Author

May, Eliot M.

Litwin, S. Bert

Tweddell, J.S.

Jaquiss, R.B.D.

Place of Publication

Milwaukee, WI

Publication Date

2005

Physical Description

Spiralbound, 93 pages

Subject

UBC MD Undergrad

Surgery

Heart Diseases-Surgery. Coronary Surgery

Abstract

Table of contents: Anomalous origin of the left coronary artery; Aortic valve replacement with ventricular septal extension. The Kono procedure; Aortic valve replacement with pulmonary autograft. The Ross procedure; Aortic stenosis; Subaortic stenosis; Critical aortic stenosis; Pupravalvar aortic stenosis; Aortopulmonary window; Arterial switch procedure; Atrial septal defect, Secundum, Primum, Sinus venosus; Atrioventricular canal; Atrioventricular septal defect; A-V canal; Blalock-Taussig shunt, central shunt procedures; Bidirectional Glenn shunt; Central shunt; Coarctation of the aorta; Corrected transposition of the great vessels; Critical aortic stenosis; Damus-Kaye-Stansel procedure; Double aortic arch; Double outlet right ventricle; Ebstein's malformation of the tricuspid valve; Endocardial cushion defect; Fontan procedure; Glenn shunt procedure; Hypoplastic left heart syndrome; Interrupted aortic arch; Jatene arterial switch; Konno procedure; L-Transposition of the vessels; Normal heart anatomy; Norwood procedure; Patent ductus arteriosus; Partial anomalous pulmonary venous connection, high SVC; Primum atrial septal defect; Pulmonary stenosis; Pulmonary stresia with ventricular septal defect; Pulmonary stresia with intact ventricular septum; Pulmonary artery band; Rastelli procedure; Ross procedure; Secundum atrial septal defect; Shunts; Single ventricle; Sinus venosus atrial septal defect; Subaortic stenosis; Switch procedure; Tetralogy of Fallot; Total anomalous pulmonary venous return; Supracardiac; Intracardiac; Infracardiac; Tricuspic atresia; Truncus arteriosus; Truncus arteriosus with interrupted aortic arch; Vascular ring; Ventricular septal defect.

ISBN

1930602277

Language

English

Material Type

Book

Call Number

REF FD 230 MAY 2005

Copies

Author

Reece, E. Albert

Hobbins, John C. (Eds).

Edition

3rd Ed.

Place of Publication

Malden, MA

Publisher

Blackwell Publishing Ltd.

Publication Date

2007

Physical Description

Paperback: 168 pages

Subject

Women's Health. Gynecology

Pregnancy/Childbirth. Obstetrics

UBC MD Undergrad

Abstract

Text covers the biology, pathology, and clinical management of disorders affecting the fetus and the mother with illustrations highlighting essential diagnostic features and treatment procedures.

ISBN

978-1-4051-3216-9

Language

English

Material Type

Book

Call Number

REF GG 100 REE 2007a

Copies

Author

Leung, Donald, Y.M.

Sampson, Hugh A.

Geha, Raif S.

Szefler, Stanley J.

Place of Publication

[St. Louis, MO]

Publisher

Mosby, Inc.

Publication Date

2003

Physical Description

Hardcover: 832 pages

Subject

Allergies

Immune System/Immune System Diseases-Symptoms

Drug Allergies

Food Allergies

Asthma

Skin. Skin Diseases

UBC MD Undergrad

Abstract

Contents: Epidemiology of allergic diseases; Natural history of allergic diseases and asthma; Genetics of allergic disease and asthma; Regulation and biology of immunoglobulin E; Inflammatory effector cells/cell migration; Developing immune system and allergy; Approach to the child wtih recurrent infections; Antibody deficiency; T-Cell immunodeficiencies; Pediatric human immunodeficiency virus infection; Complement deficiencies; White blood cell defects; Rheumatic diseases of childhood: Therapeutic principles; Autoimmune diseases; Autoimmune lymphoprolifitive syndrome; Epstein-Barr virus infections; Intravenous immune serum globulin therapy; Bone marrow transplantation; Immunizations; Gene therapy and allergy; Stem cell therapeutics: An overview; Laboratory (in vitro) analyses; In vivo testing for immunoglobulin E-mediated sensitivity; Outdoor allergens; Indoor allergens; Environmental control; Immunotherapy for allergic disease; Allergic rhinitis; Otitis media; Sinusitis; Chronic cough; Immunology of the asthmatic response; Guidelines for treatment of asthma; Functional assessment of asthma; Infections and asthma; Special considerations for infants and young children; Inner city asthma; Asthma in older children; Asthma education programs for children; Asthma and the athlete; Refractory childhood asthma: New insight into the pathogenesis, diagnosis, and management; Promoting adherence and effective self-management in patients with asthma; New directions in asthma management; Mucosal immunity: An overview; Evaluation of food allergy; Approach to feeding problems in the infant and young child; Prevention and natural history of food allergy; Enterocolitis, proctocolitis, and gastroenteritis, and proctocolitis; Food allergy, respiratory disease, and anaphylaxis; Atopic dermatitis and food hypersensitivity; Management of food allergy; Atopic dermatitis; Urticaria and angiodema; Contact dermatitis; Allergic and immunologic eye disease; Drug allergy; Latex allergy; Insect sting anaphylaxis; General treatment of anaphylasis.

ISBN

0323018025

Language

English

Material Type

Book

Call Number

REF FF 400 LEU 2003

Copies

Author

Martin, Richard J

Fanaroff, Avroy A

Walsh, Michele C

Edition

8th ed.

Place of Publication

Philadelphia, PA

Publisher

Mosby Elsevier

Publication Date

2006

Physical Description

Hardcover: pages 1 to 758

Subject

Infants (Newborn)-Diseases

Fetal Monitoring

UBC MD Undergrad

Fetal Surgery

Pregnancy/Childbirth. Obstetrics

Abstract

Updated to reflect all of the recent sweeping developments in neonatal-perinatal medicine, this 2-volume reference representing a wide range of subspecialties, offers sound practical advice based upon the best available evidence. Volume One focuses on the field of neonatal-perinatal medicine, pregnancy disorders and their impact on the fetus, and delivery room care. Volume Two concentrates on development and disorders of organ systems.

Notes

Audience

Neonatologists, Perinatologists, Neonatal Nurses

ISBN

13978032302966-7

Language

English

Material Type

Book

Call Number

REF GH 700 MAR 2006 (v.1)

Copies

Author

Martin, Richard J

Fanaroff, Avroy A

Walsh, Michele C

Edition

8th ed.

Place of Publication

Philadelphia, PA

Publisher

Mosby Elsevier

Publication Date

2006

Physical Description

Hardcover: pages 759 to 1820

Subject

Infants (Newborn)-Diseases

Pregnancy/Childbirth. Obstetrics

Fetal Monitoring

UBC MD Undergrad

Abstract

Updated to reflect all of the recent sweeping developments in neonatal-perinatal medicine, this 2-volume reference representing a wide range of subspecialties, offers sound practical advice based upon the best available evidence. Volume One focuses on the field of neonatal-perinatal medicine, pregnancy disorders and their impact on the fetus, and delivery room care. Volume Two concentrates on development and disorders of organ systems.

ISBN

13978032302966-7

Language

English

Material Type

Book

Call Number

REF GH 700 MAR 2006 (v.2)

Copies

Author

Jones, Kenneth Lyons

Edition

6th ed.

Place of Publication

Philadelphia, PA

Publisher

Elsevier Saunders

Publication Date

2006

Physical Description

Hardcover: 954 p.

Subject

Medical Encyclopedias

Birth Defects. Congenital Abnormalities

UBC MD Undergrad

Abstract

Table of Contents

1. Recognizable Patterns of Malformation

A. Chromosomal Abnormality Syndromes

Down Syndrome--Trisomy 18 Syndrome --Trisomy 13 Syndrome --Trisomy 8 Syndrome Trisomy 9 --Mosaic Syndrome --Triploidy Syndrome and Diploid/Triploid Mixoploidy Syndrome --Deletion 3p Syndrome Duplication 3q Syndrome Deletion 4p Syndrome --Deletion 4q Syndrome --Deletion 5p Syndrome --Deletion 9p Syndrome --Duplication 10q Syndrome --Aniridia–Wilms Tumor Association --Deletion 11q Syndrome --Deletion 13q Syndrome --Duplication 15q Syndrome-- Deletion 18p Syndrome-- Deletion 18q Syndrome --Cat-Eye Syndrome --XYY Syndrome --XXY Syndrome, Klinefelter Syndrome XXXY and XXXXY Syndromes XXX and --XXXX Syndromes XXXXX Syndrome --45X Syndrome

--

B. Very Small Stature, Not Skeletal Dysplasia

Brachmann–De Lange Syndrome --Rubinstein-Taybi Syndrome --Russell-Silver Syndrome --Short Syndrome --3-M Syndrome --Mulibrey Nanism Syndrome --Dubowitz Syndrome --Bloom Syndrome --Johanson-Blizzard Syndrome --Seckel Syndrome Hallermann-Streiff Syndrome

C. Moderate Short Stature, Facial, +/- Genital

Smith-Lemli-Opitz Syndrome --Kabuki Syndrome --Williams Syndrome Noonan Syndrome --Costello Syndrome Cardio-Facio-Cutaneous (CFC)Syndrome --Aarskog Syndrome --Robinow Syndrome --Opitz G/BBB Syndrome --Floating-Harbor Syndrome

D. Senile-Like Appearance

Progeria Syndrome Wiedemann-Rautenstrauch Syndrome --Werner Syndrome --Cockayne Syndrome Rothmund-Thomson Syndrome

E. Early Overgrowth with Associated Defects

Fragile X Syndrome --Sotos Syndrome --Weaver Syndrome --Marshall-Smith Syndrome --Beckwith-Wiedemann Syndrome --Simpson-Golabi-Behmel Syndrome

F. Unusual Brain and/or Neuromuscular Findings With Associated Defects

Amyoplasia Congenita Disruptive Sequence Distal Arthrogryposis Syndrome, Type 1 -- Pena-Shokeir Phenotype --Cerebro-Oculo-Facio-Skeletal (COFS) Syndrome --Lethal Multiple Pterygium Syndrome --Neu-Laxova Syndrome --Restrictive Dermopathy Meckel-Gruber Syndrome --Pallister-Hall Syndrome --X-Linked Hydrocephalus Spectrum Hydrolethalus Syndrome --Walker-Warburg Syndrome Miller-Dieker Syndrome Smith-Magenis Syndrome Ataxia-Telangiectasia Syndrome Menkes Syndrome 22q13 Deletion Syndrome --Angelman Syndrome Prader-Willi Syndrome --Cohen Syndrome --Killian/Teschler-Nicola Syndrome 1p36 --Deletion Syndrome --Fryns Syndrome Zellweger Syndrome --Freeman-Sheldon Syndrome --Myotonic Dystrophy Syndrome --Schwartz-Jampel Syndrome --Marden-Walker Syndrome --Schinzel-Giedion Syndrome --Acrocallosal Syndrome --3C Syndrome --Hecht Syndrome

G. Facial Defects As Major Feature

Moebius Sequence --Blepharophimosis-Ptosis-Epicanthus Inversus Synrome --Robin Sequence --Cleft Lip Sequence --Van Der Woude Syndrome Frontonasal Dysplasia Sequence Fraser Syndrome --Melnick-Fraser Syndrome --Branchio-Oculo-Facial Syndrome --Charge Syndrome --Waardenburg Syndrome, Types I and II-- Treacher Collins Syndrome --Marshall Syndrome --Cervico-Oculo-Acoustic Syndrome

H. Facial-Limb Defects as Major Feature

Miller Syndrome --Nager Syndrome --Townes-Brocks Syndrome --Oral-Facial-Digital Syndrome --Mohr Syndrome --Deletion 22q11.2 --Oculodentodigital Syndrome --Lenz Microphthalmia Syndrome --Oto-Palato-Digital Syndrome, Type I --Oto-Palato-Digital Syndrome, Type II --Coffin-Lowry Syndrome X-Linked ?--Thalassemia/Mental Retardation (ATR-X) Syndrome --FG Syndrome Stickler Syndrome --Catel-Manzke Syndrome --Langer-Giedion Syndrome --Tricho-Rhino-Phalangeal Syndrome, Type I --Ectrodactyly–Ectodermal Dysplasia–Clefting Syndrome --Hay-Wells Syndrome Of Ectodermal Dysplasia --Roberts Syndrome

I. Limb Defect as Major Feature

Grebe Syndrome --Poland Sequence --Ulnar-Mammary Syndrome --Popliteal Pterygium Syndrome --Escobar Syndrome --Child Syndrome --Femoral Hypoplasia-Unusual Facies Syndrome --Tibial Aplasia-Ectrodactyly Syndrome --Adams-Oliver Syndrome --Holt-Oram Syndrome --Levy-Hollister Syndrome --Fanconi Pancytopenia Syndrome --Radial Aplasia–Thrombocytopenia Syndrome --Aase Syndrome

J. Osteochondrodysplasias

Achondrogenesis, Types IA And IB --Type II Achondrogenesis-Hypochondrogenesis --Fibrochondrogenesis Atelosteogenesis, Type I --Short Rib–Polydactyly Syndrome, Type I (Saldino- Noonan Type)-- Short Rib–Polydactyly Syndrome, Type II (Majewski Type) --Thanatophoric Dysplasia --Jeune Thoracic Dystrophy --Campomelic Dysplasia Achondroplasia Hypochondroplasia --Pseudoachondroplasia Acromesomelic-- Dysplasia Spondyloepiphyseal --Dysplasia Congenita Kniest Dysplasia-- Dyggve-Melchior-Clausen Syndrome --Spondylometaphyseal Dysplasia, Kozlowski Type Metatropic Dysplasia --Geleophysic Dysplasia --Chondroectodermal Dysplasia --Diastrophic Dysplasia X-Linked --Recessive Spondyloepiphyseal --Dysplasia Tarda Multiple Epiphyseal-- Dysplasia Metaphyseal Dysplasia, --Schmid Type Metaphyseal Dysplasia, --Mckusick Type Metaphyseal Dysplasia,-- Jansen Type Shwachman-Diamond Syndrome Chondrodysplasia Punctata, --X-Linked Dominant Type Autosomal Recessive --Chondrodysplasia Punctata Hypophosphatasia --Hajdu-Cheney Syndrome --Craniometaphyseal Dysplasia --Frontometaphyseal Dysplasia

K. Osteochondrodysplasia with Osteopetrosis

Osteopetrosis: Autosomal Recessive—Lethal --Sclerosteosis --Lenz-Majewski --Hyperostosis Syndrome Pyknodysostosis --Cleidocranial Dysostosis --Yunis-Varon Syndrome

L. Craniosynostosis Syndromes

Saethre-Chotzen Syndrome --Pfeiffer Syndrome --Apert Syndrome --Crouzon Syndrome FGFR3- Associated Coronal Synostosis Syndrome --Craniofrontonasal Dysplasia --Carpenter Syndrome --Greig Cephalopolysyndactyly Syndrome --Antley-Bixler Syndrome Baller-Gerold Syndrome

M. Other Skeletal Dysplasias

Multiple Synostosis Syndrome --Spondylocarpotarsal Synostosis Syndrome --Larsen Syndrome --Multiple Exostoses Syndrome --Nail-Patella Syndrome --Meier-Gorlin Syndrome --Leri-Weill Dyschondrosteosis --Langer Mesomelic Dysplasia --Acrodysostosis --Albright Hereditary Osteodystrophy

N. Storage Disorders

Generalized Gangliosidosis Syndrome, Type I (Severe Infantile Type) --Leroy I-Cell Syndrome --Pseudo-Hurler Polydystrophy Syndrome --Hurler Syndrome --Scheie Syndrome --Hurler-Scheie Syndrome --Hunter Syndrome --Sanfilippo Syndrome --Morquio Syndrome --Maroteaux-Lamy Mucopolysaccharidosis Syndrome (Mild, Moderate, and Severe Types) Mucopolysaccharidosis VII1. *-*--

O. Connective Tissue Disorders

Marfan Syndrome-- Beals Syndrome --Shprintzen-Goldberg Syndrome --Ehlers-Danlos Syndrome --Osteogenesis Imperfecta Syndrome, Type I --Osteogenesis Imperfecta Syndrome, Type II --Fibrodysplasia Ossificans Progressiva Syndrome

P. Hamartoses

Sturge-Weber Sequence --Neurocutaneous Melanosis Sequence --Linear Sebaceous Nevus Sequence --Incontinentia Pigmenti Syndrome --Hypomelanosis of Ito Tuberous Sclerosis Syndrome --Neurofibromatosis Syndrome --McCune-Albright Syndrome-- Klippel-Trenaunay Syndrome --Proteus Syndrome --Encephalocraniocutaneous Lipomatosis Maffucci Syndrome-- Peutz-Jeghers Syndrome --Bannayan-Riley-Ruvalcaba Syndrome --Hereditary Hemorragic Telangiectasia-- Multiple Endocrine Neoplasia, Type 2b --Gorlin Syndrome --Multiple Lentigines Syndrome --Goltz Syndrome Microphthalmia–Linear --Skin Defects Syndrome

Q. Ectodermal Dysplasias

Hypohidrotic Ectodermal Dysplasia Syndrome --Rapp-Hodgkin Ectodermal Dysplasia Syndrome --Tricho-Dento-Osseous Syndrome --Clouston Syndrome --GAPO Syndrome --Pachyonychia Congenita Syndrome --Xeroderma Pigmentosa Syndrome --Senter-Kid Syndrome

R. Enviornmental Agents

Fetal Alcohol Syndrome --Fetal Hydantoin Syndrome --Fetal Valproate Syndrome --Fetal Warfarin Syndrome --Fetal Aminopterin/Methotrexate --Syndrome Retinoic Acid Embryopathy --Fetal Varicella Syndrome --Hyperthermia-Induced Spectrum of Defects

S. Miscellaneous Syndromes

Coffin-Siris Syndrome --Börjeson-Forssman-Lehmann Syndrome --Alagille Syndrome-- Melnick-Needles Syndrome --Bardet-Biedl Syndrome --Mckusick-Kaufman Syndrome --Rieger Syndrome --Peters' Plus Syndrome --Toriello-Carey Syndrome --Mowat-Wilson Syndrome --Cerebro-Costo-Mandibular Syndrome --Jarcho-Levin Syndrome --Mandibuloacral Dysplasia --Berardinelli Lipodystrophy Syndrome-- Distichiasis-Lymphedema Syndrome

T. Miscellaneous Sequences

Laterality Sequences --Holoprosencephaly Sequence --Meningomyelocele, Anencephaly, Iniencephaly Sequences Occult Spinal Dysraphism Sequence Septo-Optic --Dysplasia Sequence Athyrotic --Hypothyroidism Sequence --DiGeorge Sequence --Klippel-Feil Sequence Early Urethral Obstruction Sequence-- Exstrophy of Bladder Sequence --Exstrophy of Cloaca Sequence --Urorectal Septum Malformation --Sequence Oligohydramnios Sequence --Sirenomelia Sequence-- Caudal Dysplasia Sequence-- Amnion Rupture Sequence --Limb–Body Wall Complex

U. Spectra Of Defects

Oculo-Auriculo-Vertebral Spectrum --Oromandibular-Limb Hypogenesis Spectrum --Congenital Microgastria-Limb Reduction Complex --Sternal Malformation-Vascular Dysplasia --Spectrum Monozygotic (MZ) Twinning And Structural Defects - General

V. Miscellaneous Associations

VATER Association MURCS Association

2. Approaches to Categorical Problems of Growth Deficiency, Mental Deficiency, Arthrogryposis, Ambiguous External Genitalia 3. Morphogenesis and Dysmorphogenesis 4. Genetics, Genetic Counseling, and Prevention 5. Minor Anomalies as Clues to More Serious Problems and Toward the Recognition of Malformation Syndromes 6. Normal Standards

Notes

New to this Edition

1,000 new full-color figures and photographs.

Includes updates for every disorder, with extensive new information on the molecular basis of malformations as well as new clinical information for many disorders.

Covers 16 additional commonly seen disorders, including Deletion 1p36 syndrome * Deleletion 22q13 syndrome * Meier-Gorlin Syndrome * Short Syndrome * 3-C Syndrome * GAPO Syndrome * Lenz Microphthalmia Syndrome * Muenke Craniosynostosis * Torriello-Carey Syndrome * Mandibulo-Acral Syndrome * Mowat-Wilson Syndrome * Ulnar-Mammary Syndrome * Kaufman-McKusick Syndrome * Smith-Maginess Syndrome * Wiedeman-Rautenstrauch Syndrome * and Shprintzen-Golberg Syndrome.

Presents a wealth of new Growth Charts, plus complete revisions to existing Growth Charts.

ISBN

978-0-7216-0615-6

Language

English

Material Type

Book

Call Number

REF AB 20 JON 2006

Copies

Author

Holmes, Gregory

Moshe, Solomon

Jones, Royden H. Jr.

Place of Publication

Philadelphia, PA

Publisher

Butterworth-Heinemann

Publication Date

c2006

Physical Description

Hardcover: 859 p.

Subject

Children's Health. Pediatrics

UBC MD Undergrad

Abstract

Table of Contents

SECTION I

Basic Principles and Maturational Change

1. Basic Principles of Electroencephalography

2. Electroencephalography of the Newborn: Normal Features

3. Visual Analysis of the Neonatal Electroencephalogram

4. Normal Development of the Electroencephalogram: Infancy Through Adolescence

5. Visual Analysis of the Pediatric Electroencephalogram

6. Clinical Neurophysiology of the Motor Unit in Infants and Children

7. Maturational Changes vis-à-vis Neurophysiology Markers and the Development of Peripheral Nerves

8. Somatosensory Evoked Potentials in Pediatrics - Normal

9. Brainstem Auditory Evoked Potentials in Pediatrics - Normal

10. Visual Evoked Potentials in Pediatrics - Normal

--

SECTION II

Disorders of Cerebral Function

11. Age-Specific Seizure Disorders

12. Neurophysiology of Language and *Behavioral Disorders in Children

13. Neonatal *Electroencephalography: Abnormal Features

14. Drug Effects on the Human Electroencephalogram

15. Electroencephalography and Structural Disease of the Brain

16. Manifestations of Metabolic, Toxic, and Degenerative Diseases

17. Infectious Diseases

18. Head Trauma

19. Childhood Sleep-Wake Disorders

20. The Diagnosis of Brain Death

21. Ambulatory Electroencephalography

22. Electroencephalography in Evaluation for Epilepsy Surgery in Children

23. Long-Term Electroencephalogram and Video Monitoring

24. Intraoperative Neurophysiologic Monitoring Using Evoked Potentials

Abnormal Evoked Potentials

25. Somatosensory Evoked Potentials in Pediatrics - Abnormal

26. Brainstem Auditory Evoked Potentials in Pediatrics - Abnormal

27. Visual Evoked Potentials in Pediatrics - Abnormal

SECTION III

Neuromuscular Disorders

28. The Floppy Infant

29. Facial and Bulbar Weakness

30. Spinal Muscular Atrophies and Other Disorders of the Anterior Horn Cell

31. Plexopathies and Nerve Root Lesions

32. Focal Neuropathies in Children

33. Clinical Neurophysiology of Pediatric Polyneuropathies

34. Autonomic Testing in Childhood

35. Neuromuscular Transmission Defects

36. Muscle Disorders in Children: Neurophysiologic Contributions to Diagnosis and Management

37. Neuromuscular Problems of the Critically Ill Neonate, Child, and Adolescent

38. The Interrelation of DNA Analysis with Clinical Neurophysiology in the Diagnosis of Chronic Neuromuscular Disorder of Childhood

SECTION IV

Other Neurophysiologic Techniques

39. Magnetoencephalography (MEG)

40. Transcranial Magnetic *Stimulation: An Overview

41. Sphincter Dysfunction

Index

ISBN

0-7506-7251-x

Language

English

Material Type

Book

Call Number

REF GK 100 HOL 2006

Copies

Author

Wynbrandt, James.

Ludman, Mark D.

Edition

3rd ed.

Place of Publication

New York, NY

Publisher

Facts On File (Infobase)

Publication Date

2008

Physical Description

Hardcover, 682 p.

Subject

Genetics/Genetic Disorders-Encyclopedias

Genetic Disorders

Birth Defects. Congenital Abnormalities

Children's Health-Encyclopedias

UBC MD Undergrad

Abstract

Topics cover everything from the most basic genetic concepts to the latest screening and diagnostic techniques. Coverage includes:

autism, cancer, chromosomal abnormalities, ethics, genetic counseling, heart defects, muscular dystrophy, neural tube defects, phenylketonuria, spina bifida, and much more.

ISBN

9780816063963

Language

English

Material Type

Book

Call Number

REF GI 20 WYN 2008

Copies

Author

Rankin, Sally H.

Stallings, Karen Duffy

London, Fran

Edition

5th ed.

Place of Publication

Philadelphia, PA

Publisher

Lippincott Williams & Wilkins

Publication Date

2005

Physical Description

Paperback, 368 p.

Subject

Patient Education

Patient-Health Care Practitioner Relations. Doctor-Patient Relations.

Medical Directories. Resource Guides

UBC MD Undergrad

Abstract

This practical text/reference provides theory-based approaches to teaching patients of all ages and their families in a variety of healthcare settings.--Table of Contents: Principles of Contemporary Patient Education;

Patient Education in Nursing Practice;

Health Promotion: Models and Applications to Patient Education;

Integration of Cultural Systems and Beliefs;

Educational Theories for Teaching and Motivating Patients;

Staff Development in Patient Education: Meeting JCAHO Standards and Beyond;

Community Health Promotion: Assessment and Intervention;

Application of the Principles in Nursing Practice;

Assessment for Patient Education;

Planning: Shared Goals for Patient Education;

Educational Interventions for Patients and Families;

Patient Education Resources on the Internet;

Evaluating Patient Education Outcomes;

Case Management and Patient Education;

Community-Based Patient Education Programs

ISBN

0781748496

Language

English

Material Type

Book

Call Number

REF IA 850 RAN 2005

Copies

Author

Sperling, Mark A.

Edition

3rd ed.

Publisher

Saunders Elsevier

Publication Date

2008

Physical Description

Hardcover: 867 p.

Subject

UBC MD Undergrad

Endocrine System. Endocrine Diseases. Endocrinology

Language

English

Material Type

Book

Call Number

REF FL 250 SPE 2008

Copies

Author

Guyton, Arthur C.

Hall, John E.

Edition

11th ed.

Place of Publication

Philadelphia, PA

Publisher

Elsevier Saunders

Publication Date

2006

Physical Description

Hardcover: 1066 p.

Subject

Physiology

UBC MD Undergrad

Abstract

This textbook covers all of the major systems in the human body, while emphasizing system interaction, homeostasis, and pathophysiology.

ISBN

9780721602400

Language

English

Material Type

Book

Call Number

REF AC 300 GUY 2006

Copies

Author

Zipes, Douglas P.

Libby, Peter

Bonow, Robert O.

Braunwald, Eugene

Edition

7th ed

Place of Publication

Philadelphia, PA

Publisher

Elsevier Saunders

Publication Date

2005

Physical Description

Hardcover: 1102 p.

Subject

Cardiovascular System-Anatomy/Physiology

Heart/Heart Diseases. Cardiology

UBC MD Undergrad

Abstract

Volume 1 of this 7th edition contains 36 new chapters and full-color figures and photographs. Compared with the rather limited color-plate photographs in the sixth edition, the color photographs, figures, and tables in each chapter significantly enhance the new text. Informative chapters on the foundations of cardiovascular medicine remain, including detailed discussions of history taking, physical examination, and electrocardiography, topics often overshadowed in an era of rapidly progressive medical technology.

ISBN

9789997637383

Language

English

Material Type

Book

Call Number

REF FD 200 ZIP 2005 v.1

Copies

Author

Zipes, Douglas P.

Libby, Peter

Bonow, Robert O.

Braunwald, Eugene

Edition

7th ed

Place of Publication

Philadelphia, PA

Publisher

Elsevier Saunders

Publication Date

2005

Physical Description

Hardcover: 2183 p.

Subject

Cardiovascular System/Cardiovascular System Diseases

Heart/Heart Diseases. Cardiology

UBC MD Undergrad

Abstract

Volume 2 of this 7th edition contains 36 new chapters and full-color figures and photographs. Compared with the rather limited color-plate photographs in the sixth edition, the color photographs, figures, and tables in each chapter significantly enhance the new text. Informative chapters on the foundations of cardiovascular medicine remain, including detailed discussions of history taking, physical examination, and electrocardiography, topics often overshadowed in an era of rapidly progressive medical technology.

ISBN

9789997637390

Language

English

Material Type

Book

Call Number

REF FD 200 ZIP 2005 v.2

Copies

Author

Nussbaum, Robert L.

McInnes, Roderick R.

Willard, Huntington F.

Hamosh, Ada

Edition

7th ed.

Place of Publication

Philadelphia, PA

Publisher

Saunders Elsevier

Publication Date

2007

Physical Description

Softcover: 566 p.

Subject

Genetics

UBC MD Undergrad

Abstract

This text integrates the classic principles of human genetics with modern molecular genetics to help you diagnose and manage a wide range of genetic disorders.

ISBN

97814116030805

Language

English

Material Type

Book

Call Number

REF GI 200 NUS 2007

Copies

Author

Woodhead, Jerold C.

Edition

2nd ed.

Place of Publication

Philadelphia, PA

Publisher

Mosby Elsevier

Publication Date

2008

Physical Description

Softcover: 721 p.

Subject

Children's Health. Pediatrics

UBC MD Undergrad

Abstract

This guide offers practical guidance on the causes, clinical evaluation, and treatment of common pediatric conditions - knowledge that every student can and should master.

ISBN

9780323043335

Language

English

Material Type

Book

Call Number

REF GK 100 WOO 2008

Copies

Author

Dipchand, Anne

Friedman, Jeremy

Bismilla, Zia

Gupta, Sumit

Lam, Catherine

Edition

11th ed.

Place of Publication

[Toronto, ON]

Publisher

Saunders Elsevier

Publication Date

2009

Physical Description

Softcover: 996 p.

Subject

Children's Health. Pediatrics

UBC MD Undergrad

Abstract

This handbook offers diagnostic and therapeutic approaches to pediatric clinical problems. Representing over 50 years of expert guidance from one of the world's leading pediatric health science centers, this practical reference book provides succinct, easily accesible, and evidence-based answers for those caring for pediatric patients.

ISBN

9781897422045

Language

English

Material Type

Book

Call Number

REF GK 100 DIP 2009

Copies

Author

Hall, Judith G.

Allanson, Judith E.

Gripp, Karen W.

Slavotinek, Anne M.

Edition

2nd ed.

Place of Publication

[Toronto, ON]

Publisher

Oxford University Press

Publication Date

2007

Physical Description

Softcover: 489 p.

Subject

Genetics

Diagnostic Tests/Procedures. Physical Diagnosis

UBC MD Undergrad

Abstract

This book provides a comprehensive collection of data on a variety of physical measurements for use in the evaluation of children and adults with dysmorphic features, structural anomalies, and genetic syndromes. It has been written as a practical manual that can be carried to the ward or in the field for evaluating individuals with unusual physical features.

ISBN

9780195301496

Language

English

Material Type

Book

Call Number

REF FA 140 HAL 2007

Copies

Author

Dugani, Sagar (ed.)

Lam, Danica (ed.)

Edition

25th ed.

Place of Publication

[Toronto, ON]

Publisher

Toronto Notes for Medical Students, Inc.

Publication Date

2009

Physical Description

Softcover: [alternative paging]

Subject

Medical Directories. Resource Guides

UBC MD Undergrad

Abstract

The classic Canadian compilation of notes to assist medical students in studying for the MCCQE I and USMLE II exams.

ISBN

9780980939705

Language

English

Material Type

Book

Call Number

REF AB 22 TOR 2009

Copies

Author

Hebert, Philip C.

Edition

2nd edition

Place of Publication

Oxford, UK

Publisher

Oxford University Press

Publication Date

2008

Physical Description

Paperback: p 290.

Subject

Medical Ethics

Physicians

UBC MD Undergrad

Abstract

This book offers healthcare trainees and practitioners alike a comprehensive, usable guide to biomedical ethics today. This text works through questions of moral principles relevant to a diverse and growing number of healthcare professionals. Rather than focus on theory, the text takes an applied, case-study based approach that makes complex ethical issues real and relatable. Updates to this edition include new discussions on reproductive technology and reproductive choice, medical professionalism, and managing error. Also new are thoroughly updated references, expanded theoretical coverage, and case studies that reflect team ethics. This is an ideal text for second-and third-year one-semester ethics courses offered in medical schools, health sciences departments, and nursing programs.

ISBN

978-0-19-542841-4

Language

English

Material Type

Book

Call Number

REF IC 100 HEB 2008

Copies

Author

Murray, Robert K.

Bender, David A.

Botham, Kathleen M.

Kennelly, Peter J.

Rodwell, Victor W.

Weil, P. Anthony

Edition

28th Ed.

Place of Publication

New York, NY

Publisher

McGraw-Hill Companies, Inc.

Publication Date

2009

Physical Description

Softcover: 693 pages

Subject

Biochemistry

UBC MD Undergrad

Abstract

Comprehensive, concise, and up-to-date this resource shows the link between biochemistry and the molecular basis of health and disease and can be used for USMLE review. This edition includes a conversion to full-color artwork. NEW to this edition: Full-color presentation, including 600+ illustrations; Every chapter opens with a Summary of the Biomedical Importance and concludes with a Summary reviewing the topics covered; Two all-new chapters: "Free Radicals and Antioxidant Nutrients" and "Biochemical Case Histories" which offers an extensive presentation of 16 clinical conditions; A new appendix containing basic clinical laboratory results and an updated one with a list of important websites and online journals; NEW or updated coverage of important topics including the Human Genome Project and computer-aided drug delivery.

ISBN

978-0-07-162591-3

Language

English

Material Type

Book

Call Number

REF AB 50 MUR 2009

Copies