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Softcover. Condizione: Très bon. Ancien livre de bibliothèque avec équipements. Couverture différente. Edition 1995. Ammareal reverse jusqu'à 15% du prix net de cet article à des organisations caritatives. ENGLISH DESCRIPTION Book Condition: Used, Very good. Former library book. Different cover. Edition 1995. Ammareal gives back up to 15% of this item's net price to charity organizations.

Paperback. Condizione: Brand New. 199 pages. 9.00x6.00x0.50 inches. In Stock.

Condizione: Very good.

Condizione: As New. Unread book in perfect condition.

Condizione: New. In.

PF. Condizione: New.

Condizione: New.

Condizione: new. Amsterdam & New York : North-Holland, 1995. Paperback. viii,294 pp. Includes bibliographical references and indexes. (Koninklijke Academie van Wetenschappen. Verhandelingen, Afd. Natuurkunde, Tweede reeks, deel 95). Condition : new copy. ISBN 9780444857996. Keywords : MEDiCINE,

Condizione: New. Peroxisomal disorders constitute a major research front in clinical genetics, paediatrics and cell biology. This illustrative account of laboratory methods for the diagnosis of peroxisomal disorders methods should allow laboratories to introduce these methods into their repertoire. Editor(s): Roels, F. Series: Journal of Inherited Metabolic Disease. Num Pages: 226 pages, 85 black & white illustrations, biography. BIC Classification: MJC; MJG. Category: (P) Professional & Vocational. Dimension: 235 x 155 x 13. Weight in Grams: 410. . 1997. Reprinted from the Journal of Inherited Metabolic . paperback. . . . .

Paperback. Condizione: Brand New. reprint edition. 232 pages. 9.30x6.15x0.54 inches. In Stock.

Condizione: New.

Condizione: New. Peroxisomal disorders constitute a major research front in clinical genetics, paediatrics and cell biology. This illustrative account of laboratory methods for the diagnosis of peroxisomal disorders methods should allow laboratories to introduce these methods into their repertoire. Editor(s): Roels, F. Series: Journal of Inherited Metabolic Disease. Num Pages: 226 pages, 85 black & white illustrations, biography. BIC Classification: MJC; MJG. Category: (P) Professional & Vocational. Dimension: 235 x 155 x 13. Weight in Grams: 410. . 1997. Reprinted from the Journal of Inherited Metabolic . paperback. . . . . Books ship from the US and Ireland.

Condizione: Very good.

20x14,50 cm. original softcover, stapled. 16 pp. many ills (some in color). -(back cover slightly stained).

169pp.geïll., 29cm., in de reeks "Rijksarchief in Limburg" vol.18, enkele stempeltjes, goede staat, N73458.

Taschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - Peroxisomal disorders constitute a major research front in clinical genetics, paediatrics and cell biology. Since 1983, the metabolic defect in some 20 different peroxisomal disorders has been described. The best known conditions include Zellweger syndrome, rhizomelic chondrodysplasia punctata and X-linked adrenoleukodystrophy and, in the most recent edition of The Metabolic and Molecular Basis Inherited Disease, edited by Scriver and colleagues, more than 100 pages are now devoted to the subject. Progress in our understanding of these conditions, and their diagnosis, results from the application of a variety of laboratory investigations. These include microscopic studies, analysis of metabolites (very long-chain fatty acids, bile acids, and plasmalogens), enzyme studies (peroxisomal beta-oxidation pathway and dihydroxyacetone phosphate acyltransferase), immunodetection of peroxisomal (membrane) proteins and molecular analysis of mutant DNA. In order to encourage a greater awareness in this field and the diagnostic protocols required, an international course was organised in Gent, Belgium, in May 1994, on the clinical and biochemical diagnosis of peroxisomal disorders. A number of international experts in the field who provided intensive hands-on experience over 3.5 days, have now collected their course work and reviews together in this Handbook. The volume is introduced by Sidney Goldfischer, who in 1973 was the first to recognise the absence of peroxisomes in Zellweger syndrome, but whose observations were not fully appreciated for a further decade. This handbook provides the most comprehensive and detailed account of laboratory methods for the diagnosis of peroxisomal disorders. The methods are clearly presented and well illustrated, and should allow laboratories to introduce these methods into their repertoire. Audience: Paediatricians, neurologists, clinical biochemists, pathologists, genetic counsellors, obstetricians, and GPs interested in the recognition, diagnosis and prenatal prevention of peroxisomal disorders.

Condizione: Very good.

Taschenbuch. Condizione: Neu. Neuware - Many grade-school children have difficulties sitting still and concentrating. Fantasy stories may help them to better concentrate, to better perceive their own feelings and to achieve a higher level of self-confidence. Fantasy stories are also appropriate for reducing feelings of stress - a phenomenon now not unknown to even the youngest children. They provide a feeling of inner peace, relaxation and creativity, and they strengthen the children s optimism in life and their sense of reality.Two goblins and a cloud dragon accompany the children through the fantasy stories and provide an easy introduction to new and fascinating worlds. They tell the story of some of the little sensory joys that may be discovered in everyday life: the wind in your face, sand running through the fingers of your hands, the smell of fresh mint, the sound of bubbling water .The insightful drawings by the author round off the joy provided children in reading these stories, which can be used either as introductory or as meditative images. They are also available in color from the publisher s website.

Taschenbuch. Condizione: Neu. Traumflüge | Fantasiereisen für die Grundschule | Angelika Schütgens | Taschenbuch | 124 S. | Deutsch | 2013 | Vandenhoeck & Ruprecht | EAN 9783525701553 | Verantwortliche Person für die EU: Vandenhoeck & Ruprecht, Theaterstr. 13, 37073 Göttingen, ute[dot]schnueckel[at]brill[dot]com | Anbieter: preigu.

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Peroxisomal disorders constitute a major research front in clinical genetics, paediatrics and cell biology. Since 1983, the metabolic defect in some 20 different peroxisomal disorders has been described. The best known conditions include Zellweger syndrome, rhizomelic chondrodysplasia punctata and X-linked adrenoleukodystrophy and, in the most recent edition of The Metabolic and Molecular Basis Inherited Disease, edited by Scriver and colleagues, more than 100 pages are now devoted to the subject. Progress in our understanding of these conditions, and their diagnosis, results from the application of a variety of laboratory investigations. These include microscopic studies, analysis of metabolites (very long-chain fatty acids, bile acids, and plasmalogens), enzyme studies (peroxisomal beta-oxidation pathway and dihydroxyacetone phosphate acyltransferase), immunodetection of peroxisomal (membrane) proteins and molecular analysis of mutant DNA. In order to encourage a greater awareness in this field and the diagnostic protocols required, an international course was organised in Gent, Belgium, in May 1994, on the clinical and biochemical diagnosis of peroxisomal disorders. A number of international experts in the field who provided intensive hands-on experience over 3.5 days, have now collected their course work and reviews together in this Handbook. The volume is introduced by Sidney Goldfischer, who in 1973 was the first to recognise the absence of peroxisomes in Zellweger syndrome, but whose observations were not fully appreciated for a further decade. This handbook provides the most comprehensive and detailed account of laboratory methods for the diagnosis of peroxisomal disorders. The methods are clearly presented and well illustrated, and should allow laboratories to introduce these methods into their repertoire. Audience: Paediatricians, neurologists, clinical biochemists, pathologists, genetic counsellors, obstetricians, and GPs interested in the recognition, diagnosis and prenatal prevention of peroxisomal disorders. 236 pp. Englisch.

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Peroxisomal disorders constitute a major research front in clinical genetics, paediatrics and cell biology. Since 1983, the metabolic defect in some 20 different peroxisomal disorders has been described. The best known conditions include Zellweger syndro.

Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Peroxisomal disorders constitute a major research front in clinical genetics, paediatrics and cell biology. Since 1983, the metabolic defect in some 20 different peroxisomal disorders has been described. The best known conditions include Zellweger syndrome, rhizomelic chondrodysplasia punctata and X-linked adrenoleukodystrophy and, in the most recent edition of The Metabolic and Molecular Basis Inherited Disease, edited by Scriver and colleagues, more than 100 pages are now devoted to the subject.Progress in our understanding of these conditions, and their diagnosis, results from the application of a variety of laboratory investigations. These include microscopic studies, analysis of metabolites (very long-chain fatty acids, bile acids, and plasmalogens), enzyme studies (peroxisomal beta-oxidation pathway and dihydroxyacetone phosphate acyltransferase), immunodetection of peroxisomal (membrane) proteins and molecular analysis of mutant DNA.In order to encourage a greater awareness in this field and the diagnostic protocols required, an international course was organised in Gent, Belgium, in May 1994, on the clinical and biochemical diagnosis of peroxisomal disorders. A number of international experts in the field who provided intensive hands-on experience over 3.5 days, have now collected their course work and reviews together in this Handbook. The volume is introduced by Sidney Goldfischer, who in 1973 was the first to recognise the absence of peroxisomes in Zellweger syndrome, but whose observations were not fully appreciated for a further decade. This handbook provides the most comprehensive and detailed account of laboratory methods for the diagnosis of peroxisomal disorders. The methods are clearly presented and well illustrated, and should allow laboratories to introduce these methods into their repertoire.Audience: Paediatricians, neurologists, clinical biochemists, pathologists, genetic counsellors, obstetricians, and GPs interested in the recognition, diagnosis and prenatal prevention of peroxisomal disorders.Springer-Verlag KG, Sachsenplatz 4-6, 1201 Wien 236 pp. Englisch.