Schutgens (23 results)

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

Condition: New.

Condition: As New. Unread book in perfect condition.

Condition: as new. Preadviezen uitgebracht door W.J.M. Voermans, R.J.B. Schutgens, A.C.M. Meuwese. Den Haag : Boom juridisch, 2017. Paperback. 192 pp. illustraties ; 25 cm. (VAR-reeks (Vereniging voor Bestuursrecht), 158). Condition : as new copy. ISBN 9789462903814. Keywords : RECHT, Preadviezen VAR Geschriften van de Vereniging voor Administratief Recht (VAR) staats- & bestuursrecht.…

Condition: very good. Deventer : Kluwer, 2013. Paperback. v,273 pp. (Handelingen Nederlandse Juristen-Vereniging ; jrg. 143/2013-1). Condition : very good copy. ISBN 9789013116533. Keywords : RECHT, Handelingen NJV.

Condition: 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.

Condition: 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. . . . . …

Condition: New. In English.

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

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

Condition: 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. …

Condition: as new. Oisterwijk : Wolf Legal Productions, [2014]. Paperback. xiv,801 pp. illustraties. 24 cm. Proefschrift Open Universiteit Heerlen - Nederland is een land van commissies. Sommige zijn zinvol: ze stellen een analyse op die verheldert, succes benoemt of falen aan de kaak stelt. Een soort commissies komen veel voor. Dat zijn de onafhankelijke visitatiecommissies die een totale organisatie of een bepaalde eenheid kritisch bezien. Zijn die commissies nuttig of niet? In het hoger onderwijs beoordelen visitatiecommissies de kwaliteit van de opleidingen. Ook hebben commissies per stadsbestuur bekeken of de doelstellingen van het grotestedenbeleid behaald zijn. Visitatie leidt niet alleen tot verantwoording, maar kan ook een aanzet geven tot verbetering. In dit boek wordt een vergelijking gemaakt tussen enerzijds de visitatie van gemeentebesturen op bestuurskracht met anderzijds de visitaties van opleidingen en het grotestedenbeleid. Wat is in essentie de kwaliteit van al dat visiteren in deze drie sectoren? Herkennen de gevisiteerden zich in de analyses en uitkomsten? Onderschrijven ze de bevindingen? Het visiteren deugt in tal van opzichten. Er is sprake van -evidence based policy-. Of het nu gaat om het bestel, het proces, de conclusies of het leren - de analyse is op hoofdlijnen positief. Het boek eindigt met een ijking van de -Beginselen van goed visiteren-. Deze verklaren grotendeels waarom de uitvoering van visitaties succesvol verloopt. De auteur laat zien dat van beleidshomeopathie geen sprake is. Commissies bieden geen heilzame drankjes waarvan de werking alleen ontstaat als je erin gelooft. Uiteraard kan een visitatie ook wel discussie oproepen of leiden tot neveneffecten. Visiteren, zoals blijkt uit "Kijken met vreemde ogen", heeft meerwaarde. Condition : as new copy. ISBN 9789462401808. Keywords : RECHT, staats- & bestuursrecht.…

Taschenbuch. Condition: 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.…

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

Condition: As New.

Condition: As New.

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Taschenbuch. Condition: 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. …

paperback. Condition: Gut. 124 Seiten; 9783525701553.3 Gewicht in Gramm: 500.

PF. Condition: New. This item is printed on demand. Brand new book, sourced directly from publisher. Dispatch time is 6-7 days from our warehouse. Book will be sent in robust, secure packaging to ensure it reaches you securely.

Taschenbuch. Condition: 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.…

Kartoniert / Broschiert. Condition: 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. Condition: 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. …