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Growth and Development
Contributing journals to this collection:
AAP Grand Rounds,
NeoReviews,
Pediatrics,
and Pediatrics in Review
Citations 1-10 of 245 total displayed.
- ARTICLES
Clinical and Genetic Analysis of Unclassifiable Inherited Bone Marrow Failure Syndromes
- Juliana T. Teo, Robert Klaassen, Conrad V. Fernandez, Rochelle Yanofsky, John Wu, Josette Champagne, Mariana Silva, Jeffrey H. Lipton, Jossee Brossard, Yvan Samson, Sharon Abish, MacGregor Steele, Kaiser Ali, Uma Athale, Lawrence Jardine, John P. Hand, Elena Tsangaris, Isaac Odame, Joseph Beyene, and Yigal Dror
Pediatrics 2008; 122: e139-e148.
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- Articles
Turner Syndrome
- Melissa L. Loscalzo
Pediatr. Rev. 2008; 29: 219-227.
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- In Brief
Fears and Phobias
- Jacques Benun, Carol Lewis, Matthew Siegel, and Janet R. Serwint
Pediatr. Rev. 2008; 29: 250-251.
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- 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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