Sickle cell-hemoglobin Caribbean--a benign syndrome

Priapism in Homozygous Sickle Cell Disease: A 40-year Study of the Natural History.

The West Indian medical journal·2015

Iron Deficiency among Jamaican Adolescents.

The West Indian medical journal·2015

Pattern of pregnancy weight gain in homozygous sickle cell disease and effect on birth size.

The West Indian medical journal·2011

Venous incompetence, poverty and lactate dehydrogenase in Jamaica are important predictors of leg ulceration in sickle cell anaemia.

British journal of haematology·2008

Lamotrigine poisoning presenting as seizures: a case of deliberate poisoning.

Child abuse & neglect·2007

Dominant influence of gamma-globin promoter polymorphisms on fetal haemoglobin expression in sickle cell disease.

Cellular and molecular biology (Noisy-le-Grand, France)·2004

Molecular Epidemiology of δβ-Thalassemia and Hereditary Persistence of Fetal Hemoglobin (HPFH) in the Quanzhou Childbearing-Age Population, China.

Hemoglobin·2026

Compound Heterozygous Hemoglobin Minneapolis-Laos and Codon 41/42 (-TTCT) in a Thai Female Adult: A Case Report and Literature Review.

Hemoglobin·2026

Hb F-SickKids (HBG2: C.308A > G): A Novel γ-Globin Variant Associated with Transient Neonatal Cyanosis.

Hemoglobin·2026

Pyruvate Kinase Activation in the Management of Thalassemia and Sickle Cell Disease.

Hemoglobin·2026

Genotypic Characterization of Hemoglobinopathies in Azerbaijan: A Review of 10 Years at a Referral Center.

Hemoglobin·2026

Successful Management of Transfusion-Dependent Unstable Hemoglobin Perth with Splenectomy: First Report from Iran and Literature Review.

Hemoglobin·2026

First reported North American calcium binding protein 2-related non-syndromic hearing loss.

BMJ case reports·2026

Steatocystoma Simplex of the Orbit: Expanding the Differential for Pediatric Eye Masses.

Cureus·2026

The second species of Cyanocypus He & Zhou (Coleoptera: Staphylinidae: Staphylininae) with remarks on the systematic position of the genus.

Zootaxa·2026

Late-diagnosed Nonclassical 21-hydroxylase Deficiency in Two Elderly Men with Adrenal Incidentalomas: Clinical Clues to the Underlying Diagnosis.

Internal medicine (Tokyo, Japan)·2026

Oxalate Nephropathy-Induced Acute Kidney Injury following Use of an Organic Hair-Treatment Product in an 8-Year-Old Child: A Case Report.

Case reports in nephrology and dialysis·2026

Related Experiment Videos

Sickle cell-hemoglobin Caribbean--a benign syndrome

Related Concept Videos

Priapism in Homozygous Sickle Cell Disease: A 40-year Study of the Natural History.

Iron Deficiency among Jamaican Adolescents.

Pattern of pregnancy weight gain in homozygous sickle cell disease and effect on birth size.

Venous incompetence, poverty and lactate dehydrogenase in Jamaica are important predictors of leg ulceration in sickle cell anaemia.

Lamotrigine poisoning presenting as seizures: a case of deliberate poisoning.

Dominant influence of gamma-globin promoter polymorphisms on fetal haemoglobin expression in sickle cell disease.

Molecular Epidemiology of δβ-Thalassemia and Hereditary Persistence of Fetal Hemoglobin (HPFH) in the Quanzhou Childbearing-Age Population, China.

Compound Heterozygous Hemoglobin Minneapolis-Laos and Codon 41/42 (-TTCT) in a Thai Female Adult: A Case Report and Literature Review.

Hb F-SickKids (<i>HBG2</i>: C.308A > G): A Novel γ-Globin Variant Associated with Transient Neonatal Cyanosis.

Pyruvate Kinase Activation in the Management of Thalassemia and Sickle Cell Disease.

Genotypic Characterization of Hemoglobinopathies in Azerbaijan: A Review of 10 Years at a Referral Center.

Successful Management of Transfusion-Dependent Unstable Hemoglobin Perth with Splenectomy: First Report from Iran and Literature Review.

First reported North American calcium binding protein 2-related non-syndromic hearing loss.

Steatocystoma Simplex of the Orbit: Expanding the Differential for Pediatric Eye Masses.

<b>The second species of <i>Cyanocypus</i> He & Zhou (Coleoptera: Staphylinidae: Staphylininae) with remarks on the systematic position of the genus</b>.

Late-diagnosed Nonclassical 21-hydroxylase Deficiency in Two Elderly Men with Adrenal Incidentalomas: Clinical Clues to the Underlying Diagnosis.

Oxalate Nephropathy-Induced Acute Kidney Injury following Use of an Organic Hair-Treatment Product in an 8-Year-Old Child: A Case Report.

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Sickle cell-hemoglobin Caribbean--a benign syndrome

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