Zobrazeno 1 - 10
of 163
pro vyhledávání: '"anemia syndrome"'
Autor:
Francesca Di Candia, Valentina Di Iorio, Nadia Tinto, Riccardo Bonfanti, Claudio Iovino, Francesco Maria Rosanio, Ludovica Fedi, Fernanda Iafusco, Francesca Arrigoni, Rita Malesci, Francesca Simonelli, Andrea Rigamonti, Adriana Franzese, Enza Mozzillo
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-8 (2023)
Abstract Background Individuals with thiamine-responsive megaloblastic anemia (TRMA) mainly manifest macrocytic anemia, sensorineural deafness, ocular complications, and nonautoimmune diabetes. Macrocytic anemia and diabetes may be responsive to high
Externí odkaz:
https://doaj.org/article/f16f0562ac8a44fe9e76fe144d6f5725
Autor:
Yosef Manla, Obada Kholoki, Feras Bader, Oshin Kanwar, Emna Abidi, Wasim S. El Nekidy, Fadi Hijazi, Nizar Attallah
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
Background and aimLittle is known about the burden of cardiorenal syndrome (CRS) and cardiorenal anemia syndrome (CRAS) in the Middle East Region. Furthermore, whether the occurrence rates of CRAS differ across heart failure (HF) phenotypes is not wi
Externí odkaz:
https://doaj.org/article/99d58d681d6f4314ad236c3da94f9a23
Publikováno v:
Revista GICOS, Vol 7, Iss 3, Pp 35-53 (2022)
La anemia es el descenso de la concentración de hemoglobina e incapacidad de eritropoyesis para compensar la pérdida excesiva de eritrocitos. La población más vulnerable al síndrome anémico (SA) son personas mayores de 60 años, quienes represe
Externí odkaz:
https://doaj.org/article/004729dd3e8c4d8d9439f4fea0ae8528
Akademický článek
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Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
BackgroundPatients with chronic kidney disease (CKD) are at high risk of developing heart failure and anemia, which is defined as type 4 cardiorenal-anemia syndrome (CRAS). CRAS aggravates the deterioration of both kidney and heart function, ultimate
Externí odkaz:
https://doaj.org/article/8ea500234189414e9960710bdaa50a4a
Publikováno v:
Clinical Case Reports, Vol 8, Iss 6, Pp 991-994 (2020)
Abstract The case of thiamine‐responsive megaloblastic anemia (TRMA) presented here speculates the need early diagnosis, continuous monitoring, follow‐up, and regulated treatment plan for the patients. Complications and systemic manifestations ar
Externí odkaz:
https://doaj.org/article/e57d3005260c40d8805a93273cb339de
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-5 (2019)
Abstract Background Phenotypic difference is general in Mendelian disease. Due to the extremely low incidence for a single disease, phenotype spectrum needs to be expanded. Meanwhile, earlier knowledge says patients who suffered from two kinds of dif
Externí odkaz:
https://doaj.org/article/d59b2affcec24362a30b6ff3f733a5df
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: Thiamine-responsive megaloblastic anemia syndrome (TRMA) is a rare autosomal recessive hereditary disease due to mutations in SLC19A2. Some cases show familial inheritance.Case report: A female patient (from a gravida 1, para 1 mother) of
Externí odkaz:
https://doaj.org/article/59850e3120964d1ea67f0dcd3ffcd3ab
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
G. N. Gorokhovskaya, V. L. Yun
Publikováno v:
Медицинский совет, Vol 0, Iss 2, Pp 85-92 (2014)
The article tells about the etiology and pathogenesis of iron deficiency, clinical manifestations and principles of treatment of iron deficiency anemia. The choice of drug therapy is highlighted. The advantages of non-ionic iron preparations (Maltofe
Externí odkaz:
https://doaj.org/article/0ba2ea5ccd4f4826a854d33682421a70