(Q28213878)

2

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L Rampoldi

3

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M Ho

4

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C Dobson-Stone

5

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F Tison

6

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W A Symmans

7

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M Oechsner

8

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W Kalckreuth

9

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J M Watt

10

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A J Corbett

11

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H H Hamdalla

12

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A G Marshall

13

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I Sutton

14

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M T Dotti

15

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A Malandrini

16

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R H Walker

17

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G Daniels

18

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A P Monaco

A new phenotype (McLeod) in the Kell blood-group system

19

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language of work or name

English

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publication date

December 2001

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language of work

Annals of Neurology

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volume

50

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issue

6

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page(s)

755-64

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cites work

1 reference

Benign X-linked myopathy with acanthocytes (McLeod syndrome). Its relationship to X-linked muscular dystrophy

21 January 2018

1 reference

Normal dystrophin in McLeod myopathy

21 January 2018

1 reference

McLeod syndrome: a distinct form of neuroacanthocytosis. Report of two cases and literature review with emphasis on neuromuscular manifestations

21 January 2018

1 reference

A novel frameshift mutation in the McLeod syndrome gene in a Japanese family

21 January 2018

1 reference

A case of McLeod syndrome with unusually severe myopathy

21 January 2018

1 reference

Unusual muscle pathology in McLeod syndrome

21 January 2018

1 reference

Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein

21 January 2018

1 reference

Functional and structural aspects of the Kell blood group system

21 January 2018

1 reference

Analysis of deletions in three McLeod patients: exclusion of the XS locus from the Xp21.1-Xp21.2 region

21 January 2018

1 reference

Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a family

21 January 2018

1 reference

Cerebral involvement in McLeod syndrome

21 January 2018

1 reference

Reduction of striatal glucose metabolism in McLeod choreoacanthocytosis

21 January 2018

1 reference

Diagnostic tests for choreoacanthocytosis

21 January 2018

1 reference

Benign normolipoproteinaemic acanthocytosis

21 January 2018

1 reference

The first example of the McLeod phenotype in a Japanese baby with chronic granulomatous disease

21 January 2018

1 reference

Patients with features similar to Huntington's disease, without CAG expansion in huntingtin

21 January 2018

1 reference

A conserved sorting-associated protein is mutant in chorea-acanthocytosis

21 January 2018

1 reference

The gene encoding a newly discovered protein, chorein, is mutated in chorea-acanthocytosis

21 January 2018

1 reference

Endothelin and dopamine release

21 January 2018

1 reference

Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome)

21 January 2018

1 reference

Morphology and physiology of the McLeod erythrocyte. I. Scanning electron microscopy and electrolyte and water transport properties

21 January 2018

1 reference

21 January 2018

1 reference