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22 in total

1. CONGENITAL NONPROGRESSIVE MYOPATHY. CENTRAL CORE DISEASE AND NEMALINE MYOPATHY IN ONE FAMILY.

Authors: A K AFIFI; J W SMITH; H ZELLWEGER
Journal: Neurology Date: 1965-04 Impact factor: 9.910

2. Amylo-1, 6-glucosidase in muscle tissue in generalized glycogen storage disease.

Authors: B ILLINGWORTH; G T CORI; C F CORI
Journal: J Biol Chem Date: 1956-01 Impact factor: 5.157

3. The myotonic discharge in various neurological syndromes: a neurophysiological analysis.

Authors: J Brumlik; B Drechsler; T M Vannin
Journal: Electromyography Date: 1970 Nov-Dec

4. Alpha-1,4-glucosidase activity in leucocytes and lymphocytes of 2 adult patients with glycogen-storage disease type II, (Pompe's disease).

Authors: D Seiler; R Kelleter; H W Kölmel; R Heene
Journal: Experientia Date: 1973-08-15

5. Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies.

Authors: A G Engel
Journal: Brain Date: 1970 Impact factor: 13.501

6. Spontaneous electrical activity in muscle. Description of two patients with motor neurone disease.

Authors: A A Eisen; G Karpati
Journal: J Neurol Sci Date: 1971-02 Impact factor: 3.181

7. Adult myopathy from glycogen storage disease due to acid maltase deficiency.

Authors: P Hudgson; D Gardner-Medwin; M Worsfold; R J Pennington; J N Walton
Journal: Brain Date: 1968-09 Impact factor: 13.501

8. Correlation between electromyographic findings and muscle biopsy in ccases of neuromuscular diseease.

Authors: I Hausmanowa-Petrusewicz; H Jedrzejowska
Journal: J Neurol Sci Date: 1971-05 Impact factor: 3.181

9. Pre-clinical muscular dystrophy: histopathological changes observed on muscle biopsy.

Authors: P Hudgson; G W Pearce; J N Walton
Journal: Brain Date: 1967-09 Impact factor: 13.501

10. alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).

Authors: H G HERS
Journal: Biochem J Date: 1963-01 Impact factor: 3.857

6 in total

Review 1. The natural course of non-classic Pompe's disease; a review of 225 published cases.

Authors: Léon P F Winkel; Marloes L C Hagemans; Pieter A van Doorn; M Christa B Loonen; Wim J C Hop; Arnold J J Reuser; Ans T van der Ploeg
Journal: J Neurol Date: 2005-08 Impact factor: 4.849

2. The symptomatology, morphology and biochemistry of glycogenosis type II (Pompe) in the adult.

Authors: G K Schlenska; R Heene; G Spalke; D Seiler
Journal: J Neurol Date: 1976-06-14 Impact factor: 4.849

3. [Mitigated adult forms of acid maltase deficiency (Pompe's disease). Morphologic and pathobiochemical studies].

Authors: D Pongratz; G Hübner; T Deufel; O H Wieland
Journal: Klin Wochenschr Date: 1983-08-01

4. [Pseudodystrophic muscle glycogenosis in adults. (Acid maltase deficiency syndrome) (author's transl)].

Authors: F Gullotta; H Stefan; H Mattern
Journal: J Neurol Date: 1976 Impact factor: 4.849

5. Acid maltase deficiency in non-identical adult twins. A morphological and biochemical study.

Authors: J J Martin; T de Barsy; W R den Tandt
Journal: J Neurol Date: 1976-08-06 Impact factor: 4.849

6. [High frequency discharges as a non-specific EMG activity in adult acid maltase deficiency (author's transl)].

Authors: F Manz
Journal: Arch Psychiatr Nervenkr (1970) Date: 1980

6 in total