Научная литература
booksshare.net -> Добавить материал -> Медицина -> Алексеева Н.А. -> "Анемии" -> 308

Анемии - Алексеева Н.А.

Алексеева Н.А. Анемии — Спб.: Гипократ, 2004. — 512 c.
ISBN 5-8232-0243-1
Скачать (прямая ссылка): anemii2004.pdf
Предыдущая << 1 .. 302 303 304 305 306 307 < 308 > 309 310 311 312 313 314 .. 316 >> Следующая

— knockout mice / Z.He, J.Russel // Blood.—2001,—Vol. 97,—P. 1099.
Hejna J. Localization of the Fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3 / J.Hejna, C.Timmers, C.Reifsteck // Am. J. Hum. Genet.— 2000.— Vol. 66,— № 5.—P. 1540.
Hillmen P. Congenital paroxysmal nocturnal hacmoglobinuria / P.Hillmen. S.Riehards, A.Baker II Blood.— 1998 — Vol. 92. Suppl. 1, Pt. I.—P. 154.
Hirono A. Three cases of hereditary nonsp-hcrocytic hemolytic anemia associated with red blood cell glutathione deficiency / A.Hirono, H.lyori, l.Sekine // Blood.—
1996.— Vol. 87,—P. 2071.
Hoffacker V. Thymomas alter the T-cell subset composiyion in the blood a potential mechanism for thymoma—associated autoimmune disease / V,Hoffacker, A.Schultz. J.Tiesinga I/ Blood —2000.— Vol. 96.—P. 3872.
Hromec A. Kongenitale Atransferriniimie /
A.Hromee, J.Payer, Z.Killinger // Dtsch, Med. Wschr.— 1994 — Bd. 119,— S. 663.
Huang C. Molecular biology and genetics of the Rh blood group system / C.Huang, P.Liu, J.Chcng // Semin. Hematol.— 2000.—Vol. 37.—P. 150.
Huang R.-F.S. Folate deficiency induced a ccll cycle specific apoptosis in HepG2 cells / R.-F.S Huang, Y.-H.Ho. H.-L.Lin //J. Nulr.—1999,—Vol. 129 —P. 25.
Huang C.-H. Rh50 glycoprotein gene and Rhmiii disease: a silent splice donor is
trans to a Gly279oGlu missensc mutation in the conversed transmcmbrane segment /
C.-H.Huang, Z.Liu, G.Cheng // Blood -1998.—Vof. 93,—P. 1176.
Huber P. Investigation of Fanconi anemia protein interactions by yeast two-hybrid analysis / P.Huber, A.Medhurst, H.Yous-soufian // FEBS Lett.—2000,—Vol. 268,—P. 73.
Hvas A.-H. Increased plasma methylmalonic acid level does not predict clinical manifestations of vitamin В12 deficiency /
A.-H.Hvas. J.Ellegaard, E.Nexo II Arch. Intern. Med —2001,—Vol. 161,—P. 1534.
Hyland C. A novel single missense mutation identified along the RH50 gene in a composite heterozygous Rhnuii blood donor of the regulator type / C.Hyland,
B.Ch?rif-Zahar, N.Cowley // Blood.— 1998.—Vol. 91,—P. 1458.
Ingram C. Evaluation of DNA analysis for evidence of apoptosis in megaloblastic anaemia / C.Ingram, A.Davidoff, E.Ma-rais // Brit. J. Haematol - 1997.— Vol. 96.—P. 576.
Inoue T. Homozygous missensc mutation (band 3 Fukuoka: GI30R): a mild form of hereditary spherocytosis with near-normal band 3 content and minimal changes of membrane ultrastructural despite moderate protein 4.2 deficiency / T.Inoue. A.Kanzaki. M.iCaku Ч Brit. J. Haematol.—1998.—Vol. 102.—P. 932. lolascon A. Results of the last two years research on CD A / A.lolascon It Pediatr. Res.—2001.—Vol. 50,—P. 136. lolascon A, UGT1 promoter polymorphism accounts from increased neonatal appearance of hereditary spherocytosis /
A.lolascon, M.Faienza, A.Moretti II Blood —1998,—Vol. 91,—P. 1093. lolascon A. Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis) / A.lolascon, G.Stewart, J.Ajetunmobi IJ Blood.— 1999.— Vol. 93.—P. 3120. lsolato P. Neonatal and fetal mcthylenctctra-hydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations / P.lsolato, O.Wells, J.Donnely // Am, J. Hum. Genet.
2000.—Vol. 67,—P. 986.
Ivankovic C. A ease of McLeod syndrome with fatal outcome: development of nn
500
І,НІ,ІІИ» ІІІ'АФИЧЄСКИИ список
tibody In high |нч|иічісу antigen!) pointed to diagnosis / I'lvnnkovil, //ivkovic,
B.Jerun-Slrujlt // Vox Sung. 2000.— Vol. 79, Suppl 74 P. 134
Janssen H. Factor V l.cidcn mutation, prothrombin gene mutation, and deficiencies in coagulation inhibitors associated with Budd—Chiary syndrome and portal veins thrombosis: results of a case — control study / H.Janssen, J.Meinardi,
F.VIegaar // Blood.—2000,—Vol. 96 — P. 2364.
Jocnje H. Complementation analysis on Fan-coni anemia: assignment of the reference FA —H patient to group A / H.Joenje, M.Levitus, Q.Waisfisz II Am. J. Hum. Genet.— 2000,— Vol. 67,—P. 759.
Jocnje H. Evidence for at least eight Fanconi anemia genes / H.Joenje, A.Oostra, M.Wijker // Am. J. Hum. Genet.—
1997,—Vol. 61.—P. 940.
Kaplan M Onset of jaundice in glucose-6-phosphate dehydrogenase- deficient neonates / M.Kaplan, N.Algur, C.Hammerman // Pediatrics.— 2001.— Vol. 108.— P. 956.
Кчріап M. Glucose-6-phosphate dehydrogenase-deficient neonates: A potential cause for concern in North America / M.Kaplan, C.Hammerman I/ Pediatrics.—
2000,— Vol. 106 — P. 1478.
Kaplan M. Differing pathogenesis of perinatal bilirubinemia in glucose-6-phosphate dehydrogenase-deficient versus-normal neonates I M.Kaplan, C.Hammerman, P.Renbaum // Pediatr. Res.— 2001.— Vol. 50,—P. 532.
Kappas A. A single dose of Sn- mesoporphyrin prevents development of severe hyperbilirubinemia in glucose-6-phosphate dehyd-rogcnase-dcficient newborns / A.Kappas,
G.Drummond, T.Valacs II Pediatrics.—
2001,—Vol. 108,—P. 25.
Karadlmilris A. Abnormal T-ccll repertoire is
consistent with immune process underlying the pathogenesis of paroxysmal nocturnal hemoglobinuria I A.Karadimitris, J.Manavalan, H .Thaler II Blood.—
Предыдущая << 1 .. 302 303 304 305 306 307 < 308 > 309 310 311 312 313 314 .. 316 >> Следующая

Реклама

c1c0fc952cf0704ad12d6af2ad3bf47e03017fed

Есть, чем поделиться? Отправьте
материал
нам
Авторские права © 2009 BooksShare.
Все права защищены.
Rambler's Top100

c1c0fc952cf0704ad12d6af2ad3bf47e03017fed