Results 71 to 80 of about 153,345 (297)

Drug‐induced liver injury associated with selective androgen receptor modulators in an adolescent patient

open access: yesJPGN Reports, EarlyView.
ABSTRACT Selective androgenic receptor modulators (SARMs) have similar properties to anabolic steroids but bind to androgen receptors in a tissue‐specific manner. Studies have investigated the benefits of SARMs in promoting bone and muscle growth while limiting the adverse effects of androgenic stimulation of other organs.
David J. Katibian   +3 more
wiley   +1 more source

Management of rivaroxaban- or apixaban-associated major bleeding with prothrombin complex concentrates: a cohort study.

open access: yesBlood, 2017
A. Majeed   +9 more
semanticscholar   +1 more source

Prothrombin and Haemorrhage [PDF]

open access: yesBMJ, 1954
Anne C. Donald   +4 more
openaire   +3 more sources

Porto‐sinusoidal vascular disorder in a pediatric patient with prolidase deficiency: A case report

open access: yesJPGN Reports, EarlyView.
Abstract Prolidase deficiency (PD) is a rare autosomal recessive disorder affecting collagen turnover, leading to diverse clinical manifestations including dermatologic lesions, hepatosplenomegaly, and vascular anomalies. Liver involvement in PD is poorly understood, with few reported cases.
Melissa Castro   +5 more
wiley   +1 more source

A case of amebic colitis: A potentially fatal mimicker of inflammatory bowel disease

open access: yesJPGN Reports, EarlyView.
ABSTRACT Amebiasis, caused by Entamoeba histolytica, can present diagnostic challenges due to its diverse clinical manifestations and potential for misdiagnosis, particularly in regions with low incidence rates. We report a case of a 9‐year‐old girl initially diagnosed with inflammatory bowel disease but later confirmed to have amebic colitis.
Fadhel Al Ateeqi   +2 more
wiley   +1 more source

Acquired Haemophilia Occurring in Association With Bullous Pemphigoid

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Acquired haemophilia A (AHA) is a rare condition due to neutralizing antibodies against Factor VIII and can result in severe bleeding manifestations. The association of AHA with bullous pemphigoid (BP) is rare, most frequently observed in the elderly, and has been attributed to cross‐reactive antibodies targeting Factor VIII and BPAG2 protein.
Wen Yang Benjamin Ho   +3 more
wiley   +1 more source

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