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

Obstetrical & gynecological survey, 2008-06, Vol.63 (6), p.361-363

2008

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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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Sickle Reticulocytes Adhere to VCAM-1

Blood, 1995-01, Vol.85 (1), p.268-274

1995

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Phosphodiesterase-4 Inhibition Reduces Ischemic/Reperfusion Liver Injury in a Mouse Model for Sickle Cell Disease

Blood, 2008-11, Vol.112 (11), p.1444-1444

2008

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Acquisition of mutans streptococci and caries prevalence in pediatric sickle cell anemia patients receiving long-term antibiotic therapy

Pediatric dentistry, 2005-05, Vol.27 (3), p.186

2005

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Editorial: The acute chest syndrome of sickle cell disease

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

Platt, Orah S

2000

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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

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

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

Mutations in HFM1 in Recessive Primary Ovarian Insufficiency

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

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

Sickle Reticulocytes Adhere to VCAM-1

Phosphodiesterase-4 Inhibition Reduces Ischemic/Reperfusion Liver Injury in a Mouse Model for Sickle Cell Disease

Acquisition of mutans streptococci and caries prevalence in pediatric sickle cell anemia patients receiving long-term antibiotic therapy

Editorial: The acute chest syndrome of sickle cell disease

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