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Pediatric Academic Productivity: Pediatric Benchmarks for the h- and g-Indices

The Journal of pediatrics, 2016-02, Vol.169, p.272-276

2016

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A Proposed Job Description for the Modern Division Director

The Journal of pediatrics, 2013-10, Vol.163 (4), p.932-933.e1

2013

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The Next 7 Great Achievements in Pediatric Research

Pediatrics (Evanston), 2017-05, Vol.139 (5)

2017

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Screening Student Athletes for Sickle Cell Trait — A Social and Clinical Experiment

The New England journal of medicine, 2010-09, Vol.363 (11), p.997-999

2010

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Pulmonary hypertension and nitric oxide depletion in sickle cell disease

Blood, 2010-08, Vol.116 (5), p.687-692

2010

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Impact of the Putative Differentiating Agent Sodium Phenylbutyrate on Myelodysplastic Syndromes and Acute Myeloid Leukemia

Clinical cancer research, 2001-08, Vol.7 (8), p.2330-2339

2001

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Improving teaching on an inpatient pediatrics service: a retrospective analysis of a program change

BMC medical education, 2012-10, Vol.12 (1), p.92-92, Article 92

2012

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Hospitalization rates and costs of care of patients with sickle‐cell anemia in the state of Maryland in the era of hydroxyurea

American journal of hematology, 2006-12, Vol.81 (12), p.927-932

2006

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The Barker hypothesis: how pediatricans will diagnose and prevent common adult-onset diseases

Transactions of the American Clinical and Climatological Association, 2009, Vol.120, p.199-207

Dover, George J

2009

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Augmentation by Erythropoietin of the Fetal-Hemoglobin Response to Hydroxyurea in Sickle Cell Disease

The New England journal of medicine, 1993-01, Vol.328 (2), p.73-80

1993

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Child health research funding and policy: imperatives and investments for a healthier world

Pediatrics (Evanston), 2010-06, Vol.125 (6), p.1259

2010

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The genetics revolution and primary care pediatrics

JAMA : the journal of the American Medical Association, 2008-01, Vol.299 (4), p.451

2008

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Short-chain fatty acid derivatives induce fetal globin expression and erythropoiesis in vivo

Blood, 2002-12, Vol.100 (13), p.4640-4648

2002

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Role of Cyclic Nucleotides in Fetal Hemoglobin Induction in Cultured CD34 + Cells

Experimental hematology, 2006-09, Vol.34 (9), p.1150-1160

2006

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Pulsed-dosing with oral sodium phenylbutyrate increases hemoglobin F in a patient with sickle cell anemia

Pediatric blood & cancer, 2008-02, Vol.50 (2), p.357-359

2008

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Utilizing electronic health record data to determine the health of the medication process after the relocation of a children's hospital

Studies in health technology and informatics, 2013, Vol.192, p.210

2013

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Screening for iron deficiency anemia by dietary history in a high-risk population

Pediatrics (Evanston), 2000-06, Vol.105 (6), p.1254

2000

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Extended Therapy with Intravenous Arginine Butyrate in Patients with β-Hemoglobinopathies

The New England journal of medicine, 1995-06, Vol.332 (24), p.1606-1610

1995

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Erythropoietic activity in patients with sickle cell anaemia before and after treatment with hydroxyurea

British journal of haematology, 1999-05, Vol.105 (2), p.491-496

1999

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Fatal intramuscular bleeding misdiagnosed as suspected nonaccidental injury

Pediatrics (Evanston), 1995-05, Vol.95 (5), p.771

1995

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Hematologic Responses of Patients with Sickle Cell Disease to Treatment with Hydroxyurea

The New England journal of medicine, 1990-04, Vol.322 (15), p.1037-1045

1990

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Induction of fetal hemoglobin synthesis in children with sickle cell anemia on low-dose oral sodium phenylbutyrate therapy

Journal of pediatric hematology/oncology, 2002-12, Vol.24 (9), p.737-741

2002

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Treatment of Sickle Cell Anemia with Hydroxyurea and Erythropoietin

The New England journal of medicine, 1990-08, Vol.323 (6), p.366-372

1990

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Sustained Induction of Fetal Hemoglobin by Pulse Butyrate Therapy in Sickle Cell Disease

Blood, 1999-03, Vol.93 (6), p.1790-1797

1999

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The role of heterocellular hereditary persistence of fetal haemoglobin in β0‐thalassaemia intermedia

British journal of haematology, 2001-09, Vol.114 (4), p.899-906

2001

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Pediatric Academic Productivity: Pediatric Benchmarks for the h- and g-Indices

A Proposed Job Description for the Modern Division Director

The Next 7 Great Achievements in Pediatric Research

Screening Student Athletes for Sickle Cell Trait — A Social and Clinical Experiment

Pulmonary hypertension and nitric oxide depletion in sickle cell disease

Impact of the Putative Differentiating Agent Sodium Phenylbutyrate on Myelodysplastic Syndromes and Acute Myeloid Leukemia

Improving teaching on an inpatient pediatrics service: a retrospective analysis of a program change

Hospitalization rates and costs of care of patients with sickle‐cell anemia in the state of Maryland in the era of hydroxyurea

The Barker hypothesis: how pediatricans will diagnose and prevent common adult-onset diseases

Augmentation by Erythropoietin of the Fetal-Hemoglobin Response to Hydroxyurea in Sickle Cell Disease

Child health research funding and policy: imperatives and investments for a healthier world

The genetics revolution and primary care pediatrics

Short-chain fatty acid derivatives induce fetal globin expression and erythropoiesis in vivo

Role of Cyclic Nucleotides in Fetal Hemoglobin Induction in Cultured CD34 + Cells

Pulsed-dosing with oral sodium phenylbutyrate increases hemoglobin F in a patient with sickle cell anemia

Utilizing electronic health record data to determine the health of the medication process after the relocation of a children's hospital

Screening for iron deficiency anemia by dietary history in a high-risk population

Extended Therapy with Intravenous Arginine Butyrate in Patients with β-Hemoglobinopathies

Erythropoietic activity in patients with sickle cell anaemia before and after treatment with hydroxyurea

Fatal intramuscular bleeding misdiagnosed as suspected nonaccidental injury

Hematologic Responses of Patients with Sickle Cell Disease to Treatment with Hydroxyurea

Induction of fetal hemoglobin synthesis in children with sickle cell anemia on low-dose oral sodium phenylbutyrate therapy

Treatment of Sickle Cell Anemia with Hydroxyurea and Erythropoietin

Sustained Induction of Fetal Hemoglobin by Pulse Butyrate Therapy in Sickle Cell Disease

The role of heterocellular hereditary persistence of fetal haemoglobin in β0‐thalassaemia intermedia

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