Author

Schwartz, David T.

Edition

1st ed.

Place of Publication

New York, NY

Publisher

McGraw-Hill Companies, Inc.

Publication Date

2008

Physical Description

Hardcover, 562 p., ill.

Subject

Radiology

UBC MD Undergrad

Abstract

"Emergency Radiology: Case Studies" is a one-of-a-kind text specifically designed to help you fine-tune your emergency radiographic interpretation and problem-solving skills. Illustrated with hundreds of high-resolution images, this reference covers the full range of clinical problems in which radiographic studies play a key role. Dr. David Schwartz, a leading educator, takes you step-by-step through the radiographic analysis of medical, surgical, and traumatic disorders, giving you an unparalleled review of the use and interpretation of radiographic studies in emergency diagnosis.

ISBN

9780071409179

Language

English

Material Type

Book

Call Number

REF EC 100 SCH 2008

Copies

Author

Tintinalli, Judith E.

Stapczynski, J. Stephan

Ma, O. John et al

Edition

8th

Place of Publication

New York, NY

Publisher

McGraw-Hill Education

Publication Date

2016

Physical Description

Hardcover, 2134 p. ill.

Subject

Emergency Medicine

Abstract

The most widely used and highly regarded textbook and reference of emergency medicine -- Endorsed by the American College of Emergency Physicians

The 8th edition of Tintinalli s Emergency Medicine provides the depth and breadth of coverage that reflects the complexity and expertise needed to practice emergency medicine successfully in today's fast paced environments. It is an important contemporary clinical emergency care resource for physicians, NPs, and PAs who practice emergency medicine and for emergency medicine and pediatric emergency medicine fellows.

ISBN

9780071794763

Language

English

Material Type

Book

Call Number

REF EB 800 TIN 2016

Copies

Author

Tintinalli, Judith E.

Stapczynski, J. Stephan

Ma, O. John et al

Edition

6th

Place of Publication

New York, NY

Publisher

McGraw-Hill Education

Publication Date

2003

Physical Description

Hardcover, 2016pp

Subject

Emergency Medicine

Abstract

Covers the gamut of emergency medicine practice in brief, clinically focused chapters. New to this edition are chapters on bioterroism and weapons of mass destruction, pharmacology of antimicrobials, antifungals, and antivirals, principles of drug interactions, endocarditis, and abdominal and pelvic pain in the non-pregnant patient. Pharmacologic considerations, tables of vital differential diagnoses, and observation criteria throughout are new features reflecting developments in this dynamic specialty.

ISBN

978-0071388757

Language

English

Material Type

Book

Call Number

REF EB 800 TIN 2003

Copies

Editor

Wolfsthal, Susan D.

Edition

7th ed.

Place of Publication

Philadelphia, PA

Publisher

Wolters Kluwer

Publication Date

2012

Physical Description

Paperback, 712 p., ill.

Subject

UBC MD Undergrad

Internal Medicine

Abstract

NMS Medicine, Seventh Edition, is the ideal reference and review text for medical students in the internal medicine clerkship. The book provides medical students with a comprehensive and meticulously organized review of internal medicine and USMLE-style questions and case studies to reinforce key topics and concepts. Features include 500 USMLE-style questions in vignette format for self-study and assessment, a comprehensive exam, and a convenient outline format.

ISBN

9781608315819

Language

English

Material Type

Book

Call Number

REF AB 60 WOL 2012

Copies

Author

Spiegelman, Paul

Berrett, Britt

Place of Publication

New York, NY

Publisher

An Inc. Original

Publication Date

2013

Physical Description

Hardcover, 208 p.

Subject

Change Management

Administration

Hospitals

Leadership/Coaching

Abstract

Patients Come Second shakes up the traditional healthcare model, arguing that in order to care for and retain patients, leaders must first create exceptional teams and find ways to engage nurses, administrative staff, physicians, supervisors, and even housekeeping staff and switchboard operators. By connecting employees' work with a higher purpose and equipping them with the tools to become leaders themselves, patient care can be dramatically transformed. And with continuing healthcare changes on the horizon and ever-rising pressure to acquire and keep patients, doing so now is more important than ever.

ISBN

9780988842809

Language

English

Material Type

Book

Call Number

REF JB 200 SPI 2013

Copies

Author

St. Pierre, Michael

Buerschaper, Cornelius

Simon, Robert

Edition

2nd Ed.

Place of Publication

Berlin, Germany

Publisher

Springer-Verlag

Publication Date

2011

Physical Description

Hardcover: 346 pages

Subject

Emergency Care Services. Emergency Room. ER

Emergency Medicine

Safety

Abstract

Critical situations in acute and emergency care are one of the great clinical challenges because of the uncertainty, high stakes, time pressure, and stress that are involved. This book provides a comprehensive outline of all the human factors issues relevant to patient safety during acute care. Following an initial section discussing the basic principles of human behavior and decision making, the various influences on safe patient care are discussed in depth. These are divided into three interacting groups: individual factors, team factors, and organizational factors. Relevant psychological theories are carefully examined, and case studies and descriptions of proven strategies help to ground these theories in daily practice. This newly revised edition will help both physicians and non-physicians to better understand the principles of human behavior and decision making in critical situations and thus to provide safer treatment.

ISBN

9783642196997

Language

English

Material Type

Book

Call Number

REF EB 800 STP 2011

Copies

Website

PHSA Users:

http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp16131&site=pfi-live

UBC Users:

http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_B&C=cell

Corporate Author

Massachusetts Institute of Technology

Place of Publication

Cambridge, Ma.

Publisher

Elsevier

Publication Date

1974 - present.

ISSN

0092-8674

Language

English

Material Type

Serial

Frequency

Biweekly

Holdings

CFRI/Study & Learning Commons - Print: v.76:1-v.98:4 (1994-1998); v.104:1-v.156:3+suppls. (2001-2014).

Missing: v.78:7, v.79:2 (1994); v.80:7, v.81:6, v.82:4,7 (1995); v.84:7, v.85:1, v.86:1,7 (1996); v.88:7, v.90:3,7 (1997); v.92:1,4,7, v.93:3-5, v.94, v.95:1-3,5,6 (1998); v.96:2,7, v.97:1-6 (1999); v.104:6 (2001); v.111:4 (2002); v.117:1 (2004); v.141:4 (2010).

Online: 1974 to present.

Website

PHSA Users:

http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp161531&site=pfi-live

UBC Users:

http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_B&C=cell+metabolism

Place of Publication

Cambridge, MA

Publisher

Cell Press

Publication Date

2005 to Present

ISSN

1550-4131

Language

English

Material Type

Serial

Frequency

Monthly

Holdings

CFRI/Study & Learning Commons - Print: v.1-v.11:1 (2005-2010)

Missing: v.2:1-2,5 (2005); v.3:6 (2006); v.5:1 (2007); v.8:5-6 (2008); v.10:3 (2009)

Online: 2005 to present

Website

PHSA Users:

http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp341298&site=pfi-live

UBC Users:

http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_M&C=molecular+cell

Place of Publication

Philadelphia, PA

Publisher

Elsevier Inc.

Publication Date

1997 - Present.

ISSN

1097-2765

Language

English

Material Type

Serial

Frequency

Bimonthly

Holdings

CFRI/Study & Learning Commons - Print: v.3:4-10 (2005); v.4:1,2 (2006).

Online: 1997 to present.

Website

PHSA Users:

http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp39453&site=pfi-live

UBC Users:

http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_B&C=Journal+of+Cell+Biology

Place of Publication

New York, NY

Publisher

Rockefeller University Press

Publication Date

1955 - Present

ISSN

0021-9525

Language

English

Material Type

Serial

Holdings

CFRI/Study & Learning Commons - Print: v.144:1-v.148:2 (1999-2000).

Online: 1955 to present.

Website

PHSA Users:

http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp49650&site=pfi-live

UBC Users:

http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_M&C=Molecular+Biology+of+the+Cell

Alternate Title

MBoC

Place of Publication

[Bethesda, MD]

Publisher

The American Society for Cell Biology

Publication Date

1989 - Present.

ISSN

1059-1524

Language

English

Material Type

Serial

Frequency

Bimonthly

Holdings

CFRi/Study & Learning Commons - Print: v.5:3-4,6 (1994); v.9:1-v.14:1 (1998-2003) + suppls.

Missing: v.11:5 (2000); v.13:4 (2002).

Online: 1989 to present.

Website

PHSA Users:

http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp78330&site=pfi-live

UBC Users:

http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_M&C=Nature+cell+biology

Alternate Title

Nat. Cell Biol.

Place of Publication

London, UK.

Publisher

Nature Publishing Group

Publication Date

1999 - Present.

ISSN

1465-7392

Language

English

Material Type

Serial

Frequency

Monthly

Holdings

CFRI/Study & Learning Commons - Print: v.4:2-v.16:6 (2002-2014).

Missing: v.4:1 (2002); v.11:8 (2009).

Online: 1999 to present.

Website

PHSA Users:

Not available online.

UBC Users:

http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=I_M&C=0962-8924

Place of Publication

Cambridge, Ma.

Publisher

Elsevier Inc.

Publication Date

1990 - Present.

ISSN

0962-8924

Language

English

Material Type

Serial

Frequency

Monthly

Holdings

CFRI/Study & Learning Commons - Print: v.4:10-v.8:12 (1994-1998); v.9:1,6 (1999); v.11:12-v.24:2 (2001-2014).

Missing: v.4:11 (1994); v.5:1 (1995); v.8:3 (1998); v.9:2-5,7-12 (1999); v.10:all (2000); v.13:12 (2003); v.14:1-2 (2004).

Online: 1990 to present.

Website

UBC Users:

http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_B&C=current+opinion+in+cell+biology

Place of Publication

[United Kingdom]

Publisher

Elsevier B.V.

Publication Date

1989 - Present

ISSN

0955-0674

Language

English

Material Type

Serial

Frequency

Bimonthly

Holdings

CFRI/Study & Learning Commons - Print: v.10:1-v.18:1 (1998-2006).

Missing: v.10:2 (1998); v.11:3,6 (1999); v.12:6 (2000); v.13:1-2 (2001); v.14:1,3 (2002); v.v.15:5-6 (2003); v.16:3 (2004); v.17:4 (2005); v.18:2-6 (2006).

Online: 1989 to present.

Author

Toy, Eugene

Patlan, John

Warner, Mark T.

Edition

5th ed.

Place of Publication

New York, NY

Publisher

McGraw-Hill Education

Publication Date

2017

Physical Description

Paperback, 588 p.

Subject

Internal Medicine

Abstract

Experience with clinical cases is key to mastering the art and science of medicine. This book provides 60 true-to-life cases that illustrate essential concepts in Internal Medicine. Each case includes a discussion correlated to key concepts, definitions of key terms, clinical pearls, and board-style review questions to reinforce your learning.

ISBN

9780071843355

Language

English

Material Type

Book

Call Number

REF AB 60 TOY 2017

Copies

Author

Hui, David

Leung, Alexander A.

Padwal, Raj

Edition

4th ed.

Place of Publication

Cham, Switzerland

Publisher

Springer

Publication Date

2016

Physical Description

Paperback, 546 p., ill.

Subject

Internal Medicine -- Handbooks

UBC MD Undergrad

Internal Medicine

Abstract

This fully updated 4th edition provides an integrated symptom- and issue-based approach with easy access to high yield clinical information. For each topic, carefully organized sections on different diagnoses, investigations, and treatments are designed to facilitate patient care and examination preparation. Numerous clinical pearls and comparison tables are provided to help enhance learning, and international units (US and metric) are used to facilitate application in everyday clinical practice.

The book covers many highly important, rarely discussed topics in medicine (e.g., smoking cessation, obesity, transfusion reactions, needle stick injuries, code status discussion, interpretation of gram stain, palliative care), and new chapters on end-of-life care and depression have been added. The fourth edition includes many reader-friendly improvements such as better formatting, intuitive ordering of chapters, and incorporation of the most recent guidelines for each topic. Approach to Internal Medicine continues to serve as an essential reference for every medical student, resident, fellow, practicing physician, nurse, and physician assistant.

ISBN

9783319118208

Language

English

Material Type

Book

Call Number

REF AB 60 HUI 2016

Copies

Website

UBC Users:

http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_M&C=Human+gene+therapy

Place of Publication

Baltimore, MD

Publisher

Mary Ann Liebert, Inc.

Publication Date

1990 - Present

ISSN

1043-0342

Language

English

Material Type

Serial

Frequency

Monthly

Holdings

CFRI/Study & Learning Commons - Print: v.5:9 (1994); v.6:1-v.13:18 (1995-2002).

Missing: v.8:8 (1997); v.10:17 (1999); v.11:3,4,6-18 (2000); v.12:1-12,14,17,18 (2001); v.13:5 (2002).

Online: 2006 to 2014.

Website

PHSA Users:

http://search.ebscohost.com/login.aspx?direct=true&db=edspub&AN=edp33596&site=pfi-live

UBC Users:

http://gw2jh3xr2c.search.serialssolutions.com/?SS_searchTypeJournal=yes&V=1.0&L=GW2JH3XR2C&S=AC_T_M&C=human+molecular+genetics

Place of Publication

Oxford, England

Publisher

Oxford University Press

Publication Date

1992 - Present

ISSN

0964-6906

Language

English

Material Type

Serial

Frequency

Bimonthly

Holdings

CFRI/Study & Learning Commons - Print: v.3:1-v.8:13 (1994-1999); v.9:15-16 (2000); v.10:1-16,19,20,22-25 (2001); v.11:17,20 (2002); v.12:13 (2003).

Missing: v.4:8 (1995); v.5:8 (1996); v.6:8,10 (1997).

Online: 1992 to present.

Website

PHSA Users:

http://web.b.ebscohost.com/pfi/detail/detail?vid=2&sid=1ca4387a-7b18-48a7-8383-517069a00ce3%40sessionmgr101&hid=118&bdata=JnNpdGU9cGZpLWxpdmU%3d#AN=edp3739&db=edspub

UBC Users:

http://gw2jh3xr2c.search.serialssolutions.com/?sid=sersol&SS_jc=AMERJOUROFHU&title=American%20journal%20of%20human%20genetics

Alternate Title

AJHG

Corporate Author

The American Society of Human Genetics

Publisher

Cell Press

ISSN

0002-9297

Material Type

Serial

Frequency

Monthly

Holdings

CFRI/Study & Learning Commons - Print: v.4:1-v.97:6 (1994-2012);

v.93:12-v.94:1 + suppls. (2013-2014)

Missing: v.59:3-5 (1996); v.61:1(1997); v.80:2(2007); v.85:2(2009); v.91:4-5(2009)

Online: 1949 to present (Full Text Delay: 6 months)

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