Concepedia

Author

J. Kint

Ghent University Hospital

Also Known As

J A Kint, J KINT, J Kint, J. A. KINT, J. A. Kint, J. KINT, J. Kint, J.A. KINT, J.A. Kint, Jos A. Kint

55

Publications

1.8K

Citations

20

H-Index

87

Concepts

All Affiliations

Ghent University HospitalGhent UniversityUniversitair Ziekenhuis BrusselKarolinska InstitutetRijksmuseum
JK

About

J. Kint is an author at Ghent University Hospital specializing in medicine, pathology, and pharmacology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

15

20

1.3K

2

Engineering

3

3

105

3

Public Health

2

2

105

4

Health Sciences

1

1

34

5

Natural Sciences

1

1

73

J. Kint

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32

Publications

1.7K

Citations

20

H-Index

YearCitations

Fabry's Disease: Alpha-Galactosidase Deficiency

J. Kint

Science

1970

470

Methods of study of the invasion of malignant C3H-mouse fibroblasts into embryonic chick heart in vitro

M. Mareel, J. Kint, C. Meyvisch

Virchows Archiv B Cell Pathology

1979

213

Mucopolysaccharidosis: Secondarily Induced Abnormal Distribution of Lysosomal Isoenzymes

J. Kint, G. Dacremont, D. Carton,

Science

1973

109

A new thin-layer method for phenolic substances and coumarins

C. F. van Sumere, G Wolf, H. Teuchy,

Journal of Chromatography A

1965

102

Seminal plasma alpha-glucosidase activity and male infertility

Ayman M. Mahmoud, Joel Geslevich, J. Kint,

Human Reproduction

1998

94

Biochemical studies in relation to the possible germination regulatory role of naturally occurring coumarin and phenolics

C. F. van Sumere, J. Cottenie, J. De Greef,

Recent advances in phytochemistry

1972

73

A new variant of the carbohydrate deficient glycoproteins syndrome

V. Ramaekers, Helena Stibler, J. Kint,

Journal of Inherited Metabolic Disease

1991

66

Hereditary fructose intolerance: A difficult diagnosis in the adult

Norbert Lameire, Monique Mussche, Gaston Baele,

The American Journal of Medicine

1978

55

Carbohydrate‐deficient glycoprotein syndrome type II

Jaak Jaeken, Paul De Cock, Helena Stibler,

Journal of Inherited Metabolic Disease

1993

41

Gml-ganglioside accumulation and β-galactosidase deficiency in a case of Gml-gangliosidosis (Landing disease)

G. Dacremont, J. Kint

Clinica Chimica Acta

1968

40

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