Results 151 to 160 of about 345,333 (344)

55 Oxymetholone Therapy of Aplastic Anemia [PDF]

open access: bronze, 1967
Donald M. Allen   +4 more
openalex   +1 more source

Quality control improvement at Jana DCS Sdn. Bhd. [PDF]

open access: yes, 2020
Jana DCS Sdn. Bhd. is one of the companies that run the service of air conditioning system supply in Nusajaya, Johor, Malaysia. Quality improvement is one of the most important part when talking about a company, mostly companies that operate in service ...
Abd Wahab, Muhammad Badrul Amin   +4 more
core  

Increased Plasma ST2 Levels Precede the Development of Severe Acute GvHD and Chronic GvHD After Pediatric Hematopoietic Stem Cell Transplantation

open access: yesPediatric Blood &Cancer, Volume 72, Issue 11, November 2025.
ABSTRACT Background The suppressor of tumorigenesis 2 (ST2) has emerged as one of the most promising biomarkers for predicting mortality of acute graft‐versus‐host disease (aGvHD) when measured at the onset of symptoms, but detailed time course studies are needed to understand the potential of ST2 as a risk marker of both aGvHD and chronic graft‐versus‐
Nakisa Kamari‐Kany   +6 more
wiley   +1 more source

تعيين ميزان بقا و عوامل موثر بر آن در کودکان مبتلا به آنمی آپلاستيک اکتسابی [PDF]

open access: yes, 2004
آنمی آپلاستيک يک سندرم بالينی به صورت پان سيتوپنی در خون محيطی است که در اثر کاهش يا عدم توليد سلولهای خونی، بدون وجود شواهدی از بيماری ديگر در مغز استخوان ايجاد می‌شود. اين بيماری به 2 شکل اکتسابی و ارثی(مانند آنمی فانکونی) وجود دارد.
آهنچی, نوید   +2 more
core  

APLASTIC ANEMIA AND HEALTH OF THE ORAL CAVITY- CLINICAL CONSIDERATIONS

open access: yesRomanian Journal of Oral Rehabilitation, 2022
Aplastic anemia is a non-oncological haematological disease, which is a challenge for specialists due to the severity of the clinical symptoms. It is characterized by hypocellularity of the bone marrow and its secondary pancytopenia.
Cristina Claudia Tărniceriu   +7 more
doaj  

CLINICAL APPLICABILITY OF PROPOSED ALGORITHM FOR IDENTIFYING INDIVIDUALS AT RISK FOR HEREDITARY HEMATOLOGIC MALIGNANCIES [PDF]

open access: yes, 2017
Over the past decade, more than 12 genes have been identified to cause hereditary predispositions to hematologic malignancies. These syndromes are characterized by an increased risk to develop myelodysplastic syndrome (MDS), acute myeloid leukemia (AML),
Clifford, Maggie
core   +1 more source

First Report of MPL c.23T>G (p.M8R) Variant in Congenital Amegakaryocytic Thrombocytopenia: A Case Report

open access: yeseJHaem, Volume 6, Issue 5, October 2025.
ABSTRACT Congenital amegakaryocytic thrombocytopenia is a rare inherited bone marrow failure syndrome primarily caused by MPL gene mutations. It presents with severe neonatal thrombocytopenia and typically progresses to pancytopenia. We report the first disease‐associated case of the MPL variant c.23T>G, identified through whole‐exome sequencing in an ...
Atbin Latifi, Sina Yousefian
wiley   +1 more source

The Experience of Caring for Haematopoietic Stem Cell Transplant Patients From the Perspective of Haematology Nurses: A Qualitative Descriptive Study

open access: yesNursing Open, Volume 12, Issue 10, October 2025.
ABSTRACT Aim This study aimed to explore the experiences of haematology nurses while caring for patients undergoing haematopoietic stem cell transplantation. Design A qualitative descriptive study was conducted. Methods We conducted semi‐structured interviews with 18 haematology nurses in six hospitals between May 2022 and December 2023.
Ying Qian   +4 more
wiley   +1 more source

Cutaneous Finding in Anti Thymocyte Globulin Induced Serum Sickness

open access: yesIranian Journal of Allergy, Asthma and Immunology, 2006
Polyclonal anti-thymocyte globulin (ATG) is used as an immunosuppressive agent in the treatment of aplastic anemia (AA). Serum sickness is a recognized side effect of ATG.
Seyed Hesamedin Nabavizadeh   +2 more
doaj  

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