Výsledky vyhledávání - "Dania A, Monagel"

Akademický článek

Neurological abnormalities among pediatric patients with sickle cell disease in Saudi Arabia: a single-center retrospective study

Autor: Ziad T. Basuni, Dania A. Monagel, Areej Taha, Nehal Ahmed, Amany Ahmed

Publikováno v: Frontiers in Pediatrics, Vol 11 (2024)

IntroductionSickle cell disease (SCD) is a common inherited blood disorder characterized by the production of abnormal sickle-shaped red blood cells. SCD can lead to various complications including neurological issues. Early detection and treatment a

Externí odkaz: https://doaj.org/article/6d32467fbda0459585f9534aa8bcfc47

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Akademický článek

Renal outcomes in pediatric patients with sickle cell disease: a single center experience in Saudi Arabia

Autor: Dania A. Monagel, Shatha S. Algahtani, Lian A. Karawagh, Wafa D. Althubaity, Sara A. Azab, Deena F. Haneef, Naglla Elimam

Publikováno v: Frontiers in Pediatrics, Vol 11 (2023)

BackgroundSickle cell nephropathy (SCN) is a significant complication of sickle cell disease (SCD) with an asymptomatic onset in childhood and potential progression to chronic kidney disease (CKD). The clinical findings of SCN include hyposthenuria,

Externí odkaz: https://doaj.org/article/6595ee9acb09446e8bed7e0d79f9103e

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Akademický článek

The perception of pediatric sickle cell anemia patient's caregivers toward hematopoietic stem cell transplantation (single-center experience, Saudi Arabia)

Autor: Dania A. Monagel, Naglla Alemam, Manar Betar, Fay N. Alnafisi, Dania E. Faidah, Reema E. Aloteibi, Muhammad Khan, Israa A. Malli

Publikováno v: Frontiers in Pediatrics, Vol 11 (2023)

BackgroundSickle cell disease (SCD) is a relatively common genetic disorder in Saudi Arabia characterized by the predominance of sickle hemoglobin (HbS). Although multiple supportive care options exist for patients with SCD, hematopoietic stem cell t

Externí odkaz: https://doaj.org/article/acf06b3e17754837b2c9dbd79bb79d21

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Akademický článek

New SAMD9L heterozygous mutation leading to myelodysplastic syndrome and acute myeloid leukemia: A case report and review of the literature

Autor: Dania A. Monagel

Publikováno v: Cancer Reports, Vol 6, Iss 4, Pp n/a-n/a (2023)

Abstract Background SAMD9L mutation is linked to the development of myeloid neoplasm. The mutation has a wide range of clinical presentations involving neurological, immunological, and hematological manifestations. Until now, limited data regarding d

Externí odkaz: https://doaj.org/article/1ebfbd1848a14f91b76a4c4070c442c0

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Gonadal health in recipients of nonmyeloablative hematopoietic stem cell transplantation in children and adolescents with sickle cell disease

Autor: Richelle C, Waldner, Gregory M T, Guilcher, Dania A, Monagel, Josephine, Ho, Sunil, Desai, Elizabeth T, Rosolowsky

Publikováno v: Pediatric Hematology and Oncology. :1-6

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11612294ab65cc9271cc25db46b3eca3
https://doi.org/10.1080/08880018.2022.2138659

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Clinical and pathological characteristics of extra-cranial germ cell tumors

Autor: Dania A. Monagel, Aletani Tala, Alghamdi Arwa, Banjar Sereen, Hakeem Ilana, Hannef Deena, Ahmed Omaima, Elimam Naglla

Publikováno v: Saudi Medical Journal. 44:498-499

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::414e5e7c6b1c5aa9b913d2bcf870c66d
https://doi.org/10.15537/smj.2023.44.5.20230070

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Pulmonary function in children and adolescents with sickle cell disease after nonmyeloablative hematopoietic cell transplantation

Autor: Dania A. Monagel, Gregory M. T. Guilcher, Alberto Nettel‐Aguirre, Glenda N. Bendiak

Publikováno v: Pediatric Blood & Cancer. 69

Pulmonary complications are common in sickle cell disease (SCD). The use of standard myeloablative conditioning regimens may increase the risk of lung injury. We report serial pulmonary function testing (PFT) outcomes in children with SCD who underwe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f447095ca349a72bb456f2732cf534b
https://doi.org/10.1002/pbc.29927

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Neuropsychological, behavioral, and quality‐of‐life outcomes in children and adolescents with sickle cell disease treated with nonmyeloablative matched sibling donor hematopoietic cell transplantation: A case series

Autor: Taryn B. Fay‐McClymont, Dania A. Monagel, Gurpreet Singh, Fiona Schulte, Brian L. Brooks, William S. MacAllister, Naddley Désiré, Aleksandra Mineyko, Marsha Vasserman, Michael T. Leaker, Tony H. Truong, Ravi Shah, Victor A. Lewis, Keith Owen Yeates, Gregory M. T. Guilcher

Publikováno v: Pediatric Blood & Cancer. 69

Despite advances in the treatment of sickle cell disease (SCD), cerebrovascular and cognitive insults can have lifelong consequences. Hematopoietic cell transplantation (HCT) is an established curative therapy, and recent studies have demonstrated ef

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c935fada1637f0a9d62de1a38003649
https://doi.org/10.1002/pbc.29893

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Clinical features at diagnosis of sickle cell disease prior to universal newborn screening in Alberta

Autor: Dania A Monagel, Jessica Monteiro, Jennifer Thull-Freedman, Angela Ruzycki, Michael Leaker, MacGregor Steele

Publikováno v: Paediatricschild health. 27(8)

Objectives Sickle cell disease (SCD) is an inherited multisystem disorder with complications starting in the first year of life. Newborn screening (NBS) can identify infants with SCD and is associated with decreased morbidity and mortality. Variation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47a19afd423d79d315d7f81830ce06be
https://pubmed.ncbi.nlm.nih.gov/36583074

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