william nyhan (54 risultati)

Soft cover. Condizione: Fine. Illustrated by John A. Craig. 32 pp with color illustrations.

Hardcover. Condizione: Near Fine condition. Condizione sovraccoperta: Near Fine dust jacket. First Printing of the First Edition. New York: Grosset & Dunlap, Publishers, 1976. Near Fine condition in Near Fine dust jacket. Clean, square, tight, unmarked copy. Sharp corners. Dust Jacket is bright & shiny. Not price clipped (12.95). Illustrated with charts, drawings, and photos. Original two-tone binding (brown cloth spine and yellow boards). Not a book club edition. No remainder mark. No owner's name or bookplate. "A valuable primer of how genes and chromosomes work in heredity and in hereditary diseases." - Jonas Salk. From the Dust Jacket: "The authors provide detailed information about sickle cell anemia, cystic fibrosis, Tay-Sachs disease, the Down syndrome, and other common inherited disorders linked to race, age, or ethnic background. Also considered are viruses, drugs, X rays, food additives and other possible environmental factors involved in birth defects and genetic diseases." Glossary. Bibliography. Index. First Printing of the First Edition. Hardcover. Near Fine condition/Near Fine dust jacket. 8vo. 320pp. Great Packaging, Fast Shipping.

Encuadernación de tapa blanda. Condizione: Bueno. Nyhan, William L. (Doctor en Medicina y Filosofía) y Edward Edelson. El factor hereditario. Los genes, los cromosomas, la familia y usted. México, Editores Asociados, 1986. Características: Buen estado general. Rústica plastificada. Tapas ligeramente sucias debido al paso del tiempo. Guardas limpias. Cantos limpios. Incluye varias ilustraciones en blanco y negro. 393 p. (19.5 x 14.5 cm) Peso: 500 g. (4336).

192pp. 8vo Trade Paperback. Praeger Special Studies in U.S. Economic, Social, & Political Issues. Papers from the: Workshop on Government & the Media, Aspen, Colorado, August, 1972. Interviews & papers from over 50 participants, including Fred Friendly, McGeorge Bundy et al. Light cover wear/soil, text clean/tight: VG.

Wraps. Craig, John A. (illustratore). Presumed first edition/first printing. [2], 32, [12] p. Includes illustrations. Most illustrations in color. Bibliography. The Novartis Foundation produces Symposia, in which groups of leading scientists from a range of topics across biology, chemistry and medicine assembled to present papers and discuss results. The Novartis Foundation, originally known as the Ciba Foundation, is well known to scientists and clinicians around the world. From WIkipdeia: "Cytogenetics is a branch of genetics that is concerned with the study of the structure and function of the cell, especially the chromosomes. [1] It includes routine analysis of G-banded chromosomes, other cytogenetic banding techniques, as well as molecular cytogenetics such as fluorescent in situ hybridization (FISH) and comparative genomic hybridization (CGH)." From Wikipedia: "William Leo Nyhan (born March 13, 1926) is an American physician who is currently Professor of Pediatrics at UC San Diego School of Medicine in La Jolla, California. He has also held positions at Johns Hopkins University School of Medicine, University of Miami School of Medicine. In addition, Nyhan has served on a number of advisory committees, pediatric advisory boards, and on the board of research foundations. His over 56 years of experience and interests in areas of research span a wide variety of disorders of amino acid metabolism. These include 4-Hydroxybutyric aciduria, 3-methylglutaconyl-Co A hydratase deficiency, multiple carboxylase deficiency, methylmalonic acidemia, and propionic acidemia. He is most-widely known as the co-discoverer of Lesch-Nyhan syndrome. Currently, he is involved in the ongoing development of tandem mass spectrometry for use in newborn screening and research, and is involved in identifying the cause(s) of progressive neurologic disability in MMA after liver transplantation. Nyhan has studied the neuropathology of propionic acidemia (PA) including the manifestation of basal ganglia infarction and the neurologic non-metabolic presentation of PA. Current research includes evaluating the use of dichloroacetate (DCA) in treating a broad range of patients with mitochondrial disease leading to lactic acidemia." Good. Cover has some wear and soiling.

2nd ed. XVII, 605 p. Hardcover. 2nd ed. Versand aus Deutschland / We dispatch from Germany via Air Mail. Einband bestoßen, daher Mängelexemplar gestempelt, sonst sehr guter Zustand. Imperfect copy due to slightly bumped cover, apart from this in very good condition. Stamped. Sprache: Englisch.

Condizione: As New. Unread book in perfect condition.

Condizione: Very Good. Condizione sovraccoperta: None. 754 pages, illustrated throughout with photos and charts in b&w. Green cloth, silver titles to front and spine, no dust jacket. Previous owner's signature on front fly leaf, else a very crisp, clean copy. Record # 401701.

Condizione: New.

Condizione: New.

Condizione: As New. Unread book in perfect condition.

Hardcover. 4to. Several tears and some rubbing to dust jacket, o/wise good condition. 765pp. ISBN 0471652253. 11436.

Condizione: New. pp. 680 1st Edition.

Condizione: New. pp. 680.

Condizione: New. pp. 680.

Hardcover. Condizione: new. Hardcover. This book focuses on clinical presentations that may be caused by inherited metabolic diseases. Its symptom- and system-based approach will help clinicians with and without detailed knowledge of human biochemistry in all specialties to reach a correct diagnosis and institute the optimal treatment program. The book summarizes the central elements of inherited metabolic diseases and describes clearly how to carry out an efficient yet complete diagnostic work-up, thereby guiding the clinician from the presenting symptoms and signs through to effective initial management. After an introduction to the different disorders, the book explains when to consider an inborn metabolic error and which initial tests to order. Core aspects such as structured communication, guidelines, transition, pregnancy, maternal care and how to respond to various medical emergencies are covered. Therapeutic concepts such as dietary treatment are delineated and practical advice provided on the quite different treatment approaches required for individual diseases. An extensive section structured according to organ systems outlines the correct approach in the context of specific symptoms and signs. The value of each of the potential investigations is explained, with precise advice on the interpretation of results. The inclusion of algorithms, tables, lists, and charts facilitates rapid decision making and information retrieval, and the appendices include a helpful guide to differential diagnosis based on clinical and biochemical phenotypes. This new updated edition of Inherited Metabolic Diseases will be an invaluable aid for the busy clinician and an excellent quick reference for metabolic and genetic specialists. This book focuses on clinical presentations that may be caused by inherited metabolic diseases. This new updated edition of Inherited Metabolic Diseases will be an invaluable aid for the busy clinician and an excellent quick reference for metabolic and genetic specialists. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.

Condizione: New.

Condizione: New. pp. 896.

Condizione: New. pp. 896.

Condizione: New. Satisfaction Guaranteed or your money back.

Condizione: New. pp. 896.

Condizione: New.

Condizione: As New. Unread book in perfect condition.

Hardcover. Condizione: new. Hardcover. In a field where even experts may find that years have elapsed since they last encountered a child with a given disorder, it is essential for the clinician to have a comprehensive source of practical and highly illustrated information covering the whole spectrum of metabolic disease to refer to.The content is divided into sections of related disorders, including disorders of amino acid metabolism, lipid storage disorders, and mitochondrial diseases for ease of reference, with an introductory outline where appropriate summarizing the biochemical features and general management issues. Within the sections, each chapter deals with an individual disease, opening with a useful summary of major phenotypic expression including clear and helpful biochemical pathways, identifying for the reader exactly where the defect occurs.Throughout the book, plentiful photographs, often showing extremely rare disorders, are an invaluable aid to diagnosis.Key Features Fully updated to incorporate all new developments in the field Brand new chapters cover methylmalonic aciduria of ACSF3 deficiency, branched chain keto acid dehydrogenase deficiency, serine deficiencies, purine nucleoside phosphorylase deficiency, antiquitin deficiency, and others Excellent and detailed clinical descriptions, with numerous valuable hints and suggestions for management Helpful explanatory algorithms and decision trees, and high-quality illustrative material including biochemical pathways and an unrivaled photographic collection, which enhance clinical applicabilityThe fourth edition of this highly regarded book, authored by two of the foremost authorities in pediatric metabolic medicine, continues to provide incomparable insight into the problems associated with metabolic diseases and remains invaluable to pediatricians, geneticists, and general clinicians worldwide. The fourth edition of this highly regarded book, authored by some of the foremost authorities in pediatric metabolic medicine, provides an invaluable insight into the problems associated with metabolic diseases. Throughout the book, plentiful photographs, often showing extremely rare disorders, are an invaluable aid to diagnosis. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.

Condizione: As New. Unread book in perfect condition.

Condizione: Sehr gut. Zustand: Sehr gut | Seiten: 720 | Sprache: Englisch | Produktart: Bücher | Keine Beschreibung verfügbar.

Gebunden. Condizione: New. William L. Nyhan, MD, PhD, is Professor of Pediatrics and Founding Director of The William L. Nyhan Biochemical Genetics and Metabolomics Laboratory at the University of California, San Diego.Georg F. Hoffmann, MD,

Hardcover. Condizione: Like New. Like New. book.

Book/CD-ROM. Condizione: Brand New. 4th edition. 855 pages. 11.00x8.25x1.75 inches. In Stock.

Taschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - This book focuses on clinical presentations that may be caused by inherited metabolic diseases. Its symptom- and system-based approach will help clinicians with and without detailed knowledge of human biochemistry in all specialties to reach a correct diagnosis and institute the optimal treatment program. The book summarizes the central elements of inherited metabolic diseases and describes clearly how to carry out an efficient yet complete diagnostic work-up, thereby guiding the clinician from the presenting symptoms and signs through to effective initial management. After an introduction to the different disorders, the book explains when to consider an inborn metabolic error and which initial tests to order. Core aspects such as structured communication, guidelines, transition, pregnancy, maternal care and how to respond to various medical emergencies are covered. Therapeutic concepts such as dietary treatment are delineated and practical advice provided on the quite different treatment approaches required for individual diseases. An extensive section structured according to organ systems outlines the correct approach in the context of specific symptoms and signs. The value of each of the potential investigations is explained, with precise advice on the interpretation of results. The inclusion of algorithms, tables, lists, and charts facilitates rapid decision making and information retrieval, and the appendices include a helpful guide to differential diagnosis based on clinical and biochemical phenotypes. This new updated edition of Inherited Metabolic Diseases will be an invaluable aid for the busy clinician and an excellent quick reference for metabolic and genetic specialists.