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

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

Ness, Bryan D. (ed.)

Knight, Jeffrey A. (ed.)

Edition

Revised Edition

Place of Publication

Pasadena, Ca.

Publisher

Salem Press, Inc.

Publication Date

2004

Physical Description

Hardcover: 440 p.

Subject

Genetics

Genetics/Genetic Disorders-Encyclopedias

UBC MD Undergrad

Abstract

This encyclopedia provides a thorough yet accessible overview of genetics. This revised edition adds 64 new overview essays to the 172 original entries.

ISBN

1587651491

Language

English

Material Type

Book

Call Number

REF GI 20 NES 2004 v.1

Copies

Author

Ness, Bryan D. (ed.)

Knight, Jeffrey A. (ed.)

Edition

Revised Edition

Place of Publication

Pasadena, Ca.

Publisher

Salem Press, Inc.

Publication Date

2004

Physical Description

Hardcover: 863 p.

Subject

Genetics

Genetics/Genetic Disorders-Encyclopedias

UBC MD Undergrad

Abstract

This encyclopedia provides a thorough yet accessible overview of genetics. This revised edition adds 64 new overview essays to the 172 original entries.

ISBN

1587651491

Language

English

Material Type

Book

Call Number

REF GI 20 NES 2004 v.2

Copies

Author

Sadler, T.W.

Edition

9th Ed.

Place of Publication

Philadelphia, PA

Publisher

Lippincott Williams & Wilkins

Publication Date

2004

Physical Description

Softcover; 534 pages; 1 CD

Subject

Embryology

UBC MD Undergrad

Abstract

This text covers aspects of embryology that would be of interest to medical students and their instructors. It is structured by chronology and then by system. Also included is Simbryo, an electronic supplement consisting of Flash animation showing the evolution of early embryonic development.

ISBN

0781743109

Language

English

Material Type

Book

Call Number

REF AB 55 SAD 2004

Copies

Author

Moore, Keith L.

Persaud, T.V.N.

Edition

8th Ed.

Place of Publication

Philadelphia, PA

Publisher

Saunders Elsevier

Publication Date

2008

Physical Description

Softcover: 522 pages

Subject

Embryology

UBC MD Undergrad

Abstract

This text examines all aspects of human development, emphasizing both basic concepts and relevant clinical problems. The book presents a week-by-week and stage-by-stage view of how fetal organs and systems develop, why and when birth defects occur, and what roles the placenta and fetal membranes play in development.

ISBN

9781416037064

Language

English

Material Type

Book

Call Number

REF AB 55 MOO 2008

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

Rimoin, David L.

Pyeritz, Reed E.

Korf, Bruce R. (Eds).

Edition

5th Ed.

Place of Publication

Philadelphia, PA

Publisher

Churchill Livingstone Elsevier

Publication Date

2007

Physical Description

Hardcover: 1082 pages

Subject

Genetics

UBC MD Undergrad

Abstract

This 3 volume text emphasizes application as well as the theory of medical genetics across the full spectrum of inherited disorders. Get expert clinical advice and guidance from over 250 of the world's most trusted authorities in medical genetics.

Volume 1 covers: Basic principles; General principles; Approaches to clinical problems; Approaches to specific disorders.

ISBN

9780443068706

Language

English

Material Type

Book

Call Number

REF GI 200 RIM 2007 VOL 1

Copies

Author

Rimoin, David L.

Pyeritz, Reed E.

Korf, Bruce R. (Eds).

Edition

5th Ed.

Place of Publication

Philadelphia, PA

Publisher

Churchill Livingstone Elsevier

Publication Date

2007

Physical Description

Hardcover: pages: 1083-2284

Subject

Genetics

UBC MD Undergrad

Abstract

This 3 volume text emphasizes application as well as the theory of medical genetics across the full spectrum of inherited disorders. Get expert clinical advice and guidance from over 250 of the world's most trusted authorities in medical genetics.

Volume 2 covers: Cardiovascular disorders; Respiratory disorders; Renal disorders; Gastrointestinal disorders; Hematologic disorders; Immunologic disorders; Endocrinologic disorders; Metabolic disorders.

ISBN

9780443068706

Language

English

Material Type

Book

Call Number

REF GI 200 RIM 2007 VOL 2

Copies

Author

Rimoin, David L.

Pyeritz, Reed E.

Korf, Bruce R. (Eds).

Edition

5th Ed.

Place of Publication

Philadelphia, PA

Publisher

Churchill Livingstone Elsevier

Publication Date

2007

Physical Description

Hardcover: pages: 2285-3872

Subject

Genetics

UBC MD Undergrad

Abstract

This 3 volume text emphasizes application as well as the theory of medical genetics across the full spectrum of inherited disorders. Get expert clinical advice and guidance from over 250 of the world's most trusted authorities in medical genetics.

Volume 3 covers: Metabolic disorders; Mental and Behaviour disorders; Neuromuscular disorders; Opthalmologic disorders; Deafness; Craniofacial disorders; Dermatologic disorders; Connective tissue disorders; Skeletal disorders.

ISBN

9780443068706

Language

English

Material Type

Book

Call Number

REF GI 200 RIM 2007 VOL 3

Copies

Author

Sadock, Benjamin

Sadock, Virginia

Edition

3rd edition

Place of Publication

Philadelphia, PA

Publisher

Lippincott Williams & Wilkins

Publication Date

2008

Physical Description

xiv, 738 p. ; 27 cm.

Subject

Mental Disorders

Mental Health/Illness

Psychiatrist

UBC MD Undergrad

Abstract

This textbook contains relevant clinical material from the Kaplan and Sadock's Synopsis of Psychiatry, Tenth Edition and includes updated information on recently introduced psychiatric drugs. The book is DSM-IV-TR compatible and replete with case studies and tables, including DSM-IV-TR tables. Chapters offer step-by-step guidance on the clinical examination, the psychiatric report, medical assessment of the psychiatric patient, laboratory tests, and signs and symptoms. The major portion of the book covers all psychiatric and substance-related disorders, with special chapters on children, adolescents, and the elderly. Also included are chapters on emergency psychiatry, forensic psychiatry, ethics, and palliative and end-of-life care.

ISBN

9780781787468

Language

English

Material Type

Book

Call Number

REF CD 05 SAD 2008

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

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

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

McMillan, Julia A.

Feigin, Ralph D.

DeAngelis, Catherine D.

Jones Jr., M. Douglas

Place of Publication

Philadelphia, PA

Publisher

Lippincott Williams & Wilkins

Publication Date

2006

Physical Description

Hardcover: 2723 p.

Subject

Children's Health. Pediatrics

UBC MD Undergrad

Abstract

This book is designed to meet the needs of the student of pediatrics, whether a medical student, a busy pediatric house officer, or a practitioner. It is divided into 5 parts: General Pediatrics; The Fetus and the Newborn; Ambulatory Pediatrics; The Sick or Hospitalized Patient; and The Pediatrician's Companion: Important Things You Forget to Remember.

ISBN

9780781738941

Language

English

Material Type

Book

Call Number

REF GK 100 MCM 2006

Copies

Author

Lawrence, Peter F.

Place of Publication

Philadelphia, PA

Publisher

Lippincott Williams & Wilkins

Publication Date

2007

Physical Description

Softcover: 443 p.

Subject

Surgery

UBC MD Undergrad

Abstract

Employing more than 200 illustrations, this book demonstrates relevant anatomy and common surgical approaches. It provides information on treatment options, imaging modalities, operative techniques, laparoscopic and robotic surgery, surgical devices and products, and postoperative care.

Notes

*March 24/14 - Marked as missing

ISBN

9780781750042

Language

English

Material Type

Book

Call Number

REF ED 100 LAW 2007

Copies

Author

Lucente, Frank E.

Gady, Har-El

Edition

5th Ed.

Place of Publication

Philadelphia, PA

Publisher

Lippincott Williams & Wilkins

Publication Date

2004

Physical Description

Paperback: 504 pages

Subject

Ear/Nose/Throat. Ear/Nose/Throat Diseases *Otolaryngology

UBC MD Undergrad

Abstract

This pocket manual presents step-by-step guidelines on patient workup, differential diagnosis, and therapy for more than 40 symptoms occurring in the head and neck region.

ISBN

0781747074

Language

English

Material Type

Book

Call Number

REF FI 100 LUC 2004

Copies

Author

Doherty, Gerard M.

Edition

1st ed.

Place of Publication

New York, NY

Publisher

McGraw-Hill Medical

Publication Date

2005

Physical Description

Paperback, 472 p.

Subject

Surgery

UBC MD Undergrad

Abstract

Essential coverage of surgery! In the popular one-disorder-per-page format, this pocket guide features bulleted, high-yield information on over 400 common surgical diagnoses. With key equations and formulae, a clinical pearl per page, plus references, this book truly is essential in critical care.

ISBN

9780071423144

Language

English

Material Type

Book

Call Number

REF ED 100 DOH 2005

Copies

Author

Welbury, Richard R.

Duggal, Monty S.

Hosey, Marie-Therese

Place of Publication

Oxford, UK

Publisher

Oxford University Press

Publication Date

2005

Physical Description

Paperback: 443 pages

Subject

Dental Care-Children

Dental Care. Dentistry

UBC MD Undergrad

Abstract

An essential textbook for both the theroretical knowledge and practice of pediatric dentistry.

ISBN

0198565836

Language

English

Material Type

Book

Call Number

REF FJ 100.5 WEL 2005

Copies