2026
article
OpenAlex
Amir Ali Hamidieh, Mina Mokaram, Amirali Kalantari, Leila Jafari et autres
BACKGROUND: Fanconi anemia (FA) is the most common inherited bone marrow failure syndrome. Iran, with a high rate of consanguineous marriage and considerable ethnic diversity, represents a high-risk context for FA. We established the Iranian Fanconi Anemia Registry (IRFAR) to provide the …
ir
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2026
article
OpenAlex
Amirali Kalantari, Zahra Karimizadeh, Atoosa Eftekhar, Rashin Mohseni et autres
Chronic and complex wounds are a major burden worldwide, and a considerable number remain unresponsive to traditional therapy. Cord blood-derived platelet gel (CBPG) is a novel allogeneic wound therapy providing a fibrin-based scaffold enriched with neonatal platelet-derived growth factors, including high concentrations …
ir
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2026
article
OpenAlex
Shirin Hekmatirad, Fatemeh Gholizadeh, Saeed Montazeri, Laleh Sharifi et autres
Bladder cancer (BC) exhibits high inter- and intra-patient heterogeneity, limiting the efficacy of standard treatments and underscoring the need for personalized therapeutic models. We established patient-derived organoids (PDOs) from 31 clinical BC specimens, achieving an 80.65% success rate. These organoids preserved distinct …
ir
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2026
article
OpenAlex
Atieh Karimzadeh, Sadaf Setareh Azar, Yalda Karamlou, Amirali Kalantari et autres
ir
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2026
article
OpenAlex
Shafie Rahmati, Amir Ali Hamidieh, Maryam Behfar, Leila Jafari et autres
Performance of centrifugal blood component separators in apheresis is highly dependent on operational parameters such as rotational speed and inlet flow rate. However, fixed-protocol systems limit multi-objective optimization and adaptability to donor variability. To investigate the coupled effects of rotational speed and …
ir
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2026
article
OpenAlex
Anahita Razaghian, Mohsen Badalzadeh, Amir Ali Hamidieh, Raheleh Shokouhi Shoormasti et autres
PURPOSE: Wiskott-Aldrich syndrome (WAS) is an X-linked immunodeficiency characterized by eczema, microthrombocytopenia, and recurrent infections. This study evaluates the frequency of clinical manifestations and overall outcomes in WAS patients, comparing those who received hematopoietic stem cell transplantation (HSCT) with those who did …
ir
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2026
preprint
OpenAlex
Neda Parvini, Amir Ali Hamidieh, Fardin Fathi, Abbas Ali Amini et autres
ir
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2025
article
OpenAlex
Mahdiyeh Movahedi, Leila Moradi, Zahra Alizadeh, Mojtaba Tabatabaei Yazdi et autres
Background: Severe congenital neutropenia (SCN) is commonly treated with granulocyte colony-stimulating factor (G-CSF) to reduce neutropenia and the associated risk of infections. Pegfilgrastim, a long-acting form of G-CSF, provides the benefit of less frequent dosing; however, its application in SCN has not …
ir
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2025
conference-abstract
OpenAlex
Robert Chiesa, Michael H. Albert, Patrick Gilbert, Jeroen Knippenberg et autres
Abstract Introduction Osteopetrosis (OP) is a group of rare inherited conditions characterized by dysfunctional osteoclasts, leading to hypocalcemia, cytopenia, bone fractures, compression of cranial nerves and vision loss. Hematopoietic stem cell transplantation (HSCT) is the only curative approach for most children with …
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2025
article
OpenAlex
Leila Jafari, Pooya Ashkevari, Sarina Ansari, Mona Delkhah et autres
BACKGROUND: A significant challenge in extracorporeal photopheresis (ECP) in developing countries is the high cost of apheresis equipment. Additionally, obtaining proper IV access in pediatric patients is considerably more difficult than in adult patients. To address the limitations of applying ECP for …
ir, fr
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Accès ouvert
2025
article
OpenAlex
Batool Pouraboli, Maryam Maleki, Nahid Dehghan Nayeri, Amir Ali Hamidieh et autres
BACKGROUND: Pediatric hematopoietic stem cell transplantation (HSCT) is a complex process that impacts the entire family. The traumatic nature of the pediatric HSCT period makes this a particularly vulnerable time for parents, leading to coping challenges. This study aimed to explore parents' …
ir
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2025
article
OpenAlex
Abbas Khosravi, Abtin Ghasempour, Mostafa Paridar, Pargol Mashati et autres
Megakaryocytes (MKs), which are differentiated from megakaryocytic–erythrocytic progenitors, generate platelets (PLTs) by expanding and branching their cellular fragments under the influence of cytokines and intercellular mechanisms such as autophagy and release of reactive oxygen species (ROS) in the bone marrow. Autophagy is …
ir, us
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