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Health & Medicine Assessment of children hearing

Assessment of hearing in children Hearing impairment in children is not uncommon 2-4 per 1000 newborns will have permanent childhood hearing loss More common in low socioeconomic…

Business Beyond Pills: Designing a Winning Drug Delivery Strategy for the New Era of Biologics

L E K . C O ML.E.K. Consulting / Executive Insights EXECUTIVE INSIGHTS INSIGHTS @ WORK® VOLUME XVII, ISSUE 7 Beyond Pills: Designing a Winning Drug Delivery Strategy for…

Documents Cardiomyopathy in Children And Adolescents: What Begins in Childhood… James W. Wiggins, Jr. MD...

Slide 1Cardiomyopathy in Children And Adolescents: What Begins in Childhood… James W. Wiggins, Jr. MD FAAP, FACC St. Vincent Healthcare Pediatric Cardiology, Billings,…

Documents Fact and Fallacy in Neonatal Screening Dennis K.K. Au Au.D. Division of Otorhinolaryngology...

Slide 1 Fact and Fallacy in Neonatal Screening Dennis K.K. Au Au.D. Division of Otorhinolaryngology Department of Surgery University of Hong Kong Medical Centre Slide 2 Early…

Documents Deaf-Blind

Deaf-Blind ASL I Spring 2009 Final Ms. Maclin MBHS Links: www.deafblindinfo.org/FAQ.asp http://www.msab.state.mn.us/DBC/notable_deafblind_people.htm http://www.actionfund.org/ohsay/saysee18.htm…

Documents Lysosomal Storage Disorders and Treatment

International Journal of PharmTech Research CODEN (USA): IJPRIF ISSN : 0974-4304 Vol.2, No.2, pp 1082-1091, April-June 2010 Lysosomal Storage Disorders and Treatment T.E.G.K.MURTHY2,

Documents Mucopolysaccharidosis I, II, and VI: Brief review and guidelines for treatment

C:\Typeset\SBG\33-4\2010-050\2010-050.vpMucopolysaccharidosis I, II, and VI: Brief review and guidelines for treatment Roberto Giugliani1,2, Andressa Federhen1,2, Maria Verônica

Documents Mucopolysaccharidosis type II: Identification of 30 novel mutations among Latin American patients

Mucopolysaccharidosis type II: Identification of 30 novel mutations among Latin American patientsContents lists available at ScienceDirect Molecular Genetics and Metabolism

Documents Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment...

J. Edmond Wraith & Maurizio Scarpa & Michael Beck & Olaf A. Bodamer & Linda De Meirleir & Nathalie Guffon & Allan Meldgaard Lund & Gunilla Malm

Documents Clinical, biochemical and molecular characteristics of Filipino patients with mucopolysaccharidosis....

Clinical, biochemical and molecular characteristics of Filipino patients with mucopolysaccharidosis type II - Hunter syndromeRESEARCH Open Access Clinical, biochemical and