G m addison (148 resultados)

Hardcover. Condición: Near Fine. Estado de la sobrecubierta: Good. Reprint. Reprint. Original green cloth. Near Fine in Good Dust Jacket with some smudging, edge wear, and edge tears.

Soft cover. Condición: Very Good. No Jacket. First Edition. 20 cases to improve diagnostic skills. Slight edge wear. No inscriptions (H33A).

Condición: Fair. 1963. Popular Edition. 191 pages. Pictorial dust jacket over green cloth. Black and white photographs throughout with colour frontispiece. Pages and photographs are lightly tanned throughout. Water staining to most pages, with some pages slightly stuck together. Creasing to some pages. Severe cracking to hinges causing boards to be loose. Boards have light shelf-wear with corner bumping. Slight crushing to spine ends. Unclipped jacket has light edgewear with tears and creasing. Water staining to both panels. Wear marks overall.…

Soft cover. Condición: Good. No Dust Jacket. (No Date) 32 pp. Original gray staple-bound wraps, moderately soiled. Edges darkened. Covers almost detached. All edges gilt. Neat inscription to previous owner on half-title page. Light foxing throughout. Illust. w/ b/w drawings. Mary E. Butler; Giacomelli; H. Bannermann; H. Whatley; Robert Ellice Mack; W. G. Addison; A. M. Clausen; G. H. Thompson; A. Wilde Parsons; Julius Luz; George Clausen (ilustrador). …

Condición: Good. 1959. hardback. Fine in fine cloth covers, lacking dust wrapper. Covers showing some wear and age, remains a fine copy. . . . .

Condición: New.

PAP. Condición: New. New Book. Shipped from UK. Established seller since 2000.

Cloth. Condición: Very Good. Estado de la sobrecubierta: No d/j as Published. Type: Book Proceedings of the 25th Annual Symposium of the SSIEM, Sheffield, UK, Sept. 1987. Combined supplements of Journal of inherited metabolic disease, Vol. II (1988). Embraces many of the major aspects of the study of inborn errors of metabolism.Small mark near spine on base of front board.278pp.…

PAP. Condición: New. New Book. Shipped from UK. Established seller since 2000.

Condición: New.

Paperback. Condición: New. Brand new book, sourced directly from publisher. Dispatch time is 24-48 hours from our warehouse. Book will be sent in robust, secure packaging to ensure it reaches you securely.

Condición: As New. Unread book in perfect condition.

Condición: As New. Unread book in perfect condition.

Paperback. Condición: New. Brand new book, sourced directly from publisher. Dispatch time is 24-48 hours from our warehouse. Book will be sent in robust, secure packaging to ensure it reaches you securely.

Condición: Good. 1959. hardback. Fine in fine cloth covers, lacking dust wrapper. Covers showing some wear and age, remains a fine copy. . . . . Books ship from the US and Ireland.

Condición: Good. Your purchase helps support Sri Lankan Children's Charity 'The Rainbow Centre'. Ex-library, so some stamps and wear, but in good overall condition. Our donations to The Rainbow Centre have helped provide an education and a safe haven to hundreds of children who live in appalling conditions.…

Condición: New.

Condición: New.

Paperback or Softback. Condición: New. Inherited Disorders of Vitamins and Cofactors: Proceedings of the 22nd Annual Symposium of the Ssiem, Newcastle Upon Tyne, September 1984. Book.

Paperback or Softback. Condición: New. Organic Acidurias: Proceedings of the 21st Annual Symposium of the Ssiem, Lyon, September 1983 the Combined Supplements 1 and 2 of Journal of Inherite. Book.

Paperback or Softback. Condición: New. Inherited Metabolic Diseases and the Brain. Book.

Paperback or Softback. Condición: New. Practical Developments in Inherited Metabolic Disease: DNA Analysis, Phenylketonuria and Screening for Congenital Adrenal Hyperplasia: Proceedings of. Book.

Paperback. Condición: New. The first symposium of the Society for the Study ofInborn valuable overview of advances in the application of Errors of Metabolism (SSIEM) on the organic acid urias chemical analysis of amniotic fluid to their early prenatal was held in Leeds in 1971 and published by the Society in diagnosis. The continuing complexity of diagnosis, 1972 (the 9th Annual SSIEM Symposium). Although biochemistry and aetiology ofthe dicarboxylic acid urias relatively few of these disorders were recognized at that has been admirably reduced by the papers from Dr time, the symposium was prompted by the then recent Gregersen and Dr Goodman, with Dr Goodman clearly identification between 1966 and 1970 of isovaleric identifying the primary defect in the polycystic variant of acidaemia, methylmalonic aciduria, propionic aci- multiple acyl CoA dehydrogenase deficiency ("glutaric daemia, pyroglutamic aciduria and 3-methylcrotonyl- aciduria type II") as a deficiency of electron transfer glycinuria. Identification and diagnosis of diseases of this flavoprotein (ETF) dehydrogenase.Dr Engel's paper kind had greatly improved primarily through the also provides a useful overview from currently available application of gas chromatography and mass spectro- data of the place of L-carnitine in the organic acid urias, metry to medicine, although the complexity of the an area in which rapid developments are occurring. The underlying biochemistry and the genetic heterogeneity of emerging understanding of the aetiologies of the the organic acidurias was not then realised. Softcover reprint of the original 1st ed. 1984.…

Condición: New.

Condición: New.

Condición: New.

Condición: New.

Paperback. Condición: New. Softcover reprint of the original 1st ed. 1986.

Condición: As New. Unread book in perfect condition.

Condición: As New. Unread book in perfect condition.