Karl S. Roth and James C. M. Chan

Renal Tubular Acidosis: A New Look at an Old Problem
Clin Pediatr (Phila) 2001 40: 533-543. [Abstract] [PDF] [References]  

Sithembiso C. Velaphi and Jeffrey M. Perlman

Neonatal Adrenal Hemorrhage: Clinical and Abdominal Sonographic Findings
Clin Pediatr (Phila) 2001 40: 545-548. [Abstract] [PDF] [References]  

Paul L. Geltman, Alan F. Meyers, and Howard Bauchner

Daily Multivitamins with Iron to Prevent Anemia in Infancy: A Randomized Clinical Trial
Clin Pediatr (Phila) 2001 40: 549-554. [Abstract] [PDF] [References]  

Kathleen A. Burklow, Lisa M. Vaughn, Kristin S. Valerius, and Janet R. Schultz

Parental Expectations Regarding Discussions on Psychosocial Topics During Pediatric Office Visits
Clin Pediatr (Phila) 2001 40: 555-562. [Abstract] [PDF] [References]  

Karyn L. Hunnicutt

A 6-Year-Old Child with Abdominal Pain
Clin Pediatr (Phila) 2001 40: 563-565. [PDF] [References]  

Paul S. Bergeson and J. Chris Shaw

Are Infants Really Obligatory Nasal Breathers?
Clin Pediatr (Phila) 2001 40: 567-569. [PDF] [References]  

Matthew D. Curry, Pamela G. Larsen, Christopher J. Mansfield, and Kathleen D. Leonardo

Impacts of a Flood Disaster on an Ambulatory Pediatric Clinic Population
Clin Pediatr (Phila) 2001 40: 571-574. [PDF] [References]  

Alessandro Ventura, Sergio Facchini, C. Amantidu, M. F. Andreotti, A. Andrighetto, A. Baggiani, F. Benedetti, S. Bonati, I. Buonaterra, M. Capozzo, E. Ciscato, F. Cracco, G. Ferrari, M. Fornale, F. Fusco, E. Laverda, M. Mardiciaro, E. Nicolussi, L. Pasinato, D. Pittarello, E. Pizio, R. Salvadori, D. Sambugaro, S. Sassolino, V. Spavanello, C. T. Visan, G. Ziglio, and V. Zuffellato

Searching for Celiac Disease in Pediatric General Practice
Clin Pediatr (Phila) 2001 40: 575-577. [PDF] [References]  

Irwin A. Schafer

Gentamicin-Mediated Suppression of Hurler Syndrome Stops Mutations Restores a Low Level of ox-L-Iduronidase Activity and Reduces Lysosomal Glycosaminoglycan Accumulation
Clin Pediatr (Phila) 2001 40: 579-580. [PDF]  

Irwin A. Schafer

Primary Systemic Carnitine Deficiency is Caused by Mutations in a Gene Encoding Sodium-Ion-Dependent Carnitine Transporter
Clin Pediatr (Phila) 2001 40: 580. [PDF]  

Irwin A. Schafer

A Mutation in the Rett Syndrome Gene, MECP2, Causes X-linked Mental Retardation and Progressive Spasticity in Males
Clin Pediatr (Phila) 2001 40: 581. [PDF]  

Irwin A. Schafer

High-Frequency Hearing Loss Correlated With Mutation in the GJB2 Gene
Clin Pediatr (Phila) 2001 40: 581-582. [PDF]  

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