Results 111 to 120 of about 20,435 (244)

Hemoglobinopathies and preimplantation diagnostics

, 2022
Hemoglobinopathies constitute some of the most common inherited disorders worldwide. Manifestations are very severe, patient management is difficult and treatment is not easily accessible.
Mamas, T., Kakourou, G., Vrettou, C., Traeger-Synodinos, J.   +3 more
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Cerebral Blood Transit in Sickle Cell Anemia

Journal of Magnetic Resonance Imaging, Volume 64, Issue 3, Page 738-750, September 2026.
ABSTRACT Background Sickle cell anemia (SCA) patients upregulate cerebral blood flow to compensate for decreased arterial oxygen content. Such hyperemic conditions can manifest as venous hyperintense signal on arterial spin labeling (ASL) MRI, which may reflect faster capillary blood transit, altered oxygen extraction fraction (OEF), and infarct risk ...
Wesley T. Richerson, Megan A. Aumann, Alexander K. Song, Samantha Davis, Lauren Milner, Maria Garza, Dann Martin, L. Taylor Davis, Sumit Pruthi, Lori C. Jordan, Manus J. Donahue   +10 more
wiley   +1 more source

A study of hemoglobinopathies and hemoglobin variants by high-performance liquid chromatography and correlation with red blood cell indices in antenatal mothers

Asian Journal of Medical Sciences
Background: Hemoglobinopathies are the most commonly inherited red cell disorder around the world. In India, hemoglobinopathies show wide variation of prevalence in different regions and different populations.
Arnab Sinha , Suchismita Chakrabarti , Ruplekha Mitra Mustaphi   +2 more
doaj   +1 more source

Beta Thalassemia and Chronic Myeloid Leukemia: Dual Diagnosis Under the Microscope

International Journal of Laboratory Hematology, Volume 48, Issue 5, Page 931-933, October 2026.
Paige Muir, Mohammad Bahmanyar, Hamish Nicolson, Hayley Merkeley   +3 more
wiley   +1 more source

Patent Foramen Ovale: Epidemiology, Risk Factors, Pathophysiology, Clinical Features, Diagnosis, and Management

MedComm, Volume 7, Issue 9, September 2026.
The clinical manifestations of PFO. Although the majority of PFOs are benign and asymptomatic, they can present with a variety of clinical manifestations, or coexisting with other diseases and aggravating their symptoms, including cerebral diseases (such as CS, epilepsy, TIA, or migraine), systemic embolism (such as embolism in renal artery, coronary ...
Linlin Meng, Xiaotong Zhang, Guangrui Sun, Honggang Dai, Xiao Meng, Cheng Zhang, Yun Zhang   +6 more
wiley   +1 more source

Rheumatoid arthritis in patients with hemoglobinopathies

, 2011
Rheumatoid arthritis (RA) in patients suffering from hemoglobinopathies is an important clinical problem, but the correlation between these diseases is still imperfectly known.
Pliakou, X. I., Bourantas, K. L., Damigos, D., Briasoulis, E., Koutsouka, F. P., Voulgari, P. V.   +5 more
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Relationship between hemoglobinopathies and male infertility: a scoping review [PDF]

Infertility is a common issue that threatens couples worldwide. Infertility can result from the male or female partner alone, or both partners. It can be due to multiple factors related to the patient’s overall health or lifestyle.
Yassin, Mohamed, Jolo, Lolwa, Eliwa, Ahmed, Al-Jubouri, Abdullah M., Haithm, Yunes, Al-Qahtani, Noof   +5 more
core   +1 more source

Mirror Syndrome (Ballantyne Syndrome): Prenatal Diagnosis, Pathophysiology, and the Role of Fetal Therapy—A Narrative Review

Prenatal Diagnosis, Volume 46, Issue 10, Page 1617-1625, September 2026.
ABSTRACT Mirror syndrome is a rare maternal–fetal condition associated with fetal hydrops and a high risk of adverse maternal and fetal perinatal outcomes. Its diagnosis is challenging due to the lack of standardized diagnostic criteria and its clinical and biochemical overlap with preeclampsia.
Riccardo Tudisco, Pauline Latapie, Anita Romiti, Alexandra Benachi, Maelig Abgral, Alexandre J. Vivanti   +5 more
wiley   +1 more source

Society for Maternal‐Fetal Medicine Special Statement: Checklists for persons with sickle cell disease in pregnancy

Pregnancy, Volume 2, Issue 5, September 2026.
Abstract This article presents checklists designed to guide clinicians in the comprehensive management of pregnant individuals with sickle cell disease, including prepregnancy, antepartum, delivery, and postpartum care, as well as the specific management of vaso‐occlusive crises.
Society for Maternal‐Fetal Medicine (SMFM), Nicolina Smith, Rebecca F. Hamm, Jessica Peterson, Alexandra DeRusso Forrest, Nicole A. Smith, Jourdan E. Triebwasser, SMFM Patient Safety and Quality Committee   +7 more
wiley   +1 more source

Hemoglobinopathies types and their peculiarities in India

Hemoglobinopathies, including thalassemias and sickle cell disorders are among the most prevalent inherited autosomal recessive blood disorders globally and pose significant public health challenges in India.
Ткаченко, Олена Вікторівна, Tkachenko, О. V., Sharma, D.   +2 more
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