Results 121 to 130 of about 68,882 (316)

Low rates of endothelial cell dysfunction and transplant‐related mortality in 537 children receiving fludarabine–treosulfan conditioning for all transplant indications: A retrospective multicentre study on behalf of the UK Paediatric BMT group

British Journal of Haematology, EarlyView.
Thomas Altmann, Kanchan Rao, Ramya Hanasoge‐Nataraj, Katharine Patrick, Ben Carpenter, Rachael Hough, Anna‐Maria Ewins, Sanjay Tewari, Oana Mirci‐Danicar, Mary Slatter, Robert Wynn, Su Han Lum   +11 more
wiley   +1 more source

Analysis of Late Complications Associated With Hematopoietic Stem Cell Transplantation in Patients With Dyskeratosis Congenita

Pediatric Blood &Cancer, Volume 72, Issue 8, August 2025.
ABSTRACT Background Dyskeratosis congenita (DKC) is a genetic disorder frequently complicated by bone marrow failure (BMF). Hematopoietic stem cell transplantation (HSCT) remains the only curative treatment option for BMF in DKC. However, late complications of DKC, especially pulmonary fibrosis (PF), pose significant challenges.
Takashi Koike, Shohei Yamamoto, Mayuko Shibata, Kohei Otsuka, Yumiko Sugishita, Ryota Kaneko, Naoko Kawabata, Sachio Fujita, Kosuke Akiyama, Daisuke Toyama, Miharu Yabe, Atsushi Uchiyama, Hiromasa Yabe   +12 more
wiley   +1 more source

Skin microvascular vasodilatory capacity in offspring of two parents with Type 2 diabetes [PDF]

, 2001
Aims<br/> Microvascular dysfunction occurs in Type 2 diabetes and in subjects with fasting hyperglycaemia. It is unclear whether this dysfunction relates to dysglycaemia.
A. C. Shore, A. Rumley, A. T. Hattersley, B. C. Lee, Balletshofer, Caballero, G. D. Lowe, Hattersley, J. E. Tooke, J. M. Humphreys, Jaap, Jaap, Jaap, Juhan-Vague, Lee, Levy, Matthews, Noon, P. M. Clark, Pimenta, Radder, Serne, Shore, Tattersal, Tooke, UKPDS Study Group., Viswanathan   +26 more
core   +1 more source

Synergistic effects of ADAMTS13 deficiency and complement activation in pathogenesis of thrombotic microangiopathy.

Blood, 2019
Severe deficiency of plasma ADAMTS13 activity is the primary cause of thrombotic thrombocytopenic purpura (TTP) while an overwhelming activation of complement via analternative pathway results in an atypical hemolytic uremic syndrome (aHUS), two ...
Liang Zheng, Di Zhang, W. Cao, W. Song, X. L. Zheng   +4 more
semanticscholar   +1 more source

Clinical effects of combination therapy with continuous renal replacement therapy and continuous intravenous sodium infusion therapy

Therapeutic Apheresis and Dialysis, Volume 29, Issue 4, Page 543-556, August 2025.
Abstract Introduction This single‐center retrospective study investigated the clinical effects of combination therapy involving continuous renal replacement therapy (CRRT) and continuous intravenous sodium infusion therapy (cIVNa) in critically ill patients with prerenal acute kidney injury (AKI) who were expected to experience insufficient plasma ...
Akinori Yamaguchi, Atsuyoshi Mita, Kosuke Sonoda, Koji Hashimoto, Hiroshi Imamura, Yuji Kamijo   +5 more
wiley   +1 more source

Pauci-immune glomerulonephritis in individuals with disease associated with levamisole-adulterated cocaine: a series of 4 cases. [PDF]

, 2014
Exposure to levamisole-adulterated cocaine can induce a distinct clinical syndrome characterized by retiform purpura and/or agranulocytosis accompanied by an unusual constellation of serologic abnormalities including antiphospholipid antibodies, lupus ...
Butcher, Brad, Carlson, Adam Q, Graf, Jonathan, Imboden, John B, Jen, Kuang-Yu, Sam, Ramin, Tuot, Delphine S   +6 more
core   +2 more sources

Monoclonal gammopathy‐associated thrombotic microangiopathy

American journal of hematology/oncology, 2019
To the Editor: Thrombotic microangiopathy (TMA) represents a heterogeneous group of clinical syndromes with end-organ damage resulting from endothelial injury secondary to a variety of etiologies.
J. Yui, D. Garceau, K. Jhaveri, R. Wanchoo, V. Bijol, I. Glezerman, H. Hassoun, A. Dispenzieri, S. Russell, N. Leung   +9 more
semanticscholar   +1 more source

Case Report: Hematopoietic Stem Cell Transplantation to Treat Severe Acquired Aplastic Anemia in a Pediatric Kidney Transplant Recipient

Pediatric Transplantation, Volume 29, Issue 5, August 2025.
ABSTRACT Background Hematopoietic stem cell transplantation (HSCT) in solid organ transplant recipients has been reported in adults. However, data on children are scarce. We report a case of an allogeneic HSCT in a 14‐year‐old girl to treat idiopathic very severe aplastic anemia (SAA). Case Presentation The girl developed end‐stage renal disease at the
Gintarė Mierkienė, Goda Elizabeta Vaitkevičienė, Karolis Ažukaitis, Augustina Jankauskienė, Jelena Rascon   +4 more
wiley   +1 more source

Recent advances in hypertension and cardiovascular toxicities with vascular endothelial growth factor inhibition [PDF]

, 2017
No abstract ...
Danser, A.H. Jan, Herrmann, Joerg, Lang, Ninian N., Touyz, Rhian M., van den Meiracker, Anton H.   +4 more
core   +1 more source

Cutaneous manifestations of dermatomyositis in individuals with dark skin: A review of reported cases

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Edgar Akuffo‐Addo, Samia Rahman, Kaitlyn Ramsay, Vincent Piguet, Marissa Joseph   +4 more
wiley   +1 more source