-
1
-
-
0001216951
-
A new phenotype (McLeod) in the Kell blood-group system
-
Allen FH, Krabbe SMR, Corcoran PA : A new phenotype (McLeod) in the Kell blood-group system. Vox Sang 6: 555-560, 1961
-
(1961)
Vox Sang
, vol.6
, pp. 555-560
-
-
Allen, F.H.1
Krabbe, S.M.R.2
Corcoran, P.A.3
-
3
-
-
2542541812
-
A betalipoproteinemia
-
ed by Rowland LP, Williams & Wilkins, Baltimore
-
Rowland LP, Pedley TA : A betalipoproteinemia. In Merritt's textbook of neurology, 9th ed, ed by Rowland LP, Williams & Wilkins, Baltimore, 1995, pp 594-596
-
(1995)
Merritt's Textbook of Neurology, 9th Ed
, pp. 594-596
-
-
Rowland, L.P.1
Pedley, T.A.2
-
4
-
-
0023910762
-
Localization of the McLeod locus (XK) within Xp21 by deletion analysis
-
Bertelson CJ, Pogo AO, Chaudhuri A, et al : Localization of the McLeod locus (XK) within Xp21 by deletion analysis. Am J Hum Genet 42 : 703-711, 1988
-
(1988)
Am J Hum Genet
, vol.42
, pp. 703-711
-
-
Bertelson, C.J.1
Pogo, A.O.2
Chaudhuri, A.3
-
5
-
-
0019466439
-
Elevated serum creatine phosphokinase in subjects with McLeod syndrome
-
Marsh WL, Marsh NJ, Moore A, et al : Elevated serum creatine phosphokinase in subjects with McLeod syndrome. Vox Sang 40 : 403-411, 1981
-
(1981)
Vox Sang
, vol.40
, pp. 403-411
-
-
Marsh, W.L.1
Marsh, N.J.2
Moore, A.3
-
6
-
-
0025181425
-
The Kell blood group system : A review
-
Marsh WL, Redman CM : The Kell blood group system : a review. Transfusion 30 : 158-167,1990
-
(1990)
Transfusion
, vol.30
, pp. 158-167
-
-
Marsh, W.L.1
Redman, C.M.2
-
7
-
-
0019468751
-
Choreoacanthocytosis. Clues to clinical diagnosis
-
Sasaki T, Mawatari S, Iwashita H, et al : Choreoacanthocytosis. Clues to clinical diagnosis. Arch Neurol 38 : 335-338, 1981
-
(1981)
Arch Neurol
, vol.38
, pp. 335-338
-
-
Sasaki, T.1
Mawatari, S.2
Iwashita, H.3
-
8
-
-
0028263898
-
Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein
-
Ho M, Chelly J, Carter N, et al : Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein. Cell 77 : 869-880, 1994
-
(1994)
Cell
, vol.77
, pp. 869-880
-
-
Ho, M.1
Chelly, J.2
Carter, N.3
-
9
-
-
0017714137
-
Haematological changes associated with the McLeod phenotype of the Kell blood group system
-
Wimer BM, Marsh WL, Taswell HF, et al : Haematological changes associated with the McLeod phenotype of the Kell blood group system. Br J Haematol 36:219-224, 1977
-
(1977)
Br J Haematol
, vol.36
, pp. 219-224
-
-
Wimer, B.M.1
Marsh, W.L.2
Taswell, H.F.3
-
10
-
-
0020472883
-
Cardiomyopathy associated with the syndrome of amyotrophic chorea and acanthocytosis
-
Faillace RT, Kingston WJ, Nanda NC, et al: Cardiomyopathy associated with the syndrome of amyotrophic chorea and acanthocytosis. Ann Intern Med 96:616-617, 1982
-
(1982)
Ann Intern Med
, vol.96
, pp. 616-617
-
-
Faillace, R.T.1
Kingston, W.J.2
Nanda, N.C.3
-
11
-
-
0020565680
-
An individual with McLeod syndrome and the Kell blood group antigen K (K 1)
-
Marsh WL, Schnipper EF, Johnson CL, et al : An individual with McLeod syndrome and the Kell blood group antigen K (K 1). Transfusion 23:336-338, 1983
-
(1983)
Transfusion
, vol.23
, pp. 336-338
-
-
Marsh, W.L.1
Schnipper, E.F.2
Johnson, C.L.3
-
12
-
-
0020516749
-
Benign X-linked myopathy with acanthocytes (McLeod syndrome). Its relationship to X-linked muscular dystrophy
-
Swash M, Schwartz MS, Carter ND, et al : Benign X-linked myopathy with acanthocytes (McLeod syndrome). Its relationship to X-linked muscular dystrophy. Brain 106 : 717-733, 1983
-
(1983)
Brain
, vol.106
, pp. 717-733
-
-
Swash, M.1
Schwartz, M.S.2
Carter, N.D.3
-
13
-
-
0020961737
-
McLeod syndrome (hemolysis, acanthocytosis, and increased serum creatine kinase) : Potential confusion with polymyositis
-
Zyskowski LP, Bunch TW, Hoagland HC, et al : McLeod syndrome (hemolysis, acanthocytosis, and increased serum creatine kinase) : potential confusion with polymyositis. Arthritis Rheum 26 : 806-808, 1983
-
(1983)
Arthritis Rheum
, vol.26
, pp. 806-808
-
-
Zyskowski, L.P.1
Bunch, T.W.2
Hoagland, H.C.3
-
14
-
-
0026073577
-
Neuoacanthocytosis. A clinical, haematological and pathological study of 19 cases
-
Hardie RJ, Pullon HWH, Harding AE, et al : Neuoacanthocytosis. A clinical, haematological and pathological study of 19 cases Brain 114 : 13-49, 1991
-
(1991)
Brain
, vol.114
, pp. 13-49
-
-
Hardie, R.J.1
Pullon, H.W.H.2
Harding, A.E.3
-
15
-
-
0026781027
-
McLeod syndrome : A distinct form of neuroacanthocytosis. Report of two cases and literature review with emphasis on neuromuscular manifestations
-
Witt TN, Danek A, Reiter M, et al : McLeod syndrome : a distinct form of neuroacanthocytosis. Report of two cases and literature review with emphasis on neuromuscular manifestations. J Neurol 239 : 302-306, 1992
-
(1992)
J Neurol
, vol.239
, pp. 302-306
-
-
Witt, T.N.1
Danek, A.2
Reiter, M.3
-
16
-
-
0028232725
-
A family of McLeod syndrome, masquerading as chorea-acanthocytosis
-
Takashima H, Sakai T, Iwashita H, et al : A family of McLeod syndrome, masquerading as chorea-acanthocytosis. J Neurol Sci 124 : 56-60, 1994
-
(1994)
J Neurol Sci
, vol.124
, pp. 56-60
-
-
Takashima, H.1
Sakai, T.2
Iwashita, H.3
-
17
-
-
0028227820
-
Atypical McLeod syndrome manifested as X-linked chorea-acanthocytois, neuromyopathy and dilated cardiomyopathy : Report of a family
-
Malandrini A, Fabrizi GM, Truschi F, et al : Atypical McLeod syndrome manifested as X-linked chorea-acanthocytois, neuromyopathy and dilated cardiomyopathy : report of a family. J Neurol Sci 124 : 89-94, 1994
-
(1994)
J Neurol Sci
, vol.124
, pp. 89-94
-
-
Malandrini, A.1
Fabrizi, G.M.2
Truschi, F.3
-
18
-
-
0025348463
-
Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome)
-
Carter ND, Morgan JE, Monaco AP, et al : Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome). J Med Genet 27: 345-347, 1990
-
(1990)
J Med Genet
, vol.27
, pp. 345-347
-
-
Carter, N.D.1
Morgan, J.E.2
Monaco, A.P.3
-
20
-
-
0029928980
-
A novel point mutation in the McLeod syndrome gene in neuroacanthocytosis
-
Ho MF, Chalmers RM, Davis MB, et al : A novel point mutation in the McLeod syndrome gene in neuroacanthocytosis. Ann Neurol 39 : 672-675, 1996
-
(1996)
Ann Neurol
, vol.39
, pp. 672-675
-
-
Ho, M.F.1
Chalmers, R.M.2
Davis, M.B.3
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