Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Domnita Crisan"'
Publikováno v:
Annals of clinical and laboratory science. 47(1)
Medical literature has documented an association between acute hepatic failure and coarse, bright-green neutrophilic inclusions. Upon identification of these unique inclusions patients have been reported to have poor outcomes and usually die within 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::31112f0d77d162ce4806e39917d63ad3
https://pubmed.ncbi.nlm.nih.gov/28249918
https://pubmed.ncbi.nlm.nih.gov/28249918
Publikováno v:
Diagnostic Molecular Pathology. 22:156-160
FLT3 is one of the most frequently mutated genes in acute myeloid leukemia. Previous studies have reported FLT3 mutation in as many as 9.2% of myeloproliferative neoplasms (MPNs) and myelodysplastic/myeloproliferative neoplasms (MDS/MPNs), as well as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9e597ed3219ee48c65ecd347d9f18a5
https://doi.org/10.1097/pdm.0b013e31828564fe
https://doi.org/10.1097/pdm.0b013e31828564fe
Autor:
Bobby L. Boyanton, Domnita Crisan
Publikováno v:
Laboratory Hematology Practice
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7454a7fc94a8ab30916103573a2ecdb2
https://doi.org/10.1002/9781444398595.ch13
https://doi.org/10.1002/9781444398595.ch13
Publikováno v:
European Journal of Haematology. 46:77-84
33 cases of chronic granulocytic leukemia (CGL) were reassessed to determine if, by strict morphologic criteria. Philadelphia chromosome (Ph1)-negative CGL exists as a diagnostic entity and if Ph1-positive CGL could be distinguished from Ph1-negative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d82f2e5f214a25e154097a9770ad8cf
https://doi.org/10.1111/j.1600-0609.1991.tb00526.x
https://doi.org/10.1111/j.1600-0609.1991.tb00526.x
Publikováno v:
The Journal of Molecular Diagnostics. 8:420-425
Venous thromboembolic events (VTEs) affect an estimated 1 in 1000 people annually, resulting in ∼50,000 deaths, with prevalence increasing with age. The genetic contributors to thrombosis have been described and further explored within the last 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9aa40dfbbeb8411bcccccdf1134e805e
https://doi.org/10.2353/jmoldx.2006.060014
https://doi.org/10.2353/jmoldx.2006.060014
Autor:
Domnita Crisan, Joan C. Mattson, Lelia Yu, Rebecca C. Hankin, Arthur B. Eisenbrey, Bruce H. Davis, Waqar A. Khan, Abdul Al Saadi
Publikováno v:
American Journal of Clinical Pathology. 116:41-50
We describe 2 male patients in whom hepatosplenic gamma/delta T-cell lymphoma (HSTL) developed 6 and 10 years after renal transplantation. The onset was abrupt with systemic symptoms, cytopenia, and hepatosplenomegaly. The histologic examination of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f141c77d487b5dc06501c9d9502ad140
https://doi.org/10.1309/tc9u-fav7-0qbw-6dfc
https://doi.org/10.1309/tc9u-fav7-0qbw-6dfc
Autor:
Jeanne Carr, Domnita Crisan
Publikováno v:
The Journal of Molecular Diagnostics. 2:105-115
Cardiovascular diseases (CVD) represent a paradigm for the complex interplay of environmental risk factors and multiple genetic risk factors. Genetic abnormalities that are disease-causing, however, are less frequent than genetic factors that confer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e026f1bbdfc290d7d4ba77909300ee4
https://doi.org/10.1016/s1525-1578(10)60624-1
https://doi.org/10.1016/s1525-1578(10)60624-1
Autor:
Domnita Crisan
Publikováno v:
Clinics in Laboratory Medicine. 20:49-69
This article reviews the molecular lesions that occur in the clonal hematopoietic disorders classified as myelodysplastic syndromes (MDS). A systematization of these molecular lesions is attempted based on the types of molecular abnormalities. Charac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9c72385c765e42b2aceca3fd0bcae26
https://doi.org/10.1016/s0272-2712(18)30076-3
https://doi.org/10.1016/s0272-2712(18)30076-3
Publikováno v:
Molecular Diagnosis. 5:33-38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4dac626b695edc6f9ee5f12e7decb74
https://doi.org/10.2165/00066982-200005010-00009
https://doi.org/10.2165/00066982-200005010-00009
Publikováno v:
Molecular Diagnosis. 3:163-170
Background: Hairy cell leukemia (HCL) is a slowly progressive lymphoproliferative disorder that tends to afflict middle-aged adults, especially men. Blastic transformation of this form of leukemia is extremely rare. To date, a single case has been re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c81f64f733c148e44ea3662287cb5d17
https://doi.org/10.1016/s1084-8592(98)80035-0
https://doi.org/10.1016/s1084-8592(98)80035-0