Blood. 1498 Vol. 92,—P. 2229.
Kulinei A. Hereditary coproporphyria hi Germany: clinical- biochemical studies m 53 patients / A.Kuhnel, U.Gross, M Don. // Clin. Biochcm.—2000. Vol. И
P. 465.
l.amoril J Neonatal hemolytic anemia dm to inherited harderoporphynii clinUnl characteristics and molecular basis / J I .i moril, ll.Puy, L.Gouya II Blood 1998.—Vol. 91. P. 1453.
LamorilJ. Characterization ol mulatiniut l'<> gene in British patientN daiiionairali'* absence of genetype-phenotype corirluii on and identifies relationship bi’lwtrn hereditary coproporphyria and ІШіЬіо porphyriu / J.Lamoril, ll.Puy, S.Whatk'V Ч Am. J.. Hum. (Icnct. .MHII
Vol 6b P. 1130.
SOI
ЬИЬІІИОІРАФИЧЕскии список
Ltmdau О. l-amilial hemolytic uremic syndrome associated with complement factor 11 deficiency / I).Landau, ll.Shalev,
G. Levy-Finer // J. Pediatr.— 2001.— Vol. 138.— P. 12.
Lecomte M. H ereditary pyropoikilocytosis and ellipttocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expression / M.Lecomtc, D.Dhermy, M.Gar-barz II Hum. Genet.— 1987.— Vol. 77.—P. 329.
Lecomte M. L’clliptocyto.se hcrtkiitaire en Afrique dc l’Ouest: frequence et repartition des variants de la spectrine / M.Lecomte,
D.Dhermy, H.Gautcro // C. R. Acad. Sc. (Paris).— 1988,— Vol. 306,— P. 43.
Lecomte M. Severe recessive poikilocytic anaemia with a new spcctrin a chain variant / M.Lecomte, C.Feo. H.Gautcro // Brit. J. Haematol.— 1990.— Vol. 74.— P. 497.
Lee E. A case of autoimmune haemolytic anaemia with an IgA anti-Ce autoantibody / E.Lee, R.Knight И Vox Sang.—
2000.— Vol. 79, Suppl. I.—P. 130.
Lee E. Rituxan in the treatment of cold agglutinin disease / E.Lee, B.Kueck II Blood —1998,—Vol. 92,—P. 3490.
Lee L. Advances in hepatocyte transplantation: a myth becomes reality / L.Lee II J. Clin. Invest.—2001.—Vol. 108.— P. 367.
Lee S. Functional and structural aspects of the Kell blood group system I S.Lee,
D.Russo, C.Redman // Transf. Med. Rev.— 2000,— Vol. 14,—P. 93.
Lenzner C. Molecular analysis of 29 pyruvate kinase-deficient patients from central Europe with hereditary hemolytic anemia / C.Lenzner, P.Nurnberg, G.Jaco-basch II Blood.— 1997,—Vol. 89.— P. 1793.
Leonard J. Inborn errors of metabolism around time of birth / J.Leonard, A.Mar-ris II Lancet— 2000,— Vol. 356,— P. 583.
Leonard M. Plasma zinc status, growth, and maturation in children with sickle cell disease I M.Leonard, B.Zcmel, D.Kawc-hak // J. Pediatr.—1998,—Vol. 132.— P. 467.
Levi S. Analysis of ferritin in lymphoblastoid cell lines and in Lens of subjects with hereditary hyperferritincmia-cataract syn-
drome / S.Levi, D.Girclli, F.Perronc II Blood.—1998,—Vol. 91,—P. 4180.
Levy M. Thromboses ct anticorps antiphos-pholipidcs dans lc lupus drythemateux disscmine a debut pediatrique / M.Levy, dc Oca M.Montes, O.Meter // Arch. Fr. Pediatr.— 1992.— Vol. 49.— P. 249.
LiJ. N on-transformed colony-derived stromal ccll lines from normal human marrows.
II. Phenotypic characterization and differentiation pathway I J .Li. L.Sensebil. P.Hcrvii II Exp. Hematol.— 1993.— Vol. 23,— P. 133.
Lin J.-D. The role of apoptosis in autoimmune thyroid disorders and thyroid cancer / J.-D.Lin U Br. Med. J.—2001-Vol. 322 —P. 1525
Liozon E. Thymoma-associated pancytopenia: effectiveness of cyclosporine A / E.Liozon, M.Touati, A.AIIegraud // Ann. Hematol.— 1998.—Vol. 77.—P. 175.
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