Severe course of glycogen storage disease type II (Pompe's Disease) without development of cardiomegalia

Pathology - Research and Practice ◽

10.1016/s0344-0338(86)80164-9 ◽

1986 ◽

Vol 181 (5) ◽

pp. 627-630 ◽

Author(s):

K. Ullrich ◽

H. Gröbe ◽

R. Korinthenberg ◽

D.B. von Bassewitz

Keyword(s):

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Pompe’S Disease ◽

Pompe's Disease

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Orphan designation: miglustat, Treatment of glycogen storage disease type II (Pompe's disease)

Case Medical Research ◽

10.31525/cmr-ea52d0 ◽

2019 ◽

Author(s):

Keyword(s):

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Orphan Designation ◽

Pompe’S Disease ◽

Pompe's Disease

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Increased Excretion of a Glucose-Containing Tetrasaccharide in the Urine of a Patient with Glycogen Storage Disease Type II (Pompe's Disease)

European Journal of Clinical Investigation ◽

10.1111/j.1365-2362.1974.tb02358.x ◽

1974 ◽

Vol 4 (6) ◽

pp. 429-433 ◽

Author(s):

P. Hallgren ◽

G. Hansson ◽

K. G. Henriksson ◽

A. Häger ◽

A. Lundblad ◽

...

Keyword(s):

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Pompe’S Disease ◽

Pompe's Disease

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Galactosemia to Glycogen Storage Disease Type II (Pompe's Disease)

Neonatology ◽

10.1017/cbo9780511547270.021 ◽

2011 ◽

pp. 157-166

Keyword(s):

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Pompe’S Disease ◽

Pompe's Disease

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

Cellular and Molecular Life Sciences ◽

10.1007/bf01930409 ◽

1973 ◽

Vol 29 (8) ◽

pp. 972-973 ◽

Author(s):

D. Seiler ◽

R. Kelleter ◽

H. W. Kölmel ◽

R. Heene

Keyword(s):

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Adult Patients ◽

Type Ii ◽

Pompe’S Disease ◽

Glucosidase Activity ◽

Pompe's Disease

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Hydrocephalus associated with glycogen storage disease type II (pompe’s disease)

Pediatric Neurology ◽

10.1016/s0887-8994(99)00064-8 ◽

1999 ◽

Vol 21 (3) ◽

pp. 674-676 ◽

Author(s):

Mustafa Sahin ◽

Adre J du Plessis

Keyword(s):

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Pompe’S Disease ◽

Pompe's Disease

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Enzyme patterns in glycogen storage disease type II (Pompe's disease)

10.1016/0026-0495(66)90125-9 ◽

1966 ◽

Vol 15 (7) ◽

pp. 641-648 ◽

Author(s):

Ghodsi Mekanik ◽

R.Lawrence Smith ◽

Robert M. MacLeod

Keyword(s):

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Pompe’S Disease ◽

Pompe's Disease ◽

Enzyme Patterns

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Comparative pathology of the canine model of glycogen storage disease type II (Pompe's disease)

Journal of Inherited Metabolic Disease ◽

10.1007/bf01805484 ◽

1985 ◽

Vol 8 (1) ◽

pp. 38-46 ◽

Author(s):

H. C. Walvoort ◽

J. A. M. A. Dormans ◽

T. S. G. A. M. van den Ingh

Keyword(s):

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Canine Model ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Comparative Pathology ◽

Pompe’S Disease ◽

Pompe's Disease

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Glycogen Storage Disease Type II (Pompe’s Disease): Electrocardiographic and Echocardiographic Features

Pediatric Cardiology ◽

10.1007/978-1-4613-8598-1_297 ◽

1986 ◽

pp. 1124-1125

Author(s):

J. Lam ◽

L. J. Lubbers ◽

M. S. J. Naeff ◽

G. Losekoot

Keyword(s):

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Pompe’S Disease ◽

Pompe's Disease

Download Full-text

Increased Excretion of a Glucose-Containing Tetrasaccharide in the Urine of a Patient with Glycogen Storage Disease Type II (Pompe's Disease)

European Journal of Clinical Investigation ◽

10.1111/j.1365-2362.1974.tb00416.x ◽

1974 ◽

Vol 4 (1) ◽

pp. 429-433 ◽

Author(s):

P. Hallgren ◽

G. Hansson ◽

K. G. Henriksson ◽

A. Hager ◽

A. Lundblad ◽

...

Keyword(s):

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Pompe’S Disease ◽

Pompe's Disease

Download Full-text

Orphan designation: miglustat, Treatment of glycogen storage disease type II (Pompe's disease)

Case Medical Research ◽

10.31525/cmr-ea7c24 ◽

2019 ◽

Author(s):

Keyword(s):

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Orphan Designation ◽

Pompe’S Disease ◽

Pompe's Disease

Download Full-text