Haematological Changes Associated with the McLeod Phenotype of the Kell Blood Group System

No abstract is available for this paper.

• Publication year

  1977

• Venue

  British Journal of Haematology

• Publication date

  1977-06-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1111/j.1365-2141.1977.tb00642.xPMID 871435
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Kx Antigen, The McLeod Phenotype, and Chronic Granulomatous Disease: Further Studies 1

  1976cited by this paper
• Chronic Granulomatous Disease and the Kell Blood Groups

  1975cited by this paper
• Antigens of the Kell blood group system on neutrophils and monocytes: their relation to chronic granulomatous disease.

  1975cited by this paper
• Living Blood Cells and Their Ultrastructure

  1972cited by this paper
• Kell phenotypes in chronic granulomatous disease: a potential trnsfusion hazard.

  1971cited by this paper
• Morphology of normal erythrocyte and acanthocyte using Nomarski optics and the scanning electron microscope.

  1970cited by this paper
• The discocyte-echinocyte equilibrium of the normal and pathologic red cell.

  1970cited by this paper
• Hematological observations on the anemia associated with blood type Rhnull.

  1970cited by this paper
• A ‘New’ Antibody Associated with the Kell Blood Group System

  1968cited by this paper
• A newly defined X-linked trait in man with demonstration of the Lyon effect in carrier females.

  1967cited by this paper
• In vitro bactericidal capacity of human polymorphonuclear leukocytes: diminished activity in chronic granulomatous disease of childhood.

  1967cited by this paper
• A New Phenotype (McLeod) in the Kell Blood‐group System *

  1961cited by this paper

• Systematic review of phenotypes in McLeod syndrome and case report of a progressive supranuclear palsy in a female carrier

  2024cites this paper
• XK-Associated McLeod Syndrome: Nonhematological Manifestations and Relation to VPS13A Disease

  2022cites this paper
• Effect of cryopreservation on a rare McLeod donor red blood cell concentrate

  2021cites this paper
• Enhancement of red blood cell transfusion compatibility using CRISPR‐mediated erythroblast gene editing

  2018cites this paper
• Characterization of a Drosophila model for Chorea‐Acanthocytosis

  2017cites this paper
• Characterization of a Drosophila model for Chorea‐Acanthocytosis

  2017cites this paper
• Clinicogenetic and functional studies in rare hereditary neurodegenerative movement disorders

  2016cites this paper
• Management of Neuroacanthocytosis Syndromes

  2015cites this paper
• Untangling the Thorns: Advances in the Neuroacanthocytosis Syndromes

  2015cites this paper
• Kell and Kx Blood Group Systems

  2013cites this paper
• Ablation of the Kell/Xk complex alters erythrocyte divalent cation homeostasis.

  2013cites this paper
• Brain, blood, and iron: perspectives on the roles of erythrocytes and iron in neurodegeneration.

  2012cites this paper
• The functional importance of blood group‐active molecules in human red blood cells

  2011cites this paper
• A NEW EXPLANATION FOR THE REPRODUCTIVE WOES AND MIDLIFE DECLINE OF HENRY VIII*

  2010cites this paper
• Spontaneously arising red cells with a McLeod-like phenotype in normal donors.

  2009cites this paper
• The McLeod syndrome without acanthocytes.

  2008cites this paper
• 5 – Morfología de las células sanguíneas normales y patológicas

  2008cites this paper
• Cerebral Involvement in McLeod Syndrome: The First Autopsy Revisited

  2008cites this paper
• McLeod myopathy revisted – More neurogenic and less benign

  2007cites this paper
• McLeod phenotype without the McLeod syndrome

  2007cites this paper
• McLeod syndrome: a neurohaematological disorder

  2007cites this paper
• McLeod myopathy revisited: more neurogenic and less benign.

  2007cites this paper
• Blood cell morphology in health and disease

  2006cites this paper
• Neurodegenerative Diseases: Neuroacanthocytosis

  2005cites this paper
• Neuroacanthocytosis: new developments in a neglected group of dementing disorders.

  2005influential citation
• Blood group antigens in health and disease

  2005cites this paper
• McLeod Syndrome: A Clinical Review

  2004influential citation
• Levine-Critchley Syndrome of Neuroacanthocytosis: A Clinical Review

  2004cites this paper
• Red blood cell blood group antigens: structure and function.

  2004cites this paper
• Molecular genetics of chorea-acanthocytosis

  2004cites this paper
• Schizophrenia as a manifestation of X-linked Mcleod-Neuroacanthocytosis syndrome.

  2004cites this paper
• A McLeod phenotype detected by random screening for K:‐4 [Kp(b–)] blood donors in Brazil

  2004cites this paper
• Neuroacanthocytosis Syndromes: What Links Red Blood Cells and Neurons?

  2004cites this paper
• Financial Support for Letter Writing ?

  2004cites this paper
• McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement

  2003cites this paper
• McLeod syndrome resulting from a novel XK mutation

  2003cites this paper
• Other Adult-Onset Movement Disorders with a Genetic Basis

  2003cites this paper
• Malignant MCLeod myopathy

  2002cites this paper
• The genetics of primary dystonias and related disorders.

  2002cites this paper
• Point mutations causing the McLeod phenotype

  2002cites this paper
• Mcleod syndrome: A novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings

  2001cites this paper
• McLeo dNeuroacanthocytosis :Genotype an dPhenotype

  2001cites this paper
• Kell and XK immunohistochemistry in McLeod myopathy

  2001cites this paper
• Acanthocytosis and neurological disorders

  2001cites this paper
• McLeod neuroacanthocytosis: Genotype and phenotype

  2001cites this paper
• A novel mutation of the McLeod syndrome gene in a Japanese family.

  2000cites this paper
• Blood groups and diseases associated with inherited abnormalities of the red blood cell membrane.

  2000cites this paper
• Kell, Kx and the McLeod syndrome.

  1999cites this paper
• Late appearance of acanthocytes during the course of chorea-acanthocytosis.

  1999cites this paper
• A novel frameshift mutation in the McLeod syndrome gene in a Japanese family.

  1999cites this paper
• Letters to the Editor

  1997cites this paper
• [Myelodysplastic syndromes: unusual and mild forms].

  1997cites this paper
• Analysis of the McLeod syndrome gene in three patients with neuroacanthocytosis.

  1997cites this paper
• Human erythrocyte antigen expression: its molecular bases.

  1997cites this paper
• McLeod - Neuroakanthozytose: Ein zu selten diagnostiziertes Syndrom?

  1996cites this paper
• A novel point mutation in the mcleod syndrome gene in neuroacanthocytosis

  1996cites this paper
• Genetic Abnormalities in Blood Group Serology

  1995cites this paper
• Kell Blood Group System and the McLeod Syndrome

  1995cites this paper
• Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.

  1994cites this paper
• Application of the MAIEA Assay to the Kell Blood Group System

  1994cites this paper
• Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a family.

  1994cites this paper
• [McLeod syndrome].

  1993cites this paper
• The Kell blood group system and the McLeod phenotype.

  1993cites this paper
• Choreo-acanthocytosis like phenotype without acanthocytes: clinicopathological case report

  1993cites this paper
• McLeod syndrome: a distinct form of neuroacanthocytosis

  1992cites this paper
• The use of recombinant granulocyte‐colony‐stimulating factor for granulocyte harvest

  1992cites this paper
• The first example of the McLeod phenotype in a Japanese baby with chronic granulomatous disease

  1992cites this paper
• Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.

  1992cites this paper
• Characterization of murine monoclonal antibodies directed against the Kell blood group glycoprotein

  1991cites this paper
• [Hypothyroidism and acanthocytes: diagnostic significance of blood smear].

  1991cites this paper
• Neuroacanthocytosis. A clinical, haematological and pathological study of 19 cases.

  1991cites this paper
• Reduced membrane protein methylation in red cells of the McLeod blood group phenotype

  1991cites this paper
• The Kell blood group system: a review

  1990cites this paper
• Biological roles of blood group antigens.

  1990cites this paper
• Abnormal membrane physical properties of red cells in McLeod syndrome

  1990cites this paper
• Effect of phosphatidylserine on the shape of McLeod red cell acanthocytes

  1989cites this paper
• Acanthocytosis associated with myelodysplasia.

  1989cites this paper
• Acanthocytosis and neurological impairment--a review.

  1989cites this paper
• Shape determinants of McLeod acanthocytes

  1989cites this paper
• Localization of the McLeod locus (XK) within Xp21 by deletion analysis.

  1988cites this paper
• Biochemical studies on McLeod phenotype red cells and isolation of Kx antigen

  1988cites this paper
• Recent developments in the Kell blood group system.

  1987cites this paper
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  1987cites this paper
• Kell blood group antigens are part of a 93,000-dalton red cell membrane protein.

  1986cites this paper
• Human granulocytes lack red cell Kx antigen

  1986cites this paper
• The phospholipid organisation in the membranes of McLeod and Leach phenotype erythrocytes

  1985cites this paper
• [Acanthocytosis in chronic septic granulomatosis: the McLeod syndrome].

  1985cites this paper
• Immunogenetics, Chemistry and Clinical Significance of Red Cell Antigens

  1984cites this paper
• Inborn errors of oxygen-dependent microbial killing by neutrophils.

  1984cites this paper
• Isolation of Kell‐active protein from the red cell membrane

  1984cites this paper
• An individual with McLeod syndrome and the Kell blood group antigen K(K1)

  1983cites this paper
• Benign X-linked myopathy with acanthocytes (McLeod syndrome). Its relationship to X-linked muscular dystrophy.

  1983cites this paper
• Depressed blood group antigens on red cells from a Mexican donor

  1983cites this paper
• Mcleod syndrome (hemolysis, acanthocytosis, and increased serum creatine kinase): potential confusion with polymyositis.

  1983cites this paper
• Spur cell anemia.

  1982cites this paper
• Structural and Biochemical Analysis of the McLeod Erythrocyte Membrane

  1982cites this paper
• Jk(a−b−) red blood cells resist urea lysis

  1982cites this paper
• Inactivation of Kell blood group antigens by 2‐aminoethylisothiouronium bromide

  1982cites this paper
• Kx: its relationship to chronic granulomatous disease and genetic linkage with Xg.

  1981cites this paper
• Elevated Serum Creatine Phosphokinase in Subjects with McLeod Syndrome

  1981cites this paper