-
1
-
-
84954086077
-
Hereditary nonspherocytic hemolytic anemia with high activity of erythrocyte ATPase. XII International Congress of Pediatrics; November-December, 1968; Mexico City, Mexico
-
Yokoyama M, Nakamura H, Takabe Y, Nagata K, Izumi Y. Hereditary nonspherocytic hemolytic anemia with high activity of erythrocyte ATPase. XII International Congress of Pediatrics; November-December, 1968; Mexico City, Mexico. Memoir. 1968;3:697.
-
(1968)
Memoir
, vol.3
, pp. 697
-
-
Yokoyama, M.1
Nakamura, H.2
Takabe, Y.3
Nagata, K.4
Izumi, Y.5
-
2
-
-
0016847164
-
Hemoglobin Hirosaki (α43 [CE 1] Phe → Leu), a new unstable variant
-
Ohba Y, Miyaji T, Matsuoka M, Yokoyama M, Numakra H. Hemoglobin Hirosaki (α43 [CE 1] Phe → Leu), a new unstable variant. Biochem Blophys Acta. 1975;405:155-160.
-
(1975)
Biochem Blophys Acta
, vol.405
, pp. 155-160
-
-
Ohba, Y.1
Miyaji, T.2
Matsuoka, M.3
Yokoyama, M.4
Numakra, H.5
-
3
-
-
0025982028
-
Further cases of Hb Hirosaki in two Japanese families
-
Ohba Y, Yamamoto K, Hattori Y, et al. Further cases of Hb Hirosaki in two Japanese families. Int J Hematol. 1991;54:15-23.
-
(1991)
Int J Hematol
, vol.54
, pp. 15-23
-
-
Ohba, Y.1
Yamamoto, K.2
Hattori, Y.3
-
4
-
-
0017857437
-
Further studies on hemoglobin Hirosaki: Demonstration of its presence at low concentration
-
Ohba Y, Miyaji T, Matsuoka M, Yokoyama M. Further studies on hemoglobin Hirosaki: demonstration of its presence at low concentration. Hemoglobin. 1978;2:281-286.
-
(1978)
Hemoglobin
, vol.2
, pp. 281-286
-
-
Ohba, Y.1
Miyaji, T.2
Matsuoka, M.3
Yokoyama, M.4
-
5
-
-
0019033923
-
Clinical features and metabolic aspects of red blood cells in Hb Hirosaki disease
-
Yokoyama M, Izumi Y, Ohba Y, Miyaji T. Clinical features and metabolic aspects of red blood cells in Hb Hirosaki disease [in Japanese with English abstract]. Rinsho Ketsueki. 1980;21:953-960.
-
(1980)
Rinsho Ketsueki
, vol.21
, pp. 953-960
-
-
Yokoyama, M.1
Izumi, Y.2
Ohba, Y.3
Miyaji, T.4
-
6
-
-
0019829049
-
Clinical features and biochemical aspects of red blood cells in Hb Hirosaki
-
Yokoyama M, Kudo Y, Sato Y, Izumi Y, Ohba Y, Miyaji T. Clinical features and biochemical aspects of red blood cells in Hb Hirosaki. Tohoku J Exp Med. 1981;133:187-196.
-
(1981)
Tohoku J Exp Med
, vol.133
, pp. 187-196
-
-
Yokoyama, M.1
Kudo, Y.2
Sato, Y.3
Izumi, Y.4
Ohba, Y.5
Miyaji, T.6
-
7
-
-
33645602409
-
Two cases of hereditary nonspherocytic hemolytic anemia in a family
-
Matsuda S, Yoshinaka H, Yanagihara T, et al. Two cases of hereditary nonspherocytic hemolytic anemia in a family [in Japanese]. Naika. 1978;41:312-315.
-
(1978)
Naika
, vol.41
, pp. 312-315
-
-
Matsuda, S.1
Yoshinaka, H.2
Yanagihara, T.3
-
8
-
-
0038413904
-
A new hemoglobin variant, Hb Fukui [α139(HC1)Lys-→ Asn(AAA→AAC)(α2)]
-
Harano T, Suetsugu Y, Harano K, Aung Myint Than, Hong Y-F, Kuroda A. A new hemoglobin variant, Hb Fukui [α139(HC1)Lys-→ Asn(AAA→AAC) (α2)]. Hemoglobin. 2003;7:117-121.
-
(2003)
Hemoglobin
, vol.7
, pp. 117-121
-
-
Harano, T.1
Suetsugu, Y.2
Harano, K.3
Than, A.M.4
Hong, Y.-F.5
Kuroda, A.6
-
9
-
-
0015422248
-
A simple method for the detection of unstable haemoglobins
-
Carrell RW, Kay RA. A simple method for the detection of unstable haemoglobins. Br J Haematol. 1972;23:615-619.
-
(1972)
Br J Haematol
, vol.23
, pp. 615-619
-
-
Carrell, R.W.1
Kay, R.A.2
-
10
-
-
0023551292
-
A novel globin structural mutant, Showa-Yakushiji (β 110 Leu-Pro) causing a β-thalassemia phenotype
-
Kobayashi Y, Fukumaki Y, Komatsu N, Ohba Y, Miyaji T, Miura Y. A novel globin structural mutant, Showa-Yakushiji (β 110 Leu-Pro) causing a β-thalassemia phenotype. Blood. 1987;70:1688-1691.
-
(1987)
Blood
, vol.70
, pp. 1688-1691
-
-
Kobayashi, Y.1
Fukumaki, Y.2
Komatsu, N.3
Ohba, Y.4
Miyaji, T.5
Miura, Y.6
-
11
-
-
0025223737
-
Three-base deletion in exon 3 of the β-globin gene produced a novel variant (β Gunma) with a thalassemia-like phenotype
-
Fucharoen S, Fucharoen G, Fukumaki Y, et al. Three-base deletion in exon 3 of the β-globin gene produced a novel variant (β Gunma) with a thalassemia-like phenotype. Blood. 1990;76:1894-1896.
-
(1990)
Blood
, vol.76
, pp. 1894-1896
-
-
Fucharoen, S.1
Fucharoen, G.2
Fukumaki, Y.3
-
12
-
-
0014685074
-
The Croonian Lecture, 1968: The haemoglobin molecule
-
Perutz MF. The Croonian Lecture, 1968: the haemoglobin molecule. Proc R Soc Lond B Biol Sci. 1969;173:113-140.
-
(1969)
Proc R Soc Lond B Biol Sci
, vol.173
, pp. 113-140
-
-
Perutz, M.F.1
-
13
-
-
0014816536
-
Haemolytic anaemia due to haemoglobin Torino
-
Prato V, Gallo E, Ricco G, Mazza U, Bianco G, Lehmann H. Haemolytic anaemia due to haemoglobin Torino. Br J Haematol. 1970;19:105-115.
-
(1970)
Br J Haematol
, vol.19
, pp. 105-115
-
-
Prato, V.1
Gallo, E.2
Ricco, G.3
Mazza, U.4
Bianco, G.5
Lehmann, H.6
-
14
-
-
0014210525
-
Haemoglobin hammersmith (β42 [CD1] Phe→Ser)
-
Dacie JV, Shinton NK, Gaffney PJ, Carrell RW, Lehmann H. Haemoglobin Hammersmith (β42 [CD1] Phe→Ser). Nature. 1967; 216:663-665.
-
(1967)
Nature
, vol.216
, pp. 663-665
-
-
Dacie, J.V.1
Shinton, N.K.2
Gaffney, P.J.3
Carrell, R.W.4
Lehmann, H.5
-
15
-
-
0015160591
-
Hemoglobin Louisville (β42 [CD1] Phe→Leu): An unstable variant causing mild hemolytic anemia
-
Keeling MM, Ogden LL, Wrightstone RN, et al. Hemoglobin Louisville (β42 [CD1] Phe→Leu): an unstable variant causing mild hemolytic anemia. J Clin Invest. 1971;50:2395-2401.
-
(1971)
J Clin Invest
, vol.50
, pp. 2395-2401
-
-
Keeling, M.M.1
Ogden, L.L.2
Wrightstone, R.N.3
|