Results 61 to 70 of about 9,394 (232)

Orthotopic liver transplantation in children. Two-year experience with 47 patients [PDF]

open access: yes, 1984
During a 24-month period (May 1981 to May 1983), 47 pediatric patients (ranging in age from 7 months to 18 years) underwent orthotopic liver transplantation using cyclosporine and prednisone.
Gartner, JC   +5 more
core  

Recurrent temporal bone tenosynovial giant cell tumor with chondroid metaplasia: the use of imaging to assess recurrence [PDF]

open access: yes, 2014
Tenosynovial giant cell tumor (TGCT) is a benign proliferative lesion of unclear etiology. It is predominantly monoarticular and involves the synovium of the joint, tendon sheath, and bursa.
Fernandez, M.   +6 more
core   +1 more source

Leuprorelin‐Induced Thrombocytopenia Successfully Treated With Surgical Resection of the Injection Site

open access: yesIJU Case Reports, EarlyView.
ABSTRACT Introduction Drug‐induced thrombocytopenia (DITP) can be caused by many kinds of drugs. Its treatment generally involves discontinuation of the responsible drug. Case Presentation A 70‐year‐old man received a subcutaneous injection of long‐acting (24‐week) leuprorelin depot as androgen deprivation therapy for prostate cancer.
Ryota Mori   +18 more
wiley   +1 more source

All‐in‐one optical microfiber with an interface for MRSA in biofilms: Integrating rapid quantitative analysis and synergistic antimicrobial therapy

open access: yesInfoMat, EarlyView.
Aiming at the management of MRSA biofilms, an all‐in‐one optical microfiber that integrated rapid quantitative analysis with synergistic antimicrobial therapy is developed. The prepared interfacial‐functionalized optical microfiber demonstrates the ability to detect MRSA concentrations in infection sites, enhance therapeutic efficacy, and assess ...
Pengwei Chen   +7 more
wiley   +1 more source

Langerhans cell histiocytosis: current concepts in dentistry and case report [PDF]

open access: yes, 2016
Langerhans cell histiocytosis (LCH), which is a rare granulomatous pediatric disease of unknown etiology, is characterized by the idiopathic proliferation and accumulation of abnormal and clonal Langerhans cells or their ...
Alejo-Gonzalez, Francisco   +4 more
core  

Eruptive Xanthomata Manifesting in Tattoos

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Eruptive xanthomata represent a rare, but important pruritic dermatosis for which an accurate diagnosis can prevent life‐threatening complications. We present the case of a 29‐year‐old female with no prior medical history who presented to clinic for evaluation of a pruritic papular eruption of 2 weeks' duration.
Connor Stonesifer   +4 more
wiley   +1 more source

A Macrophage Phenotype for a Constitutive, Class II Antigen-Expressing, Human Dermal Perivascular Dendritic Cell [PDF]

open access: yes, 1989
A previously uncharacterized population of class II antigen-bearing dendritic cells that are intimately associated with the dermal microvasculature was identified in normal human skin using a double-label, indirect immunofluorescence technique.
Matsubara, Tsukasa   +2 more
core   +1 more source

Efficacy of Calcipotriol/Betamethasone Ointment in Facial Discoid Dermatosis

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Facial Discoid Dermatosis (FDD) is a rare chronic skin condition characterised by persistent, annular erythematous and desquamative papules on the face. Its aetiology is unclear, making differential diagnosis challenging. Key clinical features include pink‐orange, minimally scaling lesions limited to the face, sudden onset with long‐term ...
Alberto Murtas   +4 more
wiley   +1 more source

Hemophagocytic Lymphohistiocytosis syndrome (HLH) associated with acute pancreatitis: A case report

open access: yesClinical Case Reports, 2023
Hemophagocytic Lymphohistiocytosis syndrome is fatal hyper‐inflammatory condition due to over‐activation of the immune system, being of primary and secondary types. This case report emphasizes the difficulty and challenge in and of the HLH diagnosis, and
Ahmed Mohamad Mechi   +2 more
doaj   +1 more source

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