January 2012 - Volume 54 - Issue 1 - Contributor Index

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Gahl, William A.

Congenital Hepatic Fibrosis and Portal Hypertension in Autosomal Dominant Polycystic Kidney Disease

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Gallinger, Steve

Juvenile Polyposis Syndrome, SMAD4 Mutations, and Hereditary Hemorrhagic Telangiectasia

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Gao, Wen-Yi

Proton Pump Inhibitor Use in Infants: FDA Reviewer Experience

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Garay-Sánchez, Paloma

Manifestations and Evolution of Wilson Disease in Pediatric Patients Carrying ATP7B Mutation L708P

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Garcia, Angelica

Congenital Hepatic Fibrosis and Portal Hypertension in Autosomal Dominant Polycystic Kidney Disease

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García-Luzardo, María R.

Manifestations and Evolution of Wilson Disease in Pediatric Patients Carrying ATP7B Mutation L708P

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García-Villarreal, Luis

Manifestations and Evolution of Wilson Disease in Pediatric Patients Carrying ATP7B Mutation L708P

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Gasparini, Paolo

Delayed Diagnosis of Glycogen Storage Disease Type III

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Geerlings, Arjan

Human Milk Probiotic Lactobacillus fermentum CECT5716 Reduces the Incidence of Gastrointestinal and Upper Respiratory Tract Infections in Infants

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Giersiepen, K.

European Society for Pediatric Gastroenterology, Hepatology, and Nutrition Guidelines for the Diagnosis of Coeliac Disease

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Goco, Norman

Infant Stunting Is Associated With Short Maternal Stature

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Goetz, Joëlle

Are Immunoglobulin A Anti-gliadin Antibodies Helpful in Diagnosing Coeliac Disease in Children Younger Than 2 Years?

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Gokhale, Ranjana

Thalidomide Use and Outcomes in Pediatric Patients With Crohn Disease Refractory to Infliximab and Adalimumab

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González-Santana, Daniel

Manifestations and Evolution of Wilson Disease in Pediatric Patients Carrying ATP7B Mutation L708P

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Gosiewski, Tomasz

Horizontal Distribution of the Fecal Microbiota in Adolescents With Inflammatory Bowel Disease

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Gradinger, Abigail B.

Juvenile Polyposis Syndrome, SMAD4 Mutations, and Hereditary Hemorrhagic Telangiectasia

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Griebel, Donna

Proton Pump Inhibitor Use in Infants: FDA Reviewer Experience

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Gryfe, Rob

Juvenile Polyposis Syndrome, SMAD4 Mutations, and Hereditary Hemorrhagic Telangiectasia

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Guandalini, Stefano

Author's Response

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Gunay-Aygun, Meral

Congenital Hepatic Fibrosis and Portal Hypertension in Autosomal Dominant Polycystic Kidney Disease

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