(Q34660441)

3 August 2017

1 reference

title

McLeod syndrome: a neurohaematological disorder (English)

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3 August 2017

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Jung HH

1

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3 August 2017

Danek A

series ordinal

2

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3 August 2017

Frey BM

series ordinal

3

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3 August 2017

publication date

1 August 2007

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3 August 2017

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3 August 2017

volume

93

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3 August 2017

issue

2

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3 August 2017

page(s)

112-121

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Neurologic phenotypes associated with acanthocytosis.

3 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

McLeod neuroacanthocytosis: genotype and phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Molecular basis of Kell blood group phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Purification and partial characterization of the erythrocyte Kx protein deficient in McLeod patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

The ced-8 gene controls the timing of programmed cell deaths in C. elegans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

The Kell blood group system: Kell and XK membrane proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Identification of two new members, XPLAC and XTES, of the XK family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

The Kell and XK proteins of the Kell blood group are not co-expressed in the central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Association of XK and Kell blood group proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Kell and XK immunohistochemistry in McLeod myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Expression profiles of mouse Kell, XK, and XPLAC mRNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

International Society of Blood Transfusion Committee on Terminology for Red Cell Surface Antigens: Cape Town report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Molecular basis of the Kell-null phenotype: a mutation at the splice site of human KEL gene abolishes the expression of Kell blood group antigens

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Molecular defects underlying the Kell null phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

McLeod phenotype without the McLeod syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Testing for acanthocytosis A prospective reader-blinded study in movement disorder patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Mechanisms of suicidal erythrocyte death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Fas-, caspase 8-, and caspase 3-dependent signaling regulates the activity of the aminophospholipid translocase and phosphatidylserine externalization in human erythrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Relationship of phospholipid distribution to shape change in Ca(2+)-crenated and recovered human erythrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Clinical aspects of chronic granulomatous disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

The genetic basis of chronic granulomatous disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Cerebral involvement in McLeod syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Neuropsychiatry of the basal ganglia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

White matter abnormalities on MRI in neuroacanthocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Reduction of striatal glucose metabolism in McLeod choreoacanthocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Cerebral metabolic alterations in McLeod syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

A case of McLeod syndrome with unusually severe myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Malignant McLeod myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Unusual muscle pathology in McLeod syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

Point mutations causing the McLeod phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1423-0410.2007.00949.X

10.1111/J.1423-0410.2007.00949.X

21 January 2018

Identifiers

DOI

1 reference

3 August 2017

1 reference