Results 91 to 100 of about 832 (157)

Transient imaging changes accompany ‘spinal ICANS’ following CAR T‐cell therapy for large B‐cell lymphoma in adults

British Journal of Haematology, Volume 207, Issue 6, Page 2632-2637, December 2025.
Frederick W. Vonberg, Daniel Rice‐Wilson, Imran Malik, Stephen Keddie, Nikos Gorgoraptis, Shamzah Araf, Sunita Khanal, Silvia Montoto, Shenbagaram Kasivisvanathan, Ben Uttenthal, Katerina Panopoulou, Harpreet Hyare, Maeve O'Reilly, Aisling S. Carr, Claire Roddie   +14 more
wiley   +1 more source

Incidence of hypophosphataemia in patients on parenteral nutrition

, 2007
OBJECTIVE - To determine the effect of parenteral nutrition on plasma phosphate levels and to evaluate the incidence of refeeding hypophosphataemia.
Marvin, V, Davis, J, May, C, Livingstone, C   +3 more
core  

A case of Gitelman syndrome with severe hyponatraemia and hypophosphataemia

, 2013
Gitelman syndrome (GS) is a renal tubular disorder of the thiazide-sensitive sodium chloride cotransporter, which is located in the distal tubule of the loop of Henle. We present a rare case of GS complicated by severe hyponatraemia and hypophosphataemia.
Yaqub, Sonia, Masood, Qamar, Ali, Absar, Kashif, Waqar   +3 more
core  

SGK3 promoter deletion in late-onset hypophosphatemic rickets, a possible genetic cause of the disease

Orphanet Journal of Rare Diseases
Background Hypophosphataemic rickets (HR) is a group of rare hereditary renal phosphate wasting disorders caused by mutations in the PHEX, FGF23, DMP1, ENPP1, CLCN5, SGK3, SLC9A3R1, SLC34A1 or SLC34A3.
Ahmet Uçar, Najla Albader, Amal Qattan, Huda A. BinEssa, Ebru Mısırlı Özdemir, Mustafa Özdemir, Minjing Zou, Ali S. Alzahrani, Yufei Shi   +8 more
doaj   +1 more source

Mechanisms of hypophosphataemia in alcoholic patients

, 1997
The aim of our study was to determine the possible pathophysiological mechanisms of hypophosphataemia in a group of 127 patients admitted to hospital for alcohol-related causes.
Elisaf, M. S., Siamopoulos, K. C.
core  

Treatment-resistant hypophosphataemia after ferric carboxymaltose: expanding the spectrum of 6H syndrome (hypophosphataemia, hyperphosphaturia, hypovitaminosis D, hypocalcaemia, secondary hyperparathyroidism, high fibroblast growth factor-23)

European Journal of Case Reports in Internal Medicine
Background: Ferric carboxymaltose (FCM) is widely used to treat iron deficiency anaemia (IDA), particularly in patients with gastrointestinal disease who are intolerant of oral iron. While generally well tolerated, FCM is increasingly recognised to cause
Luqmaan Rashid
doaj   +1 more source

Routine blood-based immune signatures in endogenous Cushing’s syndrome: associations with cortisol excess and selected complication burden

Frontiers in Endocrinology
BackgroundRoutine blood-based markers capture glucocorticoid-related immune-cell redistribution, but whether these measures are associated with complementary biochemical measures of cortisol excess and clinical complication burden in endogenous Cushing’s
Yunjia Cai, Yunjia Cai, Shuwen Tan, Siyuan Liu, Miao Wang, Tiemin Liu, Guixia Wang   +6 more
doaj   +1 more source

Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Hypophosphataemia at a large academic hospital in South Africa

, 2008
Aim: The aim of this study was to determine the most common causes of hypophosphataemia (≤ 0.5 mmol/l) in a hospital population in order to identify patient groups at risk of developing the condition.
Zemlin A.E., Erasmus R.T., Hoffmann M., Meyer W.P.   +3 more
core   +1 more source

Tumor-induced phosphopenic osteomalacia: modern approaches to diagnostics and treatment

Современная ревматология
Phosphopenic osteomalacia (PPOM) is a rare variant of paraneoplastic syndrome caused by tumor synthesis of fibroblast growth factor 23 (FGF23). FGF23 secretion leads to a decrease in phosphate reabsorption and calcitriol levels, which leads to the ...
A. A. Kondrashov, D. Yu. Andriyashkina, N. A. Demidova, Yu. M. Sahakyan, A. A. Klimenko   +4 more
doaj   +1 more source