Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Habib Moshref Razavi"'
Autor:
Habib Moshref Razavi, Agata Minor
Publikováno v:
Clinical Case Reports, Vol 12, Iss 7, Pp n/a-n/a (2024)
Key Clinical Message This is a case of an elderly patient diagnosed with acute myeloid leukemia (AML). While morphological findings, including numerous long, slender, cigar‐shaped Auer rods, suggested AML with t(8;21), cytogenetic and FISH analysis
Externí odkaz:
https://doaj.org/article/3e1ff831e5d34f0ba731e3a535e4cd61
Publikováno v:
Clinical Case Reports, Vol 11, Iss 6, Pp n/a-n/a (2023)
Key Clinical Message No formal treatment guidelines for MDS/MPN‐RS‐T exist. With salient features such as anemia and thrombocytosis, management is individualized and aims to address anemia, thrombosis, and in some cases acquired von Willebrand's
Externí odkaz:
https://doaj.org/article/d772380453cf4050b65d34f087f4519e
Publikováno v:
Case Reports in Hematology, Vol 2023 (2023)
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is an aggressive hematologic malignancy which is associated with a distinctive morphologic appearance. However, the morphology is not specific, and diagnostic characterization requires integration
Externí odkaz:
https://doaj.org/article/49b4d2ca0b6e405796617b07554375f8
Autor:
Habib Moshref Razavi, Samuel Krikler
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss 1, Pp 140-141 (2022)
Externí odkaz:
https://doaj.org/article/0da6a2d51fec428fb7b11f6819c1be3f
Autor:
Habib Moshref Razavi, Richard Yu
Publikováno v:
Clinical Case Reports, Vol 9, Iss 5, Pp n/a-n/a (2021)
Abstract Isolated schistocytosis is a hematological emergency. Clinically significant schistocytosis requires 1% red cell fragments in a high power field. These include triangular fragments, crescents, helmet cells, keratocytes, or microspherocytes.
Externí odkaz:
https://doaj.org/article/deb0febc761d4d73bea183ac1cfddda8
Autor:
Eric McGinnis, Habib Moshref Razavi
Publikováno v:
Clinical Case Reports, Vol 7, Iss 9, Pp 1685-1688 (2019)
Abstract Gaucher disease is a clinically heterogeneous disorder of glucocerebroside metabolism and may present incidentally late in life with unexplained thrombocytopenia, splenomegaly, or bony lesions. Clinicians should be aware that patients with G
Externí odkaz:
https://doaj.org/article/89f407cf41ca41bfac4b3fe23f25bb66
Autor:
Habib Moshref Razavi
Publikováno v:
eJHaem, Vol 2, Iss 4, Pp 897-898 (2021)
Externí odkaz:
https://doaj.org/article/f37b782bd3714d23958701e6c01fc1f8
Autor:
Habib Moshref Razavi
Publikováno v:
Turkish Journal of Hematology, Vol 38, Iss 2, Pp 151-152 (2021)
Externí odkaz:
https://doaj.org/article/81e824775dcf46fd984fc9de0ca4e19c
Autor:
Julia Varghese, Habib Moshref Razavi
Publikováno v:
eJHaem, Vol 2, Iss 2, Pp 303-304 (2021)
Externí odkaz:
https://doaj.org/article/b68912eb0db44f8997b00f4132860bf6
Publikováno v:
Case Reports in Hematology, Vol 2020 (2020)
A previously well 49-year-old patient presented to our hospital with symptomatic hypercalcaemia complaining of polyuria and polydipsia, as well as abdominal and lower back pain (serum/ionized calcium at 3.66 milli mole/l and 1.90 milli moles/l). At a
Externí odkaz:
https://doaj.org/article/ceef3ae282bc47baa5e0c36c381329d9