Vitamin D levels are low in adult patients with sickle cell disease in Jamaica and West Africa

[1]  Christine L. Taylor,et al.  Dietary Reference Intakes for Calcium and Vitamin D , 2016, Pediatric Clinical Practice Guidelines & Policies.

[2]  R. Cooper,et al.  Comparison of Patients from Nigeria and the USA Highlights Modifiable Risk Factors for Sickle Cell Anemia Complications , 2014, Hemoglobin.

[3]  C. Palacios,et al.  Is vitamin D deficiency a major global public health problem? , 2014, The Journal of Steroid Biochemistry and Molecular Biology.

[4]  A. Luke,et al.  25‐hydroxyvitamin D levels in African American and Nigerian women , 2013, American journal of human biology : the official journal of the Human Biology Council.

[5]  I. Kema,et al.  Vitamin D status indicators in indigenous populations in East Africa , 2013, European Journal of Nutrition.

[6]  M. Gershwin,et al.  The Implication of Vitamin D and Autoimmunity: a Comprehensive Review , 2013, Clinical Reviews in Allergy & Immunology.

[7]  S. Ofori-Acquah,et al.  High dose vitamin D therapy for chronic pain in children and adolescents with sickle cell disease: results of a randomized double blind pilot study , 2012, British journal of haematology.

[8]  C. Cooper,et al.  A global representation of vitamin D status in healthy populations , 2012, Archives of Osteoporosis.

[9]  Frederick G. Strathmann,et al.  3-epi-25 hydroxyvitamin D concentrations are not correlated with age in a cohort of infants and adults. , 2012, Clinica chimica acta; international journal of clinical chemistry.

[10]  U. Ekelund,et al.  Protocol for the modeling the epidemiologic transition study: a longitudinal observational study of energy balance and change in body weight, diabetes and cardiovascular disease risk , 2011, BMC public health.

[11]  I. Osunkwo.  Complete resolution of sickle cell chronic pain with high dose vitamin D therapy: a case report and review of the literature. , 2011, Journal of pediatric hematology/oncology.

[12]  P. Lips,et al.  Worldwide status of vitamin D nutrition , 2010, The Journal of Steroid Biochemistry and Molecular Biology.

[13]  A. Hoofnagle,et al.  A rubber transfer gasket to improve the throughput of liquid-liquid extraction in 96-well plates: application to vitamin D testing. , 2010, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[14]  N. Jablonski,et al.  Human skin pigmentation as an adaptation to UV radiation , 2010, Proceedings of the National Academy of Sciences.

[15]  William Wheeler,et al.  Genome-wide association study of circulating vitamin D levels , 2010, Human molecular genetics.

[16]  I. Chen,et al.  Prevalence of vitamin D deficiency in adults with sickle cell disease. , 2010, Journal of the National Medical Association.

[17]  F. Cantatore,et al.  Vitamin D and the Immune System , 2010, The Journal of Rheumatology.

[18]  M. Lehtinen,et al.  The Effects of Storage Time and Sampling Season on the Stability of Serum 25-Hydroxy Vitamin D and Androstenedione , 2009, Nutrition and cancer.

[19]  J. Souberbielle,et al.  Osteopenia and vitamin D deficiency in children with sickle cell disease , 2009, European journal of haematology.

[20]  T. Pieber,et al.  Vitamin D status and arterial hypertension: a systematic review , 2009, Nature Reviews Cardiology.

[21]  N. Jablonski,et al.  Vitamin D and the evolution of human depigmentation. , 2009, American journal of physical anthropology.

[22]  D. Cole,et al.  Common genetic variants of the vitamin D binding protein (DBP) predict differences in response of serum 25-hydroxyvitamin D [25(OH)D] to vitamin D supplementation. , 2009, Clinical biochemistry.

[23]  B. Zemel,et al.  High risk of vitamin D deficiency in children with sickle cell disease. , 2008, Journal of the American Dietetic Association.

[24]  J. Norris,et al.  Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans. , 2008, The Journal of clinical endocrinology and metabolism.

[25]  J. Aloia.  African Americans, 25-hydroxyvitamin D, and osteoporosis: a paradox. , 2008, The American journal of clinical nutrition.

[26]  M. Holick,et al.  Sickle cell bone disease: Response to vitamin D and calcium , 2008, American journal of hematology.

[27]  S. Pocock,et al.  The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. , 2008, Journal of clinical epidemiology.

[28]  Michael J. Pencina,et al.  Vitamin D Deficiency and Risk of Cardiovascular Disease , 2008, Circulation.

[29]  K. Badenhoop,et al.  CYP2R1 (vitamin D 25‐hydroxylase) gene is associated with susceptibility to type 1 diabetes and vitamin D levels in Germans , 2007, Diabetes/metabolism research and reviews.

[30]  S. Pocock,et al.  The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. , 2007, Preventive medicine.

[31]  M. Holick.  Vitamin D deficiency. , 2007, The New England journal of medicine.

[32]  G. Velho,et al.  Vitamin D endocrine system and the genetic susceptibility to diabetes, obesity and vascular disease. A review of evidence. , 2005, Diabetes & metabolism.

[33]  G. Chaplin.  Geographic distribution of environmental factors influencing human skin coloration. , 2004, American journal of physical anthropology.

[34]  B. Zemel,et al.  Low vitamin D status in children with sickle cell disease. , 2004, The Journal of pediatrics.

[35]  S. Nicolai,et al.  A review of evidence , 2015 .

[36]  E. Michos.  Vitamin D deficiency and the risk of incident Type 2 diabetes. , 2009, Future cardiology.

[37]  D. Black,et al.  Serum 25-hydroxyvitamin D is unaffected by multiple freeze-thaw cycles. , 2005, Clinical chemistry.