s aboutalebi
Volume 2, Issue 3 , January 2022, Pages 121-121
Abstract
The COVID–19 pandemic has affected all aspects of health care services. To protect health care workers and patientsfrom the risk of disease transmission, policies were changed to enable widespread use of telecommunicationstechnology in lieu of face to face clinical visits. we decided on establishing ...
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The COVID–19 pandemic has affected all aspects of health care services. To protect health care workers and patientsfrom the risk of disease transmission, policies were changed to enable widespread use of telecommunicationstechnology in lieu of face to face clinical visits. we decided on establishing the telerehabilitation setting based on thescientific methods and an evidence-based protocol.now running this program and we hope that these recent changesin rules and regulation in health delivery services can provide unprecedented research opportunities to study theimplementation and outcomes of telerehabilitation.
s shahbeigi; m bolourchian
Volume 2, Issue 3 , January 2022, Pages 122-125
Abstract
Antiphospholipid syndrome (APS) is an autoimmune disease categorized by recurrent thrombotic eventsand/or obstetrics complications with persistently positive antiphospholipid antibodies. APS could be presentedwith non-thrombotic features, the most important of which are neurological dysfunctions such ...
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Antiphospholipid syndrome (APS) is an autoimmune disease categorized by recurrent thrombotic eventsand/or obstetrics complications with persistently positive antiphospholipid antibodies. APS could be presentedwith non-thrombotic features, the most important of which are neurological dysfunctions such as migraine,epilepsy, multi-infarct dementia and chorea. But among them, one of the less common cases is extrapyramidalmanifestation, namely athetosis. we report a case of primary APS presenting with an unusual neurologicalmanifestation (left hand athetosis) in which due to the positivity of antiphospholipid antibodies(aPL) withoutthrombotic features or pregnancy complications and SLE, she was diagnosed as non-thrombotic primary APS.In this case report, we purpose to discuss our case in the light of current knowledge on APS and share ourtreatment approach.
n mansouri; n varma; f Shaveisi Zadeh; n Safavi Naieni; h Allahmoradi; z Sasaninezhad
Volume 2, Issue 3 , January 2022, Pages 126-130
Abstract
Background: beyond the 15% of cancers in humans can be related to virus infections, which in case, Hepatitis BVirus (HBV) improves the leukemia’s risk, particularly Acute Myeloid Leukemia.Materials and Methods: This prospective study which was conducted since 2010 to 2020 in affected individualswith ...
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Background: beyond the 15% of cancers in humans can be related to virus infections, which in case, Hepatitis BVirus (HBV) improves the leukemia’s risk, particularly Acute Myeloid Leukemia.Materials and Methods: This prospective study which was conducted since 2010 to 2020 in affected individualswith chronic and acute myeloid leukemia as well as the controls. Staining based on Cytochemical approach,immunophenotyping, Cytogenetic and molecular cytogenetics, Elisa, Enzyme Immuno assessment and WesternBloting, were as a main subject of lab manipulation .Results: In a sample of control patient hepatitis B virus was diagnosed (%0.004) and four infected with leukemicpatients (%3).In leukemic patients when compared with controls, differences revealed statistical significant(P=0.0047).Conclusion: As a results, the prevalence of HBV infection in affected people with leukemias was higher than inpatients who were as non malignant controls.We suggest that this issue warrants further investigation by largeconsortium studies. Cell, Gene and Therapy, Vol.2, Number 4, Winter 1st, 2021; 126- 130
z Sasaninezhad; n mansouri; n Safavi Naeini; m ghadiani; m Rezaei Tavirani; h Allahmoradi
Volume 2, Issue 3 , January 2022, Pages 131-135
Abstract
Background: According to the literature, there are a number of chronic and acute myeloid leukemias withunique, complex chromosome translocations. This study aims to conduct a brief review of the incidenceof complex chromosome translocations in myeloid leukemia and reports a case of myeloid leukemia withcomplex ...
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Background: According to the literature, there are a number of chronic and acute myeloid leukemias withunique, complex chromosome translocations. This study aims to conduct a brief review of the incidenceof complex chromosome translocations in myeloid leukemia and reports a case of myeloid leukemia withcomplex chromosome translocations.Methods: We conducted a web-based search for all peer review articles published on the subject ofcomplex chromosome tranlsocations in chronic and acute myeloid leukemia in MEDLINE, PubMed andMitelman (http://cgapanci.nih.gov/chromosomes/Mitelman) databases in addition to other pertinent webreferences. In addition, we performed conventional cytogenetic studies of 24- to 72-h cultures on bonemarrow/peripheral blood cells obtained from the current case. Cells were finally treated by the giemsatrypsin-giemsa banding technique.Results: The result of this case revealed an abnormal karyotype that had a novel complex translocationwhich involved chromosomes 2, 5, 9, and 22. We performed karyotyping after the initiation ofchemotherapy. Karyotyping results showed a complex karyotype 46,XX, t(2;5;9;22).Conclusion: This study discusses a case of chronic myeloid leukemia with complex chromosometranslocations and may provide novel information regarding these translocations in leukemias. Cell, Geneand Therapy, Vol.2, Number 4, Winter 1st, 2021; 131- 135
f mohammadi; s shahbeigi
Volume 2, Issue 3 , January 2022, Pages 136-139
Abstract
Guillain-Barre syndrome GBS is a rapid-onset limb weakness caused by the immune system damaging theperipheral nervous system. An early diagnosis and treatment is very necessary in this condition. We shouldconsider similar conditions such as spontaneous spinal epidural hematoma (SSEH) and differentiate ...
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Guillain-Barre syndrome GBS is a rapid-onset limb weakness caused by the immune system damaging theperipheral nervous system. An early diagnosis and treatment is very necessary in this condition. We shouldconsider similar conditions such as spontaneous spinal epidural hematoma (SSEH) and differentiate thiscondition as well.
h.r farmai; a.r Khatoonabadi
Volume 2, Issue 3 , January 2022, Pages 140-141
Abstract
Background: The world is changing due to everyday development in technology and communication devicesfacilities. Using these communication devices have evolved social communication, education and also healthcare services.Results: there are some challenges, such as lack of high-quality studies and little ...
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Background: The world is changing due to everyday development in technology and communication devicesfacilities. Using these communication devices have evolved social communication, education and also healthcare services.Results: there are some challenges, such as lack of high-quality studies and little acceptance from the therapist.Therefore, it is critical to work on validating assessment tools for telerehabilitation conditions. Besides, there isa need for working on modifying treatments methods and assess their efficacy in a different group of patientswith high-quality studies.
z Sasaninezhad; s shir mohammadi
Volume 2, Issue 3 , January 2022, Pages 142-145
Abstract
Rubella virus is an RNA virus that has RNA genome and belonging to genus Rubivirus and familyMatonaviridae, and Rubella is a viral infection which can cause fetal death or congenital defects. The WorldHealth Organization (WHO) recognizes 12 genotypes for Rubella virus genome include 1B, 1C, 1D, 1E, 1F,1G, ...
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Rubella virus is an RNA virus that has RNA genome and belonging to genus Rubivirus and familyMatonaviridae, and Rubella is a viral infection which can cause fetal death or congenital defects. The WorldHealth Organization (WHO) recognizes 12 genotypes for Rubella virus genome include 1B, 1C, 1D, 1E, 1F,1G, 1H, 1I, 1J, 2A, 2B, and 2C, and 1provisional genotype, 1a. Genotype1E,which has been confirmed as themost frequent genotype in China, has circulated continuouslysince its first isolation in 2001.Despite recent developments in wholegenome sequencing technologies, the number of available completegenome sequences of rubella virus is still less than 50 in GenBank. Among these sequences are only 13complete genome sequences of genotype 2B isolates The genome of RV is a single molecule of positivestrandRNA of approximately 10 kb with a GC content of 69.5 %, by far the most of any RNA virus sequencedto date.16 The 5' end of the RNA has a 7-methyl-guanosine cap.
