Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 [McArdle's syndrome (myopathy in muscle phosphorylase deficiency)].

Literature DB >> 6031735

[McArdle's syndrome (myopathy in muscle phosphorylase deficiency)].

K Schimrigk, H G Mertens, K Ricker, J Führ, P Eyer, D Pette.

Abstract

Entities: Disease

Mesh：

Substances：

Year: 1967 PMID： 6031735 DOI： 10.1007/bf01745732

Source DB: PubMed Journal: Klin Wochenschr ISSN： 0023-2173

× No keyword cloud information.

24 in total

1. [Proportionally constant groups in relation to the differentiation of enzyme activity patterns of skeletal muscles in rabbits].

Authors: D PETTE; T BUECHER
Journal: Hoppe Seylers Z Physiol Chem Date: 1963-03

2. [Electron microscopic research on myotonic muscular dystrophy].

Authors: W WECHSLER; H HAGER
Journal: Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr Date: 1961

3. A metabolic myopathy due to absence of muscle phosphorylase.

Authors: C M PEARSON; D G RIMER; W F MOMMAERTS
Journal: Am J Med Date: 1961-04 Impact factor: 4.965

4. Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle.

Authors: R SCHMID; R MAHLER
Journal: J Clin Invest Date: 1959-11 Impact factor: 14.808

5. Familial cirrhosis of the liver with storage of abnormal glycogen.

Authors: D H ANDERSEN
Journal: Lab Invest Date: 1956 Jan-Feb Impact factor: 5.662

6. Histochemical demonstration of branching enzyme (amylo-1,4-1,6-transglucosidase) in animal tissues.

Authors: T TAKEUCHI
Journal: J Histochem Cytochem Date: 1958-05 Impact factor: 2.479

7. The determination of glycogen in liver and muscle by use of anthrone reagent.

Authors: N V CARROLL; R W LONGLEY; J H ROE
Journal: J Biol Chem Date: 1956-06 Impact factor: 5.157

8. Myopathy due to a defect in muscle glycogen breakdown.

Authors: B McARDLE
Journal: Clin Sci Date: 1951-02 Impact factor: 6.124

9. A FUNCTIONAL DISORDER OF MUSCLE ASSOCIATED WITH THE ABSENCE OF PHOSPHORYLASE.

Authors: W F Mommaerts; B Illingworth; C M Pearson; R J Guillory; K Seraydarian
Journal: Proc Natl Acad Sci U S A Date: 1959-06 Impact factor: 11.205

10. [On enzyme activity patterns in regard to the differentiation of skeletal muscles].

Authors: T Bücher; D Pette
Journal: Verh Dtsch Ges Inn Med Date: 1965

9 in total

1. Steroid myopathy complicating McArdle's disease.

Authors: F L Mastaglia; J P McCollum; P F Larson; P Hudgson
Journal: J Neurol Neurosurg Psychiatry Date: 1970-02 Impact factor: 10.154

2. [Energy providing metabolism of muscles in periodic paralysis].

Authors: H G Mertens; M Lurati; K Schimrigk; J Führ; S Hofer; D Pette
Journal: Klin Wochenschr Date: 1969-05-01

3. McArdle's disease: two clinical expressions in the same pedigree.

Authors: A Papadimitriou; P Manta; R Divari; A Karabetsos; E Papadimitriou; N Bresolin
Journal: J Neurol Date: 1990-07 Impact factor: 4.849

4. Influence of local cooling on the muscle contracture and paresis of McArdle's disease.

Authors: K Ricker; G Hertel
Journal: J Neurol Date: 1977-07-20 Impact factor: 4.849

Review 5. The glycogen storage diseases.

Authors: B E Ryman
Journal: J Clin Pathol Suppl (R Coll Pathol) Date: 1974

6. Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.

Authors: S Iyengar; H Kalinsky; S Weiss; M Korostishevsky; M Sadeh; Y Zhao; K K Kidd; B Bonne-Tamir
Journal: J Med Genet Date: 1997-05 Impact factor: 6.318