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Hydroxyurea for the Treatment of Sickle Cell Anemia

The New England journal of medicine, 2008-03, Vol.358 (13), p.1362-1369

Platt, Orah S

2008

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Association between Microdeletion and Microduplication at 16p11.2 and Autism

The New England journal of medicine, 2008-02, Vol.358 (7), p.667-675

2008

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SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

Genetics in medicine, 2008-08, Vol.10 (8), p.586-592

2008

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Mortality In Sickle Cell Disease -- Life Expectancy and Risk Factors for Early Death

The New England journal of medicine, 1994-06, Vol.330 (23), p.1639-1644

1994

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Abnormal modulation of cell protective systems in response to ischemic/reperfusion injury is important in the development of mouse sickle cell hepatopathy

Haematologica (Roma), 2011-01, Vol.96 (1), p.24-32

2011

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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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Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort

American journal of hematology, 2019-05, Vol.94 (5), p.522-527

2019

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Quantitative trait loci for baseline white blood cell count, platelet count, and mean platelet volume

Mammalian genome, 2005-10, Vol.16 (10), p.749-763

2005

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Preventing Stroke in Sickle Cell Anemia

The New England journal of medicine, 2005-12, Vol.353 (26), p.2743-2745

Platt, Orah S

2005

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Quantitative trait loci for baseline erythroid traits

Mammalian genome, 2006-04, Vol.17 (4), p.298-309

2006

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Prevention and management of stroke in sickle cell anemia

Hematology, 2006, Vol.2006 (1), p.54-57

Platt, Orah S

2006

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Quantitative trait loci for peripheral blood cell counts: a study in baboons

Mammalian genome, 2007-05, Vol.18 (5), p.361-372

2007

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Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss

Physiological genomics, 2009-08, Vol.38 (3), p.281-290

2009

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Protective effects of phosphodiesterase‐4 (PDE‐4) inhibition in the early phase of pulmonary arterial hypertension in transgenic sickle cell mice

The FASEB journal, 2008-06, Vol.22 (6), p.1849-1860

2008

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The Acute Chest Syndrome of Sickle Cell Disease

The New England journal of medicine, 2000-06, Vol.342 (25), p.1904-1907

Platt, Orah S

2000

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Silent Cerebral Infarcts in Sickle Cell Anemia: A Risk Factor Analysis

Pediatrics (Evanston), 1999-03, Vol.103 (3), p.640-645

1999

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Age- and gender-dependent obesity in individuals with 16p11.2 deletion

Journal of genetics and genomics, 2011-09, Vol.38 (9), p.403-409

2011

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Genetic influences on peripheral blood cell counts: a study in baboons

Blood, 2005-08, Vol.106 (4), p.1210-1214

2005

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Transposing Sequences between Fetal and Adult Hemoglobins Indicates Which Subunits and Regulatory Molecule Interfaces Are Functionally Related

Biochemistry (Easton), 2000-04, Vol.39 (13), p.3774-3781

2000

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Pain in Sickle Cell Disease: Rates and Risk Factors

The New England journal of medicine, 1991-07, Vol.325 (1), p.11-16

1991

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Mutations in HFM1 in Recessive Primary Ovarian Insufficiency

The New England journal of medicine, 2014-03, Vol.370 (10), p.972-974

2014

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Sickle cell anemia as an inflammatory disease

The Journal of clinical investigation, 2000-08, Vol.106 (3), p.337-338

Platt, O S

2000

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Bone Marrow Transplantation in Sickle Cell Anemia — The Dilemma of Choice

The New England journal of medicine, 1996-08, Vol.335 (6), p.426-428

1996

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Easing the Suffering Caused by Sickle Cell Disease

The New England journal of medicine, 1994-03, Vol.330 (11), p.783-784

Platt, Orah S

1994

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Safety of Hydroxyurea in Children With Sickle Cell Anemia: Results of the HUG-KIDS Study, a Phase I/II Trial

Blood, 1999-09, Vol.94 (5), p.1550-1554

1999

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Hydroxyurea for the Treatment of Sickle Cell Anemia

Association between Microdeletion and Microduplication at 16p11.2 and Autism

SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

Mortality In Sickle Cell Disease -- Life Expectancy and Risk Factors for Early Death

Abnormal modulation of cell protective systems in response to ischemic/reperfusion injury is important in the development of mouse sickle cell hepatopathy

Pulmonary hypertension and nitric oxide depletion in sickle cell disease

Heritability of fetal hemoglobin, white cell count, and other clinical traits from a sickle cell disease family cohort

Quantitative trait loci for baseline white blood cell count, platelet count, and mean platelet volume

Preventing Stroke in Sickle Cell Anemia

Quantitative trait loci for baseline erythroid traits

Prevention and management of stroke in sickle cell anemia

Quantitative trait loci for peripheral blood cell counts: a study in baboons

Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss

Protective effects of phosphodiesterase‐4 (PDE‐4) inhibition in the early phase of pulmonary arterial hypertension in transgenic sickle cell mice

The Acute Chest Syndrome of Sickle Cell Disease

Silent Cerebral Infarcts in Sickle Cell Anemia: A Risk Factor Analysis

Age- and gender-dependent obesity in individuals with 16p11.2 deletion

Genetic influences on peripheral blood cell counts: a study in baboons

Transposing Sequences between Fetal and Adult Hemoglobins Indicates Which Subunits and Regulatory Molecule Interfaces Are Functionally Related

Pain in Sickle Cell Disease: Rates and Risk Factors

Mutations in HFM1 in Recessive Primary Ovarian Insufficiency

Sickle cell anemia as an inflammatory disease

Bone Marrow Transplantation in Sickle Cell Anemia — The Dilemma of Choice

Easing the Suffering Caused by Sickle Cell Disease

Safety of Hydroxyurea in Children With Sickle Cell Anemia: Results of the HUG-KIDS Study, a Phase I/II Trial

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