Literature DB >> 3083284

Adult muscle phosphorylase "b" kinase deficiency.

J M Abarbanel, N Bashan, R Potashnik, A Osimani, S W Moses, Y Herishanu.   

Abstract

A 35-year-old man had severe exercise intolerance and cramps. Venous blood lactate did not rise after ischemic exercise, and electromyographically silent contracture of hand muscles appeared. Histochemistry and electronmicroscopy of a muscle biopsy revealed subsarcolemmal and intermyofibrillar accumulation of glycogen. Biochemical studies showed moderately increased amount of glycogen. Total phosphorylase activity was normal, but the active form "a" was 27% of normal. Phosphorylase kinase activity was 12% of the normal value and was normal in leukocytes and erythrocytes.

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Year:  1986        PMID: 3083284     DOI: 10.1212/wnl.36.4.560

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  13 in total

Review 1.  Molecular genetics of phosphorylase kinase: cDNA cloning, chromosomal mapping and isoform structure.

Authors:  M W Kilimann
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

Review 2.  Phosphorylase b kinase deficiency in man: a review.

Authors:  I E Van den Berg; R Berger
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  Autosomal recessive phosphorylase kinase deficiency in liver, caused by mutations in the gene encoding the beta subunit (PHKB).

Authors:  I E van den Berg; E A van Beurden; J B de Klerk; O P van Diggelen; H E Malingré; M M Boer; R Berger
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

4.  Phosphorylase b kinase deficiency in a boy with glycogenosis affecting both liver and muscle.

Authors:  M Madlom; G T Besley; P T Cohen; V J Marrian
Journal:  Eur J Pediatr       Date:  1989-10       Impact factor: 3.183

5.  I/Lyn mouse phosphorylase kinase deficiency: mutation disrupts expression of the alpha/alpha'-subunit mRNAs.

Authors:  P K Bender; P A Lalley
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

6.  Phosphorylase kinase in leukocytes and erythrocytes of a patient with glycogen storage disease type IX.

Authors:  N Bashan; R Potashnik; T Ehrlich; S W Moses
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

7.  Enzymatic analysis in lymphocytes and erythrocytes from six patients with different phenotypes of phosphorylase kinase deficiency.

Authors:  M Kikuchi; J Aikawa; S Ishizawa; Y Igarashi; K Narisawa; K Tada
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

Review 8.  Fatal infantile hypertrophic cardiomyopathy secondary to deficiency of heart specific phosphorylase b kinase.

Authors:  M Elleder; Y S Shin; A Zuntová; P Vojtovic; V Chalupecký
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1993

Review 9.  Muscle glycogenosis.

Authors:  S W Moses
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

10.  X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase alpha subunit.

Authors:  I E van den Berg; E A van Beurden; H E Malingré; H K van Amstel; B T Poll-The; J A Smeitink; W H Lamers; R Berger
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

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