Daniels G - Search Results

1

McLeod neuroacanthocytosis: genotype and phenotype.

Danek A, Rubio JP, Rampoldi L, Ho M, Dobson-Stone C, Tison F, Symmans WA, Oechsner M, Kalckreuth W, Watt JM, Corbett AJ, Hamdalla HH, Marshall AG, Sutton I, Dotti MT, Malandrini A, Walker RH, Daniels G, Monaco AP. Danek A, et al. Among authors: daniels g. Ann Neurol. 2001 Dec;50(6):755-64. doi: 10.1002/ana.10035. Ann Neurol. 2001. PMID: 11761473

2

Chorein detection for the diagnosis of chorea-acanthocytosis.

Dobson-Stone C, Velayos-Baeza A, Filippone LA, Westbury S, Storch A, Erdmann T, Wroe SJ, Leenders KL, Lang AE, Dotti MT, Federico A, Mohiddin SA, Fananapazir L, Daniels G, Danek A, Monaco AP. Dobson-Stone C, et al. Among authors: daniels g. Ann Neurol. 2004 Aug;56(2):299-302. doi: 10.1002/ana.20200. Ann Neurol. 2004. PMID: 15293285

3

A combination of the effects of rare genotypes at the XK and KEL blood group loci results in absence of Kell system antigens from the red blood cells.

Daniels GL, Weinauer F, Stone C, Ho M, Green CA, Jahn-Jochem H, Offner R, Monaco AP. Daniels GL, et al. Blood. 1996 Nov 15;88(10):4045-50. Blood. 1996. PMID: 8916972 Free article.

4

McLeod syndrome: a novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings.

Jung HH, Hergersberg M, Kneifel S, Alkadhi H, Schiess R, Weigell-Weber M, Daniels G, Kollias S, Hess K. Jung HH, et al. Among authors: daniels g. Ann Neurol. 2001 Mar;49(3):384-92. Ann Neurol. 2001. PMID: 11261514

5

Neuroacanthocytosis. A clinical, haematological and pathological study of 19 cases.

Hardie RJ, Pullon HW, Harding AE, Owen JS, Pires M, Daniels GL, Imai Y, Misra VP, King RH, Jacobs JM, et al. Hardie RJ, et al. Among authors: daniels gl. Brain. 1991 Feb;114 ( Pt 1A):13-49. Brain. 1991. PMID: 1998879

6

McLeod syndrome resulting from a novel XK mutation.

Singleton BK, Green CA, Renaud S, Fuhr P, Poole J, Daniels GL. Singleton BK, et al. Br J Haematol. 2003 Aug;122(4):682-5. doi: 10.1046/j.1365-2141.2003.04474.x. Br J Haematol. 2003. PMID: 12899725 Free article.

7

[Acanthocytosis in chronic septic granulomatosis: the McLeod syndrome].

Höger P, Seger R, Schenker T, Daniels GL, Irle U. Höger P, et al. Among authors: daniels gl. Monatsschr Kinderheilkd. 1985 May;133(5):296-9. Monatsschr Kinderheilkd. 1985. PMID: 4040211 German.

8

Use of domain-deletion mutants to locate Lutheran blood group antigens to each of the five immunoglobulin superfamily domains of the Lutheran glycoprotein: elucidation of the molecular basis of the Lu(a)/Lu(b) and the Au(a)/Au(b) polymorphisms.

Parsons SF, Mallinson G, Daniels GL, Green CA, Smythe JS, Anstee DJ. Parsons SF, et al. Among authors: daniels gl. Blood. 1997 Jun 1;89(11):4219-25. Blood. 1997. PMID: 9166867 Free article.

9

A study on Lu-null families in South Wales.

Rowe GP, Gale SA, Daniels GL, Green CA, Tippett P. Rowe GP, et al. Among authors: daniels gl. Ann Hum Genet. 1992 Jul;56(3):267-72. doi: 10.1111/j.1469-1809.1992.tb01151.x. Ann Hum Genet. 1992. PMID: 1449238

10

The monoclonal antibody-specific immobilization of erythrocyte antigens assay (MAIEA) in the investigation of human red-cell antigens and their associated membrane proteins.

Petty AC, Green CA, Daniels GL. Petty AC, et al. Among authors: daniels gl. Transfus Med. 1997 Sep;7(3):179-88. doi: 10.1046/j.1365-3148.1997.d01-24.x. Transfus Med. 1997. PMID: 9316217 Review.

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