Lipid Storage Disorders

Lipid Storage Disorders PDF Author: R. Salvayre
Publisher: Springer Science & Business Media
ISBN: 1461310296
Category : Science
Languages : en
Pages : 791

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Book Description
This book presents the proceedings of the meeting on "Lipid Storage Disorders" which took place in Toulouse, France, in September 14-18, 1987 and which was set up as a joint NATO Advanced Research Workshop and INSERM International Symposium. The meeting probably was the first truly international symposium devoted entirely to basic as well as applied aspects of lipid metabolism as related to the lipid storage disorders. Participants came from Europe, USA, Israel and Japan, and presented data on research in molecular biology and genetics, enzymology, cell biology as well as medical and epidemiological aspects of normal and pathological lipid metabolism. In the latter case, special attention was directed to the lysosomal B-glucosidase in relation to Gaucher disease and to sphin gomyelinase in relation to Niemann-Pick disease, and "two round" table discussions were devoted to the two respective items. But research on many other lipidoses was presented, as lectures or posters and avidly discussed. Other topics presented in special sessions were drug induced lipidoses and peroxisomal disorders. The meeting ended with a session devoted to medical aspects of disorders of lipid metabolism. The symposium which included about 50 lectures and close to 70 posters had an intense scientific character superimposed on a most pleasant and collegial atmosphere. Ample time was provided to personal discussions ; lodging of the participants in the students' residence located near the meeting place, permitted further contacts between them.

Lipid Storage Disorders

Lipid Storage Disorders PDF Author: R. Salvayre
Publisher: Springer Science & Business Media
ISBN: 1461310296
Category : Science
Languages : en
Pages : 791

Get Book Here

Book Description
This book presents the proceedings of the meeting on "Lipid Storage Disorders" which took place in Toulouse, France, in September 14-18, 1987 and which was set up as a joint NATO Advanced Research Workshop and INSERM International Symposium. The meeting probably was the first truly international symposium devoted entirely to basic as well as applied aspects of lipid metabolism as related to the lipid storage disorders. Participants came from Europe, USA, Israel and Japan, and presented data on research in molecular biology and genetics, enzymology, cell biology as well as medical and epidemiological aspects of normal and pathological lipid metabolism. In the latter case, special attention was directed to the lysosomal B-glucosidase in relation to Gaucher disease and to sphin gomyelinase in relation to Niemann-Pick disease, and "two round" table discussions were devoted to the two respective items. But research on many other lipidoses was presented, as lectures or posters and avidly discussed. Other topics presented in special sessions were drug induced lipidoses and peroxisomal disorders. The meeting ended with a session devoted to medical aspects of disorders of lipid metabolism. The symposium which included about 50 lectures and close to 70 posters had an intense scientific character superimposed on a most pleasant and collegial atmosphere. Ample time was provided to personal discussions ; lodging of the participants in the students' residence located near the meeting place, permitted further contacts between them.

Lipid Storage Diseases

Lipid Storage Diseases PDF Author: Joseph Bernsohn
Publisher:
ISBN:
Category : Medical
Languages : en
Pages : 336

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Book Description
Glossy publication advertising the commercial photographs of Getty Images, showing very high quality images of sporting moments and events, and of entertainment and news stories.

Lipid Storage Diseases

Lipid Storage Diseases PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 24

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Book Description


Lipid Storage Diseases Enzymatic Defects and Clinical Implications

Lipid Storage Diseases Enzymatic Defects and Clinical Implications PDF Author: Bernsohn J.
Publisher:
ISBN:
Category :
Languages : en
Pages :

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Lipid storage diseases : enzymatic defects and clinical implications ; [proceedings of a symposium held in Chicago, Illinois, April 23 - 24, 1970]

Lipid storage diseases : enzymatic defects and clinical implications ; [proceedings of a symposium held in Chicago, Illinois, April 23 - 24, 1970] PDF Author: Joseph Bernsohn
Publisher:
ISBN:
Category : Lipids
Languages : en
Pages : 0

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Book Description


Lipid Storage Disorders

Lipid Storage Disorders PDF Author: Louis Douste-Blazy
Publisher:
ISBN:
Category :
Languages : en
Pages : 838

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Lipid Storage Diseases

Lipid Storage Diseases PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 20

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Lipid Storage Diseases

Lipid Storage Diseases PDF Author: Joseph Bernsohn
Publisher:
ISBN:
Category : Lipidoses
Languages : en
Pages : 316

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Book Description


Lipid Storage Diseases

Lipid Storage Diseases PDF Author: J. Bernsohn
Publisher:
ISBN:
Category :
Languages : en
Pages : 0

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Book Description


Inborn Disorders of Sphingolipid Metabolism

Inborn Disorders of Sphingolipid Metabolism PDF Author: Stanley M. Aronson
Publisher: Elsevier
ISBN: 1483223582
Category : Health & Fitness
Languages : en
Pages : 530

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Book Description
Inborn Disorders of Sphingolipid Metabolism is a collection of papers presented at the Third International Symposium on the Cerebral Sphingolipidoses and Allied Diseases, held at the Isaac Albert Research Institute of the Jewish Chronic Disease Hospital and at the State University of New York, Downstate Medical Center, on October 25 and 26, 1965. This book is organized into three parts encompassing 35 chapters. Part I deals first with electron microscopic, histochemical, and morphological investigations of certain sphingolipid metabolism disorders. This part also examines several case reports on the features and symptoms of spongy degeneration of the central nervous system, familial leukodystrophy, adrenal insufficiency, and cutaneous melanosis. Part II surveys the metabolism, biosynthesis, and structure of gangliosides and sialic acids. This part also considers the nature of the lipophilic portions of the brain gangliosides. This part particularly looks into the features and clinical manifestation of Tay-Sachs disease. The third part covers the genetic and clinical aspects of the Tay-Sachs disease. This part also evaluates the genetics of the Hurler-Hunter syndrome, Batten-Spielmeyer-Vogt disease, and lipogranulomatosis syndrome. This book is of value to biochemists, histochemists, geneticists, and researchers in the allied fields of lipidosis.