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Genetics & Dysmorphology
Contributing journals to this collection:
AAP Grand Rounds,
NeoReviews,
Pediatrics,
and Pediatrics in Review
Citations 1-10 of 183 total displayed.
- Articles
Adolescent Psychological Development: A Review
- Eric Hazen, Steven Schlozman, and Eugene Beresin
Pediatr. Rev. 2008; 29: 161-168.
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- ARTICLES
Early Determinants of Fractures in Rett Syndrome
- Jennepher Downs, Ami Bebbington, Helen Woodhead, Peter Jacoby, Le Jian, Amanda Jefferson, and Helen Leonard
Pediatrics 2008; 121: 540-546.
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- STATE-OF-THE-ART REVIEW ARTICLES
Ethical, Legal, and Social Concerns About Expanded Newborn Screening: Fragile X Syndrome as a Prototype for Emerging Issues
- Donald B. Bailey, Jr, Debra Skinner, Arlene M. Davis, Ian Whitmarsh, and Cynthia Powell
Pediatrics 2008; 121: e693-e704.
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- EXPERIENCE & REASON
Successful Management of Difficult Infusion-Associated Reactions in a Young Patient With Mucopolysaccharidosis Type VI Receiving Recombinant Human Arylsulfatase B (Galsulfase [Naglazyme])
- Katherine H. Kim, Celeste Decker, and Barbara K. Burton
Pediatrics 2008; 121: e714-e717.
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- EXPERIENCE & REASON
Successful Management of Difficult Infusion-Associated Reactions in a Young Patient With Mucopolysaccharidosis Type VI Receiving Recombinant Human Arylsulfatase B (Galsulfase [Naglazyme])
- Katherine H. Kim, Celeste Decker, and Barbara K. Burton
Pediatrics peds.2007-0665.
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- REVIEW ARTICLES
Recognition and Diagnosis of Mucopolysaccharidosis II (Hunter Syndrome)
- Rick Martin, Michael Beck, Christine Eng, Roberto Giugliani, Paul Harmatz, Verónica Muñoz, and Joseph Muenzer
Pediatrics 2008; 121: e377-e386.
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- EXPERIENCE & REASON
Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation
- Agatino Battaglia, H. Eugene Hoyme, Bruno Dallapiccola, Elaine Zackai, Louanne Hudgins, Donna McDonald-McGinn, Nadia Bahi-Buisson, Corrado Romano, Charles A. Williams, Lisa L. Brailey, Sameer M. Zuberi, and John C. Carey
Pediatrics 2008; 121: 404-410.
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- ARTICLES
Risk of Vascular Anomalies With Down Syndrome
- Arin K. Greene, Sendia Kim, Gary F. Rogers, Steven J. Fishman, Bjorn R. Olsen, and John B. Mulliken
Pediatrics 2008; 121: e135-e140.
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- EXPERIENCE & REASON
A Novel Monocarboxylate Transporter 8 Gene Mutation as a Cause of Severe Neonatal Hypotonia and Developmental Delay
- Anastasios Papadimitriou, Alexandra Mihaela Dumitrescu, Antigone Papavasiliou, Andreas Fretzayas, Polyxeni Nicolaidou, and Samuel Refetoff
Pediatrics 2008; 121: e199-e202.
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- LETTERS TO THE EDITOR
Pseudo-asthma Revisited: In Reply
- Miles M. Weinberger
Pediatrics 2008; 121: 221-a--a222.
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