P. Öckerman

发表

Effects of a shift from a mixed diet to a lacto-vegetarian diet on some coronary heart disease risk markers

G. Johansson, B. Källgård, P. Öckerman, 2012 .

Acid hydrolases in skin and plasma in gargoylism. Deficiency of β-galactosidase in skin

P. Öckerman, 1968 .

Improvement of Arterial Stiffness by EDTA-Chelation in Combination with Vitamin, Mineral, Trace Element and Antioxidant Supplements

P. Öckerman, 2011 .

Identity of β-glucosidase, β-xylosidase and one of the β-galactosidase activities in human liver when assayed with 4-methylumbelliferyl-β-d-glycosides studies in cases of Gaucher's disease

P. Öckerman, 1968 .

β-Glucosidase activities in human tissues findings in Gaucher's disease

B. Hultberg, P. Öckerman, 1970 .

GLYCOSIDASES IN SKIN AND PLASMA IN HUNTER'S SYNDROME Abnormality of a β‐galactosidase in Skin

P. Öckerman, P. Köhlin, 1968, Acta paediatrica Scandinavica.

4-Methylumbelliferyl-β-glucosidase in cultured human fibroblasts from controls and patients with gaucher's disease

B. Hultberg, S. Sjöblad, P. Öckerman, 1973 .

In vitro studies of adipose tissue metabolism of glucose, glycerol and free fatty acids in glycogen storage disease type 1.

P. Öckerman, 1965 .

Mannosidosis: Isolation of oligosaccharide storage material from brain

P. Öckerman, 1969 .

Properties of 4-Methylumbelliferyl-β-Galactosidase Activities in Human Liver

B. Hultberg, P. Öckerman, 1969 .

Artificial substrates in the assay of acid glycosidases.

B. Hultberg, P. Öckerman, 1972 .

Glucose-6-phosphatase in human jejunal mucosa properties demonstrating the specific character of the enzyme activity

P. Öckerman, 1965 .

Determination of a mannose-containing trisaccharide in the urine of patients and heterozygotes of mannosidosis

A. Lundblad, S. Svensson, N. Nordén, 1975 .

THE BLEEDING DISORDER IN HEPATOMEGALIC FORMS OF GLYCOGEN STORAGE DISEASE

I. Nilsson, P. Öckerman, 1970, Acta paediatrica Scandinavica.

Glycogenosis of the central nervous system in the cat

J. Westman, B. Sandström, P. Öckerman, 2004, Acta Neuropathologica.

Isolation and characterisation of 4‐O‐β‐D‐mannopyranosyl‐2‐acetamido‐2‐deoxy‐D‐glucose from the urine of a patient with mucolipidosis II and its occurrence in normal and pathological urine

A. Lundblad, S. Svensson, L. Poenaru, 1982, FEBS letters.

Isolation and characterization of oligosaccharides from urine of patients with abnormal glycoconjugate metabolism

A. Lundblad, S. Svensson, M. Chester, 1978, Journal of Inherited Metabolic Disease.

Fluorimetric estimation of 4-methyl-umbelliferyl-α-mannosidase activity in blood plasma

P. Öckerman, 1969 .

FINE‐NEEDLE ASPIRATION BIOPSY OF HUMAN LIVER FOR ENZYMATIC DIAGNOSIS OF GLYCOGEN STORAGE DISEASE AND GARGOYLISM

A. Lundquist, P. Öckerman, 1970, Acta paediatrica Scandinavica.

Glucose-6-phosphatase assay on microgram amounts of liver tissue.

P. Öckerman, 1967 .

A GENERALISED STORAGE DISORDER RESEMBLING HURLER'S SYNDROME

P. Öckerman, 1967 .

GLYCOSIDASES IN HUMAN SKIN FIBROBLAST CULTURES

B. Hultberg, S. Sjöblad, P. Öckerman, 1975 .

Glycogenosis Type 1 (Lack of Glucose‐6‐Phosphatase) in Four Siblings

P. Öckerman, K. Kaijser, G. Brante, 1964, Acta paediatrica.

Diseases of glycoprotein storage.

P. Öckerman, 1969 .

LYSOSOMAL ENZYMES IN JUVENILE AMAUROTIC IDIOCY

P. Öckerman, 1968 .

4-Methyl-umbelliferyl-β-glucosidase activity in human blood plasma

P. Öckerman, 1968 .

Deficiency of β‐galactosidase and α‐mannosidase – Primary Enzyme Defects in Gargoylism and a New Generalized Disease?

P. Öckerman, 1967 .

Enzymic liberation of d-galactose from keratan sulfate by human tissues

P. Öckerman, 1970 .

INCIDENCE OF GLYCOGEN STORAGE DISEASE IN SWEDEN

P. Öckerman, 1972 .

Glycogenosis Type 6 (Liver Phosphorylase Deficiency) A Case Followed for Ten Years, with Normal Phosphorylase Activity in White Blood Cells and Jejunal Mucosa

P. Öckerman, K. Kaijser, H. Jelke, 1966, Acta paediatrica Scandinavica.

GLUCOSE-6-PHOSPHATASE IN HUMAN JEJUNAL MUCOSA. LACK OF ACTIVITY IN GLYCOGENOSIS OF CORI'S TYPE 1.

P. Öckerman, 1964 .

SEPARATION OF PHOSPHORYLATED GLYCOLYTIC INTERMEDIATES, NUCLEOTIDES AND GLYCOGEN IN BLOOD CELLS, USING DIETHYLAMINOETHYL-SEPHADEX IN COLUMNS.

P. Öckerman, 1963 .

Phosphorylated glycolytic intermediates in liver and blood cells in members of a family with glycogenosis type I.

P. Öckerman, 1963 .

Very-Low-Calorie Diets. An Improved Procedure with Exclusive Loss of Fat, Very Good Acceptance and Positive Effects on Health

P. Öckerman, 1992 .

Glucose, glycerol and free fatty acids in glycogen storage disease type 1. Blood levels in the fasting and non-fasting state. Effect of glucose and adrenalin administration.

P. Öckerman, 1965 .

GLYCEROL IN PLASMA IN GLYCOGENOSIS OF CORI'S TYPE I.

P. Öckerman, 1963 .

A TECHNIQUE FOR THE ENZYMATIC DIAGNOSIS OF GLYCOGEN STORAGE DISEASE ON VERY SMALL TISSUE SPECIMENS

P. Öckerman, P. A. öckerman, 1968 .

Problems in the Chemical Diagnosis of Glycoprotein Storage Diseases

N. Nordén, P. Öckerman, L. Szabó, 1972 .

Mannosidosis: a clinical and histopathologic study.

B. Kjellman, I. Gamstorp, A. Brun, 1969, The Journal of pediatrics.

Splenic transplantation in a case of Gaucher's disease.

L. Hagenfeldt, L. Svennerholm, C. Groth, 1971, Lancet.

Mannosidosis in angus cattle: Partial characterization of two mannose containing oligosaccharides

A. Lundblad, N. Nordén, R. Jolly, 1973, FEBS letters.

Gargoylism: hydrolysis of β-galactosides and tissue accumulation of galactose- and mannose-containing compounds

B. Hultberg, A. Dahlqvist, A Dahlqvist, 1970 .