Results 91 to 100 of about 16,341 (256)

Implant Renal Injury‐Responsive Cells to Supplement Erythropoietin and Protect Kidney Injury

MedComm, Volume 6, Issue 11, November 2025.
Insufficient erythropoietin (EPO) production in injured kidneys leads to anemia and further exacerbates kidney damage. We constructed an injury‐responsive EPO‐producing (iREP) element that senses signals of kidney damage and drives the synthesis and secretion of native EPO.
Hao Nie, Chen Liang, Yingxin He, Siyu Wang, Xiaopeng Zhang, Jun Duan, Jieli Huang, Chen Yu, Yujia Wang, Zixian Zhao, Wei Zuo, Ting Zhang   +11 more
wiley   +1 more source

A riboflavin transporter deficiency presenting as pure red cell aplasia: a pediatric case report

Frontiers in Pediatrics
IntroductionRiboflavin transporter deficiency (RTD) is a rare genetic disorder that affects riboflavin transport, leading to impaired red blood cell production and resulting in pure red cell aplasia.
Jingying Cheng, Jiafeng Yao, Shasha Zhao, Lingling Fu, Liqiang Zhang, Jin Jiang   +5 more
doaj   +1 more source

Parvovirus B 19 (PVB19) induced pure red cell aplasia (PRCA) in immunocompromised patient after liver transplantation [Izolirana aplazija crvene krvne loze uzrokovana infekcijom Parvovirusom B 19 nakon transplantacije jetre] [PDF]

, 2010
Presented here is a case of human parvovirus B19 (PVB19) induced pure red-cell aplasia (PRCA) in immunocompromised patient after orthotopic liver transplantation (OLT).
Filipec Kanižaj, Tajana, Guštin, Denis, Kardum-Skelin, Ika, Kocman, Branislav, Mrzljak, Anna, Čolić Cvrlje, Vesna, Šušterčić, Dunja   +6 more
core  

An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement [PDF]

, 1981
An 81-year-old man from a family with a history of oculopharyngeal muscular dystrophy (OPMD) involving 6 members over 4 generations is described. The patient first noted drooping of his eyelids at the age of 65.
Aarli, Adams, Amyot, Barbeau, Bosch, Bray, Campanella, Cohen, Cox, Coërs, Croft, Direkze, Dutil, Fried, Fuchs, Goto, Graef von, Graf, Hartmann, Hayes, Julien, Kearns, Kiloh, Krause, Lakin, Lees, Lewis, Liversedge, Lundberg, Man, Maningand, Mater, Matsunaga, Murphy, Myrianthopoulos, Nicolaissen, Peterman, Radu, Rebeiz, Roberts, Satoyoshi, Saucier, Schmitt, Schmitt, Schotland, Schwarz, Szobar, Taylor, Victor, Zellweger   +49 more
core   +1 more source

Good's Syndrome Presenting With Weaning Failure From Ventilation and Myasthenia Gravis in a Post‐Thymectomy Patient

Respirology Case Reports, Volume 13, Issue 11, November 2025.
This case highlights the importance of long‐term vigilance in patients with thymoma, even after apparently successful resection, as Good's syndrome may manifest years later. Clinicians should maintain a high index of suspicion for Good's syndrome in any thymectomized patient presenting with unexplained infections, diarrhoea, or autoimmune complications,
Asmita Anilkumar Mehta, Aditya Ashok, Lakshmi Priya Valathara Pradeep, Suchitra Sivadas, George Justin Mothi   +4 more
wiley   +1 more source

Pure red cell aplasia.

Pahlavi medical journal, 1976
The so-called pure red cell aplasia or hypoplasia may occur in various instances: 1- Congenital form, usually occuring in childhood; 2-Drug-induced types; 3-The forms associated with thymoma, carcinoma and hypogamma-globulinemia; and 4-As an isolated syndrome.
M, Mehzad, G, Shafa, M, Noury
openaire   +3 more sources

Isoniazid-induced pure red cell aplasia

BMJ Case Reports, 2018
The pure red cell aplasia (PRCA) is an uncommon side effect of isoniazid. We describe a 28-year-old man who developed a severe anaemia caused by PRCA. The patient received antituberculous therapy including isoniazid for his pulmonary tuberculosis. On discontinuation of isoniazid, the anaemia recovered promptly.
Subraya Krishna Holla, Basavaprabhu Achappa, Pavan Manibettu Raguram, Sitamahalakshminagasai Yerramsetti   +3 more
openaire   +3 more sources

Drug Candidate BIO101 for Spinal Muscular Atrophy as Monotherapy or Combined With the Antisense Oligonucleotide ASO‐10‐27

Journal of Cachexia, Sarcopenia and Muscle, Volume 16, Issue 5, October 2025.
ABSTRACT Background Spinal muscular atrophy (SMA) is a neuromuscular disease caused by loss of survival of motor neuron (SMN) protein inducing progressive muscle weakness and atrophy due to motor neurons degeneration. Despite benefits of SMN restoration therapies in patients, motor defects are still persistent.
Cynthia Bézier, Steve Cottin, Parvin Nazari Hashemi, Mirella El Khoury, Zoé Clerc, Christine Balducci, Delphine Sapaly, Laure Weill, René Lafont, Stanislas Veillet, Pierre J. Dilda, Frédéric Charbonnier, Mathilde Latil, Olivier Biondi   +13 more
wiley   +1 more source

Linezolid-Induced Pure Red Cell Aplasia: A Case Report

Infection and Drug Resistance, 2022
Xiao-Yan Yang, Lin Chen, Ji-Na Gu, Cheng-Jun Zeng, Dan-Mei Pan Infectious Diseases Department, Hwa Mei Hospital, University of Chinese Academy of Sciences, Ningbo, 315010, People’s Republic of ChinaCorrespondence: Lin Chen, Infectious Diseases department,
Yang XY, Chen L, Gu JN, Zeng CJ, Pan DM
doaj  

Canine autoimmune hemolytic anemia: management challenges. [PDF]

, 2016
Immune-mediated hemolytic anemia is one of the most common manifestations of canine immune-mediated disease, yet treatment regimens remain nonstandardized and, in some cases, controversial.
Skelly, Barbara J, Swann, James W
core   +2 more sources